Resultats de la cerca - Besse, Céline

Lentiviral Transduction of CD34(+) Cells Induces Genome-Wide Epigenetic Modifications per Yamagata, Yoshiaki, Parietti, Véronique, Stockholm, Daniel, Corre, Guillaume, Poinsignon, Catherine, Touleimat, Nizar, Delafoy, Damien, Besse, Céline, Tost, Jörg, Galy, Anne, Paldi, András

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Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children per Fradin, Delphine, Boëlle, Pierre-Yves, Belot, Marie-Pierre, Lachaux, Fanny, Tost, Jorg, Besse, Céline, Deleuze, Jean-François, De Filippo, Gianpaolo, Bougnères, Pierre

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Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure per Caburet, Sandrine, Zavadakova, Petra, Ben-Neriah, Ziva, Bouhali, Kamal, Dipietromaria, Aurélie, Charon, Céline, Besse, Céline, Laissue, Paul, Chalifa-Caspi, Vered, Christin-Maitre, Sophie, Vaiman, Daniel, Levi, Giovanni, Veitia, Reiner A., Fellous, Marc

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Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia per Brucato, Nicolas, Fernandes, Veronica, Kusuma, Pradiptajati, Černý, Viktor, Mulligan, Connie J, Soares, Pedro, Rito, Teresa, Besse, Céline, Boland, Anne, Deleuze, Jean-Francois, Cox, Murray P, Sudoyo, Herawati, Stoneking, Mark, Pereira, Luisa, Ricaut, François-Xavier

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A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus per Mobuchon, Lenha, Battistella, Aude, Bardel, Claire, Scelo, Ghislaine, Renoud, Alexia, Houy, Alexandre, Cassoux, Nathalie, Milder, Maud, Cancel-Tassin, Géraldine, Cussenot, Olivier, Delattre, Olivier, Besse, Céline, Boland, Anne, Deleuze, Jean-François, Cox, David G., Stern, Marc-Henri

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Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populat... per Jabot-Hanin, Fabienne, Cobat, Aurélie, Feinberg, Jacqueline, Grange, Ghislain, Remus, Natascha, Poirier, Christine, Boland-Auge, Anne, Besse, Céline, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, Schurr, Erwin, Alcaïs, Alexandre, Hoal, Eileen G., Delacourt, Christophe, Abel, Laurent

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Papuan mitochondrial genomes and the settlement of Sahul per Pedro, Nicole, Brucato, Nicolas, Fernandes, Veronica, André, Mathilde, Saag, Lauri, Pomat, William, Besse, Céline, Boland, Anne, Deleuze, Jean-François, Clarkson, Chris, Sudoyo, Herawati, Metspalu, Mait, Stoneking, Mark, Cox, Murray P., Leavesley, Matthew, Pereira, Luisa, Ricaut, François-Xavier

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Prediction of Breast Cancer Treatment–Induced Fatigue by Machine Learning Using Genome-Wide Association Data per Lee, Sangkyu, Deasy, Joseph O, Oh, Jung Hun, Di Meglio, Antonio, Dumas, Agnes, Menvielle, Gwenn, Charles, Cecile, Boyault, Sandrine, Rousseau, Marina, Besse, Celine, Thomas, Emilie, Boland, Anne, Cottu, Paul, Tredan, Olivier, Levy, Christelle, Martin, Anne-Laure, Everhard, Sibille, Ganz, Patricia A, Partridge, Ann H, Michiels, Stefan, Deleuze, Jean-François, Andre, Fabrice, Vaz-Luis, Ines

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Human adenylate kinase 2 deficiency causes a profound haematopoietic defect associated with sensorineural deafness per Lagresle-Peyrou, Chantal, Six, Emmanuelle M., Picard, Capucine, Rieux-Laucat, Frédéric, Michel, Vincent, Ditadi, Andrea, Chappedelaine, Corinne Demerens-de, Morillon, Estelle, Valensi, Françoise, Simon-Stoos, Karen L., Mullikin, James C., Noroski, Lenora M., Besse, Céline, Wulffraat, Nicolas M., Ferster, Alina, Abecasis, Manuel M., Calvo, Fabien, Petit, Christine, Candotti, Fabio, Abel, Laurent, Fischer, Alain, Cavazzana-Calvo, Marina

