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 TitleAuthors / EditorsDate
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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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Mosquito genomics. Extensive introgression in a malaria vector species complex revealed by phylogenomics Fontaine, Michael C; Pease, James B; Steele, Aaron; Waterhouse, Robert; ... Besansky, Nora J 2015
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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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Disentangling human tolerance and resistance against HIV. Regoes, Roland R; McLaren, Paul J; Battegay, Manuel; Bernasconi, Enos; ... Fellay, Jacques 2014
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The association of cytochrome P450 genetic polymorphisms with sulfolane formation and the efficacy of a busulfan-based conditioning regimen in pediatric patients undergoing hematopoietic stem cell transplantation Uppugunduri Satyanarayana, Chakradhara Rao; Rezgui, M; Diaz, PH; Tyagi, Anuj Kumar; ... Ansari Djaberi, Marc Georges 2014
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The vitamin D receptor gene bAt (CCA) haplotype impairs the response to pegylated-interferon/ribavirin-based therapy in chronic hepatitis C patients Baur, Katharina; Mertens, Joachim C; Schmitt, Johannes; Iwata, Rika; ... Rubbia-Brandt, Laura 2012
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Fibrinogen gene regulation Fish, Richard; Neerman Arbez, Marguerite 2012
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Gene-environment interactions of selected pharmacogenes in arterial hypertension Bochud, Murielle; Guessous, Idris 2012
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Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension Guessous, Idris; Dobrinas, Maria; Kutalik, Zoltán; Pruijm, Menno; ... Bochud, Murielle 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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Psychological distress in fibromyalgia patients: a role for catechol-O-methyl-transferase Val158met polymorphism Desmeules, Jules Alexandre; Piguet, Valérie; Besson, Marie; Chabert, Jocelyne; ... Cedraschi, Christine 2012
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HLA and non-HLA polymorphisms in renal transplantation Laperrousaz, Stéphanie Lidia; Tiercy, Jean-Marie; Villard, Jean; Ferrari-Lacraz, Sylvie 2012
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Core genome conservation of Staphylococcus haemolyticus limits sequence based population structure analysis Cavanagh, Jorunn Pauline; Klingenberg, Claus; Hanssen, Anne-Merethe; Fredheim, Elizabeth Aarag; ... Sollid, Johanna Ericson 2012
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Differential contribution of PB1-F2 to the virulence of highly pathogenic H5N1 influenza A virus in mammalian and avian species Schmolke, Mirco; Manicassamy, Balaji; Pena, Lindomar; Sutton, Troy; ... García-Sastre, Adolfo 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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Ambiguous nucleotide calls from population-based sequencing of HIV-1 are a marker for viral diversity and the age of infection Kouyos, Roger D; von Wyl, Viktor; Yerly, Sabine; Böni, Jürg; ... Günthard, Huldrych F 2011
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COMT but not serotonin-related genes modulates the influence of childhood abuse on anger traits Perroud, Nader Ali; Jaussent, I.; Guillaume, Sébastien; Bellivier, F.; ... Courtet, P. 2010
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Rare genotype combination of the serotonin transporter gene associated with treatment response in severe personality disorder Perroud, Nader Ali; Salzmann, Annick; Saiz, Pilar A.; Baca-Garcia, Enrique; ... Malafosse, Alain 2010
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Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims Perroud, Nader Ali; Neidhart, Elizabeth; Petit, Brice; Vessaz, Monique; ... Guipponi, Michel 2010
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Influence of GST gene polymorphisms on busulfan pharmacokinetics in children Ansari Djaberi, Marc Georges; Lauzon-Joset, J-F; Vachon, M-F; Duval, M.; ... Krajinovic, M. 2010
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Telomere length and ApoE polymorphism in mild cognitive impairment, degenerative and vascular dementia Zekry Berger, Dina Selma; Herrmann, François; Irminger-Finger, Irmgard; Graf, Cristophe; ... Krause, Karl-Heinz 2010
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Lack of evidence for HLA-linked patterns of odorous carboxylic acids released from glutamine conjugates secreted in the human axilla Natsch, Andreas; Kuhn, Fabian; Tiercy, Jean-Marie 2010
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Evaluation de l'efficacité biologique du clopidogrel: génotype ou phénotype? Fontana, Pierre; Bonvini, Robert; Roffi, Marco; Boehlen, Françoise; ... Reny, Jean-Luc 2010
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Gap junction protein Cx37 interacts with endothelial nitric oxide synthase in endothelial cells Pfenniger, Anna; Derouette, Jean-Paul; Verma, Vandana; Lin, Xianming; ... Delmar, Mario 2010
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Impact of genetic polymorphisms and drug-drug interactions on clopidogrel and prasugrel response variability Ancrenaz, Virginie; Daali, Youssef; Fontana, Pierre; Besson, M.; ... Desmeules, Jules Alexandre 2010
