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Emmanuelle Génin

Showing results (1-10 of 119) with videos related to

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Human Genetics|June 6, 2019
Missing heritability of complex diseases: case solved?Emmanuelle Génin
Human Heredity|April 20, 2021
49th European Mathematical Genetics Meeting (EMGM) 2021Emmanuelle Génin
European Journal of Human Genetics : EJHG|March 24, 2005
Complex trait mapping in isolated populations: Are specific statistical methods required?Catherine Bourgain, Emmanuelle Génin
Human Heredity|July 24, 2015
Integration of Omics Data in Genetic EpidemiologyEmmanuelle Génin, Marcella Devoto
Human Genetics|June 6, 2020
Rare variant association testing in the non-coding genomeOzvan Bocher, Emmanuelle Génin
Human Heredity|February 10, 2015
The missing heritability paradigm: a dramatic resurgence of the GIGO syndrome in geneticsEmmanuelle Génin, Françoise Clerget-Darpoux
Human Heredity|September 1, 2016
Revisiting the Polygenic Additive Liability Model through the Example of Diabetes MellitusEmmanuelle Génin, Françoise Clerget-Darpoux
Briefings in Functional Genomics|July 10, 2014
How important are rare variants in common disease?Aude Saint Pierre, Emmanuelle Génin
Bioinformatics (Oxford, England)|April 6, 2006
ALTree: association detection and localization of susceptibility sites using haplotype phylogenetic treesClaire Bardel, Vincent Danjean, Emmanuelle Génin
BMC Proceedings|May 10, 2008
Dealing with missing phase and missing data in phylogeny-based analysisClaire Bardel, Pascal Croiseau, Emmanuelle Génin
Pageof 12

Showing results (1-10 of 119) with videos related to

Sort By:
Pageof 12
Human Genetics|June 6, 2019
Missing heritability of complex diseases: case solved?Emmanuelle Génin
Human Heredity|April 20, 2021
49th European Mathematical Genetics Meeting (EMGM) 2021Emmanuelle Génin
European Journal of Human Genetics : EJHG|March 24, 2005
Complex trait mapping in isolated populations: Are specific statistical methods required?Catherine Bourgain, Emmanuelle Génin
Human Heredity|July 24, 2015
Integration of Omics Data in Genetic EpidemiologyEmmanuelle Génin, Marcella Devoto
Human Genetics|June 6, 2020
Rare variant association testing in the non-coding genomeOzvan Bocher, Emmanuelle Génin
Human Heredity|February 10, 2015
The missing heritability paradigm: a dramatic resurgence of the GIGO syndrome in geneticsEmmanuelle Génin, Françoise Clerget-Darpoux
Human Heredity|September 1, 2016
Revisiting the Polygenic Additive Liability Model through the Example of Diabetes MellitusEmmanuelle Génin, Françoise Clerget-Darpoux
Briefings in Functional Genomics|July 10, 2014
How important are rare variants in common disease?Aude Saint Pierre, Emmanuelle Génin
Bioinformatics (Oxford, England)|April 6, 2006
ALTree: association detection and localization of susceptibility sites using haplotype phylogenetic treesClaire Bardel, Vincent Danjean, Emmanuelle Génin
BMC Proceedings|May 10, 2008
Dealing with missing phase and missing data in phylogeny-based analysisClaire Bardel, Pascal Croiseau, Emmanuelle Génin
Pageof 12