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Paper Details

Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.
Eur J Hum Genet
10
2015
CHD, FH, HumanHap550K, Illumina HumanHap550K chip, LDLR, SNPs, coronary heart disease, familial hypercholesterolemia, genetic risk variants, low-density lipoprotein receptor, low-density lipoprotein receptor (LDLR) gene, patients, premature CHD, single nucleotide polymorphisms
Author NameAffiliation
Abbas DehghanErasmus University Medical Center
Abbas DehghanErasmus University Medical Center
Hilma Holm
Yurii S AulchenkoErasmus University Medical Center, The Netherlands [2] Novosibirsk State University
Gudmar Thorleifsson
Gudmar Thorleifsson
Heribert SchunkertTechnische Universitat Munchen
Andr?? G UitterlindenErasmus University Medical Center
Andr?? G UitterlindenErasmus University Medical Center
Cornelia M van DuijnErasmus University Medical Center
Cornelia M van DuijnErasmus University Medical Center
Jose M OrdovasJean Mayer USDA HNRCA at Tufts University
Jose M OrdovasJean Mayer USDA HNRCA at Tufts University
Albert HofmanErasmus University Medical Center
Albert HofmanErasmus University Medical Center
Jacqueline C M WittemanErasmus University Medical Center
Steve E HumphriesInstitute Cardiovascular Science, University College London
John J P KasteleinAmsterdam Medical Center
Eric J G SijbrandsErasmus University Medical Center
Eric J G SijbrandsErasmus University Medical Center
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