The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.
Pyramidal cell regulation of interneuron survival sculpts cortical networks
Open accessAbstract
Complex neuronal circuitries such as those found in the mammalian cerebral cortex have evolved as balanced networks of excitatory and inhibitory neurons. Although the establishment of appropriate numbers of these cells is essential for brain function and behaviour, our understanding of this fundamental process is limited. Here we show that the survival of interneurons in mice depends on the activity of pyramidal cells in a critical window of postnatal development, during which excitatory synaptic input to individual interneurons predicts their survival or death. Pyramidal cells regulate interneuron survival through the negative modulation of PTEN signalling, which effectively drives interneuron cell death during this period. Our findings indicate that activity-dependent mechanisms dynamically adjust the number of inhibitory cells in nascent local cortical circuits, ultimately establishing the appropriate proportions of excitatory and inhibitory neurons in the cerebral cortex.
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?
In the citing paper
“Moreover, preventing programmed cell death in pyramidal cells by genetically ablating the proapoptotic Bcl-2 family members Bax and Bak (Lindsten et al., 2000) from these cells is sufficient to abolish the programmed cell death of cortical interneurons (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“Consistent with this idea, increasing or decreasing the excitability of pyramidal cells using DREADDs during the period of interneuron programmed cell death respectively enhances or diminishes the survival of cortical interneurons (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“First, long-term Ca2+ imaging experiments in vivo indicate that activity levels at the onset of the cell death period predict the fate of interneurons (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“This process seems to impact all classes of interneurons (Denaxa et al., 2018; Priya et al., 2018; Wong et al., 2018) (Figure 6A).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“This is consistent with the observation that interneuron cell death occurs progressively in vivo, with early-born infragranular layer interneurons disappearing before late-born supragranular layer interneurons (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“In other words, interneurons with relatively low levels of activity immediately before the period of interneuron cell death have an increased probability of undergoing apoptosis.”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“it is perhaps not surprising that these cells play a critical role in the survival of cortical interneurons (Figure 6B).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“Second, experimentally increasing the activity of pyramidal cells (which increases interneuron survival) non-cell autonomously represses the expression of PTEN in interneurons (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“Interestingly, PTEN levels rise in cortical interneurons during the period of programmed cell death in a temporal pattern that coincides with the normal development of interneurons, transiently increasing first in infragranular layer interneurons and, subsequently, in superficial layer interneurons (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“First, genetic deletion of PTEN from postmitotic MGE-derived interneurons dramatically increases their survival (Wong et al., 2018).”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Wong et al., 2018
In the citing paper
“This observation is in line with previous findings that the excitatory identity controls the survival and wiring of local interneurons60,61.”
From Layer 4 of mouse neocortex differs in cell types and circuit organization between sensory areas (2019) · cites this paper as [61]
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
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Raza, H., John, A., & Nemmar, A. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350087 · Cited by 47,311
(1966) · Medical Entomology and Zoology · Cited by 10,293
Signal detection theory and psychophysics
Ingleby, D. (1967) · Journal of Sound and Vibration · doi:10.1016/0022-460x(67)90197-6 · Cited by 8,616
Ultrasensitive fluorescent proteins for imaging neuronal activity
Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474
Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
Datta, S. R., Dudek, H., Tao, X., Masters, S., Fu, H., Gotoh, Y., & Greenberg, M. E. (1997) · Cell · doi:10.1016/s0092-8674(00)80405-5 · Cited by 5,689
