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 TitleAuthors / EditorsDate
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A comprehensive evaluation of the genetic architecture of sudden cardiac arrest SCD working group of the CHARGE Consortium 2018
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A frequent hypofunctional IRAK2 variant is associated with reduced spontaneous hepatitis C virus clearance Wang, Hui; El Maadidi, Souhayla; Fischer, Janett; Grabski, Elena; ... Weber, Alexander N R 2015
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Accurate, scalable and integrative haplotype estimation Delaneau, Olivier; Zagury, Jean-François; Robinson, Matthew R; Marchini, Jonathan L; Dermitzakis, Emmanouil 2019
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Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 Wang, Heming; Nandakumar, Priyanka; Tekola-Ayele, Fasil; Tayo, Bamidele O; ... Zhu, Xiaofeng 2019
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Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study Sardahaee, Farzaneh Saeedzadeh; Holmen, Turid Lingaas; Micali, Nadia; Kvaløy, Kirsti 2017
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Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes Stekelenburg, Caroline; Gerster, Karine; Blouin, Jean-Louis; Lang-Muritano, Mariarosaria; ... Schwitzgebel Luscher, Valérie 2019
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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
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Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles EPIC-CVD consortium and the CHD Exome+ consortium 2017
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Genetic loci associated with heart rate variability and their effects on cardiac disease risk Nolte, Ilja M; Munoz, M Loretto; Tragante, Vinicius; Snieder, Harold; de Geus, Eco J C 2017
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Genetic polymorphisms associated with smoking behaviour predict the risk of surgery in patients with Crohn's disease Lang, B M; Biedermann, L; van Haaften, W T; de Vallière, C; ... Misselwitz, B 2018
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Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D. Vinuela Rodriguez, Ana; McCarthy, Mark I 2020
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Genome analysis of a major urban malaria vector mosquito, Anopheles stephensi Jiang, Xiaofang; Peery, Ashley; Hall, A Brantley; Sharma, Atashi; ... Tu, Zhijian 2014
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Incorporation of GSTA1 genetic variations into a population pharmacokinetic model for IV busulfan in paediatric hematopoietic stem cell transplantation Nava, Tiago; Kassir, Nastya; Rezgui, Mohamed Aziz; Uppugunduri Satyanarayana, Chakradhara Rao; ... Bittencourt, Henrique 2018
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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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Molecular characterization of Treponema pallidum subsp. pallidum in Switzerland and France with a new multilocus sequence typing scheme Grillová, Linda; Bawa, Tanika; Mikalová, Lenka; Gayet-Ageron, Angèle; ... Bosshard, Philipp P 2018
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Molecular pathways associated with blood pressure and hexadecanedioate levels Menni, Cristina; Metrustry, Sarah J; Ehret, Georg Benedikt; Dominiczak, Anna F; ... Valdes, Ana M 2017
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New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals CHARGE EXOME BP Consortium, CHD Exome+ Consortium, Exome BP Consortium, GoT2D:T2DGenes Consortium, The UK Biobank Cardio-Metabolic Traits Consortium Blood Pressure Working Group 2017
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Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries Collaboration 2018
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Prescription d’antidépresseurs dans le traitement de la douleur : rôle de la pharmacogénétique Rodieux, Frédérique; Piguet, Valérie; Berney, Patricia Elisabeth; Desmeules, Jules Alexandre; Besson, Marie 2015
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SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease Ramirez, Alfredo; van der Flier, Wiesje M; Herold, Christine; Ramonet, David 2014
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