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Influence of autozygosity on common disease risk across the phenotypic spectrum.
Malawsky, Daniel S; van Walree, Eva; Jacobs, Benjamin M; Heng, Teng Hiang; Huang, Qin Qin; Sabir, Ataf H; Rahman, Saadia; Sharif, Saghira Malik; Khan, Ahsan; Mirkov, Masa Umicevic; Kuwahara, Hiroyuki; Gao, Xin; Alkuraya, Fowzan S; Posthuma, Danielle; Newman, William G; Griffiths, Christopher J; Mathur, Rohini; van Heel, David A; Finer, Sarah; O'Connell, Jared; Martin, Hilary C.
Affiliation
  • Malawsky DS; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. Electronic address: dm22@sanger.ac.uk.
  • van Walree E; Department of Clinical Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands; Department of Complex Trait Genetics Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU Amsterdam, Amsterdam, the Netherlands.
  • Jacobs BM; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK; Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • Heng TH; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Huang QQ; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Sabir AH; West Midlands Regional Clinical Genetics Unit, Birmingham Women's and Children's NHS FT, Birmingham, UK; Institute of Cancer and Genomics, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
  • Rahman S; Queen Square Institute of Neurology, University College London, London, UK.
  • Sharif SM; Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Khan A; Waltham Forest Council, Waltham Forest Town Hall, Forest Road, Walthamstow E17 4JF, UK.
  • Mirkov MU; Congenica Limited, BioData Innovation Centre, Wellcome Genome Campus, Hinxton, UK.
  • Kuwahara H; King Abdullah University of Science and Technology (KAUST), Computational Bioscience Research Center (CBRC), Thuwal 23955, Saudi Arabia.
  • Gao X; King Abdullah University of Science and Technology (KAUST), Computational Bioscience Research Center (CBRC), Thuwal 23955, Saudi Arabia.
  • Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
  • Posthuma D; Department of Complex Trait Genetics Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU Amsterdam, Amsterdam, the Netherlands.
  • Newman WG; Division of Evolution, Infection and Genomics, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester M13 9PL, UK; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Manchester M13 9WL, UK.
  • Griffiths CJ; Wolfson Institute of Population Health, Queen Mary University of London, London, UK; MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, London, UK.
  • Mathur R; Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • van Heel DA; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Finer S; Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK; Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • O'Connell J; 23andMe, Inc., Sunnyvale, CA, USA.
  • Martin HC; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. Electronic address: hcm@sanger.ac.uk.
Cell ; 186(21): 4514-4527.e14, 2023 10 12.
Article in En | MEDLINE | ID: mdl-37757828

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Consanguinity / Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Cell Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Consanguinity / Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Cell Year: 2023 Document type: Article