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Title
Cited by
Cited by
Year
Genetic and pharmacologic inactivation of ANGPTL3 and cardiovascular disease
FE Dewey, V Gusarova, RL Dunbar, C O’Dushlaine, C Schurmann, ...
New England Journal of Medicine 377 (3), 211-221, 2017
7892017
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease
NS Abul-Husn, X Cheng, AH Li, Y Xin, C Schurmann, P Stevis, Y Liu, ...
New England Journal of Medicine 378 (12), 1096-1106, 2018
7132018
Seasonal human coronavirus antibodies are boosted upon SARS-CoV-2 infection but not associated with protection
EM Anderson, EC Goodwin, A Verma, CP Arevalo, MJ Bolton, ME Weirick, ...
Cell 184 (7), 1858-1864. e10, 2021
4002021
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ...
Cell Genomics 2 (10), 2022
2122022
Genomics-first evaluation of heart disease associated with titin-truncating variants
CM Haggerty, SM Damrauer, MG Levin, D Birtwell, DJ Carey, AM Golden, ...
Circulation 140 (1), 42-54, 2019
1272019
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
JE Horowitz, JA Kosmicki, A Damask, D Sharma, GHL Roberts, AE Justice, ...
Nature genetics 54 (4), 382-392, 2022
1192022
Association of the V122I hereditary transthyretin amyloidosis genetic variant with heart failure among individuals of African or Hispanic/Latino ancestry
SM Damrauer, K Chaudhary, JH Cho, LW Liang, E Argulian, L Chan, ...
Jama 322 (22), 2191-2202, 2019
1112019
Genetics of height and risk of atrial fibrillation: A Mendelian randomization study
MG Levin, R Judy, D Gill, M Vujkovic, SS Verma, Y Bradford, ...
PLoS medicine 17 (10), e1003288, 2020
902020
Derivation and validation of a machine learning risk score using biomarker and electronic patient data to predict progression of diabetic kidney disease
L Chan, GN Nadkarni, F Fleming, JR McCullough, P Connolly, ...
Diabetologia 64, 1504-1515, 2021
892021
Genetic architecture of abdominal aortic aneurysm in the million veteran program
D Klarin, SS Verma, R Judy, O Dikilitas, BN Wolford, I Paranjpe, MG Levin, ...
Circulation 142 (17), 1633-1646, 2020
892020
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals
JA Kosmicki, JE Horowitz, N Banerjee, R Lanche, A Marcketta, E Maxwell, ...
The American Journal of Human Genetics 108 (7), 1350-1355, 2021
872021
Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19
JE Huffman, G Butler-Laporte, A Khan, E Pairo-Castineira, TG Drivas, ...
Nature genetics 54 (2), 125-127, 2022
822022
Primary open-angle African American glaucoma genetics (POAAGG) study: Gender and risk of POAG in African Americans
N Khachatryan, M Pistilli, MG Maguire, RJ Salowe, RM Fertig, T Moore, ...
PloS one 14 (8), e0218804, 2019
682019
Association of inherited pathogenic variants in checkpoint kinase 2 (CHEK2) with susceptibility to testicular germ cell tumors
SH AlDubayan, LC Pyle, M Gamulin, T Kulis, ND Moore, A Taylor-Weiner, ...
JAMA oncology 5 (4), 514-522, 2019
612019
Cytomegalovirus latent infection is associated with an increased risk of COVID-19-related hospitalization
C Alanio, A Verma, D Mathew, S Gouma, G Liang, T Dunn, DA Oldridge, ...
The Journal of Infectious Diseases 226 (3), 463-473, 2022
522022
Polygenic risk scores and coronary artery disease: ready for prime time?
MG Levin, DJ Rader
Circulation 141 (8), 637-640, 2020
522020
The Penn Medicine BioBank: towards a genomics-enabled learning healthcare system to accelerate precision medicine in a diverse population
A Verma, SM Damrauer, N Naseer, JE Weaver, CM Kripke, L Guare, ...
Journal of Personalized Medicine 12 (12), 1974, 2022
492022
A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes
J Park, MG Levin, CM Haggerty, DN Hartzel, R Judy, RL Kember, N Reza, ...
Genetics in Medicine 22 (1), 102-111, 2020
492020
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations
J Park, AM Lucas, X Zhang, K Chaudhary, JH Cho, G Nadkarni, A Dobbyn, ...
Nature medicine 27 (1), 66-72, 2021
442021
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
MG Levin, NL Tsao, P Singhal, C Liu, HMT Vy, I Paranjpe, JD Backman, ...
Nature Communications 13 (1), 6914, 2022
412022
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