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Emmanuelle Genin

Showing results (1-10 of 34) with videos related to

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European Journal of Human Genetics : EJHG|June 26, 2002
Comparison of family based haplotype methods using intragenic SNPs in candidate genesCatherine Bourgain, Emmanuelle Genin, Françoise Clerget-Darpoux
BMC Genetics|April 7, 2006
Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effectsEmmanuelle Cousin, Jean-Francois Deleuze, Emmanuelle Genin
Studies in Health Technology and Informatics|June 24, 2020
Secure Collapsing Method Based on Fully Homomorphic EncryptionDavid Niyitegeka, Reda Bellafqira, Emmanuelle Genin, et al.
Bioinformatics (Oxford, England)|December 4, 2018
GEMPROT: visualization of the impact on the protein of the genetic variants found on each haplotypeTania Cuppens, Thomas E Ludwig, Pascal Trouvé, et al.
Genetic Epidemiology|March 26, 2003
Does accounting for gene-environment (GxE) interaction increase the power to detect the effect of a gene in a multifactorial disease?Hana Selinger-Leneman, Emmanuelle Genin, Jill M Norris, et al.
Frontiers in Medicine|June 14, 2019
Sensitive Skin: Lessons From Transcriptomic StudiesAdeline Bataille, Christelle Le Gall-Ianotto, Emmanuelle Genin, et al.
Molecular Autism|October 25, 2011
Autism risk assessment in siblings of affected children using sex-specific genetic scoresJerome Carayol, Gerard D Schellenberg, Beth Dombroski, et al.
NAR Genomics and Bioinformatics|March 20, 2025
Enhancing the annotation of small ORF-altering variants using MORFEE: introducing MORFEEdb, a comprehensive catalog of SNVs affecting upstream ORFs in human 5'UTRsCaroline Meguerditchian, David Baux, Thomas E Ludwig, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|March 11, 2003
Deleterious genetic influence of CX3CR1 genotypes on HIV-1 disease progressionSophie Faure, Laurence Meyer, Emmanuelle Genin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 29, 2003
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54Nicolas de Roux, Emmanuelle Genin, Jean-Claude Carel, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|June 26, 2002
Comparison of family based haplotype methods using intragenic SNPs in candidate genesCatherine Bourgain, Emmanuelle Genin, Françoise Clerget-Darpoux
BMC Genetics|April 7, 2006
Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effectsEmmanuelle Cousin, Jean-Francois Deleuze, Emmanuelle Genin
Studies in Health Technology and Informatics|June 24, 2020
Secure Collapsing Method Based on Fully Homomorphic EncryptionDavid Niyitegeka, Reda Bellafqira, Emmanuelle Genin, et al.
Bioinformatics (Oxford, England)|December 4, 2018
GEMPROT: visualization of the impact on the protein of the genetic variants found on each haplotypeTania Cuppens, Thomas E Ludwig, Pascal Trouvé, et al.
Genetic Epidemiology|March 26, 2003
Does accounting for gene-environment (GxE) interaction increase the power to detect the effect of a gene in a multifactorial disease?Hana Selinger-Leneman, Emmanuelle Genin, Jill M Norris, et al.
Frontiers in Medicine|June 14, 2019
Sensitive Skin: Lessons From Transcriptomic StudiesAdeline Bataille, Christelle Le Gall-Ianotto, Emmanuelle Genin, et al.
Molecular Autism|October 25, 2011
Autism risk assessment in siblings of affected children using sex-specific genetic scoresJerome Carayol, Gerard D Schellenberg, Beth Dombroski, et al.
NAR Genomics and Bioinformatics|March 20, 2025
Enhancing the annotation of small ORF-altering variants using MORFEE: introducing MORFEEdb, a comprehensive catalog of SNVs affecting upstream ORFs in human 5'UTRsCaroline Meguerditchian, David Baux, Thomas E Ludwig, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|March 11, 2003
Deleterious genetic influence of CX3CR1 genotypes on HIV-1 disease progressionSophie Faure, Laurence Meyer, Emmanuelle Genin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 29, 2003
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54Nicolas de Roux, Emmanuelle Genin, Jean-Claude Carel, et al.
Pageof 4