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Genotyping single nucleotide polymorphisms by mass spectrometryTOST, Jörg; GUT, Ivo G.Mass spectrometry reviews (Print). 2002, Vol 21, Num 6, pp 388-418, issn 0277-7037, 31 p.Article

Serial pyrosequencing for quantitative DNA methylation analysisTOST, Iörg; EL ABDALAOUI, Hafida; GLYNNE GUT, Ivo et al.BioTechniques. 2006, Vol 40, Num 6, issn 0736-6205, 721-726 [4 p.]Article

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Genetic heterogeneity of asthma phenotypes identified by a clustering approachSIROUX, Valérie; GONZALEZ, Juan R; OMENAAS, Ernst Reidar et al.The European respiratory journal. 2014, Vol 43, Num 2, pp 439-452, issn 0903-1936, 14 p.Article

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 DiabetesTREGOUET, David-Alexandre; GROOP, Per-Henrik; NICAUD, Viviane et al.Diabetes (New York, NY). 2008, Vol 57, Num 10, pp 2843-2850, issn 0012-1797, 8 p.Article

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Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02)LIMOU, Sophie; LE CLERC, Sigrid; RATSIMANDRESY, Rojo et al.The Journal of infectious diseases. 2009, Vol 199, Num 3, pp 419-426, issn 0022-1899, 8 p.Article

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Multiple-Cohort Genetic Association Study Reveals CXCR6 as a New Chemokine Receptor Involved in Long-Term Nonprogression to AIDSLIMOU, Sophie; COULONGES, Cédric; VAN'T WOUT, Angélique B et al.The Journal of infectious diseases. 2010, Vol 202, Num 6, pp 908-915, issn 0022-1899, 8 p.Article

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's diseaseLAMBERT, Jean-Charles; HEATH, Simon; LETENNEUR, Luc et al.Nature genetics. 2009, Vol 41, Num 10, pp 1094-1099, issn 1061-4036, 6 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

HLA Has Strongest Association with IgA Nephropathy in Genome-Wide AnalysisFEEHALLY, John; FARRALL, Martin; PADMANABHAN, Sandosh et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 10, pp 1791-1797, issn 1046-6673, 7 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

Lung cancer susceptibility locus at 5p15.33MCKAY, James D; HUNG, Rayjean J; RUDNAI, Peter et al.Nature genetics. 2008, Vol 40, Num 12, pp 1404-1406, issn 1061-4036, 3 p.Article

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Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemiaQUESADA, Victor; CONDE, Laura; LOPEZ-GUERRA, Mónica et al.Nature genetics. 2012, Vol 44, Num 1, pp 47-52, issn 1061-4036, 6 p.Article

Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1JIE ZHOU; TAWK, Marcel; RENDA, Yavuz et al.American journal of human genetics. 2012, Vol 91, Num 1, pp 5-14, issn 0002-9297, 10 p.Article

Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolatesPIMENOFF, Ville N; LAVAL, Guillaume; COMAS, David et al.Pharmacogenetics and genomics (Print). 2012, Vol 22, Num 12, pp 846-857, issn 1744-6872, 12 p.Article

Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile menCHALAS BOISSONNAS, Céline; HAFIDA EL ABDALAOUI; HAELEWYN, Virginie et al.European journal of human genetics. 2010, Vol 18, Num 1, pp 73-80, issn 1018-4813, 8 p.Article

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