The DOI matches its Crossref record; 98 of the 98 references it cites were found in a registry or an index.
Germline Chd8 haploinsufficiency alters brain development in mouse
Open accessPublished version of a preprint
Abstract
The chromatin remodeling gene CHD8 represents a central node in neurodevelopmental gene networks implicated in autism. We examined the impact of germline heterozygous frameshift Chd8 mutation on neurodevelopment in mice. Chd8+/del5 mice displayed normal social interactions with no repetitive behaviors but exhibited cognitive impairment correlated with increased regional brain volume, validating that phenotypes of Chd8+/del5 mice overlap pathology reported in humans with CHD8 mutations. We applied network analysis to characterize neurodevelopmental gene expression, revealing widespread transcriptional changes in Chd8+/del5 mice across pathways disrupted in neurodevelopmental disorders, including neurogenesis, synaptic processes and neuroimmune signaling. We identified a co-expression module with peak expression in early brain development featuring dysregulation of RNA processing, chromatin remodeling and cell-cycle genes enriched for promoter binding by Chd8, and we validated increased neuronal proliferation and developmental splicing perturbation in Chd8+/del5 mice. This integrative analysis offers an initial picture of the consequences of Chd8 haploinsufficiency for brain development.
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
“Studies on CHD8 and iPS-derived ASD neurons indicate the dysregulation of proliferation and macrocephaly in ASD could be linked to the disruption of these signaling pathways and shortened G1/S transition[54, 55, 57, 94, 183, 192, 193].”
From The ASD Living Biology: from cell proliferation to clinical phenotype (2019) · cites this paper as [183]
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
Basic local alignment search tool
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669
Fiji: an open-source platform for biological-image analysis
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp616 · Cited by 41,364
WGCNA: an R package for weighted correlation network analysis
Langfelder, P., & Horvath, S. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-559 · Cited by 27,252
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Liao, Y., Smyth, G. K., & Shi, W. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btt656 · Cited by 27,219
RNA-Guided Human Genome Engineering via Cas9
Mali, P., Yang, L., Esvelt, K. M., Aach, J., Guell, M., DiCarlo, J. E., Norville, J. E., & Church, G. M. (2013) · Science · doi:10.1126/science.1232033 · Cited by 9,210
Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool
Chen, E. Y., Tan, C. M., Kou, Y., Duan, Q., Wang, Z., Meirelles, G. V., Clark, N. R., & Ma’ayan, A. (2013) · BMC Bioinformatics · doi:10.1186/1471-2105-14-128 · Cited by 7,814
Gene ontology analysis for RNA-seq: accounting for selection bias
Young, M. D., Wakefield, M. J., Smyth, G. K., & Oshlack, A. (2010) · Genome Biology · doi:10.1186/gb-2010-11-2-r14 · Cited by 7,107
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–265 of 265
Persistent cortical excitatory neuron dysregulation in adult Chd8 haploinsufficient micePreprint
Canales, C. P., Lozano, S. A., Frost, N. A., Cichewicz, K., Amaral, W. Z., Seban, N., Fenton, E., Wade, A. A., Chu, N., Smith, E. M., et al. (2025) · Research Square · doi:10.1101/2025.06.04.657776 · Cited by 3
Self-citationGene regulatory networks controlling neuronal development
Lambert, J. T., Haigh, J. L., & Nord, A. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00027-8 · Cited by 1
Self-citationLee, T., & Kim, E. (2024) · Ewha Medical Journal · doi:10.12771/emj.2024.e18 · Cited by 2
Davalan, W., Li, Q., Hale, A. T., Fan, B., Duy, P. Q., Mehta, N. H., Alper, S. L., Kundishora, A. J., Muñoz, W., Dennis, E., et al. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115473 · Cited by 1
