دنبال کردن
Shan Dong
عنوان
نقل شده توسط
نقل شده توسط
سال
KOBAS 2.0: a web server for annotation and identification of enriched pathways and diseases
C Xie, X Mao, J Huang, Y Ding, J Wu, S Dong, L Kong, G Gao, CY Li, ...
Nucleic acids research 39 (suppl_2), W316-W322, 2011
43792011
The contribution of de novo coding mutations to autism spectrum disorder
I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ...
Nature 515 (7526), 216-221, 2014
27702014
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
20372020
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ...
Neuron 87 (6), 1215-1233, 2015
15862015
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
AJ Willsey, SJ Sanders, M Li, S Dong, AT Tebbenkamp, RA Muhle, ...
Cell 155 (5), 997-1007, 2013
10232013
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
3502022
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
JY An, K Lin, L Zhu, DM Werling, S Dong, H Brand, HZ Wang, X Zhao, ...
Science 362 (6420), eaat6576, 2018
3122018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
DM Werling, H Brand, JY An, MR Stone, L Zhu, JT Glessner, RL Collins, ...
Nature genetics 50 (5), 727-736, 2018
2922018
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder
S Dong, MF Walker, NJ Carriero, M DiCola, AJ Willsey, YY Adam, ...
Cell reports 9 (1), 16-23, 2014
1992014
De novo coding variants are strongly associated with Tourette disorder
AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ...
Neuron 94 (3), 486-499. e9, 2017
1892017
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
1332018
Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex
DM Werling, S Pochareddy, J Choi, JY An, B Sheppard, M Peng, Z Li, ...
Cell reports 31 (1), 2020
1262020
Whole genome sequencing in psychiatric disorders: the WGSPD consortium
SJ Sanders, BM Neale, H Huang, DM Werling, JY An, S Dong, ...
Nature neuroscience 20 (12), 1661-1668, 2017
1042017
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus
J Gockley, AJ Willsey, S Dong, JD Dougherty, JN Constantino, ...
Molecular autism 6, 1-10, 2015
902015
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, SD Rubeis, JY An, ...
BioRxiv, 484113, 2018
492018
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, L Klei, ...
MedRxiv, 2021.12. 20.21267194, 2021
352021
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies
C Lowther, E Valkanas, JL Giordano, HZ Wang, BB Currall, K O’Keefe, ...
The American Journal of Human Genetics 110 (9), 1454-1469, 2023
222023
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Y Chen, R Dawes, HC Kim, A Ljungdahl, SL Stenton, S Walker, J Lord, ...
Nature 632 (8026), 832-840, 2024
212024
Prenatal exposure to paternal smoking and likelihood for autism spectrum disorder
B Kim, M Ha, YS Kim, YJ Koh, S Dong, HJ Kwon, YS Kim, MH Lim, ...
Autism 25 (7), 1946-1959, 2021
202021
Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families
DM Werling, H Brand, JY An, MR Stone, JT Glessner, L Zhu, RL Collins, ...
BioRxiv, 127043, 2017
202017
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مقاله‌ها 1–20