| | Title | Authors / Editors | Date |
|
unige:20601 |
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1 |
Anttila, Verneri |
2010 |
|
unige:20637 |
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 |
|
unige:21341 |
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 |
|
unige:21008 |
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 |
|
unige:20635 |
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 |
|
unige:21077 |
BRD2 and TAP-1 genes and juvenile myoclonic epilepsy |
Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed |
2010 |
|
unige:20181 |
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 |
|
unige:19676 |
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry |
Benjamin, Emelia J.; Ehret, Georg Benedikt |
2009 |
|
unige:19787 |
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 |
|
unige:19858 |
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy |
Sharp, Andrew James; Guipponi, Michel; Fuchs, Katrin; Malafosse, Alain |
2009 |
|
unige:19172 |
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 |
|
unige:11376 |
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 |
|
unige:11293 |
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 |
*genetic predisposition to disease
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