Detection of susceptibility loci by genome-wide linkage analysis

por Babron, Marie-Claude, Bourgain, Catherine, Leutenegger, Anne-Louise, Clerget-Darpoux, Françoise
Publicado em 2005

Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?

por Leutenegger, Anne-Louise, Sahbatou, Mourad, Gazal, Steven, Cann, Howard, Génin, Emmanuelle
Publicado em 2011

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 no Sci Rep (2015)

Genome-wide inbreeding estimation within Lebanese communities using SNP arrays

por Jalkh, Nadine, Sahbatou, Mourad, Chouery, Eliane, Megarbane, André, Leutenegger, Anne-Louise, Serre, Jean-Louis
Publicado no Eur J Hum Genet (2015)

Genome-wide inbreeding estimation within Lebanese communities using SNP arrays

por Jalkh, Nadine, Sahbatou, Mourad, Chouery, Eliane, Megarbane, André, Leutenegger, Anne-Louise, Serre, Jean-Louis
Publicado no Eur J Hum Genet (2015)

Detecting the dominance component of heritability in isolated and outbred human populations

por Herzig, Anthony F., Nutile, Teresa, Ruggiero, Daniela, Ciullo, Marina, Perdry, Hervé, Leutenegger, Anne-Louise
Publicado no Sci Rep (2018)

LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century

por Lesage, Suzanne , Leutenegger, Anne-Louise , Ibanez, Pablo , Janin, Sabine , Lohmann, Ebba , Dürr, Alexandra , Brice, Alexis 
Publicado em 2005

Modeling the effect of a genetic factor for a complex trait in a simulated population

por Bourgey, Mathieu, Leutenegger, Anne-Louise, Cousin, Emmanuelle, Bourgain, Catherine, Babron, Marie-Claude, Clerget-Darpoux, Françoise
Publicado em 2005

Using Genomic Inbreeding Coefficient Estimates for Homozygosity Mapping of Rare Recessive Traits: Application to Taybi-Linder Syndrome

por Leutenegger, Anne-Louise, Labalme, Audrey, Génin, Emmanuelle, Toutain, Annick, Steichen, Elisabeth, Clerget-Darpoux, Françoise, Edery, Patrick
Publicado em 2006

Estimation of the Inbreeding Coefficient through Use of Genomic Data

por Leutenegger, Anne-Louise, Prum, Bernard, Génin, Emmanuelle, Verny, Christophe, Lemainque, Arnaud, Clerget-Darpoux, Françoise, Thompson, Elizabeth A.
Publicado em 2003

Genetic and Environmental Factors Influencing the Placental Growth Factor (PGF) Variation in Two Populations

por Sorice, Rossella, Ruggiero, Daniela, Nutile, Teresa, Aversano, Mario, Husemoen, Lotte, Linneberg, Allan, Bourgain, Catherine, Leutenegger, Anne-Louise, Ciullo, Marina
Publicado em 2012

Genetics of VEGF Serum Variation in Human Isolated Populations of Cilento: Importance of VEGF Polymorphisms

por Ruggiero, Daniela, Dalmasso, Cyril, Nutile, Teresa, Sorice, Rossella, Dionisi, Laura, Aversano, Mario, Bröet, Philippe, Leutenegger, Anne-Louise, Bourgain, Catherine, Ciullo, Marina
Publicado em 2011

Variation in worldwide incidence of amyotrophic lateral sclerosis: a meta-analysis

por Marin, Benoît, Boumédiene, Farid, Logroscino, Giancarlo, Couratier, Philippe, Babron, Marie-Claude, Leutenegger, Anne Louise, Copetti, Massimilano, Preux, Pierre-Marie, Beghi, Ettore
Publicado no Int J Epidemiol (2017)

Genetic Variants Modulating CRIPTO Serum Levels Identified by Genome-Wide Association Study in Cilento Isolates

por Ruggiero, Daniela, Nappo, Stefania, Nutile, Teresa, Sorice, Rossella, Talotta, Francesco, Giorgio, Emilia, Bellenguez, Celine, Leutenegger, Anne-Louise, Liguori, Giovanna L., Ciullo, Marina
Publicado no PLoS Genet (2015)

Segregation Analysis of Phenotypic Components of Learning Disabilities. I. Nonword Memory and Digit Span

por Wijsman, Ellen M., Peterson, Do, Leutenegger, Anne-Louise, Thomson, Jennifer B., Goddard, Katrina A. B., Hsu, Li, Berninger, Virginia W., Raskind, Wendy H.
Publicado em 2000

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

por Polašek, Ozren, Hayward, Caroline, Bellenguez, Celine, Vitart, Veronique, Kolčić, Ivana, McQuillan, Ruth, Saftić, Vanja, Gyllensten, Ulf, Wilson, James F, Rudan, Igor, Wright, Alan F, Campbell, Harry, Leutenegger, Anne-Louise
Publicado em 2010

Clinical interpretation of variants identified in RNU4ATAC, a non-coding spliceosomal gene

por Benoit-Pilven, Clara, Besson, Alicia, Putoux, Audrey, Benetollo, Claire, Saccaro, Clément, Guguin, Justine, Sala, Gabriel, Cologne, Audric, Delous, Marion, Lesca, Gaetan, Padgett, Richard A., Leutenegger, Anne-Louise, Lacroix, Vincent, Edery, Patrick, Mazoyer, Sylvie
Publicado no PLoS One (2020)

Presence of Large Deletions in Kindreds with Autism

por Yu, Chang-En, Dawson, Geraldine, Munson, Jeffrey, D’Souza, Ian, Osterling, Julie, Estes, Annette, Leutenegger, Anne-Louise, Flodman, Pamela, Smith, Moyra, Raskind, Wendy H., Spence, M. Anne, McMahon, William, Wijsman, Ellen M., Schellenberg, Gerard D.
Publicado em 2002

New insights into minor splicing—a transcriptomic analysis of cells derived from TALS patients

por Cologne, Audric, Benoit-Pilven, Clara, Besson, Alicia, Putoux, Audrey, Campan-Fournier, Amandine, Bober, Michael B., De Die-Smulders, Christine E.M., Paulussen, Aimee D.C., Pinson, Lucile, Toutain, Annick, Roifman, Chaim M., Leutenegger, Anne-Louise, Mazoyer, Sylvie, Edery, Patrick, Lacroix, Vincent
Publicado no RNA (2019)

Runs of Homozygosity in European Populations

por McQuillan, Ruth, Leutenegger, Anne-Louise, Abdel-Rahman, Rehab, Franklin, Christopher S., Pericic, Marijana, Barac-Lauc, Lovorka, Smolej-Narancic, Nina, Janicijevic, Branka, Polasek, Ozren, Tenesa, Albert, MacLeod, Andrew K., Farrington, Susan M., Rudan, Pavao, Hayward, Caroline, Vitart, Veronique, Rudan, Igor, Wild, Sarah H., Dunlop, Malcolm G., Wright, Alan F., Campbell, Harry, Wilson, James F.
Publicado em 2008