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 Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history Sabbagh, Audrey; Langaney, André; Darlu, Pierre; Gérard, Nathalie; ... Poloni, Estella S. 2008
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 Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31 Villanueva, Adda; Willer, Jason R; Bryois, Julien; Dermitzakis, Emmanouil; ... Davis, Erica E 2014
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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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 Viral genotype-specific role of PNPLA3, PPARG, MTTP, and IL28B in hepatitis C virus-associated steatosis Cai, Tao; Dufour, Jean-François Jacques; Muellhaupt, Beat; Gerlach, Tilman Joern; ... Bochud, Pierre-Yves 2011
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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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 Variable-number tandem repeat analysis and multilocus sequence typing data confirm the epidemiological changes observed with Staphylococcus aureus strains isolated from bloodstream infections van der Mee-Marquet, Nathalie; Francois, Patrice; Domelier, Anne-Sophie; Arnault, Laurence; ... Quentin, Roland 2009
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 Usefulness of postmortem biochemistry in forensic pathology: illustrative case reports Palmiere, Cristian; Lesta, Maria Del Mar; Sabatasso, Sara; Mangin, Patrice; ... Sporkert, Frank 2012
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 Use of an automated multiple-locus, variable-number tandem repeat-based method for rapid and high-throughput genotyping of Staphylococcus aureus isolates Francois, Patrice; Huyghe, Antoine; Charbonnier, Yvan; Bento, Manuela; ... Schrenzel, Jacques 2005
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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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 Tuberculosis cluster in an immigrant community: case identification issues and a transcultural perspective Tardin, A.; Dominice Dao, Mélissa; Bescher Ninet, Béatrice Alice; Janssens, Jean-Paul 2009
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 Trends and projections of hepatitis C virus epidemiology in Latin America Kershenobich, David; Razavi, Homie A; Sánchez-Avila, Juan Francisco; Bessone, Fernando; ... Silva, Marcelo 2011
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 Treatment of hepatitis C in HCV mono-infected and in HIV-HCV co-infected patients: an open-labelled comparison study Gonvers, Jean-Jacques; Heim, Markus H.; Cavassini, Matthias; Mullhaupt, Beat; ... Oneta, Carl 2010
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 Treatment of chronic hepatitis C genotype 1 with triple therapy comprising telaprevir or boceprevir Rubbia-Brandt, Laura 2012
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 Transgenerational stability of the Arabidopsis epigenome is coordinated by CG methylation Mathieu, Olivier; Reinders, Jon; Caikovski, Marian; Smathajitt, Chotika; Paszkowski, Jerzy 2007
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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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 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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 The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe 2013
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 The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro Guipponi, Michel; Vuagniaux, Gregoire; Wattenhofer, Marie; Shibuya, Kazunori; ... Rossier, B. C. 2002
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 The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations Radhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos 1999
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 The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes Bruneau, Sylvia; Johnson, Kenneth R.; Yamamoto, Masakazu; Kuroiwa, Atsushi; Duboule, Denis 2001
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