The DOI matches its Crossref record; 609 of the 609 references it cites were found in a registry or an index; 147 of the 332 sources its claims cite were checked for support.
Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review
Open accessAbstract
Diffusion magnetic resonance imaging (dMRI) tractography is an advanced imaging technique that enables in vivo reconstruction of the brain's white matter connections at macro scale. It provides an important tool for quantitative mapping of the brain's structural connectivity using measures of connectivity or tissue microstructure. Over the last two decades, the study of brain connectivity using dMRI tractography has played a prominent role in the neuroimaging research landscape. In this paper, we provide a high-level overview of how tractography is used to enable quantitative analysis of the brain's structural connectivity in health and disease. We focus on two types of quantitative analyses of tractography, including: 1) tract-specific analysis that refers to research that is typically hypothesis-driven and studies particular anatomical fiber tracts, and 2) connectome-based analysis that refers to research that is more data-driven and generally studies the structural connectivity of the entire brain. We first provide a review of methodology involved in three main processing steps that are common across most approaches for quantitative analysis of tractography, including methods for tractography correction, segmentation and quantification. For each step, we aim to describe methodological choices, their popularity, and potential pros and cons. We then review studies that have used quantitative tractography approaches to study the brain's white matter, focusing on applications in neurodevelopment, aging, neurological disorders, mental disorders, and neurosurgery. We conclude that, while there have been considerable advancements in methodological technologies and breadth of applications, there nevertheless remains no consensus about the "best" methodology in quantitative analysis of tractography, and researchers should remain cautious when interpreting results in research and clinical applications.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
This review provides a high-level overview of how diffusion MRI tractography is used for quantitative mapping of brain structural connectivity, organizing methods into tractography correction, segmentation, and quantification and reviewing applications across development, aging, neurological/mental disorders, and neurosurgery. It concludes that despite methodological and application advances, there is no consensus on the “best” methodology and results should be interpreted cautiously.
Key findings
- Quantitative tractography analyses are categorized into tract-specific, hypothesis-driven analyses of named fiber tracts and connectome-based, more data-driven analyses of whole-brain structural connectivity.
- The review identifies three common processing steps—tractography correction, tractography segmentation, and tractography quantification—and discusses methodological choices, popularity, and pros/cons for each.
- In applications, the review cites developmental tractography milestones including identification of fornix and cingulum parts at 13 weeks, part of the corpus callosum at 15 weeks, and prominent radial/tangential pathways at 17 weeks; it also notes parcellation scales ranging from tens to millions of parcels, with suggestions that >2000 parcels can benefit machine learning/statistical analysis and <200 parcels can improve connectome consistency.
- The review reports no consensus on the “best” methodology for quantitative tractography analysis and emphasizes caution in biological and clinical interpretation.
Methods
- Narrative review of dMRI tractography methods and applications, not an empirical study; no original sample or dataset is analyzed.
- The methodology review is organized around three processing steps: correction of tractography biases, segmentation/identification of white matter pathways, and extraction of quantitative measures.
- The applications review covers neurodevelopment, aging, neurological disorders (with multiple sclerosis and schizophrenia as exemplars), mental disorders, and neurosurgery.
Limitations
- The paper states that there remains no consensus about the “best” methodology in quantitative tractography analysis and that researchers should remain cautious when interpreting results in research and clinical applications.
- The paper states that reconstructed streamlines are simulated entities that do not correspond directly to nerve fibers and that basic diffusion metrics are inferences from local diffusion properties rather than direct tissue measures; it also notes ongoing false-positive and false-negative anatomical accuracy issues.
- Evident from the text: as a narrative review, it does not report a systematic search strategy, inclusion criteria, or quantitative synthesis.
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Claims the paper makes
60 Partly supported · 30 No basis given · 26 Sources not found · 22 Supported · 22 No full text of the sources · 22 Own interpretation · 19 Supported so far · 12 Not checked yet · 4 Couldn’t confirm · 1 Not supported · 1 Own method · 1 Own result · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Despite focusing on different developmental ranges, these studies consistently observe significant age-related increases of FA and MD in widespread fiber tracts during postnatal growth in both cross-sectional and longitudinal population designs (Lebel and Deoni, 2018).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Disputedcites Lebel and Deoni, 2018 sourceExperimental — accuracy not yet measured
Section 3.3 (Developmental Timing; page not provided) reports that FA increases with age, but MD decreases—the opposite of the claimed MD increase. It also discusses longitudinal developmental curves, so the disagreement is specifically about MD's direction of change. (LLM, conf=0.90)
Checked by a reasoning model — may be wrong.
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Disputed
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“actually none proved effective in discriminating between true and spurious connections in the connectome networks (Maier-Hein et al., 2017; Schiavi et al., 2020a).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > False positive connections
What the sources say
- Partly supportedcites Maier-Hein et al., 2017 sourceExperimental — accuracy not yet measured
The Results (‘Tractograms contained more invalid than valid bundles’; page unavailable) report that tested tractography approaches produced more invalid than valid bundles, supporting the concern about spurious connections. But the Results (‘Statistical analysis of processing steps’; page unavailable) say filtering affected performance and one clustering approach achieved 92% validly connecting streamlines. The paper therefore does not establish that no knowledge- or data-driven filtering method proved effective at discrimination. (LLM, conf=0.85)
- Not matchedcites Schiavi et al., 2020a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“It is important to note that tractography is known to be sensitive to the choice of the underlying fiber tracking algorithms, which can further affect any subsequent quantitative analyses using the tractography data.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Brief introduction to tractography
What the sources say
- Could not verifycites Afzali et al., 2020 sourceExperimental — accuracy not yet measured
The Microstructure models > Effect of model fitting passage mentions combining global tractography with microstructure estimation, but does not compare fiber-tracking algorithms or their effects on analyses of tractography data. Searches for tractography and tracking algorithms found no passage in our copy addressing that specific claim; pages were not provided. (LLM, conf=0.72)
- Not checked — no full text of the sourcecites Alexander, 2006 source
- Not checked — no full text of the sourcecites Panagiotaki et al., 2012 source
boostedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Could not verify
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“the Anatomically-Constrained Tractography (ACT) framework (Smith et al., 2012) and similar methods (Girard and Descoteaux, 2012; Lemkaddem et al., 2014; Yeh et al., 2017) ensure that both streamline propagation and termination are constrained based on knowledge of where neuronal fibers locate, e.g., connecting between gray matter areas via the white matter.”
- Also stated in: § Termination bias · plain
“they do prevent the generation of streamlines that cannot possibly represent biological connectivity within the brain.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Termination bias
What the sources say
- Not checked — no full text of the sourcecites Smith et al., 2012 source
- Not matchedcites Girard and Descoteaux, 2012
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Lemkaddem et al., 2014 source
The Introduction states that the method places fiber endpoints in gray matter and constrains the remaining spline control points to white matter. The Methods section says it filters out fibers ending prematurely in white matter because they do not represent anatomically valid connections. These passages support the claim about anatomically constrained paths and termination. (LLM, conf=0.88)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Also stated in: § Termination bias · plain
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Possibly the earliest bias established for dMRI tractography was the fact that if the streamline algorithm simply takes a step of finite size in the direction of the local fiber orientation at the current vertex (a so-called “first-order” method), streamlines in curved bundles will tend to under-estimate the curvature, resulting in erroneous trajectories (Tournier et al., 2002).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Curvature overshoot bias
What the sources say
- Partly supportedcites Tournier et al., 2002 sourceExperimental — accuracy not yet measured
The Tracking Algorithm section describes finite steps taken in the local major-eigenvector direction. Model A reports that larger steps increase endpoint offset and that tracks can depart systematically from an ideal curved path, especially without interpolation. The copy does not establish the claimed direction of the bias—that these tracks tend to underestimate curvature. (LLM, conf=0.85)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In particular, it has been shown that tractography techniques suffer from a large number of false positives, i.e., streamlines that are reconstructed but do not correspond to real anatomical bundles”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > False positive connections
What the sources say
- Supportedcites Maier-Hein et al., 2017 source
The Results section (“Tractograms contained more invalid than valid bundles”) reports that 36 ± 17% of reconstructed streamlines connected regions not connected in the ground truth, and that invalid bundles outnumbered valid bundles. The Introduction likewise says most evaluated algorithms produced large amounts of false-positive bundles. (LLM, conf=0.92)
- Partly supportedcites Thomas et al., 2014 sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) reports that high-sensitivity tractography tends to have a high false-positive rate, supporting the concern about reconstructed pathways without anatomical support. But the paper evaluates false positives by anatomical region, not by counting individual streamlines, and says some methods and settings can achieve much lower false-positive rates. The claim overgeneralizes those findings to tractography techniques as a whole. (LLM, conf=0.85)
boosted- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“and that these erroneous connections can severely bias the estimation of connectivity (Drakesmith et al., 2015; Maier-Hein et al., 2017; Zalesky et al., 2016b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > False positive connections
What the sources say
- Supportedcites Drakesmith et al., 2015 source
The Introduction says inferred brain-network measures are sensitive to errors in edges, including false positives. In the Discussion’s “Effects of false positives” section (page not provided), the authors report that even a single false positive significantly affects inferred network metrics and that added false edges produce a strong bias in global efficiency. (LLM, conf=0.91)
- Supportedcites Maier-Hein et al., 2017 source
The Discussion (page unavailable) reports that 64% of the bundles systematically recovered by most submissions were absent from the ground truth. This supports the claim that false-positive connections can severely distort estimated connectivity, though the paper cautions that its simulation cannot quantify the effect on in vivo connectivity in absolute terms. (LLM, conf=0.90)
- Not matchedcites Zalesky et al., 2016b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“On one hand, tractography results may vary across the large set of available diffusion models (Afzali et al., 2020; Alexander, 2006; Panagiotaki et al., 2012; Yablonskiy and Sukstanskii, 2010) and tractography methods”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Brief introduction to tractography
What the sources say
- Not checked — no full text of the sourcecites Basser et al., 2000 source
- Supportedcites Behrens et al., 2007 source
The Discussion (page not provided) compares single- and multi-fibre tractography and says they can give strikingly different results for non-dominant pathways. It also describes differences among diffusion-reconstruction techniques. This supports the claim that tractography results may vary with the model or method used. (LLM, conf=0.88)
- Supportedcites Descoteaux et al., 2008 source
The Introduction says diffusion-tensor-based tractography can produce false tracts or stop prematurely. The Discussion compares different tracking approaches and reports that they reconstruct different portions of fiber bundles, supporting the claim that results vary with the model and method used. Page numbers are not available in our copy. (LLM, conf=0.90)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Every source the paper cites for this claim was checked and supports it.
