The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Cell diversity and network dynamics in photosensitive human brain organoids
Open accessAbstract
In vitro models of the developing brain such as three-dimensional brain organoids offer an unprecedented opportunity to study aspects of human brain development and disease. However, the cells generated within organoids and the extent to which they recapitulate the regional complexity, cellular diversity and circuit functionality of the brain remain undefined. Here we analyse gene expression in over 80,000 individual cells isolated from 31 human brain organoids. We find that organoids can generate a broad diversity of cells, which are related to endogenous classes, including cells from the cerebral cortex and the retina. Organoids could be developed over extended periods (more than 9 months), allowing for the establishment of relatively mature features, including the formation of dendritic spines and spontaneously active neuronal networks. Finally, neuronal activity within organoids could be controlled using light stimulation of photosensitive cells, which may offer a way to probe the functionality of human neuronal circuits using physiological sensory stimuli.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“hiPSC-derived astrocytes, which can be generated with a fast protocol in 2D layers104 or integrated in 3D systems such as spheroids and organoids105–108”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [107]
In the citing paper
“Some protocols build on the principles of spontaneous neural induction by using medium that is free of neural induction signalling molecules2,27. This promotes the generation of diverse brain regions and cell populations2,28,29.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Apart from growth factor cues, other modulators — such as scaffold support provided by the extracellular matrix — are important features of current protocols2,5,28.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Although such regional diversity is appealing, it also leads to a relatively variable outcome and the differentiation of some cells into non-ectodermal cell types28,29.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“One important issue is that organoids derived from the same cell line under the same conditions can often produce tissues with different regional identities and spatial and cellular heterogeneity28,29.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“A recent paper used droplet-based single-cell mRNA sequencing to analyse gene expression in 80,000 cells from 31 brain organoids after 3 and 6 months in vitro28. Using principal component analysis, 10 distinct populations of cells (clusters) were identified in 6-month old organoids.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“As one might expect, 6-month-old organoids presented a greater diversity of cell types than 3-month-old organoids, as well as enrichment of genes associated with neuronal and glial maturation.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Recently, it was demonstrated that photosensitive cells in retinal-like regions of brain organoids can respond to light28.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Also, the authors observed that some cell types were only produced by a subset of organoids and that organoids grown in the same bioreactor tended to be similar in terms of their ability to make cells of each cluster, suggesting that batch effects and local microenvironments are important in patterning and possibly that organoids secrete signalling factors that influence sister organoids.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“In addition to these findings, electrophysiological studies have demonstrated functional synapses in several brain organoid models25,28, and electron microscopy has confirmed the presence of structurally defined synaptic junctions28.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“Several reports suggest that long-term organoid culture can improve the correlation between the molecular signatures of organoid and endogenous cells28,52.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“For example, a large number of cells were assigned to a mesodermal lineage, emphasizing the variability inherent in the protocol.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [28]
In the citing paper
“These initial reports identified striking parallels among organoid development, human primary tissue and in vivo organogenesis”
From The organoid cell atlas (2021) · cites this paper as [10]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
(2008) · Journal of Machine Learning Research · Cited by 33,051
DAVID: Database for Annotation, Visualization, and Integrated Discovery
Dennis, G., Sherman, B. T., Hosack, D. A., Yang, J., Gao, W., Lane, H. C., & Lempicki, R. A. (2003) · Genome Biology · doi:10.1186/gb-2003-4-5-p3 · Cited by 9,327
Highly parallel genome-wide expression profiling of individual cells using nanoliter droplets.
Macosko, E. Z., Basu, A., Satija, R., Nemesh, J., Shekhar, K., Goldman, M., Tirosh, I., Bialas, A. R., Kamitaki, N., Martersteck, E. M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.05.002 · Cited by 7,110
Self-citationSpatial reconstruction of single-cell gene expression data
Satija, R., Farrell, J. A., Gennert, D., Schier, A. F., & Regev, A. (2015) · Nature Biotechnology · doi:10.1038/nbt.3192 · Cited by 7,055
Cerebral organoids model human brain development and microcephaly
Lancaster, M. A., Renner, M., Martin, C.-A., Wenzel, D., Bicknell, L. S., Hurles, M. E., Homfray, T., Penninger, J. M., Jackson, A. P., & Knoblich, J. A. (2013) · Nature · doi:10.1038/nature12517 · Cited by 5,372
Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875 · cited 1×
“Cluster c9 (17,103 cells) contained progenitors of neuroepithelial origin, including cells with an oligodendrocyte-precursor-like identity 20,26 .”
BackgroundCahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Zhang, Y., Sloan, S. A., Clarke, L. E., Caneda, C., Plaza, C. A., Blumenthal, P. D., Vogel, H., Steinberg, G. K., Edwards, M. S. B., Li, G., et al. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.013 · Cited by 2,295
Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure
Qian, X., Nguyen, H. N., Song, M. M., Hadiono, C., Ogden, S. C., Hammack, C., Yao, B., Hamersky, G. R., Jacob, F., Zhong, C., et al. (2016) · Cell · doi:10.1016/j.cell.2016.04.032 · Cited by 2,127
Generation of cerebral organoids from human pluripotent stem cells
Lancaster, M. A., & Knoblich, J. A. (2014) · Nature Protocols · doi:10.1038/nprot.2014.158 · Cited by 1,823
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 997
Organoids: A new approach in toxicity testing of nanotherapeutics
Nabi, S. U., Ali, S. I., Rather, M. A., Sheikh, W. M., Altaf, M., Singh, H., Mumtaz, P. T., Mishra, N. C., Nazir, S. U., & Bashir, S. M. (2021) · Journal of Applied Toxicology · doi:10.1002/jat.4206 · Cited by 47
Advancing preclinical models of psychiatric disorders with human brain organoid cultures
Dixon, T. A., & Muotri, A. R. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01708-2 · Cited by 49
Zhang, Z., Wang, X., Park, S. S., Song, H., & Ming, G. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.12.015 · Cited by 49
Engineered 3D immuno-glial-neurovascular human miBrain model
Stanton, A. E., Bubnys, A., Agbas, E., James, B. T., Park, D. S., Jiang, A. Y. L., Pinals, R. L., Liu, L., Truong, N., Loon, A. R., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2511596122 · Cited by 51
Models for discovery of targeted therapy in genetic epileptic encephalopathies
Maljevic, S., Reid, C. A., & Petrou, S. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14134 · Cited by 46
Functional and Sustainable 3D Human Neural Network Models from Pluripotent Stem Cells
Cantley, W. L., Du, C., Lomoio, S., DePalma, T. J., Peirent, E. R., Kleinknecht, D., Hunter, M., Tang‐Schomer, M. D., Tesco, G., & Kaplan, D. L. (2018) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b00622 · Cited by 48
Podoplanin regulates the migration of mesenchymal stromal cells and their interaction with platelets
Ward, L. S. C., Sheriff, L., Marshall, J. L., Manning, J. E., Brill, A. G., Nash, G. B., & McGettrick, H. M. (2019) · Journal of Cell Science · doi:10.1242/jcs.222067 · Cited by 44
Layer-By-Layer: The Case for 3D Bioprinting Neurons to Create Patient-Specific Epilepsy Models
Antill‐O'Brien, N., Bourke, J., & O’Connell, C. D. (2019) · Materials · doi:10.3390/ma12193218 · Cited by 49
Modeling human neurodevelopmental diseases with brain organoids
Lu, X., Yang, J., & Xiang, Y. (2022) · Cell Regeneration · doi:10.1186/s13619-021-00103-6 · Cited by 50
Principles for the design of multicellular engineered living systems
Aydin, O., Passaro, A. P., Raman, R., Spellicy, S. E., Weinberg, R. P., Kamm, R. D., Sample, M., Truskey, G. A., Zartman, J. J., Dar, R. D., et al. (2022) · APL Bioengineering · doi:10.1063/5.0076635 · Cited by 46
Bejoy, J., Wang, Z., Bijonowski, B., Yang, M., Ma, T., Sang, Q.-X., & Li, Y. (2018) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b01142 · Cited by 46
Makrygianni, E. A., & Chrousos, G. P. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.621970 · Cited by 49
Optimization of cerebral organoids: a more qualified model for Alzheimer’s disease research
Bi, F.-C., Yang, X.-H., Cheng, X.-Y., Deng, W.-B., Guo, X.-L., Yang, H., Wang, Y., Li, J., & Yao, Y. (2021) · Translational Neurodegeneration · doi:10.1186/s40035-021-00252-3 · Cited by 49
