Torthaí cuardaigh - Génin, Emmanuelle

Efficiency of multiple imputation to test for association in the presence of missing data de réir Croiseau, Pascal, Bardel, Claire, Génin, Emmanuelle

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Dealing with missing phase and missing data in phylogeny-based analysis de réir Bardel, Claire, Croiseau, Pascal, Génin, Emmanuelle

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In silico search for modifier genes associated with pancreatic and liver disease in Cystic Fibrosis de réir Trouvé, Pascal, Génin, Emmanuelle, Férec, Claude

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The Interplay between the Unfolded Protein Response, Inflammation and Infection in Cystic Fibrosis de réir Trouvé, Pascal, Férec, Claude, Génin, Emmanuelle

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

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A Weighted-Holm Procedure Accounting for Allele Frequencies in Genomewide Association Studies de réir Dalmasso, Cyril, Génin, Emmanuelle, Trégouet, David-Alexandre

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Identifying modifier genes of monogenic disease: strategies and difficulties de réir Genin, Emmanuelle, Feingold, Josué, Clerget-Darpoux, Françoise

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Dealing with missing data in family-based association studies: a multiple imputation approach de réir Croiseau, Pascal, Génin, Emmanuelle, Cordell, Heather J.

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Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants de réir Marenne, Gaëlle, Chanock, Stephen J., Malats, Núria, Génin, Emmanuelle

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Impact of the diagnosis definition on linkage detection de réir Dizier, Marie-Hélène, Génin, Emmanuelle, Babron, Marie Claude, Bourgain, Catherine

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On the use of sibling recurrence risks to select environmental factors liable to interact with genetic risk factors de réir Kazma, Rémi, Bonaïti-Pellié, Catherine, Norris, Jill M, Génin, Emmanuelle

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Sensitive Skin: Lessons From Transcriptomic Studies de réir Bataille, Adeline, Le Gall-Ianotto, Christelle, Genin, Emmanuelle, Misery, Laurent

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

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Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us? de réir Leutenegger, Anne-Louise, Sahbatou, Mourad, Gazal, Steven, Cann, Howard, Génin, Emmanuelle

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Extension of SKAT to multi-category phenotypes through a geometrical interpretation de réir Bocher, Ozvan, Marenne, Gaelle, Tournier-Lasserve, Elisabeth, Génin, Emmanuelle, Perdry, Hervé

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A mixture model approach to multiple testing for the genetic analysis of gene expression de réir Dalmasso, Cyril, Pickrell, Joseph, Tuefferd, Marianne, Génin, Emmanuelle, Bourgain, Catherine, Broët, Philippe

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Poor Survival in Rheumatoid Arthritis Associated with Bronchiectasis: A Family-Based Cohort Study de réir Puéchal, Xavier, Génin, Emmanuelle, Bienvenu, Thierry, Le Jeunne, Claire, Dusser, Daniel J.

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Power comparison of different methods to detect genetic effects and gene-environment interactions de réir Kazma, Rémi, Dizier, Marie-Hélène, Guilloud-Bataille, Michel, Bonaïti-Pellié, Catherine, Génin, Emmanuelle

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

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Rare and Low Frequency Variant Stratification in the UK Population: Description and Impact on Association Tests de réir Babron, Marie-Claude, de Tayrac, Marie, Rutledge, Douglas N., Zeggini, Eleftheria, Génin, Emmanuelle

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