High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly

por Servin, Bertrand, Faraut, Thomas, Iannuccelli, Nathalie, Zelenika, Diana, Milan, Denis
Publicado 2012

A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1

por Manes, Gaël, Hebrard, Maxime, Bocquet, Béatrice, Meunier, Isabelle, Coustes-Chazalette, Delphine, Sénéchal, Audrey, Bolland-Augé, Anne, Zelenika, Diana, Hamel, Christian P
Publicado 2011

Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes

por Fradin, Delphine, Le Fur, Sophie, Mille, Clémence, Naoui, Nadia, Groves, Chris, Zelenika, Diana, McCarthy, Mark I., Lathrop, Mark, Bougnères, Pierre
Publicado 2012

CpG Methylation Changes within the IL2RA Promoter in Type 1 Diabetes of Childhood Onset

por Belot, Marie-Pierre, Fradin, Delphine, Mai, Nga, Le Fur, Sophie, Zélénika, Diana, Kerr-Conte, Julie, Pattou, François, Lucas, Bruno, Bougnères, Pierre
Publicado 2013

Gene–environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study

por Travis, Ruth C, Reeves, Gillian K, Green, Jane, Bull, Diana, Tipper, Sarah J, Baker, Krys, Beral, Valerie, Peto, Richard, Bell, John, Zelenika, Diana, Lathrop, Mark
Publicado 2010

Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol Dependence

por Desrivières, Sylvane, Pronko, Sergey P., Lourdusamy, Anbarasu, Ducci, Francesca, Hoffman, Paula L., Wodarz, Norbert, Ridinger, Monika, Rietschel, Marcella, Zelenika, Diana, Lathrop, Mark, Schumann, Gunter, Tabakoff, Boris
Publicado 2011

Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans

por Alonso, Santos, Izagirre, Neskuts, Smith-Zubiaga, Isabel, Gardeazabal, Jesús, Díaz-Ramón, José Luís, Díaz-Pérez, José Luís, Zelenika, Diana, Boyano, María Dolores, Smit, Nico, de la Rúa, Concepción
Publicado 2008

Caution in Interpreting Results from Imputation Analysis When Linkage Disequilibrium Extends over a Large Distance: A Case Study on Venous Thrombosis

por Germain, Marine, Saut, Noémie, Oudot-Mellakh, Tiphaine, Letenneur, Luc, Dupuy, Anne-Marie, Bertrand, Marion, Alessi, Marie-Christine, Lambert, Jean-Charles, Zelenika, Diana, Emmerich, Joseph, Tiret, Laurence, Cambien, Francois, Lathrop, Mark, Amouyel, Philippe, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre
Publicado 2012

Comprehensive Linkage and Association Analyses Identify Haplotype, Near to the TNFSF15 Gene, Significantly Associated with Spondyloarthritis

por Zinovieva, Elena, Bourgain, Catherine, Kadi, Amir, Letourneur, Franck, Izac, Brigitte, Said-Nahal, Roula, Lebrun, Nicolas, Cagnard, Nicolas, Vigier, Agathe, Jacques, Sébastien, Miceli-Richard, Corinne, Garchon, Henri-Jean, Heath, Simon, Charon, Céline, Bacq, Delphine, Boland, Anne, Zelenika, Diana, Chiocchia, Gilles, Breban, Maxime
Publicado 2009

Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2

por Menzel, Stephan, Rooks, Helen, Zelenika, Diana, Mtatiro, Siana N, Gnanakulasekaran, Akshala, Drasar, Emma, Cox, Sharon, Liu, Li, Masood, Mariam, Silver, Nicholas, Garner, Chad, Vasavda, Nisha, Howard, Jo, Makani, Julie, Adekile, Adekunle, Pace, Betty, Spector, Tim, Farrall, Martin, Lathrop, Mark, Thein, Swee Lay
Publicado 2014

Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4

por Libioulle, Cécile, Louis, Edouard, Hansoul, Sarah, Sandor, Cynthia, Farnir, Frédéric, Franchimont, Denis, Vermeire, Séverine, Dewit, Olivier, de Vos, Martine, Dixon, Anna, Demarche, Bruno, Gut, Ivo, Heath, Simon, Foglio, Mario, Liang, Liming, Laukens, Debby, Mni, Myriam, Zelenika, Diana, Gossum, André Van, Rutgeerts, Paul, Belaiche, Jacques, Lathrop, Mark, Georges, Michel
Publicado 2007

Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study

por Germain, Marine, Saut, Noémie, Greliche, Nicolas, Dina, Christian, Lambert, Jean-Charles, Perret, Claire, Cohen, William, Oudot-Mellakh, Tiphaine, Antoni, Guillemette, Alessi, Marie-Christine, Zelenika, Diana, Cambien, François, Tiret, Laurence, Bertrand, Marion, Dupuy, Anne-Marie, Letenneur, Luc, Lathrop, Mark, Emmerich, Joseph, Amouyel, Philippe, Trégouët, David-Alexandre, Morange, Pierre-Emmanuel
Publicado 2011

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families

por Liang, Xueying, Pfeiffer, Ruth M., Li, Wen-Qing, Brossard, Myriam, Burke, Laura S., Wheeler, William, Calista, Donato, Fargnoli, Maria Concetta, Ghiorzo, Paola, Peris, Ketty, Bianchi-Scarra’, Giovanna, Chaudru, Valerie, Zelenika, Diana, Maeder, Dennis, Burdette, Laurie, Yeager, Meredith, Chanock, Stephen, Landi, Maria Teresa, Demenais, Florence, Tucker, Margaret A., Goldstein, Alisa M., Yang, Xiaohong R.
Publicado 2013

Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine

por Chancerel, Emilie, Lepoittevin, Camille, Le Provost, Grégoire, Lin, Yao-Cheng, Jaramillo-Correa, Juan Pablo, Eckert, Andrew J, Wegrzyn, Jill L, Zelenika, Diana, Boland, Anne, Frigerio, Jean-Marc, Chaumeil, Philippe, Garnier-Géré, Pauline, Boury, Christophe, Grivet, Delphine, González-Martínez, Santiago C, Rouzé, Pierre, Van de Peer, Yves, Neale, David B, Cervera, Maria T, Kremer, Antoine, Plomion, Christophe
Publicado 2011

TCF12 is mutated in anaplastic oligodendroglioma

por Labreche, Karim, Simeonova, Iva, Kamoun, Aurélie, Gleize, Vincent, Chubb, Daniel, Letouzé, Eric, Riazalhosseini, Yasser, Dobbins, Sara E., Elarouci, Nabila, Ducray, Francois, de Reyniès, Aurélien, Zelenika, Diana, Wardell, Christopher P., Frampton, Mathew, Saulnier, Olivier, Pastinen, Tomi, Hallout, Sabrina, Figarella-Branger, Dominique, Dehais, Caroline, Idbaih, Ahmed, Mokhtari, Karima, Delattre, Jean-Yves, Huillard, Emmanuelle, Mark Lathrop, G., Sanson, Marc, Houlston, Richard S.
Publicado 2015

Genome-Wide Population-Based Association Study of Extremely Overweight Young Adults – The GOYA Study

por Paternoster, Lavinia, Evans, David M., Aagaard Nohr, Ellen, Holst, Claus, Gaborieau, Valerie, Brennan, Paul, Prior Gjesing, Anette, Grarup, Niels, Witte, Daniel R., Jørgensen, Torben, Linneberg, Allan, Lauritzen, Torsten, Sandbaek, Anelli, Hansen, Torben, Pedersen, Oluf, Elliott, Katherine S., Kemp, John P., St. Pourcain, Beate, McMahon, George, Zelenika, Diana, Hager, Jörg, Lathrop, Mark, Timpson, Nicholas J., Davey Smith, George, Sørensen, Thorkild I. A.
Publicado 2011

Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis

por Hager, Jörg, Kamatani, Yoichiro, Cazier, Jean-Baptiste, Youhanna, Sonia, Ghassibe-Sabbagh, Michella, Platt, Daniel E., Abchee, Antoine B., Romanos, Jihane, Khazen, Georges, Othman, Raed, Badro, Danielle A., Haber, Marc, Salloum, Angelique K., Douaihy, Bouchra, Shasha, Nabil, Kabbani, Samer, Sbeite, Hana, Chammas, Elie, el Bayeh, Hamid, Rousseau, Francis, Zelenika, Diana, Gut, Ivo, Lathrop, Mark, Farrall, Martin, Gauguier, Dominique, Zalloua, Pierre A.
Publicado 2012

Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability

por Jamain, Stéphane, Cichon, Sven, Etain, Bruno, Mühleisen, Thomas W., Georgi, Alexander, Zidane, Nora, Chevallier, Lucie, Deshommes, Jasmine, Nicolas, Aude, Henrion, Annabelle, Degenhardt, Franziska, Mattheisen, Manuel, Priebe, Lutz, Mathieu, Flavie, Kahn, Jean-Pierre, Henry, Chantal, Boland, Anne, Zelenika, Diana, Gut, Ivo, Heath, Simon, Lathrop, Mark, Maier, Wolfgang, Albus, Margot, Rietschel, Marcella, Schulze, Thomas G., McMahon, Francis J., Kelsoe, John R., Hamshere, Marian, Craddock, Nicholas, Nöthen, Markus M., Bellivier, Frank, Leboyer, Marion
Publicado 2014

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

por Sun, Lei, Rommens, Johanna M, Corvol, Harriet, Li, Weili, Li, Xin, Chiang, Theodore, Lin, Fan, Dorfman, Ruslan, Busson, Pierre-François, Parekh, Rashmi V, Zelenika, Diana, Blackman, Scott, Corey, Mary, Doshi, Vishal, Henderson, Lindsay, Naughton, Kathleen, O'Neal, Wanda K, Pace, Rhonda G, Stonebraker, Jaclyn R, Wood, Sally D, Wright, Fred A, Zielenski, Julian, Clement, Annick, Drumm, Mitchell L, Boëlle, Pierre-Yves, Cutting, Garry R, Knowles, Michael R, Durie, Peter R, Strug, Lisa J
Publicado 2012

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

por Bonnet, Crystel, Grati, M'hamed, Marlin, Sandrine, Levilliers, Jacqueline, Hardelin, Jean-Pierre, Parodi, Marine, Niasme-Grare, Magali, Zelenika, Diana, Délépine, Marc, Feldmann, Delphine, Jonard, Laurence, El-Amraoui, Aziz, Weil, Dominique, Delobel, Bruno, Vincent, Christophe, Dollfus, Hélène, Eliot, Marie-Madeleine, David, Albert, Calais, Catherine, Vigneron, Jacqueline, Montaut-Verient, Bettina, Bonneau, Dominique, Dubin, Jacques, Thauvin, Christel, Duvillard, Alain, Francannet, Christine, Mom, Thierry, Lacombe, Didier, Duriez, Françoise, Drouin-Garraud, Valérie, Thuillier-Obstoy, Marie-Françoise, Sigaudy, Sabine, Frances, Anne-Marie, Collignon, Patrick, Challe, Georges, Couderc, Rémy, Lathrop, Mark, Sahel, José-Alain, Weissenbach, Jean, Petit, Christine, Denoyelle, Françoise
Publicado 2011