Chd8 Deficiency in Zebrafish Causes Autism-Like Behavioral Deficits
Wang, H.-T., Fu, X.-T., Wang, Y.-F., Liu, L., Liu, Z.-Z., & Xu, H. A. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin44414 · Cited by 1
CHD8 dysregulation in neurodevelopment: Emerging insights into autism pathophysiology
Chatterjee, D., & Maparu, K. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.149985 · Cited by 1
El‐Sehrawy, A. A. M. A., Aljumaili, O. I., Axmedov, U., Khasawneh, M. A. S., Alanazi, M. A., Smerat, A., & Basunduwah, T. S. (2026) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.70128 · Cited by 1
Homozygous CHD8 mutation intensifies ASD phenotypes and attenuates sex differences
Kim, J., Lee, S., Hwang, E., Jung, H., Lee, C., Choi, S., Lee, S., Kim, S., Moon, H., Kim, J., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03646-9 · Cited by 1
Pérez‐Sisqués, L., Bhatt, S. R., Caruso, A., Robb, J. L., Donovan, A. P. A., Bamford, R. A., Torres-Cano, A., Spring, S., Hendy, E., Gileadi, T. E., et al. (2026) · Science Advances · doi:10.1126/sciadv.adq6577 · Cited by 1
Self-citationDefective ventral neurogenesis due to midfetal Chd8 mutation drives autistic-like behavior in mice
Nitahara, K., Kawamura, A., Tashiro, A., Iwasaki, T., Horike, S.-I., Terakawa, J., Daikoku, T., Higashi, K., Kurokawa, K., Kato, K., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73416-2 · Cited by 1
The role of chromatin modifiers in common neurodevelopmental disorders
Poot, R. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814085-7.00012-x · Cited by 1
Soumier, A., Lio, G., & Demily, C. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02487-8 · Cited by 1
Chd8 haploinsufficiency impacts rearing experience in C57BL/6 mice
Tabbaa, M., & Levitt, P. R. (2024) · Genes Brain & Behavior · doi:10.1111/gbb.12892 · Cited by 1
Haigh, J. L., Adhikari, A., Copping, N. A., Stradleigh, T. W., Wade, A. A., Catta-Preta, R., Su-Feher, L., Zdilar, I., Morse, S. J., Fenton, T. A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/766634 · Cited by 1
Self-citationIncreased cortical volume without increased neuron number in heterozygous Chd8 mutant mouse cortexPreprint
Canales, C. P., Frank, S., Bennett, J., Beauregard, P., Lavenex, P., Amaral, D. G., & Nord, A. S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.11.426290 · Cited by 2
Self-citationSubtil‐Rodríguez, A., Vázquez-Chávez, E., Guerrero-Martinez, J. A., Ceballos-Chávez, M., & Reyes, J. C. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.09.507301 · Cited by 1
Ding, C., Shi, Y., Shan, S., Yuan, Y., Zhang, Y., & Qiu, Z. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.03.547590 · Cited by 1
Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutationsPreprint
Silverman, J. L., Fenton, T., Haouchine, O. Y., Hallam, E., Smith, E., Jackson, K. C., Rahbarian, D., Canales, C. P., Adhikari, A., Nord, A. S., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3246655/v1 · Cited by 1
Self-citationNovel Gain of Function Mouse Model of KCNT1-Related EpilepsyPreprint
Olguin, S. L., Davis, D., Rehman, A., Berg, S. W., Sahagún, E., Oswalt, P. S., Patil, M., Sullivan, P. D. M., Zhang, B., Bryda, E. C., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.22.666003 · Cited by 1
Self-citationWade, A. A., Lim, K. J., Catta-Preta, R., & Nord, A. S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/375238
Self-citationEllegood, J., Petkova, S. P., Kinman, A. I., Qiu, L. R., Wade, A. A., Fernandes, D., Lindenmaier, Z., Crieghton, A., Nutter, L. M. J., Nord, A. S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.31.017905
Self-citationEstablishing a transcriptome-based drug discovery paradigm for neurodevelopmental disordersPreprint
Dhindsa, R. S., Zoghbi, A. W., Krizay, D. K., Vasavda, C., & Goldstein, D. B. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.13.093468
Postzygotic and germinal de novo mutations in ASD: exploring their biological rolePreprint
Alonso-González, A., Calaza, M., Amigo, J., González‐Peñas, J., Martínez-Regueiro, Fernández‐Prieto, M., Parellada, M., Rodriguez‐Fontenla, C., & Carracedo, Á. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.21.107987
Berg, E. L., Petkova, S. P., Born, H. A., Adhikari, A., Anderson, A. E., & Silverman, J. L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.13.456299
Self-citationEllegood, J., Petkova, S. P., Kinman, A. I., Qiu, L. R., Wade, A. A., Fernandes, D., Lindenmaier, Z., Crieghton, A., Nutter, L. M. J., Nord, A. S., et al. (2020) · Research Square · doi:10.21203/rs.3.rs-90296/v1
Self-citationBen‐Ari, Y. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733499087.793568939
Jiang, K., Lin, X., Wu, J., Ying, Y., Yan, B., Wang, J., & Zou, J. (2024) · Research Square · doi:10.21203/rs.3.rs-3689329/v1
Tcf12 controls dynamic calvarial bone growth and motor learning in micePreprint
Yamada, T., Anderson-Ramirez, J., Gao, L., Chen, P., Zhang, M., Guo, T., Feng, J., Ho, T., Vorobyova, I., Maria, N. S. S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.09.574781
Weissberg, O., Getselter, D., & Elliott, E. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.16.599211
Xu, X., Wang, J., Hu, K., Su, D., Huang, Q., Fan, X., & Fan, X. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.04.626807
Autism-associated ASPM variant causes macrocephaly and social-cognitive deficits in micePreprint
Singh, S., Kim, H., Ecevitoglu, A., Chasse, R., Ludko, A. M., Sanganahalli, B. G., Gangasandra, V., Park, S. R., Yee, S., Grady, J. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.17.638753
Fenton, T. A., Petkova, S. P., Adhikari, A., & Silverman, J. L. (2025) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-025-09616-6
Self-citationThe CHD Protein, Kismet, Restricts Synaptic BMP Signaling at Glutamatergic Synapses
Klaustermeier, R. A., Hendricks, E. L., Preston, J. A., & Liebl, F. L. W. (2025) · Neuroscience Insights · doi:10.1177/26331055251379496
Михайлович, Ч. С., Gerasimenko, M., Yuhi, T., Furuhara, K., Tsuji, C., Yokoyama, S., Nakayama, K. I., Nishiyama, M., & Higashida, H. (2021) · Figshare · doi:10.6084/m9.figshare.14525969
Berg, E. L., Ching, T. M., Bruun, D. A., Rivera, J. K., Careaga, M., Ellegood, J., Lerch, J. P., Wöhr, M., Lein, P. J., & Silverman, J. L. (2020) · Figshare · doi:10.6084/m9.figshare.13468179
Self-citationKawamura, A., Abe, Y., Seki, F., Katayama, Y., Nishiyama, M., Takata, N., Tanaka, K. F., Okano, H., & Nakayama, K. I. (2020) · Figshare · doi:10.6084/m9.figshare.13279529
Ellegood, J., Petkova, S. P., Kinman, A. I., Qiu, L., Adhikari, A., Wade, A. A., Fernandes, D., Lindenmaier, Z., Creighton, A., Nutter, L. M. J., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14274167
Self-citationHaigh, J., Adhikari, A., Copping, N. A., Stradleigh, T. W., Wade, A. A., Catta-Preta, R., Su-Feher, L., Zdilar, I., Morse, S. J., Fenton, T. A., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14509699
Self-citationCopping, N. A., & Silverman, J. L. (2021) · Figshare · doi:10.6084/m9.figshare.13727617
Self-citationCherepanov, S. M., Gerasimenko, M., Yuhi, T., Furuhara, K., Tsuji, C., Yokoyama, S., Nakayama, K. I., Nishiyama, M., & Higashida, H. (2021) · Figshare · doi:10.6084/m9.figshare.14525966
Haigh, J., Adhikari, A., Copping, N. A., Stradleigh, T. W., Wade, A. A., Catta-Preta, R., Su-Feher, L., Zdilar, I., Morse, S. J., Fenton, T. A., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14509687
Self-citationBerg, E. L., Petkova, S. P., Born, H. A., Adhikari, A., Anderson, A. E., & Silverman, J. L. (2021) · Figshare · doi:10.6084/m9.figshare.16625413
Self-citationEllegood, J., Petkova, S. P., Kinman, A. I., Qiu, L., Adhikari, A., Wade, A. A., Fernandes, D., Lindenmaier, Z., Creighton, A., Nutter, L. M. J., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14274176
Self-citationHaigh, J., Adhikari, A., Copping, N. A., Stradleigh, T. W., Wade, A. A., Catta-Preta, R., Su-Feher, L., Zdilar, I., Morse, S. J., Fenton, T. A., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14509690
