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Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.
Plos Genetics|August 1, 2014
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass indexClive J Hoggart, Giulia Venturini, Massimo Mangino, et al.
Nature Communications|August 5, 2015
Rare coding variants and X-linked loci associated with age at menarcheKathryn L Lunetta, Felix R Day, Patrick Sulem, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Nature Medicine|August 1, 2022
Large-scale genome-wide association study of coronary artery disease in genetically diverse populationsCatherine Tcheandjieu, Xiang Zhu, Austin T Hilliard, et al.
Circulation|December 28, 2018
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma LevelsMaria Sabater-Lleal, Jennifer E Huffman, Paul S de Vries, et al.
European Journal of Human Genetics : EJHG|May 5, 2016
Genetic variants in RBFOX3 are associated with sleep latencyNajaf Amin, Karla V Allebrandt, Ashley van der Spek, et al.
Nature Genetics|September 13, 2011
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaqueJoshua C Bis, Maryam Kavousi, Nora Franceschini, et al.
Nature Genetics|December 17, 2009
Genome-wide association study identifies five loci associated with lung functionEmmanouela Repapi, Ian Sayers, Louise V Wain, et al.
Nature Communications|December 5, 2015
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputationMaría Soler Artigas, Louise V Wain, Suzanne Miller, et al.
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