Renner, H., Schöler, H. R., & Bruder, J. M. (2021) · Movement Disorders · doi:10.1002/mds.28775 · Cited by 47
Pagliaro, A., Finger, R., Zoutendijk, I., Bunschuh, S., Clevers, H. C., Hendriks, D. F. G., & Artegiani, B. (2023) · Nature Communications · doi:10.1038/s41467-023-43141-1 · Cited by 53
Ramani, A., Pasquini, G., Gerkau, N. J., Jadhav, V., Vinchure, O. S., Altinisik, N., Windoffer, H., Muller, S. M., Rothenaigner, I., Lin, S., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-55226-6 · Cited by 51
Krefft, O., Jabali, A., Iefremova, V., Koch, P., & Ladewig, J. (2018) · Journal of Visualized Experiments · doi:10.3791/56768 · Cited by 53
Brain Organoids—A Bottom-Up Approach for Studying Human Neurodevelopment
Karzbrun, E., & Reiner, O. (2019) · Bioengineering · doi:10.3390/bioengineering6010009 · Cited by 45
Experimental and Computational Methods for the Study of Cerebral Organoids: A Review
Poli, D., Magliaro, C., & Ahluwalia, A. D. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00162 · Cited by 47
Early Actions of Neurotransmitters During Cortex Development and Maturation of Reprogrammed Neurons
Ojeda, J., & Ávila, A. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00033 · Cited by 48
Human-Specific Genes, Cortical Progenitor Cells, and Microcephaly
Heide, M., & Huttner, W. Β. (2021) · Cells · doi:10.3390/cells10051209 · Cited by 46
Recent Trends and Perspectives in Cerebral Organoids Imaging and Analysis
Martin, C. B., Simon-Chane, C., Clouchoux, C., & Histace, A. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.629067 · Cited by 41
Current progress of cerebral organoids for modeling Alzheimer's disease origins and mechanisms
Sreenivasamurthy, S., Laul, M., Zhao, N., Kim, T., & Zhu, D. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10378 · Cited by 49
Yıldırım, M., Delepine, C., Feldman, D., Pham, V. A., Chou, S., Ip, J. P. K., Nott, A., Tsai, L., Ming, G., So, P. T. C., et al. (2022) · eLife · doi:10.7554/elife.78079 · Cited by 45
Human tau mutations in cerebral organoids induce a progressive dyshomeostasis of cholesterol
Glasauer, S. M. K., Goderie, S. K., Rauch, J. N., Guzman, E., Audouard, M., Bertucci, T., Joy, S., Rommelfanger, E., Luna, G., Keane-Rivera, E., et al. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.07.011 · Cited by 46
Stem Cell–Based Organoid Models of Neurodevelopmental Disorders
Wang, L., Owusu-Hammond, C., Sievert, D., & Gleeson, J. G. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.01.012 · Cited by 44
The Application of Biomaterials to Tissue Engineering Neural Retina and Retinal Pigment Epithelium
Hunt, N. C., Hallam, D., Chichagova, V., STEEL, D. H., & Lako, M. (2018) · Advanced Healthcare Materials · doi:10.1002/adhm.201800226 · Cited by 45
Minocycline mitigates the effect of neonatal hypoxic insult on human brain organoids
Boisvert, E. M., Means, R. E., Michaud, M., Madri, J. A., & Katz, S. G. (2019) · Cell Death & Disease · doi:10.1038/s41419-019-1553-x · Cited by 45
Retinogenesis of the Human Fetal Retina: An Apical Polarity Perspective
Quinn, P. M. J., & Wijnholds, J. (2019) · Genes · doi:10.3390/genes10120987 · Cited by 48
Application of Fused Organoid Models to Study Human Brain Development and Neural Disorders
Chen, A., Guo, Z., Fang, L., & Bian, S. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00133 · Cited by 45
Lo, L. H.-Y., & Lai, K. (2020) · Molecular Autism · doi:10.1186/s13229-020-00349-y · Cited by 47
Human Brain Organoid Models of Developmental Epilepsies
Nieto‐Estévez, V., & Hsieh, J. (2020) · Epiliepsy currents/Epilepsy currents · doi:10.1177/1535759720949254 · Cited by 44