CellProfiler: image analysis software for identifying and quantifying cell phenotypes
Carpenter, A. E., Jones, T. R., Lamprecht, M. R., Clarke, C., Kang, I. H., Friman, O., Guertin, D. A., Chang, J. H., Lindquist, R. A., Moffat, J., et al. (2006) · Genome biology · doi:10.1186/gb-2006-7-10-r100 · Cited by 5,212
Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN
Stambolic, V., Suzuki, A., de la Pompa, J. L., Brothers, G. M., Mirtsos, C., Sasaki, T., Ruland, J., Penninger, J. M., Siderovski, D. P., & Mak, T. W. (1998) · Cell · doi:10.1016/s0092-8674(00)81780-8 · Cited by 2,551
Neocortical excitation/inhibition balance in information processing and social dysfunction
Yizhar, O., Fenno, L. E., Prigge, M., Schneider, F., Davidson, T. J., O’Shea, D. J., Sohal, V. S., Goshen, I., Finkelstein, J., Paz, J. T., et al. (2011) · Nature · doi:10.1038/nature10360 · Cited by 2,454
Regulation of neuronal survival by the serine-threonine protein kinase Akt
Dudek, H., Datta, S. R., Franke, T. F., Birnbaum, M. J., Yao, R., Cooper, G. M., Segal, R. A., Kaplan, D. R., & Greenberg, M. E. (1997) · Science · doi:10.1126/science.275.5300.661 · Cited by 2,436
Cited by
Sorted by citations
Items 201–271 of 271
GABAB receptors in glial cells: from physiological regulation to pathological implications
Wang, J., Xu, L., Shen, Q., & Tang, Y. (2026) · Brain · doi:10.1093/brain/awag141 · Cited by 2
Prenatal THC exposure interferes with the neurodevelopmental role of endocannabinoid signaling
Galve‐Roperh, I., de Salas-Quiroga, A., Sánchez, S. S., & Guzmán, M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823490-7.00013-7 · Cited by 2
aGABRacadabra: A surprising new role for GABAA receptors in cortical development
Kourdougli, N., & Portera‐Cailliau, C. (2023) · Neuron · doi:10.1016/j.neuron.2022.12.019 · Cited by 2
Kawamura, N., Osuka, T., Kaneko, R., Kishi, E., Higuchi, R., Yoshimura, Y., Hirabayashi, T., Yagi, T., & Tarusawa, E. (2023) · eNeuro · doi:10.1523/eneuro.0250-23.2023 · Cited by 2
Huang, J.-Y., Hess, M., Bajpai, A., Li, X., Hobson, L. N., Xu, A. J., Barton, S. J., & Lu, H. (2025) · iScience · doi:10.1016/j.isci.2025.112104 · Cited by 2
Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2023) · doi:10.7554/elife.88313.1 · Cited by 2
Goel, A., Razak, K. A., Chubykin, A. A., & Antoine, M. W. (2025) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-025-09634-4 · Cited by 1
Lu, I.-L., Song, M., Rangel-Sandoval, C., Palacios, J. M., Kim, J., Huang, E. J., Álvarez-Buylla, A., Kriegstein, A. R., Paredes, M. F., & Rowitch, D. H. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.01.007 · Cited by 1
The GABA developmental shift in health and disease
Ben‐Ari, Y. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00012-0 · Cited by 1
Merkler, M., Ip, N. Y., & Sakata, S. (2025) · Scientific Reports · doi:10.1038/s41598-025-95968-x · Cited by 1
AAV9-mediated KCC2 upregulation enhances functional recovery following cervical spinal cord injury
Zavvarian, M.-M., Modi, A. D., Khazaei, M., Luo, Z., Velumian, A. R., Hassan, O. I., Hong, J., Ahuja, C. S., Patel, Z. H., He, M., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08734-0 · Cited by 1
Wiley, M. T., Courville, A. H., Northcutt, H., Durdanovic, I., Chowdhury, K. U., Suppiramaniam, V. D., & Reed, M. N. (2025) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2025.107568 · Cited by 1
Molero, A. E., Devakanmalai, G. S., Altun, Y., Jover‐Mengual, T., Zhang, J., Khan, N., & Mehler, M. F. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107297 · Cited by 1
Not So Innocent Bystanders in Focal Cortical Dysplasia
Wang, Y. (2021) · Epiliepsy currents/Epilepsy currents · doi:10.1177/15357597211049051 · Cited by 1
Neuronal Death: Now You See It, Now You Don’t
Balena, T., & Staley, K. J. (2024) · The Neuroscientist · doi:10.1177/10738584241282632 · Cited by 1
Gallerani, N., & Au, E. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa089 · Cited by 1
Szabó, F., Sigutova, V., Schneider, A. M., Hoerder‐Suabedissen, A., & Molnár, Z. (2024) · Journal of Anatomy · doi:10.1111/joa.14181 · Cited by 1
Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.02.502073 · Cited by 1
Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2023) · doi:10.7554/elife.88313 · Cited by 2
Marshall, A. H., Boyle, D. J., Hanson, M. A., Nagarajan, D., Bibi, N., Safa, A., Johantges, A. C., & Wester, J. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.07.597984 · Cited by 1
Dziabis, J. E., Jonathan, I. O., Horvath, B. L., Zhang, G., Patton, M. S., Smith, C. J. W., Nguyen, D. M., Jammula, M., Devlin, B. A., Monroe, S. K., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.08.692987 · Cited by 1
How the Post-Fracture Rehabilitation Choice Affects Brain Function in Older People?