In the paper
“despite the fact that white matter fibers synapse in the gray matter (Daducci et al., 2016)”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Termination bias
What the sources say
- Supportedcites Daducci et al., 2016 source
Section 2.4, “Partial fibers” (page unavailable), states that axons connect neurons located in gray matter and contrasts this with reconstructed tracts that stop prematurely in white matter. This supports the citing sentence’s point that white-matter fibers connect to neurons in gray matter. (LLM, conf=0.87)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“On the other hand, tractography results can also be sensitive to the choice of parameters (such as seeding and stopping thresholds) within a certain algorithm (Chamberland et al., 2014; Côté et al., 2013; Gong et al., 2018; Moldrich et al., 2010; Xie et al., 2020).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Brief introduction to tractography
What the sources say
- Supportedcites Chamberland et al., 2014 source
Section 2.2 says subtle variations in tractography parameters can lead to different results and specifically discusses seeding strategies and stopping criteria. The Results (section 3.4) show that fixed parameter choices can produce misleading reconstructions, including spurious streamlines. (LLM, conf=0.94)
- Not matchedcites Côté et al., 2013
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Gong et al., 2018 source
The Introduction states that varying tractography thresholds has a large impact on fiber tracking using UKFt near edema. The Discussion adds that reducing thresholds used to start and stop tractography can increase fiber-tract size, supporting the claim that results are sensitive to parameter choices within an algorithm. (LLM, conf=0.93)
plainconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
- It may state two separate claims as one. 69
- Probably not a substantial claim. 50
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Gyral bias in tractography is the bias towards generating streamlines that terminate in gyri rather than sulci (Schilling et al., 2018a; Wu et al., 2020b), which reduces the agreement of the initiations or terminations of fiber streamlines with known ground truth from tracer studies and histology (Aydogan et al., 2018; Budde and Annese, 2013).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Gyral bias
What the sources say
- Not matchedcites Schilling et al., 2018a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Wu et al., 2020b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Partly supportedcites Aydogan et al., 2018 sourceExperimental — accuracy not yet measured
The Introduction (page unavailable) reports imperfect overlap between mouse tractograms and tracer injections, supporting the general point that tractography can disagree with tracer ground truth. But the paper does not attribute that disagreement to gyral bias or preferential termination in gyri rather than sulci. The Discussion (page unavailable) describes validation using histology images as future work, not a result of this study. (LLM, conf=0.79)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Lastly, deep learning techniques have been increasingly applied for anatomical tract identification, showing high potential for future work and improvements in computational speed (Chen et al., 2021; Gupta et al., 2017a; 2018; 2017b; Lam et al., 2018; Reisert et al., 2018; Wasserthal et al., 2018; 2019; Xu et al., 2019; Zhang et al., 2020a).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Supportedcites Chen et al., 2021 source
The Introduction describes deep learning as a promising direction for white matter fiber clustering, notes multiple existing methods for tractography segmentation, and says this paper's approach demonstrated efficiency. The Conclusion reports efficiency advantages over other algorithms and identifies directions for further improvement. (LLM, conf=0.92)
- Not matchedcites Gupta et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Lam et al., 2018
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Manual streamline selection is considered to be the gold standard to delineate anatomical fiber tracts in tractography and has been widely used to validate other anatomical tract identification techniques (Poulin et al., 2019; Pujol et al., 2015; Xie et al., 2020).”
- Also stated in: § Anatomical tract identification · plain
“However, manual streamline selection is still considered to be the gold standard for benchmarked comparisons and algorithm training (Kreilkamp et al., 2019; Wasserthal et al., 2018; Zhang et al., 2010).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Supportedcites Poulin et al., 2019 source
The paper calls expert-validated streamline annotations a medical-imaging “gold standard,” while distinguishing them from biological ground truth (Annotated Datasets and Evaluation Tools, p. 4). It also reviews annotated datasets used to train or validate tractography algorithms (p. 3) and describes manually validated bundles used to train and validate a tract-segmentation method (TractSeg, p. 9). (LLM, conf=0.87)
- Partly supportedcites Kreilkamp et al., 2019 sourceExperimental — accuracy not yet measured
The Introduction (page unavailable) describes manual techniques as closest to ground truth in the absence of histological data and as a benchmark for comparing automated tractography, supporting the core of the claim. It does not establish that manual selection has been widely used to validate other tract-identification techniques; it says recent automated methods have not been extensively validated. It also does not describe using manual selections for algorithm training. (LLM, conf=0.86)
- Partly supportedcites Wasserthal et al., 2018 sourceExperimental — accuracy not yet measured
The Introduction describes manual virtual dissection as the most commonly employed way to segment white matter tracts, and §3.3 compares manual dissections with TractSeg and other methods. But §4.2 says the paper’s reference tracts are not real ground truth. The paper supports manual delineation and its use in comparisons, not the unqualified description of manual selection as a gold standard. (LLM, conf=0.84)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Also stated in: § Anatomical tract identification · plain
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In general, studies indicate that modern multi-fiber tractography is more sensitive when performing tractography and thus is more consistent across subjects and timepoints than traditional single-fiber DTI tractography (Bucci et al., 2013; Prčkovska et al., 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Partly supportedcites Bucci et al., 2013 sourceExperimental — accuracy not yet measured
The Discussion (‘Quantitative validation of fiber tracking methods’; page unavailable) reports significantly better sensitivity for q-ball than DTI, and ‘Implications for preoperative mapping’ calls probabilistic q-ball the most reproducible of the four methods tested. The paper does not establish consistency across subjects or timepoints, and cautions against generalizing from its small sample. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites Prčkovska et al., 2016 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Most widely used approaches perform a linear registration (Garyfallidis et al., 2015; O’Donnell et al., 2012), while many studies have proposed to perform non-linear approaches to enable deformations of the streamlines (Benou et al., 2019; Chandio and Garyfallidis, 2020; Olivetti et al., 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Not checked — no full text of the sourcecites Garyfallidis et al., 2015 source
- Partly supportedcites O’Donnell et al., 2012 sourceExperimental — accuracy not yet measured
The Methods (section 2.3; page unavailable) describe this paper’s tractography registration as fully affine, supporting its use as an example of linear registration. The Introduction says alignment is often performed using transformations from image-based registration, but does not establish that linear approaches are the most widely used. The nonlinear-approaches clause is attributed to other citations in the sentence, not to this paper. (LLM, conf=0.82)
- Not checked — no full text of the sourcecites Benou et al., 2019 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“There are generally two categories of methods: cortical-parcellation-based methods and fiber clustering methods (O’Donnell et al., 2013).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Supportedcites O’Donnell et al., 2013 source
The Introduction identifies parcellation-based and clustering methods as the two main categories, while also proposing hybrid methods as a third category. Section 2 explains that the former use cortical fiber endpoints and the latter group fiber trajectories, matching the citing sentence’s distinction. (LLM, conf=0.94)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“For example, the intermodality registration between dMRI and T1-weighted images can be affected by differences in image resolutions (Malinsky et al., 2013) and echo-planar imaging (EPI) distortion in dMRI data (Albi et al., 2018).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Supportedcites Malinsky et al., 2013 source
The Background describes registration of high-resolution T1 images with low-resolution diffusion-derived FA images and says the data must be preprocessed to ensure identical resolution and voxel size. This supports the resolution-difference point attributed to Malinsky et al.; the EPI-distortion point is attributed to Albi et al. and is not assessed here. (LLM, conf=0.92)
- Supportedcites Albi et al., 2018 source
The Albi et al. citation is attached to EPI distortion in dMRI, not to the image-resolution difference. The Introduction states that EPI produces geometric distortions and displaces anatomical structures; the Methods describe registering DWI data to anatomical images to correct that distortion. (LLM, conf=0.92)
plainconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“They group tractography streamlines according to their geometric trajectories, describing the structural connectivity according to the white matter anatomy (Avila et al., 2019; Chekir et al., 2014; Garyfallidis et al., 2018; Guevara et al., 2012; Li et al., 2010; O’Donnell and Westin, 2007; Román et al., 2017; Ros et al., 2013; Siless et al., 2018; 2020; Tunç et al., 2014; Vázquez et al., 2020; Wu”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Not matchedcites Avila et al., 2019
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not checked — no full text of the sourcecites Chekir et al., 2014 source
- Supportedcites Garyfallidis et al., 2018 source
The Introduction describes streamline-based segmentation of tractograms into known anatomical bundles. Section 2.2 explains that RecoBundles clusters streamlines using a distance between their trajectories and recognizes bundles by their shape. Together, these passages support the cited description of grouping streamlines to characterize white-matter pathways; no page numbers were available in our copy. (LLM, conf=0.87)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Many cortical-parcellation-based methods have also used a functional cortical parcellation computed using functional MRI data (Eickhoff et al., 2005; Glasser et al., 2016; Schaefer et al., 2018; Yeo et al., 2011).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Not checked — no full text of the sourcecites Eickhoff et al., 2005 source
- Partly supportedcites Glasser et al., 2016 sourceExperimental — accuracy not yet measured
The Methods (‘Modalities for parcellation’) confirm that Glasser et al. used task and resting-state fMRI data to construct a cortical parcellation. But the parcellation was multi-modal: it also used architectural measures, so describing this source as an example of a functional parcellation omits a defining qualification. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites Schaefer et al., 2018 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“The first category of quantitative measures are based on the tractography data alone, which are often used to define the connectivity strength (Jones, 2010; Smith et al., 2020a; Sotiropoulos and Zalesky, 2019; Yeh et al., 2020).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
What the sources say
- Not checked — no full text of the sourcecites Jones, 2010 source
- Not matchedcites Smith et al., 2020a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Sotiropoulos and Zalesky, 2019 source
In “Quantifying edges,” the paper says connection strength is most typically quantified using a function of tractography-derived streamline counts. This supports the claim that measures based on tractography data alone are used to define connectivity strength; “first category” is the citing authors’ framing. (LLM, conf=0.92)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The most popularly used cortical parcellation is the Freesurfer Desikan-Killiany cortical parcellation (Desikan et al., 2006; Fischl, 2012), while many other cortical parcellation schemes have also been widely used (Destrieux et al., 2010; Shattuck et al., 2008; Tzourio-Mazoyer et al., 2002).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Not checked — no full text of the sourcecites Desikan et al., 2006 source
- Partly supportedcites Fischl, 2012 sourceExperimental — accuracy not yet measured
The Introduction (page not provided) identifies the Desikan et al. (2006) cortical parcellation as part of FreeSurfer, and the Contributors section says Desikan and Killiany developed it. Neither passage establishes that it is the most popularly used cortical parcellation. The later clause about other schemes is cited to other sources, not Fischl (2012). (LLM, conf=0.84)
- Supportedcites Destrieux et al., 2010 source
The Destrieux citation is attached to the clause about other cortical parcellation schemes, not to the claim that Desikan–Killiany is the most popular. The Abstract identifies this paper's distinct sulco-gyral parcellation as available in FreeSurfer, and the Discussion reports that FreeSurfer, including this or an earlier atlas, had been licensed 6,700 times. (LLM, conf=0.90)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Other quantitative measures can be computed directly from tractography, such as the volume and the length of a fiber tract (Bajada et al., 2019; Behrman-Lay et al., 2015; Catani et al., 2007; Chandio et al., 2020a; Colby et al., 2012a; Grinberg et al., 2018; Rheault et al., 2020a; Song et al., 2015; Yeatman et al., 2012), have also been used.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
What the sources say
- Partly supportedcites Bajada et al., 2019 sourceExperimental — accuracy not yet measured
Section 2.4 (Length mapping; page not supplied) says the authors calculated streamline lengths directly from tractography track files and used them to create cortical tract-length maps. Our copy does not report computing fiber-tract volume as a quantitative measure; its references to volume in Section 2.3 concern image space and subject brain volume. (LLM, conf=0.88)
- Partly supportedcites Behrman-Lay et al., 2015 sourceExperimental — accuracy not yet measured
Methods §2.5 says the authors computed mean track length from tractography-derived arc lengths and used it as a quantitative measure. It does not report computing fiber-tract volume; the volume mentioned there is intracranial volume, used to normalize length. (LLM, conf=0.88)
