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Geisinger MyCode
Geisinger MyCode
Geisinger MyCode Community Health Initiative
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Title
Cited by
Cited by
Year
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
JJ Lee, R Wedow, A Okbay, E Kong, O Maghzian, M Zacher, ...
Nature genetics 50 (8), 1112-1121, 2018
19302018
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
7572017
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
6782018
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
6342017
A catalog of genetic loci associated with kidney function from analyses of a million individuals
M Wuttke, Y Li, M Li, KB Sieber, MF Feitosa, M Gorski, A Tin, L Wang, ...
Nature genetics 51 (6), 957-972, 2019
6032019
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ...
Nature genetics 50 (9), 1234-1239, 2018
5892018
Genetics of blood lipids among~ 300,000 multi-ethnic participants of the Million Veteran Program
D Klarin, SM Damrauer, K Cho, YV Sun, TM Teslovich, J Honerlaw, ...
Nature genetics 50 (11), 1514-1523, 2018
5552018
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
FE Dewey, MF Murray, JD Overton, L Habegger, JB Leader, SN Fetterolf, ...
Science 354 (6319), aaf6814, 2016
5482016
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
S Shah, A Henry, C Roselli, H Lin, G Sveinbjörnsson, G Fatemifar, ...
Nature communications 11 (1), 163, 2020
5282020
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
FE Dewey, V Gusarova, C O’Dushlaine, O Gottesman, J Trejos, C Hunt, ...
New England Journal of Medicine 374 (12), 1123-1133, 2016
4952016
Genetic identification of familial hypercholesterolemia within a single US health care system
NS Abul-Husn, K Manickam, LK Jones, EA Wright, DN Hartzel, ...
Science 354 (6319), aaf7000, 2016
4202016
Exome sequencing and characterization of 49,960 individuals in the UK Biobank
CV Van Hout, I Tachmazidou, JD Backman, JD Hoffman, D Liu, ...
Nature 586 (7831), 749-756, 2020
3912020
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study
AF Schmidt, DI Swerdlow, MV Holmes, RS Patel, Z Fairhurst-Hunter, ...
The lancet Diabetes & endocrinology 5 (2), 97-105, 2017
3832017
The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research
DJ Carey, SN Fetterolf, FD Davis, WA Faucett, HL Kirchner, U Mirshahi, ...
Genetics in medicine 18 (9), 906-913, 2016
3752016
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
3262018
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
LV Wain, N Shrine, MS Artigas, AM Erzurumluoglu, B Noyvert, ...
Nature genetics 49 (3), 416-425, 2017
2962017
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
A Tin, J Marten, VL Halperin Kuhns, Y Li, M Wuttke, H Kirsten, KB Sieber, ...
Nature genetics 51 (10), 1459-1474, 2019
2842019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
J Flannick, JM Mercader, C Fuchsberger, MS Udler, A Mahajan, J Wessel, ...
Nature 570 (7759), 71-76, 2019
2802019
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
P Gharahkhani, E Jorgenson, P Hysi, AP Khawaja, S Pendergrass, X Han, ...
Nature communications 12 (1), 1258, 2021
2182021
The IGNITE network: a model for genomic medicine implementation and research
KW Weitzel, M Alexander, BA Bernhardt, N Calman, DJ Carey, ...
BMC medical genomics 9, 1-13, 2015
2112015
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