Mitsuboshi, N., Kouzuki, M., Mochida, S., Morimoto, K., & Urakami, K. (2019) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000495937
Katsanevaki, D., & Rochefort, N. L. (2021) · Neuron · doi:10.1016/j.neuron.2021.01.010
Network and Cellular Effects of the Mu Opioid Receptor in Cortical Interneurons
Dutkiewicz, A. P. (2021) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont)
Sa'diyah, C. (2014) · SKRIPSI Jurusan Kependidikan Sekolah Dasar & Prasekolah - Fakultas Ilmu Pendidikan UM
Cayouette, M. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736929171.793568964
Genesis and Migration of Cerebral Cortical Inhibitory Interneurons: An Overview
Cook, K., & Anderson, S. A. (2022) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_186-1
Neuron‐glia crosstalk shapes brain morphogenesis
Nguyen, L. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.1004
Genesis and Migration of Cerebral Cortical Inhibitory Interneurons: An Overview
Cook, K., & Anderson, S. A. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_186
Cortical Neuron Migration in Health and Disease
Javier‐Torrent, M., & Nguyen, L. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch17
Knowles, S. J., Holter, M. C., Li, G., et al. (2023) · doi:10.7554/elife.88313.1.sa0
Dysfunctional Circuit Mechanisms of Sensory Processing in FXS and ASD: Insights from Mouse Models
Goel, A. (2023) · Springer eBooks · doi:10.1007/978-3-031-42383-3_1
Lenherr, C., Neves, G., Oliveira, M. G., & Burrone, J. (2025) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041506
Longitudinal tracking of neuronal activity from the same cells in the developing brain using Track2pPreprint
Majnik, J., Mantez, M., Zangila, S., Bugeon, S., Guignard, L., Platel, J., & Cossart, R. (2025) · eLife · doi:10.7554/elife.107540.1
Transient Early Postnatal Neuronal Hyperexcitation Results in Lasting Social Preference DeficitsPreprint
Bach, H., Nakamura-Vernet, M., Lançon, K., Drapeau, P., Mhenni, H. B., Oram, C., Martin, S., Séguéla, P., & Poulin, J.-F. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.04.674307
Negwer, M., van der Werf, I., Oudakker, A. R., van Bokhoven, H., Schubert, D., & Kasri, N. N. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.15.676416
Longitudinal tracking of neuronal activity from the same cells in the developing brain using Track2pPreprint
Majnik, J., Mantez, M., Zangila, S., Bugeon, S., Guignard, L., Platel, J., & Cossart, R. (2025) · eLife · doi:10.7554/elife.107540.2
Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721066
Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721069
Additional file 1 of WDFY3 mutation alters laminar position and morphology of cortical neurons
Schaaf, Z. A., Tat, L., Cannizzaro, N., Green, R., Rülicke, T., Hippenmeyer, S., & Zarbalis, K. S. (2022) · Figshare · doi:10.6084/m9.figshare.20131009
Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721063
Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721072
Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721060
Non-canonical role of DNA mismatch repair on sensory processing in mice
Rahman, S., Neophytou, D., Oviedo-Gray, S., Vuong, B. Q., & Oviedo, H. V. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.12.066
Reversibility and therapeutic feasibility of DNM1L-associated neurodevelopmental disorders
So, K. H., Kim, S. H., Jang, S., Sang, H. D., Yun, E.-J., Choi, H., Chae, J., & Baek, S. T. (2026) · Experimental & Molecular Medicine · doi:10.1038/s12276-026-01660-z · Cited by 1
Liaci, C., Savarese, B., Ferretti, E., Urenda, J., Lu, J., Catapano, G., Prandi, L., Camera, M., Manohar, R., Rando, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.09.710568
Compensatory attenuation of cortical apoptosis by SK2 downregulation following ketamine anesthesia
Huang, S. Y., Li, L., Wang, Y., Xu, M., Wang, Y., & Wang, Q. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1761187
Une approche tout optique pour l'étude de schémas remarquables de connectivité fonctionnelle