- Could not verifycites Catani et al., 2007 sourceExperimental — accuracy not yet measured
The tractography methods passage (Discussion; page unavailable) describes measuring the number of reconstructed pathways and fractional anisotropy, but not tract volume or length. Searches for tract volume and fiber length found no passage saying either was computed or used as a quantitative measure in this paper. (LLM, conf=0.75)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Due to these factors, several studies have demonstrated advantages of fiber clustering methods over the cortical-parcellation-based methods, including more consistent parcellation across subjects (Sydnor et al., 2018; Zhang et al., 2017) and a higher reproducibility between test-retest scans (Zhang et al., 2019).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Supportedcites Sydnor et al., 2018 source
Sydnor et al. is cited for more consistent parcellation across subjects, not for test–retest reproducibility, which the sentence attributes to Zhang et al. (2019). In the Discussion section, the paper reports that clustering produced the most consistent white matter tracts across subjects among the methods compared. (LLM, conf=0.92)
- Not matchedcites Zhang et al., 2017
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Zhang et al., 2019 source
The Zhang et al. (2019) citation is attached specifically to the test–retest claim, not the separate claim about consistency across subjects. The Discussion reports significantly higher test–retest reproducibility for fiber clustering than for the cortical-parcellation-based method across all three datasets. (LLM, conf=0.94)
boostedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“For example, researchers have used the longitudinal relaxation rate (R1), a measure sensitive to myelin, along the fiber tracts (Boshkovski et al., 2020a; Yeatman et al., 2012).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
What the sources say
- Not matchedcites Boshkovski et al., 2020a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Partly supportedcites Yeatman et al., 2012 sourceExperimental — accuracy not yet measured
The Methods section describes measuring fractional anisotropy (FA) at locations along fiber tracts, and the Discussion reports tract profiles of FA. The cited paper therefore supports the along-tract approach, but the passages do not establish that it used longitudinal relaxation rate (R1) or describe R1 as sensitive to myelin. (LLM, conf=0.88)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Most often, data are averaged across corresponding points along each streamline in the pathway, such that data can be analyzed (e.g., an along-tract or along-pathway plot) versus streamline arc length or other parameterization (Colby et al., 2012b; Corouge et al., 2006; Yeatman et al., 2012).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
What the sources say
- Not matchedcites Colby et al., 2012b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Corouge et al., 2006 source
Section 3.2.1 (p. 8) defines points at the same arc length along fibers as corresponding points. Section 3.3.1 (p. 10) computes a mean tensor at each corresponding location, and Fig. 4’s description (p. 12) says the resulting diffusion properties are plotted against location along the tract. This supports the cited paper as an example of the described approach. (LLM, conf=0.92)
- Supportedcites Yeatman et al., 2012 source
The Methods (Automated Fiber Quantification, Fiber Tract Quantification) say that each fiber is resampled to 100 equally spaced nodes. The Methods then describe averaging diffusion properties across fibers at each node to produce a tract profile, supporting the attributed along-tract analysis. (LLM, conf=0.89)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“This sampling may be done by first generating a binary mask that defines the voxels through which streamlines pass and then sampling from an underlying microstructure image within this mask (Ciccarelli et al., 2003; Heiervang et al., 2006; Kunimatsu et al., 2004; Voineskos et al., 2010). The sampling may alternatively be done by sampling microstructural measures at each point of the streamlines”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
What the sources say
- Not checked — no full text of the sourcecites Ciccarelli et al., 2003 source
- Not checked — no full text of the sourcecites Heiervang et al., 2006 source
- Supportedcites Kunimatsu et al., 2004 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Other approaches fit a medial surface representation to the pathway, such that sampled data can be represented in two dimensions and can be analyzed not only along the pathway but also across its cross-section (Chen et al., 2016b; Qiu et al., 2010; Yushkevich et al., 2009).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
What the sources say
- Not matchedcites Chen et al., 2016b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Partly supportedcites Qiu et al., 2010 sourceExperimental — accuracy not yet measured
Methods §4.3 defines the tract surface as the boundary of its volume, not a medial surface. Methods §§4.4–4.5 describe a two-dimensional surface and mapping three-dimensional FA data onto it, supporting the dimensionality-reduction part of the claim. The cited paper does not describe analysis along the pathway and across its cross-section in those terms. Page numbers are unavailable in our copy. (LLM, conf=0.88)
- Not matchedcites Yushkevich et al., 2009
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Such analyses have been applied to study, e.g., how white matter fiber tracts are affected in individuals with different disease severity (Cha et al., 2015; Chiang et al., 2016; Price et al., 2007), how tracts relate to cognitive and socio-emotional function (Zekelman et al., 2021), and how tracts are developing during human neurodevelopment and aging (Gertheiss et al., 2013; Hasan et al., 2009a;”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
What the sources say
- Supportedcites Cha et al., 2015 source
The Effects of ADHD section reports reduced fronto-accumbal tract measures in children with ADHD compared with healthy controls. The Correlation with aggression section also reports that tract measures varied with aggression among children with ADHD, supporting this paper as an example of using tractography to examine differences associated with clinical severity. The later claims about cognition and development are attached to other citations, not Cha et al. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites Chiang et al., 2016 source
- Partly supportedcites Price et al., 2007 sourceExperimental — accuracy not yet measured
Split into 3 atoms — 0 confirmed, 3 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Over the last two decades, the study of the brain as a network has become increasingly popular in the neuroscience and neuroimaging communities, giving rise to the new fields of connectomics and network neuroscience (Bassett and Sporns, 2017; Fornito et al., 2013; 2015; 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Supportedcites Bassett and Sporns, 2017 source
The Conclusion describes network neuroscience as a new field gaining momentum as networks have become ubiquitous in neurobiological research. The Network mapping and observation section identifies connectomics as the mapping of connections among neurons and brain areas. Together, these passages support the citing sentence’s broad account of growing network-based research and the emergence of these fields. (LLM, conf=0.88)
- Not matchedcites Fornito et al., 2013; 2015; 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Additional studies have analyzed tracts represented as surfaces (Chen et al., 2016b; Qiu et al., 2010; Yushkevich et al., 2009) or performed data reduction techniques to reduce the dimensionality of the point-wise measurements along tracts (Ceschin et al., 2015; Chamberland et al., 2019; Geeraert et al., 2020).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
What the sources say
- Not matchedcites Chen et al., 2016b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Qiu et al., 2010 source
Qiu et al. is cited for the first part of the sentence: analyzing tracts represented as surfaces. The Introduction says the study introduced surface representations of 23 deep white matter tracts, and the Discussion identifies construction of those representations as its main contribution. The later clause about data-reduction techniques has different citations and is not attributed to Qiu et al. (LLM, conf=0.95)
- Not matchedcites Yushkevich et al., 2009
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Construction of the connectivity matrix has been described in several reviews (Sotiropoulos et al., 2016; Yeh et al., 2020) and includes two major steps. First, parcellation of the whole-brain tractogram is needed to compute all possible fiber pathways in the brain, i.e., white matter parcels connecting all pairs of gray matter regions (as described in Section 4.2). Then, a metric of “connectivity”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Construction of a structural connectivity matrix
What the sources say
- Partly supportedcites Sotiropoulos et al., 2016 sourceExperimental — accuracy not yet measured
In Results, under “Preserving the fibre spreading pattern to the cortex supported by the 7T data” (Fig. 9; page unavailable), the paper describes constructing a connectome matrix by recording tractography-derived path probabilities between pairs of surface vertices. That supports using a connectivity metric for matrix entries, but the paper does not describe the claimed two-step procedure of parcellating a whole-brain tractogram into pathways between gray-matter regions and then assigning edge weights. It is an application of fibre-orientation estimation, not a review of connectivity-matrix construction. (LLM, conf=0.86)
- Not matchedcites Yeh et al., 2020
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Another tract-specific analysis strategy is data-driven and uses machine learning techniques to perform tasks such as disease classification and prediction (Deng et al., 2019; O’Dwyer et al., 2012; Payabvash et al., 2019; Zhang et al., 2018a), as well as prediction of behavioral measures and traits (Seguin et al., 2020a; Tian et al., 2021).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
What the sources say
- Not checked — no full text of the sourcecites Deng et al., 2019 source
- Partly supportedcites O’Dwyer et al., 2012 sourceExperimental — accuracy not yet measured
The Methods and Discussion describe using diffusion data and a support vector machine to classify healthy young APOE4 carriers and non-carriers, and the Introduction says selected voxels were used for tractography. The Discussion also reports related work classifying older subjects as having mild cognitive impairment or being healthy. This paper itself did not classify disease or predict its onset; the later citations in the citing sentence, not O’Dwyer et al., are attached to behavioral measures and traits. (LLM, conf=0.85)
- Supportedcites Payabvash et al., 2019 source
Payabvash et al. is cited for disease classification and prediction, not for the separately cited prediction of behavioral traits. The Methods describe supervised machine-learning models using tract-based measures to classify children with sensory processing disorder, and the Results report their classification performance. (LLM, conf=0.93)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“The disciplines of graph theory and network science provide a framework to quantify network properties of brain connectivity (Rubinov and Sporns, 2010) and investigate whole-brain models of structural wiring (Betzel et al., 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Not checked — no full text of the sourcecites Rubinov and Sporns, 2010 source
- Supportedcites Betzel et al., 2016 source
The citation to Betzel et al. is attached to investigating whole-brain models of structural wiring. In the Introduction, the paper describes fitting and comparing generative models of human connectomes to identify wiring rules that reproduce observed networks. (LLM, conf=0.93)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Selection of tractography filtering strategies is important and has been shown to affect the analysis of the topology of brain networks (Civier et al., 2019; Frigo et al., 2020; Yeh et al., 2016a) and affect sensitivity and specificity when analyzing the connectomes (Zalesky et al., 2016a).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Construction of a structural connectivity matrix
What the sources say
- Partly supportedcites Civier et al., 2019 sourceExperimental — accuracy not yet measured
The Introduction says methods used to construct graphs from tractograms can strongly influence connectome characteristics, and §3.2 reports that heavy pruning changes graph-theoretical metrics. But the paper tests removal of connectome connections, not a comparison of tractography filtering strategies; §4.8 says it cannot rule out effects of its fixed pipeline on topology. The sensitivity-and-specificity clause is attributed to Zalesky et al., not Civier et al. (LLM, conf=0.82)
- Supportedcites Frigo et al., 2020 source
The Abstract (Main Result) states that tractography filtering techniques change brain-network topology and alter network metrics. The Discussion and Conclusions likewise reports topological changes with SIFT2 and COMMIT. Frigo et al. is cited for this topology claim; the sentence cites Zalesky et al. separately for sensitivity and specificity. (LLM, conf=0.94)
- Not matchedcites Yeh et al., 2016a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“This modular structure constrains the flow of information through the network in a manner thought to promote functional segregation and clusters of specialized information processing (Betzel et al., 2013).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Partly supportedcites Betzel et al., 2013 sourceExperimental — accuracy not yet measured
The Introduction describes communities as preferentially interconnected nodes that can trap the flow of random walkers, a model the paper says can represent information diffusion. The Discussion links connection topology to functional coupling, but our copy does not say that modular structure promotes specialized information processing or functional segregation in those terms. No page numbers were provided for these passages. (LLM, conf=0.82)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Popular methods for community detection in structural brain networks include the Louvain algorithm and stochastic block models, though determining best practices around the utilization of these and other approaches remain an active topic of research (Fortunato and Hric, 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Partly supportedcites Fortunato and Hric, 2016 sourceExperimental — accuracy not yet measured
The Methods section (p. 22) describes popular community-detection algorithms, and the paper discusses both the Louvain method (p. 30) and stochastic block models (p. 37). The Introduction (p. 2) also says there are no clear-cut guidelines for comparing methods. These passages do not establish that Louvain and stochastic block models are popular specifically for structural brain networks. (LLM, conf=0.86)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Graph measures can be classified based on their resolution or scope—from local measures that quantify properties of individual ROIs (nodes), to mesoscale measures describing clusters of interconnected ROIs, to global measures that describe whole-brain connectivity properties (Betzel and Bassett, 2017; Fornito et al., 2016) such as network communication in the brain (Graham et al., 2020) (Fig. 4b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Supportedcites Betzel and Bassett, 2017 source
