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American Journal of Human Genetics|September 3, 2016
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal PolyneuropathiesMichaela Auer-Grumbach, Stefan Toegel, Maria Schabhüttl, et al.
Plos Medicine|February 16, 2006
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS studyStuart H Ralston, André G Uitterlinden, Maria Luisa Brandi, et al.
Annals of Internal Medicine|August 16, 2006
The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysisAndré G Uitterlinden, Stuart H Ralston, Maria Luisa Brandi, et al.
Bone|February 21, 2008
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS studyBente L Langdahl, André G Uitterlinden, Stuart H Ralston, et al.
JAMA|March 20, 2008
Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosisJoyce B J van Meurs, Thomas A Trikalinos, Stuart H Ralston, et al.
NPJ Breast Cancer|March 21, 2026
A multi-ancestry genome-wide study of tamoxifen metabolism and breast cancer recurrenceChiea Chuen Khor, Whee Sze Ong, Elaine Hsuen Lim, et al.
Nature Genetics|February 10, 2009
New susceptibility locus for coronary artery disease on chromosome 3q22.3Jeanette Erdmann, Anika Grosshennig, Peter S Braund, et al.
Circulation. Cardiovascular Genetics|June 24, 2010
Genetic determinants of major blood lipids in Pakistanis compared with EuropeansDanish Saleheen, Nicole Soranzo, Asif Rasheed, et al.
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