עקוב אחר
Anthony Marcketta
Anthony Marcketta
Regeneron Genetics Center
כתובת אימייל מאומתת בדומיין regeneron.com
כותרת
צוטט על ידי
צוטט על ידי
שנה
Computationally efficient whole-genome regression for quantitative and binary traits
J Mbatchou, L Barnard, J Backman, A Marcketta, JA Kosmicki, ...
Nature genetics 53 (7), 1097-1103, 2021
9512021
Exome sequencing and analysis of 454,787 UK Biobank participants
JD Backman, AH Li, A Marcketta, D Sun, J Mbatchou, MD Kessler, ...
Nature 599 (7886), 628-634, 2021
6942021
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
5832016
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
4712020
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MA Wilson Sayres, ...
Nature genetics 48 (6), 593-599, 2016
3782016
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
3122019
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
1472022
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
V Gusarova, C O’Dushlaine, TM Teslovich, PN Benotti, T Mirshahi, ...
Nature communications 9 (1), 2252, 2018
1422018
Genome-wide study of atrial fibrillation identifies seven risk loci and highlights biological pathways and regulatory elements involved in cardiac development
JB Nielsen, LG Fritsche, W Zhou, TM Teslovich, OL Holmen, S Gustafsson, ...
The American Journal of Human Genetics 102 (1), 103-115, 2018
1122018
Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank
CV Van Hout, I Tachmazidou, JD Backman, JX Hoffman, B Ye, AK Pandey, ...
BioRxiv, 572347, 2019
1112019
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
902021
Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe …
JE Horowitz, JA Kosmicki, A Damask, D Sharma, GHL Roberts, AE Justice, ...
MedRxiv, 2020.12. 14.20248176, 2021
232021
Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease
JE Horowitz, JA Kosmicki, A Damask, D Sharma, GHL Roberts, AE Justice, ...
MedRxiv, 2020
222020
Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals
C Gao, A Marcketta, JD Backman, C O'Dushlaine, J Staples, MAR Ferreira, ...
Genetic epidemiology 45 (6), 664-681, 2021
202021
A catalog of associations between rare coding variants and COVID-19 outcomes
JA Kosmicki, JE Horowitz, N Banerjee, R Lanche, A Marcketta, E Maxwell, ...
medRxiv, 2020.10. 28.20221804, 2021
182021
A deep catalogue of protein-coding variation in 983,578 individuals
KY Sun, X Bai, S Chen, S Bao, C Zhang, M Kapoor, J Backman, T Joseph, ...
Nature 631 (8021), 583-592, 2024
172024
Genetic association analysis of SARS-CoV-2 infection in 455,838 UK Biobank participants
JA Kosmicki, JE Horowitz, N Banerjee, R Lanche, A Marcketta, E Maxwell, ...
152020
A deep catalog of protein-coding variation in 985,830 individuals
KY Sun, X Bai, S Chen, S Bao, M Kapoor, C Zhang, J Backman, T Joseph, ...
BioRxiv, 2023
112023
Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank
SM Gaynor, T Joseph, X Bai, Y Zou, B Boutkov, EK Maxwell, O Delaneau, ...
Nature genetics 56 (11), 2345-2351, 2024
82024
Rare and common genetic variation underlying atrial fibrillation risk
OB Vad, LM Monfort, C Paludan-Müller, K Kahnert, SZ Diederichsen, ...
JAMA cardiology 9 (8), 732-740, 2024
82024
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מאמרים 1–20