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 TitleAuthors / EditorsDate
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Genetic and clinic predictors of new onset diabetes mellitus after transplantation Saigi-Morgui, Núria; Quteineh, Lina; Bochud, Pierre-Yves; Crettol, Séverine; ... Eap, Chin Bin 2019
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Transient PAX8 Expression in Islets During Pregnancy Correlates With β-Cell Survival, Revealing a Novel Candidate Gene in Gestational Diabetes Mellitus Martin-Montalvo, Alejandro; López-Noriega, Livia; Jiménez-Moreno, Carmen; Herranz, Amanda; ... Gauthier, Benoit R 2019
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Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference Young, Alexandra L; Marinescu, Razvan V; Oxtoby, Neil P; Bocchetta, Martina; ... Alexander, Daniel C 2018
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Quantifying the fitness cost of HIV-1 drug resistance mutations through phylodynamics Kühnert, Denise; Kouyos, Roger; Shirreff, George; Pečerska, Jūlija; ... Bonhoeffer, Sebastian 2018
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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 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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EASL Clinical Practice Guidelines on hepatitis E virus infection European Association for the Study of the Liver 2018
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Differential daptomycin resistance development in Staphylococcus aureus strains with active and mutated gra regulatory systems Müller, Anna; Grein, Fabian; Otto, Andreas; Gries, Kathrin; ... Sahl, Hans-Georg 2018
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NBEA: Developmental disease gene with early generalized epilepsy phenotypes Mulhern, Maureen S; Stumpel, Constance; Stong, Nicholas; Brunner, Han G; ... Sands, Tristan T 2018
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A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two families Fabre, Alexandre; Petit, Laëtitia Marie; Hansen, Lars F; Wewer, Anne V; ... Paerregaard, Anders 2018
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Mutational epidemiology of congenital fibrinogen disorders Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite 2018
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Association Between Oxytocin Receptor Genotype, Maternal Care, and Eating Disorder Behaviours in a Community Sample of Women Micali, Nadia; Crous-Bou, Marta; Treasure, Janet; Lawson, Elizabeth A 2017
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Genetic effects on gene expression across human tissues GTEx Consortium 2017
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Antimicrobial activity of ceftaroline against methicillin-resistant Staphylococcus aureus (MRSA) isolates collected in 2013-2014 at the Geneva University Hospitals Andrey, D O; Francois, Patrice; Manzano, Caroline Stéphanie; Bonetti, E J; ... Renzoni, Adriana Maria 2017
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Exploring venlafaxine pharmacokinetic variability with a phenotyping approach, a multicentric french-swiss study (MARVEL study) Lloret-Linares, Célia; Daali, Youssef; Chevret, Sylvie; Nieto, Isabelle; ... Bellivier, Frank 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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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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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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Role of Gag mutations in PI resistance in the Swiss HIV cohort study: bystanders or contributors? Kletenkov, K; Hoffmann, D; Böni, J; Yerly Ferrillo, Sabine; ... Klimkait, T 2017
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Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations Yoneyama, S; Yao, J; Guo, X; Fernandez-Rhodes, L; ... North, K E 2017
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