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 TitleAuthors / EditorsDate
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Chromosome 21: from sequence to applications Antonarakis, Stylianos 2001
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Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness Ben-Yosef, T.; Wattenhofer, M.; Riazuddin, S.; Ahmed, Z. M.; ... Morell, R. J. 2001
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The genome sequence of the malaria mosquito Anopheles gambiae Holt, Robert A 2002
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Chromosome 21: a small land of fascinating disorders with unknown pathophysiology Antonarakis, Stylianos; Lyle, Robert; Deutsch, Samuel; Reymond, Alexandre 2002
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Specific BACE1 genotypes provide additional risk for late-onset Alzheimer disease in APOE epsilon 4 carriers Gold, Gabriel; Blouin, Jean-Louis; Herrmann, François; Michon, Agnès; ... Antonarakis, Stylianos 2003
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Structure of Pseudomonas aeruginosa populations analyzed by single nucleotide polymorphism and pulsed-field gel electrophoresis genotyping Morales, Gracia; Wiehlmann, Lutz; Gudowius, Peter; Van Delden, Christian; ... Rojo, Fernando 2004
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Genetic variability of mu-opioid receptor in an obstetric population Landau, Ruth; Cahana, Alex; Smiley, R. M.; Antonarakis, Stylianos; Blouin, Jean-Louis 2004
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Modeling the influence of APOC3, APOE, and TNF polymorphisms on the risk of antiretroviral therapy-associated lipid disorders Tarr, P. E.; Taffe, Patrick; Bleiber, Gabriela; Furrer, Hansjakob; ... Telenti, Amalio 2005
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BXSB/long-lived is a recombinant inbred strain containing powerful disease suppressor loci Haywood, M. E.; Gabriel, Luisa; Rose, S. J.; Rogers, N. J.; ... Morley, B. J. 2007
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The Bxs6 locus of BXSB mice is sufficient for high-level expression of gp70 and the production of gp70 immune complexes Rankin, Joanna; Boyle, J. J.; Rose, S. J.; Gabriel, Luisa; ... Morley, B. J. 2007
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Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction? Wong Christen, Cindy Wai Yin; Christen, Thomas; Pfenniger, Anna; James, Richard William; Kwak, Brenda 2007
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A whole-genome association study of major determinants for host control of HIV-1 Fellay, Jacques; Shianna, K. V.; Ge, Dongliang; Colombo, Sara; ... Goldstein, D. B. 2007
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Connexin37: a potential modifier gene of inflammatory disease Chanson, Marc; Kwak, Brenda 2007
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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability Beckmann, J. S.; Estivill, Xavier; Antonarakis, Stylianos 2007
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Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypes Sethupathy, Praveen; Borel, Christelle; Gagnebin, Maryline; Grant, G. R.; ... Antonarakis, Stylianos 2007
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Contribution of 20 single nucleotide polymorphisms of 13 genes to dyslipidemia associated with antiretroviral therapy Arnedo, Mireia; Taffe, Patrick; Sahli, Roland; Furrer, Hansjakob; ... Tarr, P. E. 2007
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Anticoagulation orale et pharmacogénétique : perspectives pour la pratique clinique Benusiglio, Patrick Raphaël; Desmeules, Jules Alexandre; De Moerloose, Philippe; Dayer, Pierre 2007
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Chondroid cystic malformation of the lung with trisomy 8 mosaicism: a new cystic lung malformation Bouron-Dal Soglio, Dorothee; Rougemont-Pidoux, Anne-Laure; De Buys Roessingh, Anthony S.; Fetni, Raouf; ... Fournet, Jean-Christophe 2008
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Chronic active gastritis in X-linked lymphoproliferative disease Rougemont, Anne-Laure; Fournet, Jean-Christophe; Martin, Steven R.; de Saint-Basile, Geneviève; ... Le Deist, Françoise 2008
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Multiple ADH genes are associated with upper aerodigestive cancers Hashibe, Mia; Benhamou, Simone; Bouchardy Magnin, Christine 2008
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Large-scale population study of human cell lines indicates that dosage compensation is virtually complete Johnston, Colette M.; Lovell, Frances L.; Leongamornlert, Daniel A.; Stranger, Barbara E.; ... Ross, Mark T. 2008
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High-resolution mapping of expression-QTLs yields insight into human gene regulation Veyrieras, Jean-Baptiste; Kudaravalli, Sridhar; Kim, Su Yeon; Dermitzakis, Emmanouil; ... Pritchard, Jonathan K. 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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Interaction between BDNF Val66Met and childhood trauma on adult's violent suicide attempt Perroud, N.; Courtet, P.; Vincze, Ilona; Jaussent, I.; ... Malafosse, Alain 2008
