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A genetic deficiency in calpastatin and isovalerylcarnitine treatment is associated with enhanced hippocampal long-term potentiation Muller, Dominique; Molinari, I.; Soldati, L.; Bianchi, G. 1995
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Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes Sethupathy, Praveen; Borel, Christelle; Gagnebin, Maryline; Grant, G. R.; ... Antonarakis, Stylianos 2007
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SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension Won, Joong-Ho; Ehret, Georg Benedikt; Chakravarti, Aravinda; Olshen, Richard A 2011
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Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome Friese, Ryan S; Ye, Chun; Nievergelt, Caroline M; Schork, Andrew J; ... O'Connor, Daniel T 2012
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Lack of association between connexin40 polymorphisms and coronary artery disease Pfenniger, Anna; van der Laan, Sander W; Foglia, Bernard; Geindre, Sylvie Françoise; ... Kwak, Brenda 2012
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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci Liu, Chunyu; Kraja, Aldi T; Smith, Jennifer A; Brody, Jennifer A; ... Chasman, Daniel I 2016
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Next Steps for Gene Identification in Primary Hypertension Genomics Ehret, Georg Benedikt 2017
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Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry Nandakumar, Priyanka; Lee, Dongwon; Richard, Melissa A; Tekola-Ayele, Fasil; ... Chakravarti, Aravinda 2017
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala; ... Caulfield, Mark J 2018