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Gao Wang
Gao Wang
Assistant Professor at Columbia University Vagelos College of Physicians and Surgeons
Verified email at columbia.edu - Homepage
Title
Cited by
Cited by
Year
Genetic effects on gene expression across human tissues
GTEx Consortium Lead analysts: Aguet François 1 Brown Andrew A. 2 3 4 Castel ...
Nature 550 (7675), 204-213, 2017
33692017
The GTEx Consortium atlas of genetic regulatory effects across human tissues
GTEx Consortium
Science 369 (6509), 1318-1330, 2020
26962020
The impact of sex on gene expression across human tissues
M Oliva, M Muñoz-Aguirre, S Kim-Hellmuth, V Wucher, ADH Gewirtz, ...
Science 369 (6509), eaba3066, 2020
7352020
A simple new approach to variable selection in regression, with application to genetic fine mapping
G Wang, A Sarkar, P Carbonetto, M Stephens
Journal of the Royal Statistical Society Series B: Statistical Methodology …, 2020
5762020
A quantitative proteome map of the human body
L Jiang, M Wang, S Lin, R Jian, X Li, J Chan, G Dong, H Fang, ...
Cell 183 (1), 269-283. e19, 2020
3072020
Flexible statistical methods for estimating and testing effects in genomic studies with multiple conditions
SM Urbut, G Wang, P Carbonetto, M Stephens
Nature genetics 51 (1), 187-195, 2019
2982019
Exploiting the GTEx resources to decipher the mechanisms at GWAS loci
AN Barbeira, R Bonazzola, ER Gamazon, Y Liang, YS Park, ...
Genome biology 22, 1-24, 2021
2202021
Co-expression networks reveal the tissue-specific regulation of transcription and splicing
A Saha, Y Kim, ADH Gewirtz, B Jo, C Gao, IC McDowell, BE Engelhardt, ...
Genome research 27 (11), 1843-1858, 2017
1722017
RNF213 Rare Variants in an Ethnically Diverse Population With Moyamoya Disease
AC Cecchi, D Guo, Z Ren, K Flynn, RLP Santos-Cortez, SM Leal, ...
Stroke 45 (11), 3200-3207, 2014
1552014
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
1442015
Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools
FA San Lucas, G Wang, P Scheet, B Peng
Bioinformatics 28 (3), 421-422, 2012
1442012
Fine-mapping from summary data with the “Sum of Single Effects” model
Y Zou, P Carbonetto, G Wang, M Stephens
PLoS genetics 18 (7), e1010299, 2022
1412022
Genetic analyses support the contribution of mRNA N6-methyladenosine (m6A) modification to human disease heritability
Z Zhang, K Luo, Z Zou, M Qiu, J Tian, L Sieh, H Shi, Y Zou, G Wang, ...
Nature genetics 52 (9), 939-949, 2020
1372020
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease
OM de Goede, DC Nachun, NM Ferraro, MJ Gloudemans, AS Rao, ...
Cell 184 (10), 2633-2648. e19, 2021
1242021
Transcriptomic signatures across human tissues identify functional rare genetic variation
NM Ferraro, BJ Strober, J Einson, NS Abell, F Aguet, AN Barbeira, ...
Science 369 (6509), eaaz5900, 2020
1162020
Guidelines for large-scale sequence-based complex trait association studies: lessons learned from the NHLBI exome sequencing project
PL Auer, AP Reiner, G Wang, HM Kang, GR Abecasis, D Altshuler, ...
The American Journal of Human Genetics 99 (4), 791-801, 2016
1012016
Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants
S Zhang, H Zhang, Y Zhou, M Qiao, S Zhao, A Kozlova, J Shi, AR Sanders, ...
Science 369 (6503), 561-565, 2020
892020
Variant association tools for quality control and analysis of large-scale sequence and genotyping array data
GT Wang, B Peng, SM Leal
The American Journal of Human Genetics 94 (5), 770-783, 2014
842014
Mutation of ATF6 causes autosomal recessive achromatopsia
M Ansar, RLP Santos-Cortez, MAN Saqib, F Zulfiqar, K Lee, NM Ashraf, ...
Human Genetics 134, 941-950, 2015
832015
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
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