| | Title | Authors / Editors | Date |
|
unige:24639 |
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium |
McKay, James D |
2011 |
|
unige:45244 |
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease |
Krüger, Rejko; Sharma, Manu |
2011 |
|
unige:2008 |
A study of Gm allotypes and immunoglobulin heavy gamma IGHG genes in Berbers, Arabs and sub-Saharan Africans from Jerba Island, Tunisia |
Loveslati, B Y.; Sanchez-Mazas, Alicia; Ennafaa, H.; Marrakchi, R.; ... Elgaaied, A B. |
2001 |
|
unige:32178 |
A systematic survey of loss-of-function variants in human protein-coding genes |
MacArthur, Daniel G; Montgomery, Stephen; Dermitzakis, Emmanouil |
2012 |
|
unige:14331 |
A worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoprotein |
Breguet, Georges; Bütler, R.; Bütler-Brunner, E.; Sanchez-Mazas, Alicia |
1990 |
|
unige:1964 |
An apportionment of human HLA diversity |
Sanchez-Mazas, Alicia |
2007 |
|
unige:88214 |
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis |
Marchetti, Giovanna; Girelli, Domenico; Zerbinati, Carlotta; Lunghi, Barbara; ... Martinelli, Nicola |
2015 |
|
unige:8851 |
Arg16 homozygosity of the beta2-adrenergic receptor improves the outcome after beta2-agonist tocolysis for preterm labor |
Landau, Ruth; Morales, M. A.; Antonarakis, Stylianos; Blouin, Jean-Louis; Smiley, R. M. |
2005 |
|
unige:25737 |
Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease |
Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A |
2011 |
|
unige:45235 |
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study |
Ross, Owen A |
2011 |
|
unige:47588 |
ATM gene alterations in childhood acute lymphoblastic leukemias |
Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David; Sappino, Pascal |
2003 |
|
unige:1878 |
Balancing selection and heterogeneity across the classical human leukocyte antigen loci: a meta-analytic review of 497 population studies |
Solberg, Owen D.; Mack, Steven J.; Lancaster, Alex K.; Single, Richard M.; ... Thomson, Glenys |
2008 |
|
unige:21077 |
BRD2 and TAP-1 genes and juvenile myoclonic epilepsy |
Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed |
2010 |
|
unige:2538 |
Candidate genes for temporal lobe epilepsy: a replication study |
Trachsler-Salzmann, Annick; Perroud, Nader; Crespel, Arielle; Lambercy, Carmen; Malafosse, Alain |
2008 |
|
unige:9217 |
Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain |
Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A. |
1995 |
|
unige:143934 |
Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia |
Alcantara, Marion; Simonin, Mathieu; Lhermitte, Ludovic; Touzart, Aurore; ... Asnafi, Vahid |
2019 |
|
unige:135503 |
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 |
Wang, Heming; Nandakumar, Priyanka; Tekola-Ayele, Fasil; Tayo, Bamidele O; ... Zhu, Xiaofeng |
2019 |
|
unige:5537 |
Common regulatory variation impacts gene expression in a cell type-dependent manner |
Dimas, Antigone S.; Deutsch, Samuel; Stranger, Barbara E.; Montgomery, Stephen; ... Antonarakis, Stylianos |
2009 |
|
unige:19966 |
Cord blood banks collect units with different HLA alleles and haplotypes to volunteer donor banks: a comparative report from Swiss Blood stem cells |
Meyer-Monard, S.; Passweg, Jakob; Troeger, C.; Eberhard, H-P; ... Tiercy, Jean-Marie |
2009 |
|
unige:21078 |
Dimorphism of TAP-1 gene in Caucasian with juvenile myoclonic epilepsy and in Tunisian with idiopathic generalized epilepsies |
Layouni, S.; Chouchane, L.; Malafosse, Alain; Dogui, M. |
2010 |
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