Chong, Michael

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

Schmidt, A. F., Swerdlow, D. I., Holmes, M. V., Patel, R. S., Fairhurst-Hunter, Z., Lyall, D. M., Hartwig, F. P., Horta, B. L., Hyppönen, E., Power, C., et al. (2017) · The Lancet Diabetes & Endocrinology

Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology

Cited by 380

Polygenic risk score predicts prevalence of cardiovascular disease in patients with familial hypercholesterolemia

Paquette, M., Chong, M., Thériault, S., Dufour, R., Paré, G., & Baass, A. (2017) · Journal of Clinical Lipidology

Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology

Cited by 115

Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease

Sjaarda, J., Gerstein, H., Chong, M., Yusuf, S., Meyre, D., Anand, S. S., Hess, S., & Paré, G. (2018) · Journal of the American College of Cardiology

Genetic Associations and EpidemiologyAtherosclerosis and Cardiovascular Diseases

Cited by 94

Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups

Grami, N., Chong, M., Lali, R., Mohammadi-Shemirani, P., Henshall, D. E., Rannikmäe, K., & Paré, G. (2020) · Stroke

Cerebrovascular and genetic disordersGenomics and Rare Diseases

Cited by 38

Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases

Li, Y., Cheng, Y., Consolato, F., Schiano, G., Chong, M. R., Pietzner, M., Nguyen, N. Q. H., Scherer, N., Biggs, M. L., Kleber, M. E., et al. (2022) · JCI Insight

Genetic Associations and EpidemiologyRenal Diseases and Glomerulopathies

Cited by 22