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Fine–mapping of two differentiated thyroid carcinoma susceptibility loci at 2q35 and 8p12 in Europeans, Melanesians and Polynesians per Guibon, Julie, Sugier, Pierre-Emmanuel, Kulkarni, Om, Karimi, Mojgan, Bacq-Daian, Delphine, Besse, Céline, Boland, Anne, Adjadj, Elisabeth, Rachédi, Frédérique, Rubino, Carole, Xhaard, Constance, Mulot, Claire, Laurent-Puig, Pierre, Guizard, Anne-Valérie, Schvartz, Claire, Ortiz, Rosa Maria, Ren, Yan, Ostroumova, Evgenia, Deleuze, Jean-François, Boutron-Ruault, Marie-Christine, Kesminiene, Ausrele, De Vathaire, Florent, Guénel, Pascal, Lesueur, Fabienne, Truong, Thérèse

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Experimental evolution links post-transcriptional regulation to Leishmania fitness gain per Piel, Laura, Rajan, K. Shanmugha, Bussotti, Giovanni, Varet, Hugo, Legendre, Rachel, Proux, Caroline, Douché, Thibaut, Giai-Gianetto, Quentin, Chaze, Thibault, Cokelaer, Thomas, Vojtkova, Barbora, Gordon-Bar, Nadav, Doniger, Tirza, Cohen-Chalamish, Smadar, Rengaraj, Praveenkumar, Besse, Céline, Boland, Anne, Sadlova, Jovana, Deleuze, Jean-François, Matondo, Mariette, Unger, Ron, Volf, Petr, Michaeli, Shulamit, Pescher, Pascale, Späth, Gerald F.

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Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease per Bustamante, Jacinta, Arias, Andres A, Vogt, Guillaume, Picard, Capucine, Galicia, Lizbeth Blancas, Prando, Carolina, Grant, Audrey V, Marchal, Christophe C, Hubeau, Marjorie, Chapgier, Ariane, de Beaucoudrey, Ludovic, Puel, Anne, Feinberg, Jacqueline, Valinetz, Ethan, Jannière, Lucile, Besse, Céline, Boland, Anne, Brisseau, Jean-Marie, Blanche, Stéphane, Lortholary, Olivier, Fieschi, Claire, Emile, Jean-François, Boisson-Dupuis, Stéphanie, Al-Muhsen, Saleh, Woda, Bruce, Newburger, Peter E, Condino-Neto, Antonio, Dinauer, Mary C, Abel, Laurent, Casanova, Jean-Laurent

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GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients per Cox, David G., Curtit, Elsa, Romieu, Gilles, Fumoleau, Pierre, Rios, Maria, Bonnefoi, Hervé, Bachelot, Thomas, Soulié, Patrick, Jouannaud, Christelle, Bourgeois, Hugues, Petit, Thierry, Tennevet, Isabelle, Assouline, David, Mathieu, Marie-Christine, Jacquin, Jean-Philippe, Lavau-Denes, Sandrine, Darut-Jouve, Ariane, Ferrero, Jean-Marc, Tarpin, Carole, Lévy, Christelle, Delecroix, Valérie, Trillet-Lenoir, Véronique, Cojocarasu, Oana, Meunier, Jérôme, Pierga, Jean-Yves, Faure-Mercier, Céline, Blanché, Hélène, Sahbatou, Mourad, Boland, Anne, Bacq, Delphine, Besse, Céline, Deleuze, Jean-François, Pauporté, Iris, Thomas, Gilles, Pivot, Xavier

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Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort per Pivot, Xavier, Romieu, Gilles, Fumoleau, Pierre, Rios, Maria, Bonnefoi, Hervé, Bachelot, Thomas, Soulié, Patrick, Jouannaud, Christelle, Bourgeois, Hugues, Petit, Thierry, Tennevet, Isabelle, Assouline, David, Mathieu, Marie-Christine, Jacquin, Jean-Philippe, Lavau-Denes, Sandrine, Darut-Jouve, Ariane, Ferrero, Jean-Marc, Tarpin, Carole, Lévy, Christelle, Delecroix, Valérie, Trillet-Lenoir, Véronique, Cojocarasu, Oana, Meunier, Jérôme, Pierga, Jean-Yves, Agostini, Cécile, Kerbrat, Pierre, Faure-Mercier, Céline, Blanché, Hélène, Sahbatou, Mourad, Boland, Anne, Bacq, Delphine, Besse, Céline, Calvo, Fabien, Renaud, Alexia, Deleuze, Jean-François, Pauporté, Iris, Thomas, Gilles, Cox, David G.

