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Zongxiao He
Zongxiao He
Tencent
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Title
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Cited by
Year
Excess of rare, inherited truncating mutations in autism
N Krumm, TN Turner, C Baker, L Vives, K Mohajeri, K Witherspoon, ...
Nature genetics 47 (6), 582-588, 2015
6262015
Novel somatic and germline mutations in intracranial germ cell tumours
L Wang, S Yamaguchi, MD Burstein, K Terashima, K Chang, HK Ng, ...
Nature 511 (7508), 241-245, 2014
2142014
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay
JX Chong, MJ McMillin, KM Shively, AE Beck, CT Marvin, JR Armenteros, ...
The American Journal of Human Genetics 96 (3), 462-473, 2015
1362015
MECR mutations cause childhood-onset dystonia and optic atrophy, a mitochondrial fatty acid synthesis disorder
G Heimer, JM Kerätär, LG Riley, S Balasubramaniam, E Eyal, ...
The American Journal of Human Genetics 99 (6), 1229-1244, 2016
862016
Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data
Z He, BJ O’Roak, JD Smith, G Wang, S Hooker, RLP Santos-Cortez, B Li, ...
The American Journal of Human Genetics 94 (1), 33-46, 2014
832014
Autosomal-dominant multiple pterygium syndrome is caused by mutations in MYH3
JX Chong, LC Burrage, AE Beck, CT Marvin, MJ McMillin, KM Shively, ...
The American Journal of Human Genetics 96 (5), 841-849, 2015
682015
The rare-variant generalized disequilibrium test for association analysis of nuclear and extended pedigrees with application to alzheimer disease WGS data
Z He, D Zhang, AE Renton, B Li, L Zhao, GT Wang, AM Goate, R Mayeux, ...
The American Journal of Human Genetics 100 (2), 193-204, 2017
322017
mirAct: a web tool for evaluating microRNA activity based on gene expression data
Z Liang, H Zhou, Z He, H Zheng, J Wu
Nucleic acids research 39 (suppl_2), W139-W144, 2011
302011
Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population
M Shahzad, S Yousaf, YM Waryah, H Gul, T Kausar, N Tariq, U Mahmood, ...
Scientific reports 7 (1), 44185, 2017
292017
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
M Ansar, A Jan, RLP Santos-Cortez, X Wang, M Suliman, A Acharya, ...
European Journal of Human Genetics 24 (8), 1223-1227, 2016
202016
A rare variant nonparametric linkage method for nuclear and extended pedigrees with application to late-onset Alzheimer disease via WGS data
L Zhao, Z He, D Zhang, GT Wang, AE Renton, BN Vardarajan, ...
The American Journal of Human Genetics 105 (4), 822-835, 2019
182019
SEQSpark: a complete analysis tool for large-scale rare variant association studies using whole-genome and exome sequence data
D Zhang, L Zhao, B Li, Z He, GT Wang, DJ Liu, SM Leal
The American Journal of Human Genetics 101 (1), 115-122, 2017
142017
MendelProb: probability and sample size calculations for Mendelian studies of exome and whole genome sequence data
Z He, L Wang, AT DeWan, SM Leal
Bioinformatics 35 (3), 529-531, 2019
2019
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