Self-citationZhang, Y., Wang, J., Liu, X., & Liu, H. (2020) · Figshare · doi:10.6084/m9.figshare.13357394
Haigh, J., Adhikari, A., Copping, N. A., Stradleigh, T. W., Wade, A. A., Catta-Preta, R., Su-Feher, L., Zdilar, I., Morse, S. J., Fenton, T. A., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14509696
Self-citationHaigh, J., Adhikari, A., Copping, N. A., Stradleigh, T. W., Wade, A. A., Catta-Preta, R., Su-Feher, L., Zdilar, I., Morse, S. J., Fenton, T. A., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14509693
Self-citationCopping, N. A., & Silverman, J. L. (2021) · Figshare · doi:10.6084/m9.figshare.13727614
Self-citationМихайлович, Ч. С., Gerasimenko, M., Yuhi, T., Furuhara, K., Tsuji, C., Yokoyama, S., Nakayama, K. I., Nishiyama, M., & Higashida, H. (2021) · Figshare · doi:10.6084/m9.figshare.14525963
Hurley, S., Mohan, C., Suetterlin, P., Ellingford, R. A., Riegman, K. L. H., Ellegood, J., Caruso, A., Michetti, C., Brock, O., Evans, R., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14111228
Self-citationEllegood, J., Petkova, S. P., Kinman, A. I., Qiu, L., Adhikari, A., Wade, A. A., Fernandes, D., Lindenmaier, Z., Creighton, A., Nutter, L. M. J., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14274173
Self-citationJiménez, J. A., Ptacek, T., Tuttle, A. H., Schmid, R., Moy, S. S., Simon, J. M., & Zylka, M. J. (2020) · Figshare · doi:10.6084/m9.figshare.13059112
Smith, E., Canales, C. P., Kenaston, M. W., Seban, N., Wade, A. A., Fenton, E., Ardekani, C., Lozano, S., Chu, N. C., Perla, D., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.2139/ssrn.5871048
Self-citationParfenenko, M. A., Kudakaeva, A. A., Кострюкова, А. М., Pakhomova, V. P., Грознова, О. С., & Воинова, В. Ю. (2025) · Педиатрия Восточная Европа · doi:10.34883/pi.2025.13.4.002
Temporal and Cell‐Specific Regulation of Synaptic Homeostasis by the Chromatin Remodeler Chd1
Morency, D. T., Cui, T., Cai, Y., Lok, C., Nokku, R. E., Huang, R., Chu, G. L., Xie, Y., Abu‐Tayeh, S. W., He, K., et al. (2026) · Advanced Science · doi:10.1002/advs.202510538
Hayot, G. (2020) · theses.fr (ABES) · doi:10.70675/68f97142z0b02z402czaf1az7158eb30dd29
Yao, W., Wise, B. L., Lin, Y., Fan, M., Xu, S., Ju, I.-S., Berg, J. I., Silverman, J. L., Loots, G. G., & Christiansen, B. (2026) · JBMR Plus · doi:10.1093/jbmrpl/ziag085
Self-citationA Novel Variant of the CHD8 Gene in a Patient with Autism Spectrum Disorder
Falcone, E., Bauleo, A., Stefano, L. D., Brando, R., Maietta, S., Tabolacci, E., Montesanto, A., Pace, V., Apa, R., Puntorieri, D., et al. (2026) · Genes · doi:10.3390/genes17060599
Zhang, Q. H., Qiao, Y., Li, H., Zeng, J., Chen, J., Zhou, H. J., Hu, Y., & Luo, J. (2026) · Neuroscience Bulletin · doi:10.1007/s12264-026-01653-y
Lin, X., Wu, J., Ying, Y., Yan, B., Wang, J., Zou, J., & Jiang, K. (2026) · Autism Research · doi:10.1002/aur.70310
Molecular Acrobats: How CHD Remodelers Shape the Genetic Playground to License Cell Identity
Özdemir, I., & Hainer, S. J. (2026) · BioEssays · doi:10.1002/bies.70158
Chromodomain helicase DNA-binding proteins and orofacial cleft
Dehghanian, M., Hosseinzadeh, M., Abdali, H., Nouri, N., & Kazemi, M. (2026) · Journal of Research in Medical Sciences · doi:10.4103/jrms.jrms_118_26
Recent Advances in Autism Spectrum Disorder Research on Epigenetics and Personalised Medicine
Khosrofar, R., Morshedi, I., Behzadpour, M., Afzali, N., Hosseini, R. S., & Aghili, A. (2026) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.70184
Metadata
- Authors
- Gompers, A. L., Su-Feher, L., Ellegood, J., Copping, N. A., Riyadh, M. A., Stradleigh, T. W., Pride, M. C., Schaffler, M. D., Wade, A. A., Catta-Preta, R., Zdilar, I., Louis, S., Kaushik, G., Mannion, B. J., Plajzer-Frick, I., Afzal, V., Visel, A., Pennacchio, L. A., Dickel, D. E., Lerch, J. P., Crawley, J. N., Zarbalis, K. S., Silverman, J. L., & Nord, A. S.
- Affiliations
- University of California, Davis (US)
- Hospital for Sick Children (CA)
- Shriners Hospitals for Children - Northern California (US)
- Lawrence Berkeley National Laboratory (US)
- University of Toronto (CA)
- Corresponding author
- Nord, Alex S
- ORCID
- Su-Feher, Linda
- Ellegood, Jacob
- Riyadh, M Asrafuzzaman
- Stradleigh, Tyler W
- Schaffler, Melanie D
- Wade, A Ayanna
- Catta-Preta, Rinaldo
- Zdilar, Iva
- Louis, Shreya
- Mannion, Brandon J
- Afzal, Veena
- Visel, Axel
- Pennacchio, Len A
- Dickel, Diane E
- Lerch, Jason P
- Crawley, Jacqueline N
- Zarbalis, Konstantinos S
- Silverman, Jill L
- Nord, Alex S
- Venue
- Nature Neuroscience
- Published
- 2017-06-26
- Volume
- 20
- Issue
- 8
- Pages
- 1062-1073
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC6008102
- OpenAlex
- W2687519416
- Cited by
- 266
- References
- 98
- Citations by year
- 2026: 18 · 2025: 22 · 2024: 23 · 2023: 21 · 2022: 21 · 2021: 52 · 2020: 48 · 2019: 27 · 2018: 26 · 2017: 8
- FWCI
- 19.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
- Funders
- U.S. Department of Energy (-AC02-05CH11231, 05CH11231, DE AC02 05CH11231, Contract DE-AC02-05CH11231., DE-AC02-)
- University of California Berkeley (DE-AC02-05CH11231)
- Ontario Brain Institute
- Fondation Brain Canada
- MIND Institute, University of California, Davis (U54 HD 079125, HD079125)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (DE-AC02-05CH11231)
- National Institutes of Health (DE-AC02–05CH11231, GM008799, GM119831, GM007377)
- University of California, Davis (T32-GM008799, U54 HD079125, GM007377)
- Intellectual and Developmental Disabilities Research Center (U54-HD079125)
- Ciência sem Fronteiras
- National Heart, Lung, and Blood Institute (R24HL123879, UM1HL098166)
- National Human Genome Research Institute (U54HG006997, R01HG003988)
- National Institute of General Medical Sciences (T32GM008799, T32GM007377, DE-AC02-05CH11231, GM119831, GM007377, GM008799, R35GM119831)
- National Institute of Neurological Disorders and Stroke (R01NS085709)
- National Institute of Dental and Craniofacial Research (U01DE024427)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (U54HD079125)
- Lawrence Berkeley National Laboratory (UM1HL098166, AC02‐05CH11231, DE-AC02-05CH11231, R24HL123879, U54HG006997, R01HG003988, 05CH11231, U01DE024427)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
- Keywords
- CHD8, haploinsufficiency, autism spectrum disorder, brain development, chromatin remodeling, cognitive impairment, regional brain volume, neurogenesis, synaptic processes, neuroimmune signaling, RNA processing, alternative splicing, neuronal proliferation, promoter binding
- MeSH terms
- Animals, Brain, Chromatin, DNA-Binding Proteins, Mice, Transgenic, Mutation, Phenotype, Transcription Factors, Gene Expression Regulation, Developmental, Cell Cycle Proteins, Gene Regulatory Networks, Haploinsufficiency
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