フォロー
Steven A. Lubitz
Steven A. Lubitz
所属不明
確認したメール アドレス: mgh.harvard.edu
タイトル
引用先
引用先
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
AV Khera, M Chaffin, KG Aragam, ME Haas, C Roselli, SH Choi, ...
Nature genetics 50 (9), 1219-1224, 2018
28532018
50 year trends in atrial fibrillation prevalence, incidence, risk factors, and mortality in the Framingham Heart Study: a cohort study
RB Schnabel, X Yin, P Gona, MG Larson, AS Beiser, DD McManus, ...
The Lancet 386 (9989), 154-162, 2015
19772015
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
17262021
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524-537, 2018
14632018
Atrial fibrillation begets heart failure and vice versa: temporal associations and differences in preserved versus reduced ejection fraction
R Santhanakrishnan, NA Wang, MG Larson, JW Magnani, DD McManus, ...
Circulation 133 (5), 484-492, 2016
9052016
Simple risk model predicts incidence of atrial fibrillation in a racially and geographically diverse population: the CHARGE‐AF consortium
A Alonso, BP Krijthe, T Aspelund, KA Stepas, MJ Pencina, CB Moser, ...
Journal of the American Heart Association 2 (2), e000102, 2013
8942013
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ...
Nature genetics 44 (6), 670-675, 2012
7122012
Multi-ethnic genome-wide association study for atrial fibrillation
C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ...
Nature genetics 50 (9), 1225-1233, 2018
6992018
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
6932020
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
6892017
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ...
Nature 586 (7831), 763-768, 2020
5722020
Common variants in KCNN3 are associated with lone atrial fibrillation
PT Ellinor, KL Lunetta, NL Glazer, A Pfeufer, A Alonso, MK Chung, ...
Nature genetics 42 (3), 240-244, 2010
5622010
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
5552022
Genome-wide association study of PR interval
A Pfeufer, C Van Noord, KD Marciante, DE Arking, MG Larson, AV Smith, ...
Nature genetics 42 (2), 153-159, 2010
5072010
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
L Folkersen, S Gustafsson, Q Wang, DH Hansen, ÅK Hedman, A Schork, ...
Nature metabolism 2 (10), 1135-1148, 2020
4942020
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data
P Wainschtein, D Jain, Z Zheng, LA Cupples, AH Shadyab, B McKnight, ...
Nature genetics 54 (3), 263-273, 2022
4812022
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
EJ Benjamin, KM Rice, DE Arking, A Pfeufer, C Van Noord, AV Smith, ...
Nature genetics 41 (8), 879-881, 2009
4552009
Cardiac involvement in patients with sarcoidosis: diagnostic and prognostic value of outpatient testing
D Mehta, SA Lubitz, Z Frankel, JP Wisnivesky, AJ Einstein, M Goldman, ...
Chest 133 (6), 1426-1435, 2008
4372008
Lifetime risk of atrial fibrillation according to optimal, borderline, or elevated levels of risk factors: cohort study based on longitudinal data from the Framingham Heart Study
L Staerk, B Wang, SR Preis, MG Larson, SA Lubitz, PT Ellinor, ...
Bmj 361, 2018
4162018
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
LM Amendola, MO Dorschner, PD Robertson, JS Salama, R Hart, ...
Genome research 25 (3), 305-315, 2015
4002015
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