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Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Nagy, Reka; Boutin, Thibaud S; Marten, Jonathan; Huffman, Jennifer E; Kerr, Shona M; Campbell, Archie; Evenden, Louise; Gibson, Jude; Amador, Carmen; Howard, David M; Navarro, Pau; Morris, Andrew; Deary, Ian J; Hocking, Lynne J; Padmanabhan, Sandosh; Smith, Blair H; Joshi, Peter; Wilson, James F; Hastie, Nicholas D; Wright, Alan F; McIntosh, Andrew M; Porteous, David J; Haley, Chris S; Vitart, Veronique; Hayward, Caroline.
Afiliação
  • Nagy R; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Boutin TS; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Marten J; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Huffman JE; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Kerr SM; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Campbell A; Centre for Genomic and Experimental Medicine, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh, UK.
  • Evenden L; Edinburgh Clinical Research Facility, University of Edinburgh, Edinburgh, UK.
  • Gibson J; Edinburgh Clinical Research Facility, University of Edinburgh, Edinburgh, UK.
  • Amador C; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Howard DM; Division of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, UK.
  • Navarro P; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Morris A; Farr Institute of Health Informatics Research, Edinburgh, UK.
  • Deary IJ; Centre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, Edinburgh, UK.
  • Hocking LJ; Division of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.
  • Padmanabhan S; Division of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Smith BH; Medical Research Institute, University of Dundee, Dundee, UK.
  • Joshi P; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, EH8 9AG, UK.
  • Wilson JF; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, EH8 9AG, UK.
  • Hastie ND; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Wright AF; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
  • McIntosh AM; Division of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, UK.
  • Porteous DJ; Centre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, Edinburgh, UK.
  • Haley CS; Centre for Genomic and Experimental Medicine, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh, UK.
  • Vitart V; Centre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, Edinburgh, UK.
  • Hayward C; MRC Human Genetics Unit, University of Edinburgh, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.
Genome Med ; 9(1): 23, 2017 03 07.
Article em En | MEDLINE | ID: mdl-28270201
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Haplótipos / Característica Quantitativa Herdável / Polimorfismo de Nucleotídeo Único Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Genome Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Haplótipos / Característica Quantitativa Herdável / Polimorfismo de Nucleotídeo Único Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Genome Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido