Efficiency of multiple imputation to test for association in the presence of missing data

por Croiseau, Pascal, Bardel, Claire, Génin, Emmanuelle
Publicado 2007

Dealing with missing phase and missing data in phylogeny-based analysis

por Bardel, Claire, Croiseau, Pascal, Génin, Emmanuelle
Publicado 2007

In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis

por Trouvé, Pascal, Génin, Emmanuelle, Férec, Claude
Publicado 2017

The Interplay between the Unfolded Protein Response, Inflammation and Infection in Cystic Fibrosis

por Trouvé, Pascal, Férec, Claude, Génin, Emmanuelle
Publicado 2021

Selection of SNP subsets for association studies in candidate genes: comparison of the power of different strategies to detect single disease susceptibility locus effects

por Cousin, Emmanuelle, Deleuze, Jean-Francois, Genin, Emmanuelle
Publicado 2006

Opening the Black Box of Imputation Software to Study the Impact of Reference Panel Composition on Performance

por Dekeyser, Thibault, Génin, Emmanuelle, Herzig, Anthony F.
Publicado 2023

The False Dawn of Polygenic Risk Scores for Human Disease Prediction

por Herzig, Anthony F., Clerget-Darpoux, Françoise, Génin, Emmanuelle
Publicado 2022

Mitochondria, a Key Target in Amyotrophic Lateral Sclerosis Pathogenesis

por Genin, Emmanuelle C., Abou-Ali, Mélanie, Paquis-Flucklinger, Véronique
Publicado 2023

Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants

por Marenne, Gaëlle, Chanock, Stephen J., Malats, Núria, Génin, Emmanuelle
Publicado 2013

Impact of the diagnosis definition on linkage detection

por Dizier, Marie-Hélène, Génin, Emmanuelle, Babron, Marie Claude, Bourgain, Catherine
Publicado 2005

Sensitive Skin: Lessons From Transcriptomic Studies

por Bataille, Adeline, Le Gall-Ianotto, Christelle, Genin, Emmanuelle, Misery, Laurent
Publicado 2019

On the use of haplotype phylogeny to detect disease susceptibility loci

por Bardel, Claire, Danjean, Vincent, Hugot, Jean-Pierre, Darlu, Pierre, Génin, Emmanuelle
Publicado 2005

A mixture model approach to multiple testing for the genetic analysis of gene expression

por Dalmasso, Cyril, Pickrell, Joseph, Tuefferd, Marianne, Génin, Emmanuelle, Bourgain, Catherine, Broët, Philippe
Publicado 2007

Poor Survival in Rheumatoid Arthritis Associated with Bronchiectasis: A Family-Based Cohort Study

por Puéchal, Xavier, Génin, Emmanuelle, Bienvenu, Thierry, Le Jeunne, Claire, Dusser, Daniel J.
Publicado 2014

High level of inbreeding in final phase of 1000 Genomes Project

por Gazal, Steven, Sahbatou, Mourad, Babron, Marie-Claude, Génin, Emmanuelle, Leutenegger, Anne-Louise
Publicado 2015

Power comparison of different methods to detect genetic effects and gene-environment interactions

por Kazma, Rémi, Dizier, Marie-Hélène, Guilloud-Bataille, Michel, Bonaïti-Pellié, Catherine, Génin, Emmanuelle
Publicado 2007

Autism risk assessment in siblings of affected children using sex-specific genetic scores

por Carayol, Jerome, Schellenberg, Gerard D, Dombroski, Beth, Genin, Emmanuelle, Rousseau, Francis, Dawson, Geraldine
Publicado 2011

Rare and Low Frequency Variant Stratification in the UK Population: Description and Impact on Association Tests

por Babron, Marie-Claude, de Tayrac, Marie, Rutledge, Douglas N., Zeggini, Eleftheria, Génin, Emmanuelle
Publicado 2012

Accuracy of heritability estimations in presence of hidden population stratification

por Dandine-Roulland, Claire, Bellenguez, Céline, Debette, Stéphanie, Amouyel, Philippe, Génin, Emmanuelle, Perdry, Hervé
Publicado 2016

CFTR Cooperative Cis-Regulatory Elements in Intestinal Cells

por Collobert, Mégane, Bocher, Ozvan, Le Nabec, Anaïs, Génin, Emmanuelle, Férec, Claude, Moisan, Stéphanie
Publicado 2021