Recent advances in organoid engineering: A comprehensive review
Unagolla, J. M., & Jayasuriya, A. C. (2022) · Applied Materials Today · doi:10.1016/j.apmt.2022.101582 · Cited by 44
Toward the next generation of vascularized human neural organoids
Li, M., Gao, L., Zhao, L., Zou, T., & Xu, H. (2022) · Medicinal Research Reviews · doi:10.1002/med.21922 · Cited by 45
Image-Based Profiling of Synaptic Connectivity in Primary Neuronal Cell Culture
Verstraelen, P., Dyck, M. V., Verschuuren, M., Kashikar, N. D., Nuydens, R., Timmermans, J., & Vos, W. H. D. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00389 · Cited by 48
Human in vitro models for understanding mechanisms of autism spectrum disorder
Gordon, A., & Geschwind, D. H. (2020) · Molecular Autism · doi:10.1186/s13229-020-00332-7 · Cited by 45
Increased connectivity of hiPSC-derived neural networks in multiphase granular hydrogel scaffolds
Hsu, C., George, J. H., Waller, S., Besnard, C., Nagel, D. A., Hill, E. J., Coleman, M. D., Korsunsky, A. M., Cui, Z., & Ye, H. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.07.008 · Cited by 44
Recent Advances in Electrophysiological Recording Platforms for Brain and Heart Organoids
Chung, W. G., Kim, E., Song, H., Lee, J., Lee, S., Lim, K., Jeong, I., & Park, J. (2022) · Advanced NanoBiomed Research · doi:10.1002/anbr.202200081 · Cited by 42
Atomically thin bioelectronics
Kireev, D., Kutagulla, S., Hong, J., Wilson, M. N., Ramezani, M., Kuzum, D., Ahn, J., & Akinwande, D. (2024) · Nature Reviews Materials · doi:10.1038/s41578-024-00728-4 · Cited by 43
Moroz, L. L. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00100 · Cited by 41
Yang, G., & Shcheglovitov, A. (2019) · Developmental Dynamics · doi:10.1002/dvdy.100 · Cited by 46
Three-dimensional testicular organoids as novel in vitro models of testicular biology and toxicology
Sakib, S., Voigt, A. L., Goldsmith, T., & Dobrinski, I. (2019) · Current Zoology · doi:10.1093/eep/dvz011 · Cited by 45
Romero-Morales, A. I., O’Grady, B. J., Balotin, K. M., Bellan, L. M., Lippmann, E. S., & Gama, V. (2019) · HardwareX · doi:10.1016/j.ohx.2019.e00084 · Cited by 45
Ciarpella, F., Zamfir, R. G., Campanelli, A., Ren, E., Pedrotti, G., Bottani, E., Borioli, A., Caron, D., Chio, M. D., Dolci, S., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103438 · Cited by 47
Wan, J., Zhou, S., Mea, H. J., Guo, Y., Ku, H., & Urbina, B. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00480 · Cited by 45
SHANK3 deficiency leads to myelin defects in the central and peripheral nervous system
Malara, M., Lutz, A.-K., Incearap, B., Bauer, H. F., Cursano, S., Volbracht, K., Lerner, J. J., Pandey, R., Delling, J. P., Ioannidis, V., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04400-4 · Cited by 49
Applications of organoid technology to brain tumors
Wen, J., Liu, F., Cheng, Q., Weygant, N., Liang, X., Fan, F., Li, C., Zhang, L., & Liu, Z. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14272 · Cited by 44
Using brain organoids to study human neurodevelopment, evolution and disease
Kyrousi, C., & Cappello, S. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.347 · Cited by 41
The Emergence of Stem Cell‐Based Brain Organoids: Trends and Challenges
Gopalakrishnan, J. (2019) · BioEssays · doi:10.1002/bies.201900011 · Cited by 44
Recent advances in understanding neocortical development
Borrell, V. (2019) · F1000Research · doi:10.12688/f1000research.20332.1 · Cited by 44
iPSCs-Based Neural 3D Systems: A Multidimensional Approach for Disease Modeling and Drug Discovery
Costamagna, G., Andreoli, L., Corti, S. P., & Faravelli, I. (2019) · Cells · doi:10.3390/cells8111438 · Cited by 40