Section 3, “Multi-scale network analysis,” distinguishes local measures of individual nodes, global measures of the network as a whole, and an intermediate mesoscale characterized by clusters of nodes. This supports the cited classification by scope; the citing sentence’s ROIs are its application of the paper’s nodes. (LLM, conf=0.94)
- Not checked — no full text of the sourcecites Fornito et al., 2016 source
- Supportedcites Graham et al., 2020 source
Graham et al. is cited for the example ‘network communication in the brain,’ not for the preceding classification of graph measures, which is cited to other works. The editorial’s Abstract explicitly discusses communication across whole-brain networks, so it supports that example. (LLM, conf=0.93)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In light of these shortcomings, recent work has stated to focus on alternative models of connectome communication, such as network diffusion (Estrada and Hatano, 2008; Goñi et al., 2014), linear transmission models (Mišić et al., 2015), and navigation (Seguin et al., 2018) (see Avena-Koenigsberger et al., 2018 for a review).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Partly supportedcites Estrada and Hatano, 2008 sourceExperimental — accuracy not yet measured
The section “Communicability as the Green’s function of networks” (p. 4) explicitly interprets the model as particle diffusion on a complex network, supporting its citation as an alternative to shortest-path communication. The paper does not study connectomes specifically, so it does not support that setting-specific part of the sentence. (LLM, conf=0.83)
- Not matchedcites Goñi et al., 2014
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Mišić et al., 2015
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In addition, connectome networks are known to strike a balance between wiring minimization (shortest paths) and formation of connections between brain regions with similar connectivity profiles (homophily) (Betzel et al., 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Partly supportedcites Betzel et al., 2016 sourceExperimental — accuracy not yet measured
The Results section reports that the best-fitting model combines a penalty against long-distance connections with a greater probability of connecting regions that have similar connectivity profiles. However, the parenthetical “shortest paths” is inaccurate: the paper describes minimizing physical wiring distance, and its Results > Geometric model section says forming only the shortest connections increases characteristic path length. (LLM, conf=0.88)
boostedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“For instance, despite the inherent limitations of dMRI tractography in resolving axonal fiber directionality, graph measures computed on the undirected human connectome can reveal patterns of asymmetric communication, as evidenced by significant associations to the directionality of effective connectivity computed using dynamic causal modeling (Seguin et al., 2019).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Supportedcites Seguin et al., 2019 source
The Introduction states that communication measures applied to undirected brain networks reveal send-receive asymmetries in the human cortex, and that these asymmetries are significantly associated with effective-connectivity directionality derived from dynamic causal modeling. The Results section, “Senders, receivers, and effective connectivity,” reports significant correlations across pairs of subsystems, with the stated exception of the seven-subsystem partition. (LLM, conf=0.95)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“However, algorithmically, the identification of shortest paths demands individual regions to possess global knowledge of structural connectivity, a requirement unlikely to be met in decentralized systems such as the brain (Avena-Koenigsberger et al., 2019; Goñi et al., 2014; Seguin et al., 2018).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Partly supportedcites Avena-Koenigsberger et al., 2019 sourceExperimental — accuracy not yet measured
The Introduction says that routing along shortest paths relies on all elements having information about the network’s global topology. The Discussion, however, calls it an open question how a brain system gains that information and raises the possibility that it learns about its topology through feedback; it does not establish that the requirement is unlikely to be met. (LLM, conf=0.86)
- Not matchedcites Goñi et al., 2014
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Supportedcites Seguin et al., 2018 source
The introductory passage (listed under Abstract; page not provided) says that identifying shortest paths requires individual elements of nervous systems to possess global knowledge of network topology, and that this requirement is challenged because nervous systems are decentralized. The Discussion section, “Biological Plausibility and Communication Efficiency” (page not provided), likewise describes the centralized knowledge needed to compute optimal routes as biologically implausible. (LLM, conf=0.94)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“Similar studies also show that the radial and tangential pathways organization are prominent at 17 weeks but gradually disappear at later gestational ages, and all major structural pathways are already identifiable by term (Takahashi et al., 2002).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Could not verifycites Takahashi et al., 2002 sourceExperimental — accuracy not yet measured
The Results describe diffusion imaging of excised larval sea lamprey spinal cords, and the Discussion describes their axonal anatomy. Neither addresses gestational age or whether major structural pathways are identifiable by term. Searches for 17 weeks, radial and tangential pathways, and fetal development found no supporting passage. (LLM, conf=0.78)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Could not verify
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“Similar studies also show that the radial and tangential pathways organization are prominent at 17 weeks but gradually disappear at later gestational ages, and all major structural pathways are already identifiable by term (Takahashi et al., 2002).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Could not verifycites Takahashi et al., 2002 sourceExperimental — accuracy not yet measured
The Results and Discussion describe diffusion measurements in excised larval sea lamprey spinal cord; no page numbers are available in our copy. Searches for radial and tangential pathways, 17 gestational weeks, and pathways identifiable by term found no passage addressing fetal development. The lamprey findings therefore cannot verify the attributed claim. (LLM, conf=0.76)
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Could not verify
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“For instance, using ex vivo dMRI scans on fetal brain samples, researchers are able to identify the major tract parts of the fornix and cingulum bundles at 13 weeks, but a part of the corpus callosum at 15 weeks (Huang et al., 2009).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Partly supportedcites Huang et al., 2009 sourceExperimental — accuracy not yet measured
The Results (White matter tracts) say the fornix is appreciable as a major tract at 13 weeks and the corpus callosum appears at 15 weeks. But they say the cingulum bundle can be traced only after 17 weeks, not at 13 weeks. The supplied passages do not give page numbers. (LLM, conf=0.93)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Due to recent advances in methodological progress such as motion correction algorithms, in vivo tractography on the fetal brain has become available and exhibit highly agreement with ex vivo and neuroanatomical studies (Christiaens et al., 2021; Khan et al., 2019), which indicates strong potential for future prenatal brain investigations.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Partly supportedcites Christiaens et al., 2021 sourceExperimental — accuracy not yet measured
The Discussion reports that the motion-correction framework has proved effective in fetal data, supporting the methodological-progress part of the attribution. But this paper analyzes scans acquired after birth (Data and preprocessing) and does not report in vivo fetal tractography or compare it with ex vivo or neuroanatomical studies. (LLM, conf=0.85)
- Partly supportedcites Khan et al., 2019 sourceExperimental — accuracy not yet measured
The Introduction (Fetal DTI; page unavailable) reports that motion-corrected in utero DTI enabled fetal tractography. The Conclusion (page unavailable) says the authors’ atlas portrayed developmental trends seen in prior ex vivo and in utero studies, but it does not establish high agreement specifically between in vivo tractography and ex vivo or neuroanatomical studies. (LLM, conf=0.83)
boostedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“revealing a typical spatial degeneration pattern across brain systems in which prefrontal association tracts are the most vulnerable to aging, while cingulum, temporal and parietal-occipital commissural connections are relatively preserved.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Aging and lifespan tractography of the brain
What the sources say
- Partly supportedcites Davis et al., 2009 sourceExperimental — accuracy not yet measured
The Discussion (Anterior-Posterior Gradient; page unavailable) ranks age-related FA differences highest in the genu and uncinate fasciculus and lowest in the cingulum bundle and splenium, supporting greater vulnerability of anterior tracts and relative preservation of some connections. But the same section reports appreciable effects in the inferior longitudinal fasciculus, including a stronger effect in its occipito-temporal segment; the Results (Anterior-posterior trend analysis; page unavailable) also find age effects in the cingulum. The claim overstates preservation across the named connections. (LLM, conf=0.88)
- Not matchedcites Stadlbauer et al., 2008a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Partly supportedcites Sullivan et al., 2010 sourceExperimental — accuracy not yet measured
The Results (section 3.3) identify the frontal forceps as having the most prominent age-related FA decrease, and the Discussion (section 4) describes greater susceptibility in anterior than posterior bundles. But the proposed preservation is too broad: section 4 reports age-related changes in the superior cingulum, while section 3.4 reports significant age effects in temporal and parietal callosal sectors. Page numbers are unavailable in our copy. (LLM, conf=0.87)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Many studies have discovered largely adult-like topological structures including significant small-world, modular, and rich-club organization during the middle to final trimester of gestation”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Not checked — no full text of the sourcecites Brown et al., 2014 source
- Partly supportedcites Song et al., 2017 sourceExperimental — accuracy not yet measured
The Results report small-world organization in fetal structural networks at 20, 35, and 40 postmenstrual weeks (Figures 6–7; page not provided). The passages do not establish modular or rich-club organization, or characterize the topology as broadly adult-like. (LLM, conf=0.88)
- Partly supportedcites Tymofiyeva et al., 2013 sourceExperimental — accuracy not yet measured
The Results (Changes in Global Topological Properties with Age) report small-world properties at all studied ages and assess modularity. But the study examined premature and term-born neonates, infants, and adults—not fetuses during gestation—and the cited passages do not establish rich-club organization or statistical significance for every claimed property. (LLM, conf=0.86)
boostedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“tractography studies show that the basic layouts of the brain’s structural network are largely preserved until old age, such as the economical small-world character, the modular organization and rich club organization”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Aging and lifespan tractography of the brain
What the sources say
- Not matchedcites Gong et al., 2009b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Li et al., 2020c
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Partly supportedcites Wen et al., 2011 sourceExperimental — accuracy not yet measured
The Small-world properties section reports that all studied subjects’ structural networks had small-world architecture, and the Discussion says this property was preserved despite individual variation. The paper does not establish preservation across the lifespan until old age, and the passages found do not report preserved modular or rich-club organization. (LLM, conf=0.88)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“although most tracts show increased FA during childhood and adolescence and decreased FA at older ages”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Aging and lifespan tractography of the brain
What the sources say
- Supportedcites Hasan et al., 2010 source
The Results, under “Age effects” (page not supplied), report an inverted U-shaped FA trajectory for all measured pathways in both males and females. This supports increasing FA at younger ages followed by decreasing FA at older ages within the study’s 6–68-year age range. (LLM, conf=0.93)
- Not matchedcites 2009b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not checked — no full text of the sourcecites Lebel et al., 2010 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“After birth until adulthood, the brain network reshapes to improve integration capacity with the reconfigurations of decreased modularity and decreased small-worldness”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Partly supportedcites Chen et al., 2013 sourceExperimental — accuracy not yet measured
The Results (Global network properties and their age-related trajectories; page unavailable) report increased global efficiency and decreased modularity from early to late childhood, with both measures then stabilizing. The Results (Small-world efficiency of developing WM networks; page unavailable) show small-worldness values that fluctuate across age groups rather than a sustained decrease. The study begins at age 6, so it does not establish a trajectory from birth. (LLM, conf=0.88)
- Partly supportedcites Dennis et al., 2013 sourceExperimental — accuracy not yet measured
The Discussion reports decreasing small-worldness and modularity with age and says the network changes suggest increased structural integration. But the study examined people aged 12–30, so it does not establish that this pattern occurs throughout the period from birth to adulthood. (LLM, conf=0.87)
- Partly supportedcites Hagmann et al., 2010 sourceExperimental — accuracy not yet measured