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Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-path... per Curtit, Elsa, Pivot, Xavier, Henriques, Julie, Paget-Bailly, Sophie, Fumoleau, Pierre, Rios, Maria, Bonnefoi, Hervé, Bachelot, Thomas, Soulié, Patrick, Jouannaud, Christelle, Bourgeois, Hugues, Petit, Thierry, Tennevet, Isabelle, Assouline, David, Mathieu, Marie-Christine, Jacquin, Jean-Philippe, Lavau-Denes, Sandrine, Darut-Jouve, Ariane, Ferrero, Jean-Marc, Tarpin, Carole, Lévy, Christelle, Delecroix, Valérie, Trillet-Lenoir, Véronique, Cojocarasu, Oana, Meunier, Jérôme, Pierga, Jean-Yves, Kerbrat, Pierre, Faure-Mercier, Céline, Blanché, Hélène, Sahbatou, Mourad, Boland, Anne, Bacq, Delphine, Besse, Céline, Thomas, Gilles, Deleuze, Jean-François, Pauporté, Iris, Romieu, Gilles, Cox, David G.

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Accelerated genome sequencing with controlled costs for infants in intensive care units: a feasibility study in a French hospital network per Denommé-Pichon, Anne-Sophie, Vitobello, Antonio, Olaso, Robert, Ziegler, Alban, Jeanne, Médéric, Tran Mau-Them, Frédéric, Couturier, Victor, Racine, Caroline, Isidor, Bertrand, Poë, Charlotte, Jouan, Thibaud, Boland, Anne, Fin, Bertrand, Bacq-Daian, Delphine, Besse, Céline, Garde, Aurore, Prost, Adeline, Garret, Philippine, Tisserant, Émilie, Delanne, Julian, Nambot, Sophie, Juven, Aurélien, Gorce, Magali, Nizon, Mathilde, Vincent, Marie, Moutton, Sébastien, Fradin, Mélanie, Lavillaureix, Alinoë, Rollier, Paul, Capri, Yline, Van-Gils, Julien, Busa, Tiffany, Sigaudy, Sabine, Pasquier, Laurent, Barth, Magalie, Bruel, Ange-Line, Flamant, Cyril, Prouteau, Clément, Bonneau, Dominique, Toutain, Annick, Chantegret, Corinne, Callier, Patrick, Philippe, Christophe, Duffourd, Yannis, Deleuze, Jean-François, Sorlin, Arthur, Faivre, Laurence, Thauvin-Robinet, Christel

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Analysis with the exome array identifies multiple new independent variants in lipid loci per Kanoni, Stavroula, Masca, Nicholas G.D., Stirrups, Kathleen E., Varga, Tibor V., Warren, Helen R., Scott, Robert A., Southam, Lorraine, Zhang, Weihua, Yaghootkar, Hanieh, Müller-Nurasyid, Martina, Couto Alves, Alexessander, Strawbridge, Rona J., Lataniotis, Lazaros, An Hashim, Nikman, Besse, Céline, Boland, Anne, Braund, Peter S., Connell, John M., Dominiczak, Anna, Farmaki, Aliki-Eleni, Franks, Stephen, Grallert, Harald, Jansson, Jan-Håkan, Karaleftheri, Maria, Keinänen-Kiukaanniemi, Sirkka, Matchan, Angela, Pasko, Dorota, Peters, Annette, Poulter, Neil, Rayner, Nigel W., Renström, Frida, Rolandsson, Olov, Sabater-Lleal, Maria, Sennblad, Bengt, Sever, Peter, Shields, Denis, Silveira, Angela, Stanton, Alice V., Strauch, Konstantin, Tomaszewski, Maciej, Tsafantakis, Emmanouil, Waldenberger, Melanie, Blakemore, Alexandra I.F., Dedoussis, George, Escher, Stefan A., Kooner, Jaspal S., McCarthy, Mark I., Palmer, Colin N.A., Hamsten, Anders, Caulfield, Mark J., Frayling, Timothy M., Tobin, Martin D., Jarvelin, Marjo-Riitta, Zeggini, Eleftheria, Gieger, Christian, Chambers, John C., Wareham, Nick J., Munroe, Patricia B., Franks, Paul W., Samani, Nilesh J., Deloukas, Panos

