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Human Genetics
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June 6, 2019
Missing heritability of complex diseases: case solved?
Emmanuelle Génin
Human Heredity
|
April 20, 2021
49th European Mathematical Genetics Meeting (EMGM) 2021
Emmanuelle 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 Epidemiology
Emmanuelle Génin, Marcella Devoto
Human Genetics
|
June 6, 2020
Rare variant association testing in the non-coding genome
Ozvan Bocher, Emmanuelle Génin
Human Heredity
|
February 10, 2015
The missing heritability paradigm: a dramatic resurgence of the GIGO syndrome in genetics
Emmanuelle Génin, Françoise Clerget-Darpoux
Human Heredity
|
September 1, 2016
Revisiting the Polygenic Additive Liability Model through the Example of Diabetes Mellitus
Emmanuelle 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 trees
Claire Bardel, Vincent Danjean, Emmanuelle Génin
BMC Proceedings
|
May 10, 2008
Dealing with missing phase and missing data in phylogeny-based analysis
Claire Bardel, Pascal Croiseau, Emmanuelle Génin
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of 12
Search research articles
Search
Showing results (1-10 of 119) with videos related to
Sort By:
Page
of 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) 2021
Emmanuelle 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 Epidemiology
Emmanuelle Génin, Marcella Devoto
Human Genetics
|
June 6, 2020
Rare variant association testing in the non-coding genome
Ozvan Bocher, Emmanuelle Génin
Human Heredity
|
February 10, 2015
The missing heritability paradigm: a dramatic resurgence of the GIGO syndrome in genetics
Emmanuelle Génin, Françoise Clerget-Darpoux
Human Heredity
|
September 1, 2016
Revisiting the Polygenic Additive Liability Model through the Example of Diabetes Mellitus
Emmanuelle 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 trees
Claire Bardel, Vincent Danjean, Emmanuelle Génin
BMC Proceedings
|
May 10, 2008
Dealing with missing phase and missing data in phylogeny-based analysis
Claire Bardel, Pascal Croiseau, Emmanuelle Génin
Page
of 12