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Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis van Meurs, Joyce B J.; Trikalinos, Thomas A.; Ferrari, Serge Livio 2008
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TNFA -308G>A in two international population-based cohorts and risk of asthma Castro-Giner, F.; Kogevinas, M.; Mächler, M.; de Cid, R.; ... Probst-Hensch, Nicole M. 2008
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Of autoantibodies and single nucleotide polymorphisms: a brave new world? Pichard, Claude; Laviano, Alessandro; Meguid, Michael M. 2008
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Influence of ABCB1 gene polymorphisms and P-glycoprotein activity on cyclosporine pharmacokinetics in peripheral blood mononuclear cells in healthy volunteers Ansermot, Nicolas; Rebsamen, Michela; Chabert, Jocelyne; Fathi, Marc; ... Desmeules, Jules Alexandre 2008
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Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencing Nikolaev, S. I.; Iseli, Christian; Sharp, A. J.; Robyr, Daniel; ... Antonarakis, Stylianos 2009
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A genome-wide association study of testicular germ cell tumor Rapley, Elizabeth A.; Turnbull, Clare; Al Olama, Ali Amin; Dermitzakis, Emmanouil; ... Stratton, Michael R. 2009
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Common regulatory variation impacts gene expression in a cell type-dependent manner Dimas, Antigone S.; Deutsch, Samuel; Stranger, Barbara E.; Montgomery, Stephen; ... Antonarakis, Stylianos 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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Genetic and epigenetic analysis of SSAT gene dysregulation in suicidal behavior Guipponi, Michel; Deutsch, Samuel; Kohler, Karine; Perroud, Nader; ... Malafosse, Alain 2009
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HOXA1 A218G polymorphism is associated with smaller cerebellar volume in healthy humans Canu, Elisa; Boccardi, Marina; Ghidoni, Roberta; Benussi, Luisa; ... Frisoni, Giovanni 2009
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Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia Ansari Djaberi, Marc Georges; Sauty, Géraldine; Labuda, Malgorzata; Gagné, Vincent; ... Krajinovic, Maja 2009
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Contribution of genome-wide significant single-nucleotide polymorphisms and antiretroviral therapy to dyslipidemia in HIV-infected individuals: a longitudinal study Rotger, Margalida; Bayard, Cornelia; Taffe, Patrick; Martinez, Raquel; ... Tarr, P. E. 2009
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Genetics. Life after GWA studies Dermitzakis, Emmanouil; Clark, A. G. 2009
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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Ganesh, Santhi K. 2009
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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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A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parents Marini, Monica; Bocciardi, Renata; Gimelli, Stefania; Di Duca, Marco; ... Ravazzolo, Roberto 2010
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Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures Jamali, Sarah; Salzmann, Annick; Perroud, Nader Ali; Ponsole-Lenfant, Magali; ... Szepetowski, Pierre 2010
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Data analysis issues for allele-specific expression using Illumina's GoldenGate assay Ritchie, Matthew E.; Forrest, Matthew S.; Dimas, Antigone S.; Daelemans, Caroline; ... Tavare, Simon 2010
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BRD2 and TAP-1 genes and juvenile myoclonic epilepsy Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed 2010
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Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33 Dermitzakis, Emmanouil 2010
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Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder Karege, Félicien; Perroud, Nader Ali; Schurhoff, F.; Meary, A.; ... 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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Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study Rauch, Andri; Kutalik, Zoltan; Descombes, Patrick; Cai, Tao; ... Bochud, Pierre-Yves 2010
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Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations North, Kari E.; Franceschini, Nora; Avery, Christy L.; Baird, Lisa; ... Hunt, Steven C. 2010
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Rare and common regulatory variation in population-scale sequenced human genomes Montgomery, Stephen; Lappalainen, Tuuli Emilia; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil 2011
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Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes Small, Kerrin S; Hedman, Asa K; Grundberg, Elin; Nica, Alexandra; ... Dermitzakis, Emmanouil 2011
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