Omics Approach to Axonal Dysfunction of Motor Neurons in Amyotrophic Lateral Sclerosis (ALS)
Suzuki, N., Akiyama, T., Warita, H., & Aoki, M. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00194 · Cited by 46
Rosa, F., Dhingra, A., Uysal, B., Mendis, G. D. C., Loeffler, H., Elsen, G. E., Mueller, S., Schwarz, N., Castillo-Lizardo, M., Cuddy, C., et al. (2020) · Stem Cell Reports · doi:10.1016/j.stemcr.2020.05.015 · Cited by 40
Patient-Derived Midbrain Organoids to Explore the Molecular Basis of Parkinson's Disease
Galet, B., Cheval, H., & Ravassard, P. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.01005 · Cited by 47
Human retinal model systems: Strengths, weaknesses, and future directions
Eldred, K. C., & Reh, T. A. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.09.001 · Cited by 41
Generation of ‘semi-guided’ cortical organoids with complex neural oscillations
Fitzgerald, M. Q., Chu, T., Puppo, F., Blanch, R., Chillón, M., Subramaniam, S., & Muotri, A. R. (2024) · Nature Protocols · doi:10.1038/s41596-024-00994-0 · Cited by 45
Effective cryopreservation of human brain tissue and neural organoids
Xue, W., Li, H., Jin-hong, X., Yu, X., Liu, L., Liu, H., Zhao, R., & Shao, Z. (2024) · Cell Reports Methods · doi:10.1016/j.crmeth.2024.100777 · Cited by 41
Bringing Renal Biopsy Interpretation Into the Molecular Age With Single-Cell RNA Sequencing
Malone, A. F., Wu, H., & Humphreys, B. D. (2017) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2017.09.005 · Cited by 43
Bioengineering tissue morphogenesis and function in human neural organoids
Fedorchak, N. J., Iyer, N. R., & Ashton, R. S. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.05.025 · Cited by 41
Region Specific Brain Organoids to Study Neurodevelopmental Disorders
Susaimanickam, P. J., Kiral, F. R., & Park, I. (2022) · International Journal of Stem Cells · doi:10.15283/ijsc22006 · Cited by 47
Human iPSC application in Alzheimer’s disease and tau-related neurodegenerative diseases
TCW, J. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.01.043 · Cited by 39
Yang, Y., Yang, R., Kang, B., Qian, S., He, X., & Zhang, X. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113335 · Cited by 41
Translational potential of human brain organoids
Sun, A. X., Ng, H., & Tan, E. (2018) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.505 · Cited by 45
Recapitulating developmental mechanisms for retinal regeneration
Ahmad, I., Teotia, P., Erickson, H. E., & Xia, X. (2019) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2019.100824 · Cited by 42
Deconstructing and reconstructing the human brain with regionally specified brain organoids
Xiang, Y., Çakır, B., & Park, I. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.05.023 · Cited by 39
Panoutsopoulos, A. A. (2020) · The Neuroscientist · doi:10.1177/1073858420960112 · Cited by 42
Human neural organoids: Models for developmental neurobiology and disease
Guy, B., Zhang, J. S., Duncan, L. H., & Johnston, R. J. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.06.012 · Cited by 43
Three-dimensional culture models to study glioblastoma — current trends and future perspectives
Joseph, J. V., Blaavand, M. S., Daubon, T., Kruyt, F. A. E., & Thomsen, M. K. (2021) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2021.08.019 · Cited by 42
Silk scaffolding drives self-assembly of functional and mature human brain organoids
Sozzi, E., Kajtez, J., Bruzelius, A., Wesseler, M. F., Nilsson, F., Birtele, M., Larsen, N. B., Ottosson, D. R., Storm, P., Parmar, M., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1023279 · Cited by 41
