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Published in Nature genetics (01.01.2014)
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A European study of HLA-B in Stevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs
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Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome
Bujakowska, Kinga M, Zhang, Qi, Siemiatkowska, Anna M, Liu, Qin, Place, Emily, Falk, Marni J, Consugar, Mark, Lancelot, Marie-Elise, Antonio, Aline, Lonjou, Christine, Carpentier, Wassila, Mohand-Saïd, Saddek, den Hollander, Anneke I, Cremers, Frans P M, Leroy, Bart P, Gai, Xiaowu, Sahel, José-Alain, van den Born, L Ingeborgh, Collin, Rob W J, Zeitz, Christina, Audo, Isabelle, Pierce, Eric A
Published in Human molecular genetics (01.01.2015)
Published in Human molecular genetics (01.01.2015)
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Boosting GWAS using biological networks: A study on susceptibility to familial breast cancer
Climente-González, Héctor, Lonjou, Christine, Lesueur, Fabienne, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Azencott, Chloé-Agathe
Published in PLoS computational biology (18.03.2021)
Published in PLoS computational biology (18.03.2021)
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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation
Lonjou, Christine, Damiola, Francesca, Moissonnier, Monika, Durand, Geoffroy, Malakhova, Irina, Masyakin, Vladimir, Le Calvez-Kelm, Florence, Cardis, Elisabeth, Byrnes, Graham, Kesminiene, Ausrele, Lesueur, Fabienne
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Published in BMC cancer (12.05.2017)
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Linkage Disequilibrium in Human Populations
Lonjou, Christine, Zhang, Weihua, Collins, Andrew, Tapper, William J., Elahi, Eiram, Maniatis, Nikolas, Morton, Newton E.
Published in Proceedings of the National Academy of Sciences - PNAS (13.05.2003)
Published in Proceedings of the National Academy of Sciences - PNAS (13.05.2003)
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Models including pathological and radiomic features vs clinical models in predicting outcome of patients with metastatic non-small cell lung cancer treated with immunotherapy
Captier, Nicolas, Lerousseau, Marvin, Orlhac, Fanny, Hovhannisyan, Narinée, Luporsi, Marie, Lagha, Sarah, Tedesco, Anne-Sophie, Salamoun Feghali, Paulette, Lonjou, Christine, Ramtohul, Toulsie, Beaulaton, Clément, Brisse, Hervé, Vincent-Salomon, Anne, Walter, Thomas, Buvat, Irène, Girard, Nicolas, Barillot, Emmanuel
Published in Journal of clinical oncology (01.06.2023)
Published in Journal of clinical oncology (01.06.2023)
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Biological networks and GWAS: comparing and combining network methods to understand the genetics of familial breast cancer susceptibility in the GENESIS study
Climente-González, Héctor, Lonjou, Christine, Lesueur, Fabienne, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Azencott, Chloé-Agathe, Genesis Study Group
Published in PLoS computational biology (18.03.2021)
Published in PLoS computational biology (18.03.2021)
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Allelic Association under Map Error and Recombinational Heterogeneity: A Tale of Two Sites
Lonjou, Christine, Collins, Andrew, Ajioka, Richard S., Jorde, Lynn B., Kushner, James P., Morton, Newton E.
