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Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes.
Gregson, Celia L; Newell, Felicity; Leo, Paul J; Clark, Graeme R; Paternoster, Lavinia; Marshall, Mhairi; Forgetta, Vincenzo; Morris, John A; Ge, Bing; Bao, Xiao; Duncan Bassett, J H; Williams, Graham R; Youlten, Scott E; Croucher, Peter I; Davey Smith, George; Evans, David M; Kemp, John P; Brown, Matthew A; Tobias, Jon H; Duncan, Emma L.
Afiliación
  • Gregson CL; Musculoskeletal Research Unit, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK. Electronic address: celia.gregson@bristol.ac.uk.
  • Newell F; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia.
  • Leo PJ; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia.
  • Clark GR; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia.
  • Paternoster L; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Marshall M; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia.
  • Forgetta V; Department of Human Genetics, McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
  • Morris JA; Department of Human Genetics, McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
  • Ge B; Department of Human Genetics, McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada; Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada.
  • Bao X; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia.
  • Duncan Bassett JH; Molecular Endocrinology Laboratory, Department of Medicine, Imperial College London, Hammersmith Campus, London W12 0NN, UK.
  • Williams GR; Molecular Endocrinology Laboratory, Department of Medicine, Imperial College London, Hammersmith Campus, London W12 0NN, UK.
  • Youlten SE; The Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
  • Croucher PI; The Garvan Institute of Medical Research, Sydney, New South Wales, Australia; St Vincent's Clinical School, University of New South Wales Medicine, Sydney, New South Wales, Australia.
  • Davey Smith G; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Evans DM; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK; University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
  • Kemp JP; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK; University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
  • Brown MA; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia.
  • Tobias JH; Musculoskeletal Research Unit, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Duncan EL; Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology at Translational Research Institute, 37 Kent Street, Woolloongabba 4102, QLD, Australia; Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
Bone ; 114: 62-71, 2018 09.
Article en En | MEDLINE | ID: mdl-29883787
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Variación Genética / Densidad Ósea / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo / Vértebras Lumbares Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Bone Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenotipo / Variación Genética / Densidad Ósea / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo / Vértebras Lumbares Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Bone Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos