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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy Syrbe, Steffen; Hedrich, Ulrike B S; Riesch, Erik; Djémié, Tania; ... Lemke, Johannes R 2015
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Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis Vazquez, F; Rodger, M; Carrier, M; Le Gal, G; ... Gandara, E 2015
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An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis Marchetti, Giovanna; Girelli, Domenico; Zerbinati, Carlotta; Lunghi, Barbara; ... Martinelli, Nicola 2015
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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study Winkler, Thomas W; Justice, Anne E; Graff, Mariaelisa; Barata, Llilda 2015
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Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors van de Bunt, Martijn; Manning Fox, Jocelyn E; Dai, Xiaoqing; Barrett, Amy; ... Gloyn, Anna L 2015
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[What's new in internal medicine?] Laffitte, Emmanuel Alexis 2014
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Predicting stroke through genetic risk functions: the CHARGE Risk Score Project Ibrahim-Verbaas, Carla A; Fornage, Myriam; Bis, Joshua C; Choi, Seung Hoan; ... Launer, Lenore J 2014
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Genetic implication of a novel thiamine transporter in human hypertension International Consortium for Blood Pressure Genome-Wide Association Studies 2014
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Prédispositions génétiques dans l'allergie médicamenteuse : importance du HLA Bergmann, Marcel; Villard, Jean; Caubet, Jean-Christoph Roger J-P 2014
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Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31 Villanueva, Adda; Willer, Jason R; Bryois, Julien; Dermitzakis, Emmanouil; ... Davis, Erica E 2014
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High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms Kurki, Mitja I; Gaál, Emília Ilona; Kettunen, Johannes; Lappalainen, Tuuli Emilia; ... Jääskeläinen, Juha E 2014
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Non-alcoholic fatty liver disease and insulin resistance: from bench to bedside Gariani, Karim; Philippe, Jacques; Jornayvaz, François 2013
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Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study Trinquand, Amélie; Tanguy-Schmidt, Aline; Ben Abdelali, Raouf; Lambert, Jérôme; ... Asnafi, Vahid 2013
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Common noncoding UMOD gene variants induce salt-sensitive hypertension and kidney damage by increasing uromodulin expression Trudu, Matteo; Janas, Sylvie; Lanzani, Chiara; Debaix, Huguette; ... Rampoldi, Luca 2013
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A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study Peters, Ulrike; North, Kari E; Sethupathy, Praveen; Buyske, Steve; ... Kooperberg, Charles 2013
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Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations Franceschini, Nora; Fox, Ervin; Zhang, Zhaogong; Edwards, Todd L; ... Zhu, Xiaofeng 2013
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Fine Mapping and Identification of BMI Loci in African Americans Gong, Jian; Schumacher, Fredrick; Lim, Unhee; Hindorff, Lucia A; ... Peters, Ulrike 2013
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Discovery and refinement of loci associated with lipid levels Global Lipids Genetics Consortium 2013
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; ... Morris, Huw R 2013
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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study Pichler, Irene; Del Greco M, Fabiola; Gögele, Martin; Lill, Christina M; ... Pramstaller, Peter 2013
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