Analysis of KLF transcription factor family gene variants in type 2 diabetes

Por Gutiérrez-Aguilar, Ruth, Benmezroua, Yamina, Vaillant, Emmanuel, Balkau, Beverley, Marre, Michel, Charpentier, Guillaume, Sladek, Rob, Froguel, Philippe, Neve, Bernadette
Publicado em 2007

Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study

Por Ezzidi, Intissar, Mtiraoui, Nabil, Cauchi, Stéphane, Vaillant, Emmanuel, Dechaume, Aurélie, Chaieb, Molka, Kacem, Maha, Almawi, Wassim Y, Froguel, Philippe, Mahjoub, Touhami, Vaxillaire, Martine
Publicado em 2009

What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?

Por Philippe, Julien, Derhourhi, Mehdi, Durand, Emmanuelle, Vaillant, Emmanuel, Dechaume, Aurélie, Rabearivelo, Iandry, Dhennin, Véronique, Vaxillaire, Martine, De Graeve, Franck, Sand, Olivier, Froguel, Philippe, Bonnefond, Amélie
Publicado no PLoS One (2015)

A Novel Rare Missense Variation of the NOD2 Gene: Evidences of Implication in Crohn’s Disease

Por Frade-Proud’Hon-Clerc, Sara, Smol, Thomas, Frenois, Frédéric, Sand, Olivier, Vaillant, Emmanuel, Dhennin, Véronique, Bonnefond, Amélie, Froguel, Philippe, Fumery, Mathurin, Guillon-Dellac, Nathalie, Gower-Rousseau, Corinne, Vasseur, Francis
Publicado no Int J Mol Sci (2019)

Glucose-Dependent Regulation of NR2F2 Promoter and Influence of SNP-rs3743462 on Whole Body Insulin Sensitivity

Por Boutant, Marie, Ramos, Oscar Henrique Pereira, Lecoeur, Cécile, Vaillant, Emmanuel, Philippe, Julien, Zhang, Pili, Perilhou, Anaïs, Valcarcel, Beatriz, Sebert, Sylvain, Jarvelin, Mario-Ritta, Balkau, Beverley, Scott, Donald, Froguel, Philippe, Vaxillaire, Martine, Vasseur-Cognet, Mireille
Publicado em 2012

Disruption of a Novel Krüppel-like Transcription Factor p300-regulated Pathway for Insulin Biosynthesis Revealed by Studies of the c.-331 INS Mutation Found in Neonatal Diabetes Me...

Por Bonnefond, Amélie, Lomberk, Gwen, Buttar, Navtej, Busiah, Kanetee, Vaillant, Emmanuel, Lobbens, Stéphane, Yengo, Loïc, Dechaume, Aurélie, Mignot, Brigitte, Simon, Albane, Scharfmann, Raphaël, Neve, Bernadette, Tanyolaç, Sinan, Hodoglugil, Ugur, Pattou, François, Cavé, Hélène, Iovanna, Juan, Stein, Roland, Polak, Michel, Vaxillaire, Martine, Froguel, Philippe, Urrutia, Raul
Publicado em 2011

CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability

Por Montagne, Louise, Derhourhi, Mehdi, Piton, Amélie, Toussaint, Bénédicte, Durand, Emmanuelle, Vaillant, Emmanuel, Thuillier, Dorothée, Gaget, Stefan, De Graeve, Franck, Rabearivelo, Iandry, Lansiaux, Amélie, Lenne, Bruno, Sukno, Sylvie, Desailloud, Rachel, Cnop, Miriam, Nicolescu, Ramona, Cohen, Lior, Zagury, Jean-François, Amouyal, Mélanie, Weill, Jacques, Muller, Jean, Sand, Olivier, Delobel, Bruno, Froguel, Philippe, Bonnefond, Amélie
Publicado no Mol Metab (2018)

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

Por Bonnefond, Amélie, Clément, Nathalie, Fawcett, Katherine, Yengo, Loïc, Vaillant, Emmanuel, Guillaume, Jean-Luc, Dechaume, Aurélie, Payne, Felicity, Roussel, Ronan, Czernichow, Sébastien, Hercberg, Serge, Hadjadj, Samy, Balkau, Beverley, Marre, Michel, Lantieri, Olivier, Langenberg, Claudia, Bouatia-Naji, Nabila, Charpentier, Guillaume, Vaxillaire, Martine, Rocheleau, Ghislain, Wareham, Nicholas J., Sladek, Robert, McCarthy, Mark I., Dina, Christian, Barroso, Inês, Jockers, Ralf, Froguel, Philippe
Publicado em 2012

Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell function

Por Neve, Bernadette, Fernandez-Zapico, Martin E., Ashkenazi-Katalan, Vered, Dina, Christian, Hamid, Yasmin H., Joly, Erik, Vaillant, Emmanuel, Benmezroua, Yamina, Durand, Emmanuelle, Bakaher, Nicolas, Delannoy, Valerie, Vaxillaire, Martine, Cook, Tiffany, Dallinga-Thie, Geesje M., Jansen, Hans, Charles, Marie-Aline, Clément, Karine, Galan, Pilar, Hercberg, Serge, Helbecque, Nicole, Charpentier, Guillaume, Prentki, Marc, Hansen, Torben, Pedersen, Oluf, Urrutia, Raul, Melloul, Danielle, Froguel, Philippe
Publicado em 2005

Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension

Por Baron, Morgane, Maillet, Julie, Huyvaert, Marlène, Dechaume, Aurélie, Boutry, Raphaël, Loiselle, Hélène, Durand, Emmanuelle, Toussaint, Bénédicte, Vaillant, Emmanuel, Philippe, Julien, Thomas, Jérémy, Ghulam, Amjad, Franc, Sylvia, Charpentier, Guillaume, Borys, Jean-Michel, Lévy-Marchal, Claire, Tauber, Maïthé, Scharfmann, Raphaël, Weill, Jacques, Aubert, Cécile, Kerr-Conte, Julie, Pattou, François, Roussel, Ronan, Balkau, Beverley, Marre, Michel, Boissel, Mathilde, Derhourhi, Mehdi, Gaget, Stefan, Canouil, Mickaël, Froguel, Philippe, Bonnefond, Amélie
Publicado no Nat Med (2019)

Low copy number of the salivary amylase gene predisposes to obesity

Por Falchi, Mario, Moustafa, Julia Sarah El-Sayed, Takousis, Petros, Pesce, Francesco, Bonnefond, Amélie, Andersson-Assarsson, Johanna C., Sudmant, Peter H., Dorajoo, Rajkumar, Al-Shafai, Mashael Nedham, Bottolo, Leonardo, Ozdemir, Erdal, So, Hon-Cheong, Davies, Robert W., Patrice, Alexandre, Dent, Robert, Mangino, Massimo, Hysi, Pirro G., Dechaume, Aurélie, Huyvaert, Marlène, Skinner, Jane, Pigeyre, Marie, Caiazzo, Robert, Raverdy, Violeta, Vaillant, Emmanuel, Field, Sarah, Balkau, Beverley, Marre, Michel, Visvikis-Siest, Sophie, Weill, Jacques, Poulain-Godefroy, Odile, Jacobson, Peter, Sjostrom, Lars, Hammond, Christopher J., Deloukas, Panos, Sham, Pak Chung, McPherson, Ruth, Lee, Jeannette, Tai, E. Shyong, Sladek, Robert, Carlsson, Lena M.S., Walley, Andrew, Eichler, Evan E., Pattou, Francois, Spector, Timothy D., Froguel, Philippe
Publicado no Nat Genet (2014)