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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23 per Garnier, Sophie, Harakalova, Magdalena, Weiss, Stefan, Mokry, Michal, Regitz-Zagrosek, Vera, Hengstenberg, Christian, Cappola, Thomas P, Isnard, Richard, Arbustini, Eloisa, Cook, Stuart A, van Setten, Jessica, Calis, Jorg J A, Hakonarson, Hakon, Morley, Michael P, Stark, Klaus, Prasad, Sanjay K, Li, Jin, O'Regan, Declan P, Grasso, Maurizia, Müller-Nurasyid, Martina, Meitinger, Thomas, Empana, Jean-Philippe, Strauch, Konstantin, Waldenberger, Melanie, Marguiles, Kenneth B, Seidman, Christine E, Kararigas, Georgios, Meder, Benjamin, Haas, Jan, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Erdmann, Jeanette, Blankenberg, Stefan, Wichter, Thomas, Ruppert, Volker, Tavazzi, Luigi, Dubourg, Olivier, Roizes, Gérard, Dorent, Richard, de Groote, Pascal, Fauchier, Laurent, Trochu, Jean-Noël, Aupetit, Jean-François, Bilinska, Zofia T, Germain, Marine, Völker, Uwe, Hemerich, Daiane, Raji, Ibticem, Bacq-Daian, Delphine, Proust, Carole, Remior, Paloma, Gomez-Bueno, Manuel, Lehnert, Kristin, Maas, Renee, Olaso, Robert, Saripella, Ganapathi Varma, Felix, Stephan B, McGinn, Steven, Duboscq-Bidot, Laëtitia, van Mil, Alain, Besse, Céline, Fontaine, Vincent, Blanché, Hélène, Ader, Flavie, Keating, Brendan, Curjol, Angélique, Boland, Anne, Komajda, Michel, Cambien, François, Deleuze, Jean-François, Dörr, Marcus, Asselbergs, Folkert W, Villard, Eric, Trégouët, David-Alexandre, Charron, Philippe

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Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma per Machiela, Mitchell J., Hofmann, Jonathan N., Carreras-Torres, Robert, Brown, Kevin M., Johansson, Mattias, Wang, Zhaoming, Foll, Matthieu, Li, Peng, Rothman, Nathaniel, Savage, Sharon A., Gaborieau, Valerie, McKay, James D., Ye, Yuanqing, Henrion, Marc, Bruinsma, Fiona, Jordan, Susan, Severi, Gianluca, Hveem, Kristian, Vatten, Lars J., Fletcher, Tony, Koppova, Kvetoslava, Larsson, Susanna C., Wolk, Alicja, Banks, Rosamonde E., Selby, Peter J., Easton, Douglas F., Pharoah, Paul, Andreotti, Gabriella, Beane Freeman, Laura E., Koutros, Stella, Albanes, Demetrius, Mannisto, Satu, Weinstein, Stephanie, Clark, Peter E., Edwards, Todd E., Lipworth, Loren, Gapstur, Susan M., Stevens, Victoria L., Carol, Hallie, Freedman, Matthew L., Pomerantz, Mark M., Cho, Eunyoung, Kraft, Peter, Preston, Mark A., Wilson, Kathryn M., Gaziano, J. Michael, Sesso, Howard S., Black, Amanda, Freedman, Neal D., Huang, Wen-Yi, Anema, John G., Kahnoski, Richard J., Lane, Brian R., Noyes, Sabrina L., Petillo, David, Colli, Leandro M., Sampson, Joshua N., Besse, Celine, Blanche, Helene, Boland, Anne, Burdette, Laurie, Prokhortchouk, Egor, Skryabin, Konstantin G., Yeager, Meredith, Mijuskovic, Mirjana, Ognjanovic, Miodrag, Foretova, Lenka, Holcatova, Ivana, Janout, Vladimir, Mates, Dana, Mukeriya, Anush, Rascu, Stefan, Zaridze, David, Bencko, Vladimir, Cybulski, Cezary, Fabianova, Eleonora, Jinga, Viorel, Lissowska, Jolanta, Lubinski, Jan, Navratilova, Marie, Rudnai, Peter, Szeszenia-Dabrowska, Neonila, Benhamou, Simone, Cancel-Tassin, Geraldine, Cussenot, Olivier, Bueno-de-Mesquita, H.B(as)., Canzian, Federico, Duell, Eric J., Ljungberg, Börje, Sitaram, Raviprakash T., Peters, Ulrike, White, Emily, Anderson, Garnet L., Johnson, Lisa, Luo, Juhua, Buring, Julie, Lee, I-Min, Chow, Wong-Ho, Moore, Lee E., Wood, Christopher, Eisen, Timothy, Larkin, James, Choueiri, Toni K., Lathrop, G. Mark, Teh, Bin Tean, Deleuze, Jean-Francois, Wu, Xifeng, Houlston, Richard S., Brennan, Paul, Chanock, Stephen J., Scelo, Ghislaine, Purdue, Mark P.

