Chang Xiao
Chang Xiao
Children's hospital of philadelphia
Bestätigte E-Mail-Adresse bei
Zitiert von
Zitiert von
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
wANNOVAR: annotating genetic variants for personal genomes via the web
X Chang, K Wang
Journal of medical genetics 49 (7), 433-436, 2012
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
A first update on mapping the human genetic architecture of COVID-19
Writing group lead Andrews Shea J. 6 Kanai Masahiro 3 Cordioli Mattia 7, ...
Nature 608 (7921), E1-E10, 2022
DNA Methylation in the Malignant Transformation of Meningiomas
F Gao, L Shi, J Russin, L Zeng, X Chang, S He, TC Chen, SL Giannotta, ...
PLOS ONE 8 (1), e54114, 2013
High-coverage proteome analysis reveals the first insight of protein modification systems in the pathogenic spirochete Leptospira interrogans
XJ Cao, J Dai, H Xu, S Nie, X Chang, BY Hu, QH Sheng, LS Wang, ...
Cell research 20 (2), 197-210, 2010
Dynamic modular architecture of protein-protein interaction networks beyond the dichotomy of ‘date’and ‘party’hubs
X Chang, T Xu, Y Li, K Wang
Scientific reports 3 (1), 1691, 2013
Comparative proteogenomic analysis of the Leptospira interrogans virulence-attenuated strain IPAV against the pathogenic strain 56601
Y Zhong, X Chang, XJ Cao, Y Zhang, H Zheng, Y Zhu, C Cai, Z Cui, ...
Cell research 21 (8), 1210-1229, 2011
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma
LD McDaniel, KL Conkrite, X Chang, M Capasso, Z Vaksman, ...
PLoS genetics 13 (5), e1006787, 2017
Src kinase as a mediator of convergent molecular abnormalities leading to NMDAR hypoactivity in schizophrenia
A Banerjee, HY Wang, KE Borgmann-Winter, ML MacDonald, ...
Molecular psychiatry 20 (9), 1091-1100, 2015
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
YR Li, JT Glessner, BP Coe, J Li, M Mohebnasab, X Chang, J Connolly, ...
Nature communications 11 (1), 255, 2020
Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the disease
Y Liu, X Chang, CG Hahn, RE Gur, PAM Sleiman, H Hakonarson
Translational psychiatry 8 (1), 44, 2018
RNA-seq analysis of amygdala tissue reveals characteristic expression profiles in schizophrenia
X Chang, Y Liu, CG Hahn, RE Gur, PMA Sleiman, H Hakonarson
Translational psychiatry 7 (8), e1203-e1203, 2017
Hypoglycemic mechanism of polysaccharide from Cyclocarya paliurus leaves in type 2 diabetic rats by gut microbiota and host metabolism alteration
Q Li, J Hu, Q Nie, X Chang, Q Fang, J Xie, H Li, S Nie
Science China Life Sciences 64, 117-132, 2021
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene
G Van Ingen, J Li, A Goedegebure, R Pandey, YR Li, ME March, ...
Nature communications 7 (1), 12792, 2016
Systems perspectives on erythromycin biosynthesis by comparative genomic and transcriptomic analyses of S. erythraea E3 and NRRL23338 strains
YY Li, X Chang, WB Yu, H Li, ZQ Ye, H Yu, BH Liu, Y Zhang, SL Zhang, ...
Bmc Genomics 14, 1-13, 2013
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
N Mullins, J Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, 313-327, 2019
The functional genetic link of NLGN4X knockdown and neurodevelopment in neural stem cells
L Shi, X Chang, P Zhang, MP Coba, W Lu, K Wang
Human molecular genetics 22 (18), 3749-3760, 2013
Common and rare genetic risk factors converge in protein interaction networks underlying schizophrenia
X Chang, LA Lima, Y Liu, J Li, Q Li, PMA Sleiman, H Hakonarson
Frontiers in genetics 9, 434, 2018
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