Gao Wang

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2019
Позовавания	12198	10933
h-индекс	33	29
i10-индекс	50	46

2600

1300

650

1950

2014201520162017201820192020202120222023202474 113 182 259 541 796 1174 1857 2163 2336 2582

Публичен достъп

Преглед на всички

56 статии

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неналични

Въз основа на изисквания при финансирането

Съавтори

Matthew StephensUniversity of ChicagoПотвърден имейл адрес: uchicago.edu
Peter CarbonettoUniversity of ChicagoПотвърден имейл адрес: uchicago.edu
Regie Santos-CortezAssociate Professor, Otolaryngology-Head and Neck SurgeryПотвърден имейл адрес: cuanschutz.edu
Deborah A. NickersonUniversity of WashingtonПотвърден имейл адрес: uw.edu
Bo PengDepartment of Medicine, Baylor College of MedicineПотвърден имейл адрес: bcm.edu
michael bamshaduniversity of washingtonПотвърден имейл адрес: u.washington.edu
Jay ShendureProfessor of Genome Sciences, University of WashingtonПотвърден имейл адрес: uw.edu
Zongxiao HeTencentПотвърден имейл адрес: tencent.com
Paul AuerProfessor of Biostatistics, Medical College of WisconsinПотвърден имейл адрес: mcw.edu
Di ZhangBaylor College of MedicineПотвърден имейл адрес: bcm.edu
Paul ScheetUniversity of Texas MD Anderson Cancer CenterПотвърден имейл адрес: mdanderson.org
Anthony San LucasUniversity of Texas MD Anderson Cancer CenterПотвърден имейл адрес: mdanderson.org
Goncalo AbecasisUniversity of Michigan School of Public HealthПотвърден имейл адрес: umich.edu
Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann ArborПотвърден имейл адрес: umich.edu
Evan EichlerProfessor of Genome Sciences, University of WashingtonПотвърден имейл адрес: gs.washington.edu
Mengyuan KanUniversity of PennsylvaniaПотвърден имейл адрес: pennmedicine.upenn.edu
Yee Him CheungSenior Scientist, Philips ResearchПотвърден имейл адрес: columbia.edu
John N WeinsteinMD Anderson Cancer CenterПотвърден имейл адрес: mdanderson.org
Dajiang J. LiuDistinguished Professor; Vice Chair-Research; Co-Chair-Bioinfo & Genomics PhD Prgm; Director - AIПотвърден имейл адрес: psu.edu

Следене

Gao Wang

Assistant Professor at Columbia University Vagelos College of Physicians and Surgeons

Потвърден имейл адрес: columbia.edu - Начална страница

Computational genomics


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
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	3517	2017
The GTEx Consortium atlas of genetic regulatory effects across human tissues GTEx Consortium Science 369 (6509), 1318-1330, 2020	3118	2020
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	820	2020
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	705	2020
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	349	2020
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	342	2019
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	247	2021
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014	244	2014
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	182	2017
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	178	2022
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	163	2014
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	153	2020
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	153	2012
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	145	2015
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	139	2021
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	131	2020
An atlas of alternative polyadenylation quantitative trait loci contributing to complex trait and disease heritability L Li, KL Huang, Y Gao, Y Cui, G Wang, ND Elrod, Y Li, YE Chen, P Ji, ... Nature genetics 53 (7), 994-1005, 2021	130	2021
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	104	2016
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	95	2016
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	94	2020

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