Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome X Xu, X Yang, Q Wu, A Liu, X Yang, AY Ye, AY Huang, J Li, M Wang, Z Yu, ... Human mutation 36 (9), 861-872, 2015 | 125 | 2015 |
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ... Cell reports 24 (13), 3441-3454. e12, 2018 | 121 | 2018 |
The psychiatric cell map initiative: a convergent systems biological approach to illuminating key molecular pathways in neuropsychiatric disorders AJ Willsey, MT Morris, S Wang, HR Willsey, N Sun, N Teerikorpi, TB Baum, ... Cell 174 (3), 505-520, 2018 | 118 | 2018 |
Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations Y Dou, X Yang, Z Li, S Wang, Z Zhang, AY Ye, L Yan, C Yang, Q Wu, J Li, ... Human mutation 38 (8), 1002-1013, 2017 | 85 | 2017 |
Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals AY Huang, X Xu, AY Ye, Q Wu, L Yan, B Zhao, X Yang, Y He, S Wang, ... Cell research 24 (11), 1311-1327, 2014 | 66 | 2014 |
Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort X Yang, A Liu, X Xu, X Yang, Q Zeng, AY Ye, Z Yu, S Wang, AY Huang, ... Scientific reports 7 (1), 15677, 2017 | 54 | 2017 |
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations WZ Zhou, J Zhang, Z Li, X Lin, J Li, S Wang, C Yang, Q Wu, AY Ye, ... Human mutation 40 (6), 801-815, 2019 | 40 | 2019 |
A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations AY Ye, Y Dou, X Yang, S Wang, AY Huang, L Wei Genome research 28 (7), 943-951, 2018 | 33 | 2018 |
Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs AY Huang, X Yang, S Wang, X Zheng, Q Wu, AY Ye, L Wei PLoS Genetics 14 (5), e1007395, 2018 | 31 | 2018 |
A convergent molecular network underlying autism and congenital heart disease SB Rosenthal, HR Willsey, Y Xu, Y Mei, J Dea, S Wang, C Curtis, ... Cell systems 12 (11), 1094-1107. e6, 2021 | 22 | 2021 |
A whole-exome sequencing study of Tourette disorder in a Chinese population X Zhao, S Wang, J Hao, P Zhu, X Zhang, M Wu DNA and Cell Biology 39 (1), 63-68, 2020 | 13 | 2020 |
ATP1A3 mosaicism in families with alternating hemiplegia of childhood X Yang, X Yang, J Chen, S Li, Q Zeng, AY Huang, AY Ye, Z Yu, S Wang, ... Clinical Genetics 96 (1), 43-52, 2019 | 12 | 2019 |
State, MW (2018). De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ... Cell reports 24 (13), 3441-3454, 0 | 11 | |
Pleiotropy of autism-associated chromatin regulators M Lasser, N Sun, Y Xu, S Wang, S Drake, K Law, S Gonzalez, B Wang, ... Development 150 (14), 2023 | 9 | 2023 |
State, MW, Krogan, NJ, 2018. The psychiatric cell map initiative: a convergent systems biological approach to illuminating key molecular pathways in neuropsychiatric disorders AJ Willsey, MT Morris, S Wang, HR Willsey, N Sun, N Teerikorpi, TB Baum, ... Cell 174 (3), 505-520, 0 | 8 | |
Shared genetic regulatory networks contribute to neuropathic and inflammatory pain: multi-omics systems analysis F Ye, L Du, W Huang, S Wang Biomolecules 12 (10), 1454, 2022 | 6 | 2022 |
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD S Wang, B Wang, V Drury, S Drake, N Sun, H Alkhairo, J Arbelaez, ... Nature communications 14 (1), 8077, 2023 | 4 | 2023 |
A foundational atlas of autism protein interactions reveals molecular convergence B Wang, R Vartak, Y Zaltsman, ZZC Naing, K Hennick, B Polacco, ... | 4 | 2023 |
Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder S Wang, B Wang, V Drury, S Drake, N Sun, H Alkhairo, J Arbelaez, ... medRxiv, 2022.09. 22.22280248, 2022 | 1 | 2022 |