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Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability | PLOS ONE
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Analysis of protein-coding genetic variation in 60,706 humans | Nature
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Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior: Cell
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior: Cell
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Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior: Cell
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Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability | PLOS ONE
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Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature - Inga Talvik, Rikke S. Møller, Merilin Vaher, Ulvi Vaher, Line HG Larsen, Hans A. Dahl, Pilvi Ilves, Tiina