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Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747–54] per Machiela, Mitchell J., Hofmann, Jonathan N., Carreras-Torres, Robert, Brown, Kevin M., Johansson, Mattias, Wang, Zhaoming, Foll, Matthieu, Li, Peng, Rothman, Nathaniel, Savage, Sharon A., Gaborieau, Valerie, McKay, James D., Ye, Yuanqing, Henrion, Marc, Bruinsma, Fiona, Jordan, Susan, Severi, Gianluca, Hveem, Kristian, Vatten, Lars J., Fletcher, Tony, Koppova, Kvetoslava, Larsson, Susanna C., Wolk, Alicja, Banks, Rosamonde E., Selby, Peter J., Easton, Douglas F., Pharoah, Paul, Andreotti, Gabriella, Beane Freeman, Laura E., Koutros, Stella, Albanes, Demetrius, Mannisto, Satu, Weinstein, Stephanie, Clark, Peter E., Edwards, Todd E, Lipworth, Loren, Gapstur, Susan M., Stevens, Victoria L., Carol, Hallie, Freedman, Matthew L., Pomerantz, Mark M., Cho, Eunyoung, Kraft, Peter, Preston, Mark A., Wilson, Kathryn M., Gaziano, J. Michael, Sesso, Howard S., Black, Amanda, Freedman, Neal D., Huang, Wen-Yi, Anema, John G., Kahnoski, Richard J., Lane, Brian R., Noyes, Sabrina L., Petillo, David, Colli, Leandro M., Sampson, Joshua N., Besse, Celine, Blanche, Helene, Boland, Anne, Burdette, Laurie, Prokhortchouk, Egor, Skryabin, Konstantin G., Yeager, Meredith, Mijuskovic, Mirjana, Ognjanovic, Miodrag, Foretova, Lenka, Holcatova, Ivana, Janout, Vladimir, Mates, Dana, Mukeriya, Anush, Rascu, Stefan, Zaridze, David, Bencko, Vladimir, Cybulski, Cezary, Fabianova, Eleonora, Jinga, Viorel, Lissowska, Jolanta, Lubinski, Jan, Navratilova, Marie, Rudnai, Peter, Szeszenia-Dabrowska, Neonila, Benhamou, Simone, Cancel-Tassin, Geraldine, Cussenot, Olivier, Bueno-de-Mesquita, H.B(as)., Canzian, Federico, Duell, Eric J., Ljungberg, Börje, Sitaram, Raviprakash T., Peters, Ulrike, White, Emily, Anderson, Garnet L., Johnson, Lisa, Luo, Juhua, Buring, Julie, Lee, I-Min, Chow, Wong-Ho, Moore, Lee E, Wood, Christopher, Eisen, Timothy, Larkin, James, Choueiri, Toni K., Lathrop, G. Mark, Teh, Bin Tean, Deleuze, Jean-Francois, Wu, Xifeng, Houlston, Richard S., Brennan, Paul, Chanock, Stephen J., Scelo, Ghislaine, Purdue, Mark P.

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