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Orphanet Journal of Rare Diseases|April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAPSarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.The Lancet. Diabetes & Endocrinology|June 30, 2014
Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation studyKarani S Vimaleswaran, Alana Cavadino, Diane J Berry, et al.Nature Communications|January 19, 2018
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levelsXia Jiang, Paul F O'Reilly, Hugues Aschard, et al.EJNMMI Research|April 20, 2016
32nd International Austrian Winter Symposium : Zell am See, the Netherlands. 20-23 January 2016W Langsteger, A Rezaee, W Loidl, et al.Nature Genetics|October 6, 2014
Defining the role of common variation in the genomic and biological architecture of adult human heightAndrew R Wood, Tonu Esko, Jian Yang, et al.Nature|February 13, 2015
Genetic studies of body mass index yield new insights for obesity biologyAdam E Locke, Bratati Kahali, Sonja I Berndt, et al.Pageof 177