The Results report increasing network efficiency and a generally decreasing small-world index with age. But the Modularity and Module Composition results say modularity showed no consistent significant age trend, rather than a decrease. The study examined ages 2–18, not the full period from birth to adulthood. (LLM, conf=0.91)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“For instance, in Parkinson’s disease, researchers found that DBS on sub-thalamic nucleus linking to the supplementary motor area is associated with improvement in bradykinesia and rigidity, while DBS on nucleus structurally commenting to M1 is associated with improvement in tremor (Akram et al., 2017).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurosurgery
What the sources say
- Supportedcites Akram et al., 2017 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Therefore, tractography in native space becomes suitable for MS patients because it is free of registration and allows inter-subject variability of tract location and shape (Lipp et al., 2020).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurological and mental brain disorders
What the sources say
- Supportedcites Lipp et al., 2020 source
The Methods (Data analysis) state that tractography was performed in native space for MS patients. The Introduction contrasts individual tractography with probability-map methods that require inter-subject registration and assume consistent tract anatomy; the Discussion (Anatomical generalisability) says tractography is robust to individual differences in tract size and shape. Thus, “free of registration” is supported in the sense of not requiring inter-subject registration for native-space tractography, not as a claim that the study performed no registration for other analyses. (LLM, conf=0.87)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Furthermore, connectomic neuromodulation may contribute to identifying specific networks that lead to symptom-specific treatments, paving the way for personalized therapy (Horn and Fox, 2020).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurosurgery
What the sources say
- Supportedcites Horn and Fox, 2020 source
Opportunity #3 (“symptom specific networks”) explicitly says connectomic neuromodulation may identify networks that lead to symptom-specific treatments and that stimulating different networks for different symptoms could pave the way for personalized therapy. The citing sentence preserves the paper’s tentative wording. (LLM, conf=0.95)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The reconstructed streamlines are only simulated entities that do not correspond directly to nerve fibers (Jeurissen et al., 2019; Yeh et al., 2020)”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Discussion and conclusion
What the sources say
- Supportedcites Jeurissen et al., 2019 source
Section 2.3, “The virtual nature of fiber tracking,” explicitly distinguishes physical nerve fibers from reconstructed streamlines, calling the latter virtual entities related only indirectly to nerve fibers. This supports the citing sentence’s paraphrase. (LLM, conf=0.95)
- Not matchedcites Yeh et al., 2020
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“clinical studies frequently employ advanced tractography methods to reconstruct individual tract streamlines (Sbardella et al., 2013) and obtain feasible results even when brain lesions are present (Lipp et al., 2020).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurological and mental brain disorders
What the sources say
- Supportedcites Sbardella et al., 2013 source
The Introduction (page not provided) describes three-dimensional tractography as reconstructing white-matter pathways by tracking fibers and discusses more sophisticated tracking approaches. This supports the tract-reconstruction point attributed to Sbardella et al.; the separate claim about feasible results in the presence of lesions is attributed to Lipp et al., not to this source. (LLM, conf=0.88)
- Supportedcites Lipp et al., 2020 source
The Lipp citation supports the clause about obtaining feasible results in the presence of lesions. In the Discussion and Conclusions, the paper reports successful individual tract segmentation in a large cohort with MS lesions and says this is feasible even in large-scale clinical studies. The preceding claim about how frequently clinical studies use advanced methods is attached to a different citation. (LLM, conf=0.91)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Rests on an assumption: Pathological lesions of MS hinder basic tract reconstruction.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“basic diffusion metrics are only inferences based on local diffusion properties, which are not direct measures of tissue properties (Assaf et al., 2019).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Discussion and conclusion
What the sources say
- Supportedcites Assaf et al., 2019 source
In “Local measures of white matter microstructure,” the paper says basic diffusion parameters reflect local microstructure but have no one-to-one relationship with underlying tissue structure. It also says common DTI indices are nonspecific to any particular tissue compartment, supporting the distinction between diffusion-based inference and direct tissue measurement. (LLM, conf=0.92)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“The anatomical accuracy of tractography is an ongoing issue in quantitative tractography analysis, where both false positive and false negative tractography results pose challenges (Maier-Hein et al., 2017; Thomas et al., 2014).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Discussion and conclusion
What the sources say
- Supportedcites Maier-Hein et al., 2017 source
The Results sections report many invalid connections and bundles (false positives), while no submission recovered all 25 ground-truth bundles and average bundle-volume overlap was only 36% (missed connections or portions of bundles). The Discussion describes tractography’s ambiguity as an open challenge. Page numbers are not available in our copy. (LLM, conf=0.91)
- Supportedcites Thomas et al., 2014 source
The Discussion reports that tractography methods with high sensitivity tend to have low specificity and a high rate of false positives. It also explicitly describes missed tracer-labeled regions as false negatives and concludes that anatomical accuracy remains suboptimal even under ideal experimental conditions. (LLM, conf=0.93)
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“the fact it can be trivially demonstrated that both that streamline count can be erroneously modulated in the absence of a difference in connection strength and erroneously constant in the presence of a difference in connection strength (Figs. 2, 3)”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Connection density biases
boosted- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Even operating on high-resolution dMRI data, current tractography algorithms have been shown to deviate from the ground-truth fiber projections derived from histological staining, with greater streamline densities at gyral crowns than sulcal banks (Schilling et al., 2018b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Gyral bias
What the sources say
- Not matchedcites Schilling et al., 2018b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
boostedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
In the paper
“these “weights” represent an effective cross-sectional area of each streamline, which can be utilized as a direct measure of connection density (Smith et al., 2020a)”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > Connection density biases
What the sources say
- Not matchedcites Smith et al., 2020a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
In the paper
“This strategy implicitly assumes a correlation between the strength of a reconstructed edge and its validity, which can be violated in a range of ways due to the errors produced by streamlines tractography not being simply random variance.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Improving tractography quality: methods for tractography correction > False positive connections
What the sources say
- Not checked — no full text of the sourcecites Fornito et al., 2016 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The third point is that anatomical tract identification results can be highly variable across studies due to a lack of consistent fiber tract definitions, where different methods may give different results for the same target anatomical fiber tracts (Dick and Tremblay, 2012; Rheault et al., 2020a; Schilling et al., 2020b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Not checked — no full text of the sourcecites Dick and Tremblay, 2012 source
- Not matchedcites Rheault et al., 2020a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Schilling et al., 2020b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“tract-specific tractography may be more computationally efficient if the number of tracts of interest is small, while whole-brain tractography can be computationally expensive but enables tract identification or parcellation of the whole white matter.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Most of the direct segmentation approaches use a training tract segmentation dataset and thus may not require image registration or require a small amount of work for registration (e.g., a rigid volumetric registration); however, we note that curation of a training tract segmentation dataset may require extensive work compared to performing image registration.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“however, no consensus has been reached given that many existing tract identification methods have not been compared.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“tract-specific tractography may be more computationally efficient if the number of tracts of interest is small, while whole-brain tractography can be computationally expensive but enables tract identification or parcellation of the whole white matter.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“but with more modern multi-fiber tractography, reproducibility is lower, potentially due to the increase in spurious streamlines (Rheault et al., 2020a).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
What the sources say
- Not matchedcites Rheault et al., 2020a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“While using streamline-based registration can avoid the intermodality registration issue in ROI-based methods, streamline registration (especially a nonlinear registration) may be computationally heavier than volumetric registration.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“They parcellate tractography according to a cortical (and sometimes a subcortical) gray matter parcellation, focusing on the structural connectivity among different gray matter ROIs (Bassett and Bullmore, 2017; Bullmore and Sporns, 2009a; Gong et al., 2009a; Ingalhalikar et al., 2014; Sporns et al., 2005; Yeh et al., 2016b; Zalesky et al., 2012).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Not matchedcites Bassett and Bullmore, 2017
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Bullmore and Sporns, 2009a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Gong et al., 2009a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“Though relatively less used, fiber clustering tractography parcellation methods are increasingly applied to study the brain’s structural connectivity in applications such as disease classification and between-population statistical analysis (Feng et al., 2020; Ji et al., 2019; Wu et al., 2018; Zhang et al., 2018a; 2018b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
What the sources say
- Not matchedcites Feng et al., 2020
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Ji et al., 2019
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Wu et al., 2018
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“(Note that a whole-brain tractogram is required for filtering (Sections 3.3 and 5.3) and analyses of the brain as a network using a connectivity matrix (Sections 5.5 and 5.6)).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Anatomical tract identification
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“In this category of measures, tractography is generally used to define the locations in which microstructural measures are sampled.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“There are many quantitative measures that can be computed from tractography, which can be subdivided into two categories based on the source of data used to compute the measures.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Specifically, tractography segmentation is performed by extracting streamlines that connect pairs of ROIs. Therefore the resulting tractography segmentation is mainly determined by the selection of a cortical parcellation scheme.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Defining regions for quantitation: methods for tractography segmentation > Parcellation of the whole-brain tractogram
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The second category of quantitative measures computed from tractography leverages microstructural measures that are usually computed from a diffusion model (e.g., diffusion tensor model) or another quantitative imaging modality (e.g., myelin imaging).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Popularly used diffusion-modeling-based microstructural measures include the fractional anisotropy, axial, radial and mean diffusivities (FA, AD, RD and MD respectively) derived from traditional diffusion tensor model (Basser and Pierpaoli, 1996).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures computed from tractography
What the sources say
- Not checked — no full text of the sourcecites Basser and Pierpaoli, 1996 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“Another hypothesis-driven analysis uses a regression model (e.g., a generalized linear model (Dobson and Barnett, 2018) or support vector regression (Zhang and O’Donnell, 2020)) to assess correlation of the tract quantitative measurement and a behavioral or a disease symptom score.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
What the sources say
- Not matchedcites Dobson and Barnett, 2018
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Zhang and O’Donnell, 2020
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Two main strategies can be employed: using a scalar value as a summary statistic, or using data along the length of the fiber pathway.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The second strategy to quantify an individual fiber pathway is to measure the distribution of the microstructural measures along the fiber pathway.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“In particular, because of their flexible implementations, COMMIT, COMMIT2 and COMMIT2tree allow complementing tractography with biophysical models of the tissue microstructure and, thus, enable one to access more quantitative and biologically informative features of individual bundles, such as average axon diameter (Barakovic et al., 2018), myelin content (Schiavi et al., 2019) and bundle-specific”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures using filtering techniques
What the sources say
- Not matchedcites Barakovic et al., 2018
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not checked — no full text of the sourcecites Schiavi et al., 2019
- Not matchedcites Barakovic et al., 2021b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- The authors state this as an assumption: The microstructure properties corresponding to a single streamline (or a group of axons following the same trajectory) remain constant along its path on average at achievable resolution.
