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A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose

artículo científico publicado en 2008

Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

artículo científico publicado en 2020

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network

Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network

scientific article published on 22 September 2020

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

artículo científico publicado en 2012

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

artículo científico publicado en 2012

The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype

scientific article published on 08 October 2018

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