Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effects by Deleuze Jean-Francois, Cousin Emmanuelle, Genin Emmanuelle

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On the use of haplotype phylogeny to detect disease susceptibility loci by Darlu Pierre, Hugot Jean-Pierre, Danjean Vincent, Bardel Claire, Génin Emmanuelle

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Autism risk assessment in siblings of affected children using sex-specific genetic scores by Carayol Jerome, Schellenberg Gerard D, Dombroski Beth, Genin Emmanuelle, Rousseau Francis, Dawson Geraldine

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Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe by Génin Emmanuelle, Schumacher Martin, Roujeau Jean-Claude, Naldi Luigi, Liss Yvonne, Kazma Rémi, Sekula Peggy, Hovnanian Alain, Mockenhaupt Maja

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Genome-wide CNV analysis replicates the association between <it>GSTM1</it> deletion and bladder cancer: a support for using continuous measurement from SNP-array data by Marenne Gaëlle, Real Francisco X, Rothman Nathaniel, Rodríguez-Santiago Benjamin, Pérez-Jurado Luis, Kogevinas Manolis, García-Closas Montse, Silverman Debra T, Chanock Stephen J, Génin Emmanuelle, Malats Núria

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