- Not matched
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“Other summary statistics such as the median, maximum and minimum have also been employed (Boshkovski et al., 2020b; Zhang et al., 2018a; 2018b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
What the sources say
- Not matchedcites Boshkovski et al., 2020b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Zhang et al., 2018a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Zhang et al., 2018b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“For example, compared to the mean statistic, studies have shown that the median can be more robust against outliers and does not rely on the normality assumption for the distribution of the microstructure parameter along a streamline (Boshkovski et al., 2020b; Zhang et al., 2018b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
What the sources say
- Not matchedcites Boshkovski et al., 2020b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Zhang et al., 2018b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“These methods have been used to investigate properties of healthy and pathological brains, showing better performance than the standard NOS (Schiavi et al., 2020b; Smith et al., 2015a; Yeatman et al., 2014b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures using filtering techniques
What the sources say
- Not matchedcites Schiavi et al., 2020b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Smith et al., 2015a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Yeatman et al., 2014b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- The authors state this as an assumption: The microstructure properties corresponding to a single streamline (or a group of axons following the same trajectory) remain constant along its path on average at achievable resolution.
- Not matched
In the paper
“While in its original implementation SIFT (Smith et al., 2013) provides only the NOS adjusted based on voxel-wise spherical deconvolution, its evolution SIFT2 (Smith et al., 2015b) optimizes per-streamline cross-section multipliers to match a whole-brain tractogram to fixel-wise fiber densities and thus provides a value for each streamline that can be used (for example) to define the edge weights”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures using filtering techniques
What the sources say
- Not matchedcites Smith et al., 2015b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- The authors state this as an assumption: The microstructure properties corresponding to a single streamline (or a group of axons following the same trajectory) remain constant along its path on average at achievable resolution.
- Not matched
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The choice of the best summary statistic for data measured within a fiber pathway is still open.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“These methods may rely on a summary statistic per tract, or analyze data along a tract.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Once a quantitative measure has been extracted for individual fiber pathways, several options exist for tract-specific analysis, which may be hypothesis-driven using statistical analysis or data-driven using machine learning.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“One study has suggested that the maxima and minima are more discriminative than the mean value in machine-learning-based disease classification (Zhang et al., 2018a).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
What the sources say
- Not matchedcites Zhang et al., 2018a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The underling assumption comes from the fact that a streamline reconstructed from tractography cannot represent a single axon, but rather a group of axons following the same trajectory, and thus we can suppose that on average the microstructure properties the magnetic resonance signal is sensitive to at achievable resolution remain constant.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Quantitative measures using filtering techniques
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper may give no reason why it holds.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“(This is required for connectome-based analysis and is a popular approach for tract-specific analysis).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Domain of analysis: extraction of quantitative measures within white matter fiber pathways
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds. It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“One important point to note is that correction for multiple comparisons is needed if there are multiple tracts and/or multiple quantitative measurements analyzed.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Other approaches can employ streamlines of the entire tract in the statistical analyses (Chandio et al., 2020b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
What the sources say
- Not matchedcites Chandio et al., 2020b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Unlike statistical analysis methods that usually aim to find white matter structures with statistical group differences, the machine-learning-based methods aim to offer predictive relevance.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“In machine learning analysis, the quantitative measures computed from individual fiber pathways are treated as feature descriptors, which are input to a machine learning algorithm (e.g., a support vector machine) to train a model from a set of training samples with known information (e.g., labels such as disease or healthy control).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“This step is typically done by simply thresholding according to some rule or to reach a predefined density, or using filtering techniques described in Section 5.3.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Construction of a structural connectivity matrix
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Selection of a gray matter parcellation scheme (as described in Section 4.2) is the first essential consideration when constructing a structural connectivity matrix, and it has been shown to be highly consequential in connectome analysis (de Reus and Van den Heuvel, 2013; Yeh et al., 2020; Zalesky et al., 2012).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Construction of a structural connectivity matrix
What the sources say
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Along-tract analysis enables the study of local regions along the tract.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“For scalar values that are interpreted as inversely related to connectivity “strength,” such as RD, MD, or maps reflecting extracellular or isotropic/free water components of the signal, a transformation of the connectivity matrix may be performed using the reciprocal or the log function prior to any subsequent connectivity analysis (Fornito et al., 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Construction of a structural connectivity matrix
What the sources say
- Not checked — no full text of the sourcecites Fornito et al., 2016 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Another advantage of machine learning is that it can be easily applied to multimodal data.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Then the trained model can be used to predict new samples.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“In addition, connectomes are usually post-processed to reduce potential bias in the estimation of graph measures.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Construction of a structural connectivity matrix
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Commonly used multiple comparison correction methods include false discovery rate (FDR) (Benjamini and Hochberg, 1995) and Bonferroni (Holm, 1979) methods.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
What the sources say
- Not checked — no full text of the sourcecites Benjamini and Hochberg, 1995 source
- Not matchedcites Holm, 1979
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This can be advantageous in situations where the within-group heterogeneity is large (e.g., in psychiatric diseases) and thus a statistical group comparison, which essentially compares the “average patient” to the “average control,” is not informative.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Tract-specific analysis using statistical or machine learning techniques
plainconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Shortest-path-based measures include, e.g., the popular characteristic path length and network efficiency (Rubinov and Sporns, 2010).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
- Not checked — no full text of the sourcecites Rubinov and Sporns, 2010 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“A daunting number of graph theoretical measures have been proposed to study the network properties of the brain’s connectome (Bullmore and Sporns, 2009b; Iturria-Medina et al., 2008; Rubinov and Sporns, 2010).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Performing quantitative analysis: methods for tractography quantification > Graph theoretical measures and advanced structural connectome measurements
What the sources say
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“FA values of the corpus callosum declined with aging only in the genu part while not in the body and splenium parts in participants aged 22–84 years (Michielse et al., 2010).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Aging and lifespan tractography of the brain
What the sources say
- Not checked — no full text of the sourcecites Michielse et al., 2010 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
None of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“Meanwhile, both global and local alterations of the brain’s structural topology occur with aging”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Aging and lifespan tractography of the brain
What the sources say
- Not matchedcites Bi et al., 2021
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Gong et al., 2009b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Li et al., 2020c
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
None of the sources cited for this claim have been checked yet.
In the paper
“During prenatal development, the whole network becomes increasingly efficient and segregated with typical system-level refinements such as increased small-worldness (Brown et al., 2014) and increased modularity (Van Den Heuvel et al., 2015b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Not checked — no full text of the sourcecites Brown et al., 2014 source
- Not matchedcites Van Den Heuvel et al., 2015b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The nodal efficiency of provincial hubs and the strength of within-module connections (Zhao et al., 2019a) develop fast during the prenatal stage”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Not matchedcites Zhao et al., 2019a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
In the paper
“Researchers can further estimate the growth of tracts at the subsystem level by multivariate analysis; for example, one study investigated the maturational calendars of linguistic bundles and found that the dorsal pathway development falls behind the ventral pathway at birth and catches up later at the first postnatal months (Dubois et al., 2016).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
What the sources say
- Not checked — no full text of the sourcecites Dubois et al., 2016 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“It may partly reduce the ambiguity about the best intervention target and is quite suitable for brain disorders that involve several abnormal circuits, e.g., OCD (For a review, see (Baldermann et al., 2021)).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurosurgery
What the sources say
- Not checked — no full text of the sourcecites Baldermann et al., 2021 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“traditional voxel-based analysis of brain white matter is usually performed in a standard space and seems sensitive to registration error (Colby et al., 2012b).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurological and mental brain disorders
What the sources say
- Not matchedcites Colby et al., 2012b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
In the paper
“Multiple sclerosis is a demyelinating disease with multiple focal white matter lesions (Fleischer et al., 2019).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Tractography in neurological and mental brain disorders
What the sources say
- Not checked — no full text of the sourcecites Fleischer et al., 2019 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Tractography has enabled the study of the brain’s white matter connections across the lifespan in health and disease.”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Discussion and conclusion
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“while there have been considerable advancements in methodological technologies and breadth of applications”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Discussion and conclusion
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may state two separate claims as one.
The authors state this as an assumption.
Fibers are naturally organized in bundles.
“fibers are naturally organized in bundles (Mandonnet et al., 2018; Udin and Fawcett, 1988)”
The authors state this as an assumption.
The number of bundles should be low to minimize the overall wiring cost.
“the number of bundles should be low to minimize the overall wiring cost (Bullmore and Sporns, 2012)”
The paper relies on this without support.
There is no ground truth in tractography.
“given the fact that there is no ground truth in tractography”
The authors state this as an assumption.
The microstructure properties corresponding to a single streamline (or a group of axons following the same trajectory) remain constant along its path on average at achievable resolution.
“Assuming that the microstructure properties corresponding to a single streamline remain constant along its path, these methods assign a specific microstructural property to each reconstructed pathway.”
“we can suppose that on average the microstructure properties the magnetic resonance signal is sensitive to at achievable resolution remain constant.”
The paper relies on this without support.
Pathological lesions of MS hinder basic tract reconstruction.
“Since the pathological lesions of MS hinder basic tract reconstruction”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > Applications of quantitative tractography analysis > Developmental tractography of the brain
“Similar studies also show that the radial and tangential pathways organization are prominent at 17 weeks but gradually disappear at later gestational ages, and all major structural pathways are already identifiable by term (Takahashi et al., 2002).”
§ Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review > References
“478. Takahashi M, Hackney DB, Zhang G, Wehrli SL, Wright AC, O’Brien WT, Uematsu H, Wehrli FW, Selzer ME, 2002. Magnetic resonance microimaging of intraaxonal water diffusion in live excised lamprey spinal cord.”
Citations
Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · cited 1×
“Commonly used multiple comparison correction methods include false discovery rate (FDR) [42] and Bonferroni [200] methods.”
MethodA Simple Sequentially Rejective Multiple Test Procedure
(1979) · Scandinavian Journal of Statistics · doi:10.2307/4615733 · Cited by 21,526 · cited 2×
“Commonly used multiple comparison correction methods include false discovery rate (FDR) [42] and Bonferroni [200] methods.”
MethodTzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F., Etard, O., Delcroix, N., Mazoyer, B., & Joliot, M. (2002) · NeuroImage · doi:10.1006/nimg.2001.0978 · Cited by 16,319 · cited 1×
“The most popularly used cortical parcellation is the Freesurfer Desikan-Killiany cortical parcellation [117, 143], while many other cortical parcellation schemes have also been widely used [461, 118, 396].”
MethodDesikan, R. S., Ségonne, F., Fischl, B., Quinn, B. T., Dickerson, B. C., Blacker, D., Buckner, R. L., Dale, A. M., Maguire, R. P., Hyman, B. T., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.021 · Cited by 13,324 · cited 4×
“The most popularly used cortical parcellation is the Freesurfer Desikan-Killiany cortical parcellation [117, 143], while many other cortical parcellation schemes have also been widely used [461, 118, 396].”
MethodInfluentialComplex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820 · cited 12×
“Specifically, tractography segmentation is performed by extracting streamlines that connect pairs of ROIs.”
