Search Results - Bonaïti-Pellié, Catherine

Risk tables for genetic counselling in some common congenital malformations by Bonaiti-Pellié, Catherine, Smith, Charles

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Reply to Ott and Mérette by Clerget-Darpoux, Françoise, Margaritte, Patricia, Bonaïti-Pellié, Catherine

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

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Estimating penetrance from multiple case families with predisposing mutations: extension of the ‘genotype-restricted likelihood' (GRL) method by Bonaïti, Bernard, Bonadona, Valérie, Perdry, Hervé, Andrieu, Nadine, Bonaïti-Pellié, Catherine

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

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Ethics and observational studies in medical research: various rules in a common framework by Claudot, Frédérique, Alla, François, Fresson, Jeanne, Calvez, Thierry, Coudane, Henry, Bonaïti-Pellié, Catherine

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TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance? by Bonaïti, Bernard, Olsson, Malin, Hellman, Urban, Suhr, Ole, Bonaïti-Pellié, Catherine, Planté-Bordeneuve, Violaine

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Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population by Hellman, Urban, Alarcon, Flora, Lundgren, Hans Eric, Suhr, Ole, Bonaïti-Pellié, Catherine, Planté-Bordeneuve, Violaine

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PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history by Alarcon, Flora, Bourgain, Catherine, Gauthier-Villars, Marion, Planté-Bordeneuve, Violaine, Stoppa-Lyonnet, Dominique, Bonaïti-Pellié, Catherine

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Reply to "The question of heterogeneity in Marfan syndrome" by Boileau, Catherine, Junien, Claudine, Collod, Gwenaëlle, Jondeau, Guillaume, Dubourg, Olivier, Bourdarias, Jean-Pierre, Bonaïti-Pellié, Catherine, Frezal, Jean, Maroteaux, Pierre

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A second locus for Marfan syndrome maps to chromosome 3p24.2-p25 by Collod, Gwenaëlle, Babron, Marie-Claude, Jondeau, Guillaume, Coulon, Monique, Weissenbach, Jean, Dubourg, Olivier, Bourdarias, Jean-Pierre, Bonaïti-Pellié, Catherine, Junien, Claudine, Boileau, Catherine

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Analysis of Candidate Genes in Occurrence and Growth of Colorectal Adenomas by Olschwang, Sylviane, Vernerey, Déwi, Cottet, Vanessa, Pariente, Alexandre, Nalet, Bernard, Lafon, Jacques, Faivre, Jean, Laurent-Puig, Pierre, Bonithon-Kopp, Claire, Bonaiti-Pellié, Catherine

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Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes by Boileau, Catherine, Jondeau, Guillaume, Babron, Marie-Claude, Coulon, Monique, Alexandre, Jeanne-Armelle, Sakai, Lynn, Melki, Judith, Delorme, Gabriel, Dubourg, Olivier, Bonaïti-Pellié, Catherine, Bourdarias, Jean-Pierre, Junien, Claudine

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Genetic polymorphisms of MMP1, MMP3 and MMP7 gene promoter and risk of colorectal adenoma by Lièvre, Astrid, Milet, Jacqueline, Carayol, Jérôme, Le Corre, Delphine, Milan, Chantal, Pariente, Alexandre, Nalet, Bernard, Lafon, Jacques, Faivre, Jean, Bonithon-Kopp, Claire, Olschwang, Sylviane, Bonaiti-Pellié, Catherine, Laurent-Puig, Pierre

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The International Testicular Cancer Linkage Consortium: A Clinicopathologic Descriptive Analysis of 461 Familial Malignant Testicular Germ Cell Tumor Kindred by Mai, Phuong L., Friedlander, Michael, Tucker, Kathy, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A.S., Lohynska, Radka, Daugaard, Gedske, Richard, Stéphane, Bonaïti-Pellié, Catherine, Heidenreich, Axel, Albers, Peter, Bodrogi, Istvan, Geczi, Lajos, Olah, Edith, Daly, Peter A., Guilford, Parry, Fosså, Sophie D., Heimdal, Ketil, Liubchenko, Ludmila, Tjulandin, Sergei A., Stoll, Hans, Weber, Walter, Easton, Douglas F, Dudakia, Darshna, Huddart, Robert, Stratton, Michael R., Einhorn, Lawrence, Korde, Larissa, Nathanson, Katherine L., Bishop, D. Timothy, Rapley, Elizabeth A., Greene, Mark H.

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Analysis of the DND1 Gene in Men with Sporadic and Familial Testicular Germ Cell Tumors by Linger, Rachel, Dudakia, Darshna, Huddart, Robert, Tucker, Kathy, Friedlander, Michael, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A. S., Lohynska, Radka, Daugaard, Gedske, Richard, Stéphane, Chompret, Agnes, Stoppa-Lyonnet, Dominique, Bonaïti-Pellié, Catherine, Heidenreich, Axel, Albers, Peter, Olah, Edith, Geczi, Lajos, Bodrogi, Istvan, Daly, Peter A., Guilford, Parry, Fosså, Sophie D., Heimdal, Ketil, Tjulandin, Sergei A., Liubchenko, Ludmila, Stoll, Hans, Weber, Walter, Einhorn, Lawrence, McMaster, Mary, Korde, Larissa, Greene, Mark H., Nathanson, Katherine L., Cortessis, Victoria, Easton, Douglas F., Bishop, D. Timothy, Stratton, Michael R., Rapley, Elizabeth A.

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The Y Deletion gr/gr and Susceptibility to Testicular Germ Cell Tumor by Nathanson, Katherine L., Kanetsky, Peter A., Hawes, Rachel, Vaughn, David J., Letrero, Richard, Tucker, Kathy, Friedlander, Michael, Phillips, Kelly-Anne, Hogg, David, Jewett, Michael A. S., Lohynska, Radka, Daugaard, Gedske, Richard, Stéphane, Chompret, Agnès, Bonaïti-Pellié, Catherine, Heidenreich, Axel, Olah, Edith, Geczi, Lajos, Bodrogi, Istvan, Ormiston, Wilma J., Daly, Peter A., Oosterhuis, J. Wolter, Gillis, Ad J. M., Looijenga, Leendert H. J., Guilford, Parry, Fosså, Sophie D., Heimdal, Ketil, Tjulandin, Sergei A., Liubchenko, Ludmila, Stoll, Hans, Weber, Walter, Rudd, Matthew, Huddart, Robert, Crockford, Gillian P., Forman, David, Oliver, D. Timothy, Einhorn, Lawrence, Weber, Barbara L., Kramer, Joan, McMaster, Mary, Greene, Mark H., Pike, Malcolm, Cortessis, Victoria, Chen, Chu, Schwartz, Stephen M., Bishop, D. Timothy, Easton, Douglas F., Stratton, Michael R., Rapley, Elizabeth A.

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