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 TitleAuthors / EditorsDate
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Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region Berry, A.; Scott, Hamish Steele; Kudoh, J.; Talior, I.; ... Bonne-Tamir, B. 2000
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Candidate genes for temporal lobe epilepsy: a replication study Trachsler-Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain 2008
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Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter Boccardi, Marina; Scassellati, Catia; Ghidoni, Roberta; Testa, Cristina; ... Frisoni, Giovanni 2008
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Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis 2009
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Suicide attempt characteristics may orientate toward a bipolar disorder in attempters with recurrent depression Guillaume, Sébastien; Jaussent, Isabelle; Jollant, Fabrice; Rihmer, Zoltan; ... Courtet, Philippe 2010
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Probing the genome to understand suicide Uher, Rudolf; Perroud, Nader Ali 2010
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Low disease risk in relatives of north african lrrk2 Parkinson disease patients Troiano, A R; Elbaz, A; Lohmann, E; Belarbi, S; ... Brice, A 2010
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The CST3 B haplotype is associated with frontotemporal lobar degeneration Benussi, L; Ghidoni, R; Galimberti, D; Boccardi, Marina; ... Binetti, G 2010
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Status epilepticus in fragile X syndrome Gauthey, Magali; Poloni, Claudia B.; Ramelli, Gian-Paolo; Roulet-Perez, Eliane; Korff, Christian 2010
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Only one independent genetic association with rheumatoid arthritis within the KIAA1109-TENR-IL2-IL21 locus in Caucasian sample sets: confirmation of association of rs6822844 with rheumatoid arthritis at a genome-wide level of significance Hollis-Moffatt, Jade E.; Chen-Xu, Michael; Topless, Ruth; Dalbeth, Nicola; ... Merriman, T. R. 2010
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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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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Jacquemont, Sébastien 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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Apolipoprotein CIII overexpressing mice are predisposed to diet-induced hepatic steatosis and hepatic insulin resistance Lee, Hui-Young; Birkenfeld, Andreas L; Jornayvaz, François; Jurczak, Michael J; ... Shulman, Gerald I 2011
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Real-time quantitative polymerase chain reaction analysis of patients with refractory chronic periodontitis Marconcini, Simone; Covani, Ugo; Barone, Antonio; Vittorio, Orazio; ... Nicolini, Claudio 2011
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Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis Dieudé, P; Guedj, M; Truchetet, Marie-Elise; Wipff, J; ... Allanore, Y 2011
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Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals Arking, Dan E; Junttila, M. Juhani; Goyette, Philippe; Huertas-Vazquez, Adriana; ... Newton-Cheh, Christopher 2011
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Connexin 37 limits thrombus propensity by downregulating platelet reactivity Angelillo-Scherrer, Anne; Fontana, Pierre; Burnier, Laurent; Roth, Isabelle; ... Kwak, Brenda 2011
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Psoriasis Boehncke, Wolf-Henning; Mrowietz, Ulrich 2012
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An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium 2012
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