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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Sharp, Andrew James; Guipponi, Michel; Fuchs, Katrin; Malafosse, Alain 2009
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A shared HLA-DRB1 epitope in the DR beta first domain is associated with Vogt-Koyanagi-Harada syndrome in Indian patients Tiercy, Jean-Marie; Rathinam, Sivakumar R.; Gex-Fabry, Marianne; Baglivo, Edoardo 2010
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An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits Hsu, Yi-Hsiang; Zillikens, M Carola; Wilson, Scott G.; Farber, Charles R.; ... Kiel, D. P. 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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Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II) Wright, J Timothy; Morris, Clark; Clements, Suzanne E.; D'Souza, Rena; ... Zonana, Jonathan 2009
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Dissection of BXSB lupus phenotype using mice congenic for chromosome 1 demonstrates that separate intervals direct different aspects of disease Haywood, M. E.; Rogers, N. J.; Rose, S. J.; Boyle, Joseph; ... Morley, B. J. 2004
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Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study Ehret, Georg Benedikt; O'Connor, Ashley A.; Weder, Alan; Cooper, Richard S.; Chakravarti, Aravinda 2009
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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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Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1 Anttila, Verneri 2010
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Identification of 2 major loci linked to autoimmune hemolytic anemia in NZB mice Kikuchi, Shuichi; Amano, Hirofumi; Amano, Eri; Fossati-Jimack, Liliane; ... Izui, Shozo 2005
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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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SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects Lepagnol-Bestel, A-M; Maussion, G.; Boda, Bernadett; Cardona, A.; ... Simonneau, M. 2008
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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Benjamin, Emelia J.; Ehret, Georg Benedikt 2009