Published in Proceedings of the National Academy of Sciences - PNAS (15.09.1998)
Published in Proceedings of the National Academy of Sciences - PNAS (15.09.1998)
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CRB1 mutations in inherited retinal dystrophies
Bujakowska, Kinga, Audo, Isabelle, Mohand-Saïd, Saddek, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Léveillard, Thierry, Letexier, Mélanie, Saraiva, Jean-Paul, Lonjou, Christine, Carpentier, Wassila, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina
Published in Human mutation (01.02.2012)
Published in Human mutation (01.02.2012)
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WDR34, a candidate gene for non‐syndromic rod‐cone dystrophy
Solaguren‐Beascoa, Maria, Bujakowska, Kinga M., Méjécase, Cécile, Emmenegger, Lisa, Orhan, Elise, Neuillé, Marion, Mohand‐Saïd, Saddek, Condroyer, Christel, Lancelot, Marie‐Elise, Michiels, Christelle, Demontant, Vanessa, Antonio, Aline, Letexier, Mélanie, Saraiva, Jean‐Paul, Lonjou, Christine, Carpentier, Wassila, Léveillard, Thierry, Pierce, Eric A., Dollfus, Hélène, Sahel, José‐Alain, Bhattacharya, Shomi S., Audo, Isabelle, Zeitz, Christina
Published in Clinical genetics (01.02.2021)
Published in Clinical genetics (01.02.2021)
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Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinoma
Kulkarni, Om, Sugier, Pierre-Emmanuel, Guibon, Julie, Boland-Augé, Anne, Lonjou, Christine, Bacq-Daian, Delphine, Olaso, Robert, Rubino, Carole, Souchard, Vincent, Rachedi, Frédérique, Lence-Anta, Juan Jesus, Ortiz, Rosa Maria, Xhaard, Constance, Laurent-Puig, Pierre, Mulot, Claire, Guizard, Anne-Valérie, Schvartz, Claire, Boutron-Ruault, Marie-Christine, Ostroumova, Evgenia, Kesminiene, Ausrele, Deleuze, Jean-François, Guénel, Pascal, De Vathaire, Florent, Truong, Thérèse, Lesueur, Fabienne
Published in Scientific reports (26.04.2021)
Published in Scientific reports (26.04.2021)
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Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
Girard, Elodie, Eon‐marchais, Séverine, Olaso, Robert E, Renault, Anne‐laure, Damiola, Francesca, Dondon, Marie‐gabrielle, Barjhoux, Laure, Goidin, Didier, Meyer, Vincent, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Lonjou, Christine, Coignard, Juliette, Marcou, Morgane, Cavaciuti, Eve, Baulard, Céline, Bihoreau, Marie‐thérèse, Cohen‐haguenauer, Odile, Leroux, Dominique, Penet, Clotilde, Fert‐ferrer, Sandra, Colas, Chrystelle, Frébourg, Thierry, Eisinger, Francois, Adenis, Claude, Fajac, Anne, Gladieff, Laurence, Tinat, Julie, Floquet, Anne, Chiesa, Jean, Giraud, Sophie, Mortemousque, Isabelle, Soubrier, Florent, Audebert‐bellanger, Séverine, Limacher, Jean‐marc, Lasset, Christine C., Lejeune‐dumoulin, Sophie, Dreyfus, Hélène, Bignon, Yves‐jean, Longy, Michel, Pujol, Pascal, Venat‐bouvet, Laurence, Bonadona, Valerie V., Berthet, Pascaline, Luporsi, Elisabeth, Maugard, Christine, Noguès, Catherine, Delnatte, Capucine, Fricker, Jean‐pierre, Gesta, Paul, Faivre, Laurence, Lortholary, Alain, Buecher, Bruno, Caron, Olivier, Gauthier‐villars, Marion, Coupier, Isabelle, Servant, Nicolas, Boland, Anne, Mazoyer, Sylvie, Deleuze, Jean‐françois, Stoppa‐lyonnet, Dominique, Andrieu, Nadine N., Lesueur, Fabienne
Published in International journal of cancer (11.01.2019)
Published in International journal of cancer (11.01.2019)
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A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family
Audo, Isabelle, Bujakowska, Kinga, Mohand-Saïd, Saddek, Tronche, Sophie, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Lonjou, Christine, Carpentier, Wassila, Sahel, José-Alain, Bhattacharya, Shomi, Zeitz, Christina
Published in Molecular vision (2011)
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Published in Molecular vision (2011)
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No association between HLA-B and cutaneous reactions to sulphonamides in human immunodeficiency virus-infected patients
Vitezica, Z.G., Wolkenstein, P., Lonjou, C., Eliaszewicz, M., Sicard, X., Roujeau, J.-C., Hovnanian, A.
Published in British journal of dermatology (1951) (01.08.2008)
Published in British journal of dermatology (1951) (01.08.2008)
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