Tressard, T. (2019) · theses.fr (ABES) · doi:10.70675/8a629ef0zb182z4315zbf9az0c3f999e9868
Lentini, C. (2019) · theses.fr (ABES) · doi:10.70675/6816666az3fdfz41c0zb106zc7d30c1931eb
Assembling layer 1 of the neocortex : roles of Cajal-Retzius cells
Genescu, I. (2020) · theses.fr (ABES) · doi:10.70675/3fe1b21cz5c6bz4150z94e6zd77163aba0ad
Cajal-Retzius cells and Reelin in mouse cortical development and human pathologies
Riva, M. (2021) · theses.fr (ABES) · doi:10.70675/b321eca5ze455z480bzb6d4z43505d8c9faf
Impact of PV interneuron - OPC synapse disruption on cognitive functioning
Vidal, M. (2021) · theses.fr (ABES) · doi:10.70675/66c1e527zbd3ez49f6z8736ze9817c27856d
Evolution de l'activité de la région CA1 de l'hippocampe pendant le développement postnatal précoce
Dard, R. F. (2022) · theses.fr (ABES) · doi:10.70675/a8322da1z46a2z4e19zbbd3zffe1e9d8cc19
Dai, C., Wu, X.-D., Li, X., Xu, B., Pang, Y., Huang, Y., Dong, X., Wang, N., & Dong, Z. (2026) · Cell & Bioscience · doi:10.1186/s13578-026-01575-2
Venkataramanappa, S., Graf, J., Haselmann, H., Schütz, D., Storch, O., Roemer, D., Kumar, P. A., Blank-Stein, N., Mayer, C., Holthoff, K., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.07.723521
Thalamic Activity Regulates Interneuron Density in the Developing Visual Thalamus
Huerga-Gómez, I., Torres, D., Castellano-Ruiz, P., Wilson, E. S., Martini, F. J., & López‐Bendito, G. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.0247-25.2026
Umeshima, H., Hirayama, T., Adachi, R., & Tomita, K. (2026) · Gene Expression Patterns · doi:10.1016/j.gep.2026.119412
Liaci, C., Savarese, B., Ferretti, E., Urenda, J., Lu, J. J., Catapano, G., Prandi, L., Camera, M., Manohar, R., Rando, S., et al. (2026) · eLife · doi:10.7554/elife.111288
Liaci, C., Savarese, B., Ferretti, E., Urenda, J., Lu, J. J., Catapano, G., Prandi, L., Camera, M., Manohar, R., Rando, S., et al. (2026) · eLife · doi:10.7554/elife.111288.1
Taliaz, D. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1808258
Song, X., Zhang, F., Han, D., Yu, J., Xin, X., & Guo, R. (2026) · Neuroreport · doi:10.1097/wnr.0000000000002284
Christodoulou, O., Diskos, K., Velli, A., Moulos, P., Sidiropoulou, K., & Denaxa, M. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1892850
Li, Z., Wang, Y.-Z., Shi, J., Luo, Y., Shan, Y., & Zhao, G. (2026) · CNS Neuroscience & Therapeutics · doi:10.1002/cns.71170
Interneurons and network activity in the cerebral cortex: a developmental dialogue
Moissidis, M., & Marín, Ó. (2026) · Nature reviews. Neuroscience · doi:10.1038/s41583-026-01088-4
Metadata
- Authors
- Wong, F. K., Bercsenyi, K., Sreenivasan, V., Portalés, A., Fernández-Otero, M., & Marín, O.
- Affiliations
- King's College London (GB)
- Venue
- Nature
- Published
- 2018-05
- Volume
- 557
- Issue
- 7707
- Pages
- 668-673
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC6207348
- OpenAlex
- W2803681151
- Cited by
- 286
- References
- 60
- Citations by year
- 2026: 25 · 2025: 33 · 2024: 37 · 2023: 37 · 2022: 42 · 2021: 41 · 2020: 26 · 2019: 35 · 2018: 9
- FWCI
- 10.20
- Type
- journal article
- Language
- en
- Open access
- green
- kclpure.kcl.ac.uk
- Licence
- other-oa
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Research Portal (King's College London) (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Research Explorer (The University of Manchester) (submittedVersion, other-oa)
- Funders
- Wellcome Trust (103714/Z/14/Z, 103714MA)
- European Commission (H2020)
- Horizon 2020 Framework Programme
- Medical Research Council (MR/N026063/1)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- pyramidal neurons, excitation-inhibition balance, cortical development, postnatal development, neuronal cell death, activity-dependent regulation, inhibitory interneurons, excitatory synaptic input
- MeSH terms
- Animals, Cell Count, Cell Survival, Cerebral Cortex, Female, Interneurons, Male, Neural Pathways, Cell Death, Pyramidal Cells, PTEN Phosphohydrolase, Mice
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