Підписатись
Dermot F Reilly
Dermot F Reilly
Janssen
Підтверджена електронна адреса в its.jnj.com
Назва
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Посилання
Рік
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
TG and HDL Working Group of the Exome Sequencing Project, National Heart ...
New England Journal of Medicine 371 (1), 22-31, 2014
8212014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ...
Nature 518 (7537), 102-106, 2015
7592015
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
6322017
The MBOAT7-TMC4 variant rs641738 increases risk of nonalcoholic fatty liver disease in individuals of European descent
RM Mancina, P Dongiovanni, S Petta, P Pingitore, M Meroni, R Rametta, ...
Gastroenterology 150 (5), 1219-1230. e6, 2016
6182016
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
6012019
Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758-1766, 2017
5292017
Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting
P Natarajan, R Young, NO Stitziel, S Padmanabhan, U Baber, R Mehran, ...
Circulation 135 (22), 2091-2101, 2017
4972017
Circadian variation of blood pressure and the vascular response to asynchronous stress
AM Curtis, Y Cheng, S Kapoor, D Reilly, TS Price, GA FitzGerald
Proceedings of the National Academy of Sciences 104 (9), 3450-3455, 2007
4442007
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
3952016
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
3922021
Integration of proteomics and genomics in platelets: a profile of platelet proteins and platelet-specific genes
JP McRedmond, SD Park, DF Reilly, JA Coppinger, PB Maguire, ...
Molecular & Cellular Proteomics 3 (2), 133-144, 2004
3732004
The trans-ancestral genomic architecture of glycemic traits
J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ...
Nature genetics 53 (6), 840-860, 2021
3682021
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
3242018
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
P Surendran, F Drenos, R Young, H Warren, JP Cook, AK Manning, ...
Nature genetics 48 (10), 1151-1161, 2016
3142016
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
2822022
Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease
TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ...
Journal of the American College of Cardiology 69 (7), 823-836, 2017
2442017
Bioinformatic analysis of circadian gene oscillation in mouse aorta
RD Rudic, P McNamara, D Reilly, T Grosser, AM Curtis, TS Price, ...
Circulation 112 (17), 2716-2724, 2005
1792005
Genetic components of the circadian clock regulate thrombogenesis in vivo
EJ Westgate, Y Cheng, DF Reilly, TS Price, JA Walisser, CA Bradfield, ...
Circulation 117 (16), 2087-2095, 2008
1732008
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
A Teumer, Y Li, S Ghasemi, BP Prins, M Wuttke, T Hermle, A Giri, ...
Nature communications 10 (1), 4130, 2019
1472019
Phenome-wide association studies across large population cohorts support drug target validation
D Diogo, C Tian, CS Franklin, M Alanne-Kinnunen, M March, ...
Nature communications 9 (1), 1-13, 2018
1432018
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