Advancing organoid design through co-emergence, assembly, and bioengineering
Tenreiro, M. F., Branco, M. A., Cotovio, J. P., Cabral, J. M. S., Fernandes, T. G., & Diogo, M. M. (2023) · Trends in biotechnology · doi:10.1016/j.tibtech.2022.12.021 · Cited by 39
Shaping the Neurovascular Unit Exploiting Human Brain Organoids
Rizzuti, M., Melzi, V., Brambilla, L., Quetti, L., Sali, L., Ottoboni, L., Meneri, M., Ratti, A., Verde, F., Ticozzi, N., et al. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-03998-9 · Cited by 41
A 3D bioprinted cortical organoid platform for modeling human brain development
Cadena, M. A., Sing, A., Taylor, K., Jin, L., Ning, L., Salar Amoli, M., Singh, Y., Lanjewar, S. N., Tomov, M. L., Serpooshan, V., et al. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202401603 · Cited by 39
Fagiani, F., Pedrini, E., Taverna, S., Brambilla, E., Murtaj, V., Podini, P., Ruffini, F., Butti, E., Braccia, C., Andolfo, A., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101680 · Cited by 45
Biomaterial-assisted organoid technology for disease modeling and drug screening
Shao, Y., Wang, J., Jin, A., Jiang, S., Lei, L., & Liu, L. (2024) · Materials Today Bio · doi:10.1016/j.mtbio.2024.101438 · Cited by 45
Progress in iPSC-Based Modeling of Psychiatric Disorders
Hoffmann, A., Ziller, M. J., & Spengler, D. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194896 · Cited by 39
Dingle, Y. L., Liaudanskaya, V., Finnegan, L. T., Berlind, K., Mizzoni, C., Georgakoudi, I., Nieland, T. J. F., & Kaplan, D. L. (2020) · iScience · doi:10.1016/j.isci.2020.101434 · Cited by 39
A Perspective on Organoids for Virology Research
Sridhar, A., Simmini, S., Ribeiro, C. M. S., Tapparel, C., Evers, M. M., Pajkrt, D., & Wolthers, K. C. (2020) · Viruses · doi:10.3390/v12111341 · Cited by 37
Harnessing cerebral organoids for Alzheimer's disease research
Bubnys, A., & Tsai, L. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.10.003 · Cited by 41
Birtele, M., Sharma, Y., Storm, P., Kajtez, J., Wahlestedt, J. N., Sozzi, E., Nilsson, F., Stott, S., He, X., Mattsson, B., et al. (2022) · Development · doi:10.1242/dev.200504 · Cited by 38
Integrative inference of brain cell similarities and differences from single-cell genomicsPreprint
Welch, J. D., Kozareva, V., Ferreira, A. N., Vanderburg, C. R., Martin, C., & Macosko, E. Z. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/459891 · Cited by 40
Self-citationRetinal Organoids and Retinal Prostheses: An Overview
Bellapianta, A., Cetkovic, A., Bolz, M., & Salti, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23062922 · Cited by 40
Tai, D. J. C., Razaz, P., Erdin, S., Gao, D., Wang, J. P., Nuttle, X., de Esch, C. E., Collins, R. L., Currall, B., O’Keefe, K., et al. (2022) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2022.08.012 · Cited by 39
D’Antoni, C., Mautone, L., Sanchini, C., Tondo, L., Grassmann, G., Cidonio, G., Bezzi, P., Cordella, F., & Angelantonio, S. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310762 · Cited by 41
Engineering brain-on-a-chip platforms
Servais, B., Mahmoudi, N., Gautam, V., Tong, W., Ibbotson, M. R., Nisbet, D. R., & Collins, D. J. (2024) · Nature Reviews Bioengineering · doi:10.1038/s44222-024-00184-3 · Cited by 44
Mancinelli, S., & Lodato, S. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.08.001 · Cited by 38
Modeling genetic epilepsies in a dish
Niu, W., & Parent, J. M. (2019) · Developmental Dynamics · doi:10.1002/dvdy.79 · Cited by 38
Brüll, M. (2020) · ALTEX · doi:10.14573/altex.1911111 · Cited by 44
Can lab-grown brains become conscious?
