Philippe M. Frossard, PhD

Affiliations: 
Biological and Biomedical Sciences The Aga Khan University 
Area:
Genetics Stroke
Google:
"Philippe Frossard"
Mean distance: 106866
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Harshfield EL, Koulman A, Ziemek D, et al. (2019) An unbiased lipid phenotyping approach to study the genetic determinants of lipids and their association with coronary heart disease risk factors. Journal of Proteome Research
Liu DJ, Peloso GM, Yu H, et al. (2017) Exome-wide association study of plasma lipids in >300,000 individuals. Nature Genetics
Zhao W, Rasheed A, Tikkanen E, et al. (2017) Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. Nature Genetics
Howson JMM, Zhao W, Barnes DR, et al. (2017) Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nature Genetics
Saleheen D, Zhao W, Young R, et al. (2017) Loss of Cardio-Protective Effects at the ADAMTS7 Locus Due to Gene-Smoking Interactions. Circulation
Saleheen D, Natarajan P, Armean IM, et al. (2017) Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity. Nature. 544: 235-239
Stitziel NO, Khera AV, Wang X, et al. (2017) ANGPTL3 Deficiency and Protection Against Coronary Artery Disease. Journal of the American College of Cardiology
Surendran P, Drenos F, Young R, et al. (2016) Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nature Genetics
Imamura M, Takahashi A, Yamauchi T, et al. (2016) Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes. Nature Communications. 7: 10531
Nikpay M, Goel A, Won HH, et al. (2015) A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nature Genetics. 47: 1121-30
See more...