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 TitleAuthors / EditorsDate
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 Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study Langer, Thorsten; Clemens, Eva; Broer, Linda; Maier, Lara; ... Zolk, Oliver 2020
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 Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels Tin, Adrienne; Marten, Jonathan; Halperin Kuhns, Victoria L.; Li, Yong; ... Köttgen, Anna 2019
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 Single-cell transcriptomes reveal characteristic features of human pancreatic islet cell types Li, Jin; Klughammer, Johanna; Farlik, Matthias; Penz, Thomas; ... Kubicek, Stefan 2016
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 Quantitative variability of 342 plasma proteins in a human twin population Liu, Yansheng; Buil Demur, Alfonso Alberto; Collins, Ben C; Gillet, Ludovic C J; ... Aebersold, Ruedi 2015
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 The evolution of personality in patients with mild cognitive impairment Donati, A; Studer, J; Petrillo, S; Pocnet, C; ... von Gunten, A 2013
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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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 Consistency between cross-sectional and longitudinal SNP: blood lipid associations Costanza, Michael C; Beer-Borst, Sigrid; James, Richard William; Gaspoz, Jean-Michel; Morabia, Alfredo 2012
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 European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset Mathieu, Flavie; Dizier, Marie-Helene; Etain, Bruno; Jamain, Stephane; ... Bellivier, Frank 2010
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 Deciphering the code for retroviral integration target site selection Santoni, Federico; Hartley, Oliver; Luban, Jeremy 2010
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 Discovery of Plasmodium modulators by genome-wide analysis of circulating hemocytes in Anopheles gambiae Pinto, Sofia B; Lombardo, Fabrizio; Koutsos, Anastasios C; Waterhouse, Robert; ... Michel, Kristin 2009
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 Genetic structure of Europeans: a view from the North-East Nelis, Mari; Esko, Tonu; Antonarakis, Stylianos; Borel, Christelle; Gagnebin, Maryline 2009
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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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 Protein coding potential of retroviruses and other transposable elements in vertebrate genomes Zdobnov, Evgeny; Campillos, Mónica; Harrington, Eoghan D; Torrents, David; Bork, Peer 2005
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 A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q Dauvilliers, Yves; Blouin, Jean-Louis; Neidhart, Elisabeth; Carlander, Bertrand; ... Tafti, Mehdi 2004
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 Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31 Baulac, Stéphanie; Picard, Fabienne; Herman, Alexandra; Feingold, Josué; ... LeGuern, Eric 2001
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 Enhanced susceptibility to lupus contributed from the nonautoimmune C57BL/10, but not C57BL/6, genome Rozzo, S. J.; Vyse, T. J.; Menze, K.; Izui, Shozo; Kotzin, B. L. 2000
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 Maternal and paternal lineages in Albania and the genetic structure of Indo-European populations Belledi, M.; Poloni, Estella S.; Casalotti, R.; Conterio, F.; ... Excoffier, Laurent Georges Louis 2000
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 Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21 Antonarakis, Stylianos; Blouin, Jean-Louis; Lasseter, V. K.; Gehrig, Corinne; ... Pulver, A. E. 1999
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 Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping Bartoloni, Lucia; Blouin, Jean-Louis; Sainsbury, A. J.; Gos, A.; ... Antonarakis, Stylianos 1999
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 No evidence for linkage between schizophrenia and markers at chromosome 15q13-14 Curtis, L.; Blouin, Jean-Louis; Radhakrishna, U.; Gehrig, Corinne; ... Antonarakis, Stylianos 1999
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