BackgroundInfluentialComplex network measures of brain connectivity: Uses and interpretations
Rubinov, M., & Sporns, O. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.003 · Cited by 11,522
Jenkinson, M., Beckmann, C. F., Behrens, T. E. J., Woolrich, M. W., & Smith, S. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.015 · Cited by 11,314
Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526
The organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182
Selective Cortical Undercutting As a Means of Modifying and Studying Frontal Lobe Function in Man
Scoville, W. B. (1949) · Journal of neurosurgery · doi:10.3171/jns.1949.6.1.0065 · Cited by 7,374
Research works printed but not linked: 10
- Barakovic, 2021, Resolving bundle-specific intra-axonal T2 values within a voxel using diffusion-relaxation tract-based estimation, Neuroimage, 227, 117617, 10.1016/j.neuroimage.2020.117617 · DOI
- Bullmore, 2009, Complex brain networks: graph theoretical analysis of structural and functional systems, Nat. Rev. Neurosci., 10, 186, 10.1038/nrn2575 · DOI · Paper page
- Chandio, 2020, Bundle analytics, a computational framework for investigating the shapes and profiles of brain pathways across populations, Sci. Rep., 10, 1, 10.1038/s41598-020-74054-4 · DOI
- Colby, 2012, Along-tract statistics allow for enhanced tractography analysis, Neuroimage, 59, 3227, 10.1016/j.neuroimage.2011.11.004 · DOI
- Hagmann, 2008, Mapping the structural core of human cerebral cortex, PLoS Biol., 6, e159, 10.1371/journal.pbio.0060159 · DOI · Paper page
- Rheault, 2020, Common misconceptions, hidden biases and modern challenges of dMRI tractography, J. Neural Eng., 17, 011001, 10.1088/1741-2552/ab6aad · DOI
- Schilling, 2018, Confirmation of a gyral bias in diffusion MRI fiber tractography, Hum. Brain Mapp., 39, 1449, 10.1002/hbm.23936 · DOI
- Smith, 2020, Diffusion MRI fiber tractography, Vol. 1, 533
- Wu, 2020, Mitigating gyral bias in cortical tractography via asymmetric fiber orientation distributions, Med. Image Anal., 59, 101543, 10.1016/j.media.2019.101543 · DOI
- Zalesky, 2016, Connectome sensitivity or specificity: which is more important?, Neuroimage, 142, 407, 10.1016/j.neuroimage.2016.06.035 · DOI · Paper page
Cited by
Sorted by citations
Items 201–300 of 301
A Deep Approach for Volumetric Tractography Segmentation
Rocamora-García, P., Saval-Calvo, M., Villena-Martínez, V., et al. (2023) · Lecture notes in computer science · doi:10.1007/978-3-031-36616-1_46 · Cited by 1
Shaaban, C. E., & Caprihan, A. (2023) · Cerebral Circulation - Cognition and Behavior · doi:10.1016/j.cccb.2023.100175 · Cited by 1
“There are several methods for calculating both the functional connectivity (ROI [13] or seed-based [14] methods and data-driven methods [15]) and for calculating structural connectivity based on diffusion imaging (streamline tractography and probabilistic tractography [12]).”
BackgroundMethodWende, T., Hoffmann, A., Scherlach, C., et al. (2023) · Brain Connectivity · doi:10.1089/brain.2023.0033 · Cited by 1
“…were aware of the most current description of the FAT anatomy in the respective literature as well as of the technical skills to avoid false-positive and false-negative streamline results (Briggs et al., 2018a; Catani et al., 2013; Dick et al., 2019; Pascual-Diaz et al., 2020; Zhang et al., 2022).”
The aspect of structural connectivity in relation to age-related gait performance
Kim, C.-W., Kim, Y., Kim, H.-H., & Choi, J. Y. (2023) · Psychoradiology · doi:10.1093/psyrad/kkad028 · Cited by 1
PhyberSIM: a tool for the generation of ground truth to evaluate brain fiber clustering algorithms
Poo, E., Mangin, J., Poupon, C., Hernández, C., & Guevara, P. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1396518 · Cited by 1
Behroozi, M., Graïc, J., & Gerussi, T. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1411982 · Cited by 3
A Novel Deep Clustering Framework for Fine-Scale Parcellation of Amygdala Using DMRI Tractography
He, H., Zhu, C., Zhang, L., et al. (2024) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi56570.2024.10635363 · Cited by 1
“…MRI (dMRI) to parcellate the amygdala based on its white matter (WM) structural connectivity, which falls in the interest of our study. dMRI is an advanced MR technique that enables in vivo reconstruction of the brain’s WM connections, via a computational process called tractography [13], [14].”
BackgroundSelf-citationAuditory Fiber Bundle Parcellation using Text-Prompted Decomposition Networks
Gu, J., Wang, Y., Jiang, C., et al. (2024) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi56570.2024.10635523 · Cited by 1
“Diffusion MRI (dMRI) is currently the only technique that can non-invasively characterize white matter (WM) development and disorders [1].”
BackgroundUrushihata, T., & Satoh, A. (2024) · The Journal of Physiological Sciences · doi:10.1186/s12576-024-00934-3 · Cited by 2
“The diffusion tensor tractography can non-invasively depict the trajectory of a neural fiber tract [62], and provides information about anatomical connections between distant brain areas and the course, interruption, or integrity of neural pathways [63].”
BackgroundLo, Y., Chen, Y., Zhang, F., et al. (2025) · Communications in computer and information science · doi:10.1007/978-981-96-6960-8_18 · Cited by 1
Self-citationGenCPM: a toolbox for generalized connectome-based predictive modeling
Xu, B., Ding, S., Xu, W., Fredericks, C. A., & Zhao, Y. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1627497 · Cited by 2
Xia, X., Zeng, X., Gao, F., Hua, L., Huang, S., & Yuan, Z. (2023) · Human Brain Mapping · doi:10.1002/hbm.26402
“Interestingly, striatonigrostriatal spiral circuits and most other brain neural circuits could be effectively reconstruct by using in vivo tractography (Girard et al., 2020; Shimony et al., 2018; Zhang et al., 2015; Zhang et al., 2022).”
BackgroundMethodShailja, S., Grafton, S. T., & Manjunath, B. S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.11.482601 · Cited by 3
“Noise in this context refers to streamlines that are geometrically implausible due to curvature overshoot; short length because of premature termination; and spatially distant due to connection density biases [31].”
BackgroundHowell, A. M., Warrington, S., Fonteneau, C., Cho, Y., Sotiropoulos, S. N., Murray, J. D., & Anticevic, A. (2024) · eLife · doi:10.7554/elife.95018.1 · Cited by 1
Puxeddu, M. G., Seguin, C., & Sporns, O. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00165-0 · Cited by 1
Self-citationMapping the topographic organization of the human zona incerta using diffusion MRI
Haast, R. A. M., Kai, J., Taha, A., Liu, V. M., Kasa, L. W., Gilmore, G., Guye, M., KHAN, A. R., & Lau, J. C. (2026) · eLife · doi:10.1101/2024.09.05.610266 · Cited by 1
“Each step in the processing workflow involves decisions that impact subsequent steps and results (Jeurissen et al., 2019; F. Zhang et al., 2022).”
Auditory Tract Maturation in Early Infancy: Links to Speech ProductionPreprint
Liu, F., Wang, Y., Gu, J., Liu, J., Cai, X., Zhang, H., Feng, J., Wang, Z., Wu, H., & Shen, D. G. (2025) · Qeios · doi:10.1101/2024.12.31.630971 · Cited by 1
Hassanzadeh‐Behbahani, S., Zhou, L., Zekelman, L., Rushmore, J., Chen, Y., Xue, T., Karayumak, S. C., Pieper, S., Tie, Y., Yeterian, E. H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.31.666959 · Cited by 1
“For each individual’s SWM, FAT, and arcuate fasciculus connections, we studied dMRI measures of fractional anisotropy (FA) and number of streamlines (NoS), which are widely used to study brain microstructure, cognition, and development (F. Zhang et al., 2022).”
Self-citationMultimodal imaging of human fetal brain development at the mesoscopic scale using 11.7 T ex vivo MRIPreprint
Arcamone, L., Poupon, C., Adle‐Biassette, H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.08.669657 · Cited by 1
Mesoscopic mapping of the human structural connectome using high-performance global tractography
Legeay, S. (2025) · theses.fr (ABES) · doi:10.70675/f036d118z8937z4350zb52cz2c55acdaa577 · Cited by 1
Социальная мобильность государственных гражданских служащих как управляемый процесс развития карьеры
Кондрашкин, В. А. (2013) · Известия Тульского государственного университета. Гуманитарные науки
Editorial for “Early‐Onset Micromorphological Changes of Neuronal Fiber Bundles During Radiotherapy”
O’Donnell, L. J. (2022) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.28109
Self-citationHsu, C., Chong, S., Kung, Y.-C., Kuo, K.-T., Huang, C.-C., & Lin, C.-P. (2022) · bioRxiv · doi:10.1101/2022.03.14.483870
“…statistics using diffusion tensor metrics (e.g. fractional anisotropy and mean diffusivity) (Smith et al., 2006), or measuring the topological properties of the complex human brain organization using tractography-based analysis (Bastiani and Roebroeck, 2015; Yeh et al., 2021; Zhang et al., 2021).”
MethodUsefulness and Limits of Tractography for Surgery in the Precentral Gyrus—A Case Report
Wende, T., Wilhelmy, F., Kasper, J., et al. (2022) · Clinics and Practice · doi:10.3390/clinpract12020027
“However, tractography has decreased accuracy in the cortex, and misinterpretation of false negatives in the precentral gyrus can lead to hemiparesis, while misinterpretation of false positives can lead to an unnecessarily decreased extent of resection [13,14].”
BackgroundWielenga, V. H., Dijkhuizen, R. M., & van der Toorn, A. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-2926-0_12
Triển, V. Đ., & Khánh, L. (2023) · Journal of 108 - Clinical Medicine and Phamarcy · doi:10.52389/ydls.v18i5.1902
Xue, T., Karimi, H. S., Consagra, W., Zhang, F., Cai, W., O’Donnell, L. J., Ning, L., & Yogesh Rathi, A. (2023) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi53787.2023.10230707
“The diffusion model [1, 2, 3] derived from dMRI can connect the raw dMRI signal to tissue microstructure features at the cellular level [4].”
BackgroundSelf-citationPolzehl, J., & Tabelow, K. (2023) · Use R! · doi:10.1007/978-3-031-38949-8_5
Levi, R., & Politi, L. S. (2023) · European Radiology · doi:10.1007/s00330-023-10358-z
“Currently, structural connectom-ics approaches face limitations in clinical applications due to various technical challenges, including the low anatomical resolution of DTI images and the relatively high number of false-positive/false-negative tract reconstructions [10].”
