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 TitleAuthors / EditorsDate
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Characteristics of patients with chronic hepatitis C who develop hepatocellular carcinoma Kuske, Lorenz; Mensen, Armand; Müllhaupt, Beat; Negro, Francesco; ... Dufour, Jean-François Jacques 2012
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Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection Patin, Etienne; Kutalik, Zoltán; Guergnon, Julien; Bibert, Stéphanie; ... Abel, Laurent 2012
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The impact of fibrosis and steatosis on early viral kinetics in HCV genotype 1-infected patients treated with Peg-IFN-alfa-2a and ribavirin Guedjo, Hervé; Guedj, J; Negro, Francesco; Lagging, M; ... Neumann, A U 2012
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Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy Lange, Christian M; Kutalik, Zoltan; Morikawa, Kenichi; Bibert, Stéphanie; ... Bochud, Pierre-Yves 2012
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Liver kidney microsomal type 1 antibodies reduce the CYP2D6 activity in patients with chronic hepatitis C virus infection Girardin, François; Daali, Youssef; Gex-Fabry, Marianne; Rebsamen, Michela; ... Desmeules, Jules Alexandre 2012
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Appearance of a novel measles G3 strain in multiple European countries within a two month period, 2010 Brown, KE; Mulders, MN; Freymuth, F; Santibanez, S; ... Featherstone, D 2011
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Replication of association between a SCN1A splice variant and febrile seizures Le Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain 2011
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War exposure, 5-HTTLPR genotype and lifetime risk of depression Artero, Sylvaine; Touchon, Jacques; Dupuy, Anne-Marie; Malafosse, Alain; Ritchie, Karen 2011
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The architecture of gene regulatory variation across multiple human tissues: the MuTHER study Nica, Alexandra; Parts, Leopold; Glass, Daniel; Nisbet, James; ... Spector, Timothy D 2011
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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage International Stem Cell Initiative 2011
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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Saad, Mohamad; Lesage, Suzanne; Saint-Pierre, Aude; Corvol, Jean-Christophe; ... Brice, Alexis 2011
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W 2011
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Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes Strawbridge, Rona J 2011
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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
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Catechol-O-methyltransferase Val158Met polymorphism moderates anterior cingulate volume in posttraumatic stress disorder Schulz-Heik, R Jay; Schaer, Marie; Eliez, Stéphan; Hallmayer, Joachim F; ... Woodward, Steven H 2011
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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease Krüger, Rejko; Sharma, Manu 2011
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Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A 2011
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Molecular and epidemiological evaluation of strain replacement in patients previously harboring gentamicin-resistant MRSA. De Angelis, Giulia; Francois, Patrice; Lee, Andie; Schrenzel, Jacques; ... Harbarth, Stéphan Juergen 2011
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Management of hepatitis C virus (HCV) infection in drug substitution programs Witteck, Andrea; Schmid, Patrick; Hensel-Koch, Katharina; Thurnheer, Maria C; ... Moradpour, D 2011
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Epidemiology and virulence insights from MRSA and MSSA genome analysis Lazarevic, Vladimir; Beaume, Marie-Emilie; Corvaglia, Anna; Hernandez, David; ... Francois, Patrice 2011
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