Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
Year: 2018
Type: article
Study design: Observational Study
Authors: Alicia R. Martin, Konrad J. Karczewski, Sini Kerminen, Mitja I. Kurki, Antti-Pekka Sarin, Mykyta Artomov, Johan G. Eriksson, Tõnu Esko, Giulio Genovese, Aki S. Havulinna, Jaakko Kaprio, Alexandra Konradi, László Korányi, Anna Kostareva, Minna Männikkö, Andres Metspalu, Markus Perola, Rashmi B. Prasad, Olli Raitakari, Oxana Rotar, Veikko Salomaa, Leif Groop, Aarno Palotie, Benjamin M. Neale, Samuli Ripatti, Matti Pirinen, Mark J. Daly
Institutions: Broad Institute, Massachusetts General Hospital, Stanley Center for Psychiatric Research, Massachusetts Institute of Technology, Harvard University, University of Helsinki, Institute for Molecular Medicine Finland, Finnish Institute for Health and Welfare, Helsinki University Hospital, Folkhälsans Forskningscentrum, University of Tartu, ITMO University, Federal Almazov North-West Medical Research Centre, University of Oulu, University of Turku, Turku University Hospital, Lund University, Skåne University Hospital, Helsinki Institute for Information Technology
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
Funders: Helsingin Yliopisto, University of Washington, Broad Institute, European Foundation for the Study of Diabetes, Eesti Teadusagentuur, Academy of Finland, Novo Nordisk, Sydäntutkimussäätiö, Sigrid Juséliuksen Säätiö, Russian Science Foundation, Novo Nordisk Fonden, National Institutes of Health, Horizon 2020, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Human Genome Research Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G1051078291, G1061290065, G1152568796, G1569838456, G1591729927, 1/2 A Large-Scale Schizophrenia Association Study in Sweden, G1754968858, G2433343305, 1/7 Psychiatric Genomics Consortium: Finding actionable variation, G2809226964, A Platform for Large-Scale Genomic Discovery, G2900443037, G3187080867, G3942382998, G4462439720, Genomic and Metabolomic Profiling of Finnish Familial Dyslipidemia Families, G567861331, G7221506883, Utilising special human populations to quantify the impact of rare DNA sequence variants in human health, G8163728846, G8311891658, G8337069619, Biological Insights from Genetic Investigation of ANthropometric Traits (GIANT) Across the Allelic Spectrum, Center for the Study of Inflammatory Bowel Disease at Massachusetts General Hospital
OpenAlex ID: W2763810423