Brain Connectivity Using Deep Learning Algorithms
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Assessment of U-Net in the segmentation of short tracts: transferring to clinical MRI routine
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Multimodal Neuroimaging Computing: Basics and Applications in Neurosurgery
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Self-citationMethods and statistics for diffusion MRI tractometry
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Mapping the topographic organization of the human zona incerta using diffusion MRIPreprint
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Mapping the topographic organization of the human zona incerta using diffusion MRIPreprint
Haast, R. A. M., Kai, J., Taha, A., Liu, V. M., Kasa, L. W., Gilmore, G., Guye, M., KHAN, A. R., & Lau, J. C. (2025) · eLife · doi:10.7554/elife.103530
Wu, Y., & Xu, W. (2025) · Movement Disorders · doi:10.1002/mds.30136
Diffusion-Based Gray-White Matter Mapping for Quantitative Tractography in Glioma Patients
Smolders, L., Chamberland, M., Rutten, G.-J. M., Baene, W. D., van der Hofstad, R., & Florack, L. M. J. (2025) · Lecture notes in computer science · doi:10.1007/978-3-031-86920-4_2
Diffusion neuroimaging of speech acquisition in infants
Liu, F., Liu, J., Gu, J., Wang, Y., Cai, X., Wang, Z., Wu, H., Feng, J., Zhang, H., & Shen, D. G. (2026) · Communications Biology · doi:10.1038/s42003-026-10644-8
MRI and non-MRI quantifiable neuroanatomical and functional parameters are useful for tractography
Schiavi, S., Borra, E., Luca, A. D., Jones, D. K., Petit, L., & Szczupak, D. (2025) · Brain Structure and Function · doi:10.1007/s00429-025-02932-6
“In the last two decades, diffusion magnetic resonance imaging (dMRI) - derived tractography has progressively become a cornerstone in mapping the brain’s white matter pathways (Dell’Acqua et al. 2024; Jeurissen et al. 2017; Rheault et al. 2020; Yeh et al. 2020; Zhang et al. 2022).”
Self-citationHowell, A. M., Warrington, S., Fonteneau, C., Cho, Y., Sotiropoulos, S. N., Murray, J. D., & Anticevic, A. (2025) · eLife · doi:10.7554/elife.95018.2
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A new gradient-based method for analyzing brain white matter fiber geometry
Qin, J., Dong, W., Ni, H., Wu, Y., Liu, H., Yao, Z., & Lü, Q. (2025) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2025.110538
APOE Polymorphism and Brain Imaging
Obenaus, A., & Territo, P. R. (2025) · Springer eBooks · doi:10.1007/978-3-031-52641-1_69-1
Yao, Y., Ai, L., & Yao, R. (2025) · Magnetic Resonance in Medicine · doi:10.1002/mrm.70025
A simulator for the validation of tractography-based cortical surface parcellations
Poo, E., Molina, J., Mangin, J., Hernández, C., & Guevara, P. (2025) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2025.110891
Rauland, A., Meisler, S. L., Alexander‐Bloch, A. F., Bagautdinova, J., Baller, E. B., Gur, R. E., Gur, R. C., Luo, A. C., Moore, T. M., Popovych, O. V., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.02.673635
“…diffusion of water molecules and is the key modality for non-invasively estimating white matter (WM) microstructural tissue properties (Alexander et al., 2019; Le Bihan et al., 2001) and reconstructing WM fiber pathways using tractography algorithms (Jeurissen et al., 2019; F. Zhang et al., 2022).”
Charting the Normal Development of Structural Brain Connectivity in Utero Using Diffusion MRI
Karimi, D., Li, B., Taymourtash, A., Jaimes, C. E., Grant, P. E., & Warfield, S. K. (2026) · Human Brain Mapping · doi:10.1002/hbm.70609
“These stream-lines, typically weighted based on measures of tissue microstructure integrity or fiber bundle capacity, determine the strength of connections between the regions to compute a structural connectome (Smith et al. 2022; Zhang et al. 2022; Sotiropoulos and Zalesky 2019).”
Cacciaglia, R. (2025) · Neurology · doi:10.1212/wnl.0000000000214189
Qin, J., Dong, W., Ni, H., Yao, Z., Lu, Q. H., & Wu, Y. (2025) · Lecture notes in computer science · doi:10.1007/978-3-032-05169-1_43
Rominger, C., Koschutnig, K., Fink, A., & Perchtold‐Stefan, C. M. (2025) · NeuroImage · doi:10.1016/j.neuroimage.2025.121480
Tractography-based transcranial magnetic stimulation prediction using machine learningPreprint
Betioli, L. D. S., Matsuda, R. H., Marchetti, T. C., Rondinoni, C., Moraes, V. H., Júnior, M. A. D. C., Salmón, C. E. G., Tinós, R., & Baffa, O. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.11.685674
Transcriptomic divergence of network hubs in the prenatal human brain
Oldham, S., & Ball, G. (2025) · Communications Biology · doi:10.1038/s42003-025-08962-4 · Cited by 6
“We identi fi ed several hub genes with pathogenic variants linked to NDDs, including AFF2, GNAO1, and RTTN, but only weak enrichment of GWAS loci associated with ASD and SCZ.”
Fast cortical oscillations as a potential network mechanism for language processing
Traub, R. D., Cunningham, M. O., Maier, N., & Draguhn, A. (2025) · Reviews in the Neurosciences · doi:10.1515/revneuro-2025-0124
“The anatomy of fasciculi can be studied “ in bulk ” with a technique called tractography that uses MRI in living subjects (Basser et al. 1994; Mori and van Zijl 2002; Zhang et al. 2022).”
Hüttebräucker, T., Planchuelo-Gómez, Á., García‐Azorín, D., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3154214/v1
Macroscopic and microscopic imaging in neuroanatomical research
Nurein, M. A., & Gasmalla, H. E. E. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-13635-1.00008-0
Structural network topology and cognitive control in very preterm born young adults
Marek, M. J., Dieter Wolke, C., Sorg, C., Wendt, J., Menegaux, A., Hedderich, D. M., Bartmann, P., Burkhardt, M., Hildebrandt, A., & Heep, A. (2026) · NeuroImage Clinical · doi:10.1016/j.nicl.2026.103952 · Cited by 1
Geometric–Semantic Harmony: A Dual-Student Framework for One-Shot White-Matter Tract Segmentation
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Gao, X., Hui, T., Yin, X., et al. (2026) · Sensors · doi:10.3390/s26031068
“After that, several studies on enhancing direct volumetric tract segmentation have been conducted, as reviewed and discussed in [5,8].”
Similar minds age alike: an MRI similarity approach for predicting age-related cognitive decline
Gerbolés, B. Z., Sun, J., Pineda, J. D., Volpe, G., Mijalkov, M., & Pereira, J. B. (2026) · npj Aging · doi:10.1038/s41514-026-00345-1 · Cited by 1
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“In this study, we focus on FA and the number of stream-lines (NoS) measures, which are sensitive to the changes in the underlying cellular microstructure in brain tissues [10] .”
Self-citationBisten, J., von Bornhaupt, V., Gruen, J., Bauer, T., Rüber, T., & Schultz, T. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1168
Liao, A., Liu, Q., Li, Z., & Zhao, L. (2026) · Journal of Psychiatry and Brain Science · doi:10.20900/jpbs.20260003
“Structural brain connectivity, which refers to the anatomical connections between different brain regions through neural fiber bundles, is considered vital in the pathogenesis of psychiatric disorders [3,4].”
Luo, J., Zeng, X., Xiong, Y., Xu, Y., Zhou, C., Wang, Y., Yao, D., & Guo, D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.19.712967
“…considered three complementary metrics: synaptic density estimated using positron emission tomography (PET) with the synapse-specific radioligand [ 11 C]UCB-J, synaptic development indexed by the cortical dis-254 ) To further probe the synaptic basis of this gradient in vivo , multiple linear…”
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“…communication capacity of each tract (39–41) and microstructural indices provide an index of myelination and microscopic changes in the processes that extend from neurons (40,42,43) with changes in neurite density reflecting disrupted axonal integrity within the mesolimbic white matter pathways.”
Cognitive performance after stroke at a young age from a brain network perspective
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“As a result, clear and unambiguous lines are obtained showing the course of nerve pathways [12,13].”
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“Compared to the other methods, TractSeg appeared to involve larger sections of the medial fibres of the arcuate fasciculus (Wasserthal et al., 2019; Zhang et al., 2022).”
Haotian, Y., Guo, B., He, J., Sochen, N., Pasternak, O., O’Donnell, L. J., & Zhang, F. (2026) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi61048.2026.11515809
“It is an important neuroimaging tool to quantify the brain’s wiring diagram in health and disease [2].”
Self-citationKazi, A., Mora, J., Fischl, B. R., Dalca, A. V., & Aganj, I. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1786355
“…connectome provides insight into neural circuitry, connectivity patterns, and their implications for cognition and behavior, contributing to our understanding of brain development, aging, and the impact of neurological conditions on brain wiring (Hagmann et al., 2008; Zhang et al., 2022).”
Toward CT-based Tractography: Presurgical White Matter Tract Mapping in Intracerebral HemorrhagePreprint
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Multimodal Branched Transport Infers Anatomically Aligned Brain Reaction Maps
Mendico, C. (2026) · Neuroinformatics · doi:10.1007/s12021-026-09791-4
“Instead of postulating a generic transport metric, we derive a geometry-aware cost from tractography-informed anisotropy [10, 17, 18].”
Advances in diffusion MRI in multiple sclerosis
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“…magnetic resonance imaging (dMRI) is the only non-invasive method that can be used to quantify and reconstruct the brain’s structural connections (Zhang et al. 2022 ). dMRI measures the magnitude and directionality of water molecule movement in 3D space, enabling the map - ping of cerebellar…”
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“Diffusion MRI (dMRI) is an advanced imaging technique that enables the quantification of tissue microstructural features [ 1 ] and in vivo mapping of white matter (WM) fiber tracts [ 2 ] through fiber tractography.”
Self-citationGraph-Based White Matter Tractometry: Methods, Applications, and the Path to Validation
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“…analyses of white matter typically relied on region-of-interest averaging or voxel-wise comparisons, which provided useful group-level insights but offered limited ability to localize microstructural altera - tions along specific anatomical pathways (Ly et al., 2015; Zhang et al., 2022).”
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Functional reorganization of the visual cortex in blindness: a connectivity perspective
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The pathophysiology of depression in Huntington’s disease
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What's a White Matter 'Fiber'?
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Metadata
- Authors
- Zhang, F., Daducci, A., He, Y., Schiavi, S., Seguin, C., Smith, R. E., Yeh, C.-H., Zhao, T., & O’Donnell, L. J.
- Affiliations
- Brigham and Women's Hospital (US)
- University of Verona (IT)
- The University of Sydney (AU)
- The University of Melbourne (AU)
- Chang Gung University (TW)
- Beijing Normal University (CN)
- Corresponding author
- Zhang, Fan
- O’Donnell, Lauren J.
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2022-04
- Volume
- 249
- Pages
- 118870
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC9257891
- OpenAlex
- W4205798776
- Semantic Scholar
- 76c276c32a8fd376256c5061e0b0d1f8cbbb44a0
- Cited by
- 302
- References
- 598
- Citations by year
- 2026: 57 · 2025: 88 · 2024: 71 · 2023: 58 · 2022: 24
- FWCI
- 31.00
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- NeuroImage (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- arXiv (Cornell University) (submittedVersion)
- PubMed Central (submittedVersion, cc-by-nc-nd)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Minerva Access (University of Melbourne) (submittedVersion, cc-by-nc-nd)
- arXiv (Cornell University)
- Funders
- Ministry of Science and Technology, Taiwan (109-2222-E-182-001-MY3)
- National Natural Science Foundation of China (81620108016, 81801783)
- National Institutes of Health (P41EB015902, R01MH074794, R01MH119222, R01MH125860)
- National Imaging Facility
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Clinical Neurology › Cerebrovascular and genetic disorders
- Keywords
- diffusion MRI tractography, structural connectivity, white matter, connectome, white matter microstructure, brain development, brain aging, neurological disorders, mental illness, neurosurgery, method comparison
- MeSH terms
- Brain, Humans, Nerve Net, Diffusion Tensor Imaging
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