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Sheng Wang
Sheng Wang
在 ucsf.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novoSCN1A 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
1252015
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
1212018
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
1182018
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
852017
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
662014
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
542017
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
402019
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
332018
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
312018
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
222021
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
132020
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
122019
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
92023
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
62022
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
42023
A foundational atlas of autism protein interactions reveals molecular convergence
B Wang, R Vartak, Y Zaltsman, ZZC Naing, K Hennick, B Polacco, ...
42023
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
12022
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