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Homozygous loss-of-function variants in European cosmopolitan and isolate populations.
Kaiser, Vera B; Svinti, Victoria; Prendergast, James G; Chau, You-Ying; Campbell, Archie; Patarcic, Inga; Barroso, Inês; Joshi, Peter K; Hastie, Nicholas D; Miljkovic, Ana; Taylor, Martin S; Enroth, Stefan; Memari, Yasin; Kolb-Kokocinski, Anja; Wright, Alan F; Gyllensten, Ulf; Durbin, Richard; Rudan, Igor; Campbell, Harry; Polasek, Ozren; Johansson, Åsa; Sauer, Sascha; Porteous, David J; Fraser, Ross M; Drake, Camilla; Vitart, Veronique; Hayward, Caroline; Semple, Colin A; Wilson, James F.
Afiliação
  • Kaiser VB; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and vera.kaiser@igmm.ed.ac.uk.
  • Svinti V; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Prendergast JG; The Roslin Institute, The University of Edinburgh, Easter Bush, Midlothian EH25 9RG, UK.
  • Chau YY; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Campbell A; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Patarcic I; Medical School, University of Split, Soltanska 2, Split 21000, Croatia.
  • Barroso I; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Joshi PK; Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
  • Hastie ND; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Miljkovic A; Medical School, University of Split, Soltanska 2, Split 21000, Croatia.
  • Taylor MS; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Enroth S; Department of Immunology, Genetics, and Pathology, Biomedical Center, SciLifeLab Uppsala, Uppsala University, Uppsala SE-75108, Sweden and.
  • Memari Y; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Kolb-Kokocinski A; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Wright AF; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Gyllensten U; Department of Immunology, Genetics, and Pathology, Biomedical Center, SciLifeLab Uppsala, Uppsala University, Uppsala SE-75108, Sweden and.
  • Durbin R; Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
  • Rudan I; Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
  • Campbell H; Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
  • Polasek O; Medical School, University of Split, Soltanska 2, Split 21000, Croatia, Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
  • Johansson Å; Department of Immunology, Genetics, and Pathology, Biomedical Center, SciLifeLab Uppsala, Uppsala University, Uppsala SE-75108, Sweden and.
  • Sauer S; Max-Planck-Institute for Molecular Genetics, Otto-Warburg-Laboratory, Berlin, Germany.
  • Porteous DJ; Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh EH4 2XU, UK.
  • Fraser RM; Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
  • Drake C; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Vitart V; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Hayward C; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Semple CA; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and.
  • Wilson JF; MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine and Usher Institute for Population Health Sciences and Informatics, University of Edinburgh, Teviot Place, Edinburgh EH8 9AG, UK.
Hum Mol Genet ; 24(19): 5464-74, 2015 Oct 01.
Article em En | MEDLINE | ID: mdl-26173456
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: População Branca / Mutação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: População Branca / Mutação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article