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Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression Ritchie, Karen; Jaussent, Isabelle; Stewart, Robert; Dupuy, Anne-Marie; ... Malafosse, Alain 2009
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Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation Bedard, Karen; Attar Cohen, Homa; Bonnefont, Jérôme; Jaquet, Vincent; ... Krause, Karl-Heinz 2009
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Can the pharmacogenetics of GST gene polymorphisms predict the dose of busulfan in pediatric hematopoietic stem cell transplantation? Ansari Djaberi, Marc Georges; Krajinovic, Maja 2009
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Le concept de "resistance" a l'aspirine: mecanismes et pertinence clinique Reny, Jean-Luc; Bonvini, Robert; Barazer, I.; Berdague, P.; ... Fontana, Pierre 2009
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High-throughput typing of Staphylococcus aureus by amplified fragment length polymorphism (AFLP) or multi-locus variable number of tandem repeat analysis (MLVA) reveals consistent strain relatedness Melles, D. C.; Schouls, L.; Francois, Patrice; Herzig, S.; ... Schrenzel, Jacques 2009
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Genome-wide, high-resolution DNA methylation profiling using bisulfite-mediated cytosine conversion Reinders, Jon; Delucinge Vivier, Céline; Theiler, Gregory; Chollet, Didier; ... Paszkowski, Jerzy 2008
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Functional genetic variation of human miRNAs and phenotypic consequences Borel, Christelle; Antonarakis, Stylianos 2008
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Glutathione S-transferase polymorphisms, passive smoking, obesity, and heart rate variability in nonsmokers Probst-Hensch, Nicole M.; Imboden, Medea; Felber Dietrich, Denise; Barthelemy, Jean-Claude; ... Schwartz, Joel 2008
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Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis 2008
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Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers Danoy, Patrick; Michiels, Stefan; Dessen, Philippe; Pignat, Cécile; ... Benhamou, Simone 2008
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Leptin and the sympathetic connection of fat to bone Hamrick, M W.; Ferrari, Serge Livio 2008
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De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer Hernandez, David; Francois, Patrice; Farinelli, Laurent Luca Denis; Osteras, Magne; Schrenzel, Jacques 2008
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Evidence of horizontal gene transfer between human and animal commensal Escherichia coli strains identified by microarray Grasselli, Elena; Francois, Patrice; Gutacker, Michaela; Gettler, Brian; ... Piffaretti, Jean-Claude 2008
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Particularités pharmacologiques du Tramadol chez l'enfant Saudan Frei, Sonja; Habre, Walid 2007
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Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21 Lyle, Robert; Prandini, Paola; Osoegawa, Kazutoyo; ten Hallers, Boudewijn; ... Antonarakis, Stylianos 2007
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Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1 Beiraghi, Soraya; Nath, S. K.; Gaines, Matthew; Mandhyan, D. D.; ... Radhakrishna, Uppala 2007
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Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations Neerman Arbez, Marguerite; De Moerloose, Philippe 2007
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No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome Glaser, Bronwyn; Debbané, Martin; Hinard, Christine; Morris, Michael Andréw; ... Eliez, Stéphan 2006
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Influence of serotonin receptor 2A His452Tyr polymorphism on brain temporal structures: a volumetric MR study Filippini, Nicola; Scassellati, Catia; Boccardi, Marina; Pievani, Michela; ... Gennarelli, Massimo 2006
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Connexin37 protects against atherosclerosis by regulating monocyte adhesion Wong Christen, Cindy Wai Yin; Christen, Thomas; Roth, Isabelle; Chadjichristos, Christos; ... Kwak, Brenda 2006
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ATM alterations in childhood non-Hodgkin lymphoma Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David R; Sappino, Pascal 2006
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Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions Howald, C.; Merla, Giuseppe; Digilio, M. C.; Amenta, S.; ... Reymond, Alexandre 2006
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Entre sel et gènes ou pharmacogénomique des antihypertenseurs Ernandez, Thomas; Pechere, Antoinette; Dayer, Pierre; Desmeules, Jules Alexandre 2006
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ATM variants and predisposition to childhood T-lineage acute lymphoblastic leukaemia Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, D R; Sappino, Pascal 2006
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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis Naveed, Mohammed; Al-Ali, M. T.; Murthy, S. K.; Al-Hajali, Sarah; ... Radhakrishna, Uppala 2006
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