The role of CD4⁺ T-cell subsets in determining transplantation rejection or toleranceZELENIKA, Diana; ADAMS, Elizabeth; HUMM, Susan et al.Immunological reviews. 2001, Vol 182, pp 164-179, issn 0105-2896Article

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3PURDUE, Mark P; JOHANSSON, Mattias; JACOBS, Kevin B et al.Nature genetics. 2011, Vol 43, Num 1, pp 60-65, issn 1061-4036, 6 p.Article

Genome-wide association study identifies five susceptibility loci for gliomaSHETE, Sanjay; HOSKING, Fay J; HOANG-XUAN, Khe et al.Nature genetics. 2009, Vol 41, Num 8, pp 899-904, issn 1061-4036, 6 p.Article

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseMOMOZAWA, Yukihide; MNI, Myriam; FINKEL, Yigael et al.Nature genetics. 2011, Vol 43, Num 1, pp 43-47, issn 1061-4036, 5 p.Article

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15MENZEL, Stephan; GARNER, Chad; BEST, Steve et al.Nature genetics. 2007, Vol 39, Num 10, pp 1197-1199, issn 1061-4036, 3 p.Article

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesELLEUCH, Nizar; BOUSLAM, Naima; BACQ, Delphine et al.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 4, pp 307-315, issn 1364-6745, 9 p.Article

Antiviral agent Cidofovir decreases Epstein-Barr virus (EBV) oncoproteins and enhances the radiosensitivity in EBV-related malignanciesABDULKARIM, Bassam; SABRI, Siham; ZELENIKA, Diana et al.Oncogene (Basingstoke). 2003, Vol 22, Num 15, pp 2260-2271, issn 0950-9232, 12 p.Article

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European populationSAAD, Mohamad; LESAGE, Suzanne; POLLAK, Pierre et al.Human molecular genetics (Print). 2011, Vol 20, Num 3, pp 615-627, issn 0964-6906, 13 p.Article

A SUMOylation―defective MITF germline mutation predisposes to melanoma and renal carcinomaBERTOLOTTO, Corine; LESUEUR, Fabienne; MAUBEC, Eve et al.Nature (London). 2011, Vol 480, Num 7375, pp 94-98, issn 0028-0836, 5 p.Article

Genome-wide association study of HPV seropositivityDAN CHEN; MCKAY, James D; BENCKO, Vladimir et al.Human molecular genetics (Print). 2011, Vol 20, Num 23, pp 4714-4723, issn 0964-6906, 10 p.Article

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1MORANGE, Pierre-Emmanuel; BEZEMER, Irene; GALAN, Pilar et al.American journal of human genetics. 2010, Vol 86, Num 4, pp 592-595, issn 0002-9297, 4 p.Article

Incidence of Breast Cancer and Its Subtypes in Relation to Individual and Multiple Low-Penetrance Genetic Susceptibility LociREEVES, Gillian K; TRAVIS, Ruth C; LATHROP, Mark et al.JAMA, the journal of the American Medical Association. 2010, Vol 304, Num 4, pp 426-434, issn 0098-7484, 9 p.Article

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approachTREGOUËT, David-Alexandre; HEATH, Simon; ALESSI, Marie-Christine et al.Blood. 2009, Vol 113, Num 21, pp 5298-5303, issn 0006-4971, 6 p.Article

Common variants at 30 loci contribute to polygenic dyslipidemiaKATHIRESAN, Sekar; WILLER, Cristen J; VOIGHT, Benjamin F et al.Nature genetics. 2009, Vol 41, Num 1, pp 56-65, issn 1061-4036, 10 p.Article

Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese ChildrenLE STUNFF, Catherine; DECHARTRES, Agnès; ZELENIKA, Diana et al.Diabetes (New York, NY). 2008, Vol 57, Num 2, pp 494-502, issn 0012-1797, 9 p.Article

Effect of 17q21 Variants and Smoking Exposure in Early-Onset AsthmaBOUZIGON, Emmanuelle; CORDA, Eve; SCHEINMANN, Pierre et al.The New England journal of medicine. 2008, Vol 359, Num 19, pp 1985-1994, issn 0028-4793, 10 p.Article

Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color GeneKAYSER, Manfred; FAN LIU; VAN IJCKEN, Wilfred F. J et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 411-423, issn 0002-9297, 13 p.Article

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23XIFENG WU; SCELO, Ghislaine; PROKHORTCHOUK, Egor et al.Human molecular genetics (Print). 2012, Vol 21, Num 2, pp 456-462, issn 0964-6906, 7 p.Article

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA projectOUDOT-MELLAKH, Tiphaine; COHEN, William; GERMAIN, Marine et al.British journal of haematology. 2012, Vol 157, Num 2, pp 230-239, issn 0007-1048, 10 p.Article

Serial translocation by means of circular intermediates underlies colour sidedness in cattleDURKIN, Keith; COPPIETERS, Wouter; KAMATANI, Yohichiro et al.Nature (London). 2012, Vol 482, Num 7383, pp 81-84, issn 0028-0836, 4 p.Article

Chromosome 7p11.2 (EGFR) variation influences glioma riskSANSON, Marc; HOSKING, Fay J; MARIE, Yannick et al.Human molecular genetics (Print). 2011, Vol 20, Num 14, pp 2897-2904, issn 0964-6906, 8 p.Article

Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol DependenceDESRIVIERES, Sylvane; PRONKO, Sergey P; SCHUMANN, Gunter et al.Biological psychiatry (1969). 2011, Vol 69, Num 11, pp 1100-1108, issn 0006-3223, 9 p.Article

A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosumBOUKHRIS, Amir; IMED FEKI; BRICE, Alexis et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 4, pp 441-448, issn 1364-6745, 8 p.Article

Genome-wide association study identifies three loci associated with melanoma riskBISHOP, D. Timothy; DEMENAIS, Florence; BAKKER, Bert et al.Nature genetics. 2009, Vol 41, Num 8, pp 920-925, issn 1061-4036, 6 p.Article

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular DystrophyGUENEAU, Lucie; BERTRAND, Anne T; TRANCHANT, Christine et al.American journal of human genetics. 2009, Vol 85, Num 3, pp 338-353, issn 0002-9297, 16 p.Article