Browsing by Author Forgetta, V

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Showing results 1 to 8 of 8
Issue DateTitleAuthor(s)
1-Feb-2019An atlas of genetic influences on osteoporosis in humans and miceMorris, JA; Kemp, JP; Youlten, SE; Laurent, L; Logan, JG, et al
2-Mar-2016Correction: Vitamin D and risk of multiple sclerosis: a Mendelian randomization studyMokry, LE; Ross, S; Ahmad, OS; Forgetta, V; Smith, GD, et al
5-Jun-2018Genome-wide association study of extreme high bone mass: contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genesGregson, CL; Newell, F; Leo, PJ; Clark, GR; Paternoster, L, et al
4-Sep-2017Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosisKemp, JP; Morris, JA; Medina-Gomez, C; Forgetta, V; Warrington, NM, et al
4-Jan-2018Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.Medina-Gomez, C; Kemp, JP; Trajanoska, K; Luan, J; Chesi, A, et al
4-Dec-2020Sex differences in the risk of coronary heart disease associated with type 2 diabetes: a Mendelian Randomization analysisPeters, TM; Holmes, MV; Richards, JB; Palmer, T; Forgetta, V, et al
1-Dec-2020The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypesNakanishi, T; Forgetta, V; Handa, T; Hirai, T; Mooser, V, et al
25-Dec-2016Vitamin D and risk of multiple sclerosis: a Mendelian randomization studyMokry, LE; Ross, S; Ahmad, OS; Forgetta, V; Smith, GD, et al