Reardon, S. (2020) · Nature · doi:10.1038/d41586-020-02986-y · Cited by 38
Lutz, A.-K., Arévalo, A. P., Ioannidis, V., Stirmlinger, N., Demestre, M., Delorme, R., Bourgeron, T., & Boeckers, T. M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.773571 · Cited by 38
Research models of neurodevelopmental disorders: The right model in the right place
Damianidou, E., Mouratidou, L., & Kyrousi, C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1031075 · Cited by 41
Organotypic brain explant culture as a drug evaluation system for malignant brain tumors
Minami, N., Maeda, Y., Shibao, S., Arima, Y., Ohka, F., Kondo, Y., Maruyama, K., Kusuhara, M., Sasayama, T., Kohmura, E., et al. (2017) · Cancer Medicine · doi:10.1002/cam4.1174 · Cited by 35
Modeling Alzheimer’s disease with human iPS cells: advancements, lessons, and applications
Essayan-Perez, S., Zhou, B., Nabet, A. M., Wernig, M., & Huang, Y. A. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104503 · Cited by 40
Toward three-dimensional in vitro models to study neurovascular unit functions in health and disease
Robert, J., Caffrey, T. M., & Button, E. B. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.310671 · Cited by 37
Tools for studying human microglia: In vitro and in vivo strategies
Warden, A. S., Han, C. Z., Hansen, E. A., Trescott, S., Nguyen, C. T., Kim, R. Y., Schafer, D. M., Johnson, A., Wright, M., Ramírez, G., et al. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.10.008 · Cited by 38
Advances in current in vitro models on neurodegenerative diseases
Pereira, I., Lopez-Martinez, M. J., & Samitier, J. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1260397 · Cited by 35
Cerebral organoids display dynamic clonal growth and tunable tissue replenishment
Lindenhofer, D., Haendeler, S., Esk, C., Littleboy, J. B., Avalos, C. B., Naas, J., Pflug, F., van de Ven, E. G. P., Reumann, D., Baffet, A. D., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01412-z · Cited by 36
Zhang, Y., Tang, C., He, Y., Zhang, Y., Li, Q., Zhang, T., Zhao, B., Tong, A., Zhong, Q., & Zhong, Z. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117540 · Cited by 36
Exploring human brain development and disease using assembloids
Wu, S., & Nowakowski, T. J. (2025) · Neuron · doi:10.1016/j.neuron.2025.02.010 · Cited by 36
Generation and Fusion of Human Cortical and Medial Ganglionic Eminence Brain Organoids
Xiang, Y., Tanaka, Y., Patterson, B., Çakır, B., Kim, K., Cho, Y. S., & Park, I. (2018) · Current Protocols in Stem Cell Biology · doi:10.1002/cpsc.61 · Cited by 37
Blair, J. D., & Bateup, H. S. (2019) · Developmental Dynamics · doi:10.1002/dvdy.60 · Cited by 37
Metadata
- Authors
- Quadrato, G., Nguyen, T., Macosko, E. Z., Sherwood, J. L., Min Yang, S., Berger, D. R., Maria, N., Scholvin, J., Goldman, M., Kinney, J. P., Boyden, E. S., Lichtman, J. W., Williams, Z. M., McCarroll, S. A., & Arlotta, P.
- Affiliations
- Broad Institute (US)
- Harvard University (US)
- Leaflabs (United States) (US)
- McGovern Institute for Brain Research (US)
- Corresponding author
- Quadrato, Giorgia
- Arlotta, Paola
- ORCID
- Venue
- Nature
- Published
- 2017-04-26
- Volume
- 545
- Issue
- 7652
- Pages
- 48-53
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5659341
- OpenAlex
- W2609844460
- Cited by
- 1,321
- References
- 45
- Citations by year
- 2026: 118 · 2025: 131 · 2024: 167 · 2023: 131 · 2022: 162 · 2021: 168 · 2020: 178 · 2019: 137 · 2018: 91 · 2017: 35
- FWCI
- 51.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-sa)
- Funders
- National Institute of Mental Health (P50MH094271)
- National Institute of Neurological Disorders and Stroke (DP1NS087724, R01NS073124)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Keywords
- human brain organoids, cellular diversity, neuronal network dynamics, spontaneous neuronal activity, photostimulation, dendritic spines, cortical development, retinal development, single-cell gene expression, pluripotent stem cell differentiation, interneuron migration, synaptogenesis
- MeSH terms
- Brain, Cell Line, Cell Separation, Cerebral Cortex, Dendrites, Humans, Light, Nerve Net, Neural Pathways, Organ Specificity, Organoids, Retina, Time Factors, Sequence Analysis, RNA, Photoreceptor Cells, Vertebrate, Gene Expression Profiling, Pluripotent Stem Cells, Neurogenesis, Single-Cell Analysis, Transcriptome, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review