Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

Finland provides unique opportunities to investigate population and medical genomics because of its adoption of unified national electronic health records, detailed historical and birth records, and serial population bottlenecks. We assembled a comprehensive view of recent population history (≤100 g...

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Detalhes bibliográficos
Publicado no:Am J Hum Genet
Main Authors: Martin, Alicia R., Karczewski, Konrad J., Kerminen, Sini, Kurki, Mitja I., Sarin, Antti-Pekka, Artomov, Mykyta, Eriksson, Johan G., Esko, Tõnu, Genovese, Giulio, Havulinna, Aki S., Kaprio, Jaakko, Konradi, Alexandra, Korányi, László, Kostareva, Anna, Männikkö, Minna, Metspalu, Andres, Perola, Markus, Prasad, Rashmi B., Raitakari, Olli, Rotar, Oxana, Salomaa, Veikko, Groop, Leif, Palotie, Aarno, Neale, Benjamin M., Ripatti, Samuli, Pirinen, Matti, Daly, Mark J.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5986696/
https://ncbi.nlm.nih.gov/pubmed/29706349
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2018.03.003
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