The Common P446L Polymorphism in GCKR Inversely Modulates Fasting Glucose and Triglyceride Levels and Reduces Type 2 Diabetes Risk in the DESIR Prospective General French Populatio...

Por Vaxillaire, Martine, Cavalcanti-Proença, Christine, Dechaume, Aurélie, Tichet, Jean, Marre, Michel, Balkau, Beverley, Froguel, Philippe
Publicado em 2008

Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French population

Por Cheyssac, Claire, Lecoeur, Cécile, Dechaume, Aurélie, Bibi, Amina, Charpentier, Guillaume, Balkau, Beverley, Marre, Michel, Froguel, Philippe, Gibson, Fernando, Vaxillaire, Martine
Publicado em 2006

Conserved Intramolecular Disulfide Bond Is Critical to Trafficking and Fate of ATP-binding Cassette (ABC) Transporters ABCB6 and Sulfonylurea Receptor 1 (SUR1)/ABCC8

Por Fukuda, Yu, Aguilar-Bryan, Lydia, Vaxillaire, Martine, Dechaume, Aurelie, Wang, Yao, Dean, Michael, Moitra, Karobi, Bryan, Joseph, Schuetz, John D.
Publicado em 2011

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)

Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations

Por Riveline, Jean-Pierre, Rousseau, Elise, Reznik, Yves, Fetita, Sabrina, Philippe, Julien, Dechaume, Aurélie, Hartemann, Agnès, Polak, Michel, Petit, Catherine, Charpentier, Guillaume, Gautier, Jean-François, Froguel, Philippe, Vaxillaire, Martine
Publicado em 2012

Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene

Por Bonnefond, Amélie, Philippe, Julien, Durand, Emmanuelle, Dechaume, Aurélie, Huyvaert, Marlène, Montagne, Louise, Marre, Michel, Balkau, Beverley, Fajardy, Isabelle, Vambergue, Anne, Vatin, Vincent, Delplanque, Jérôme, Le Guilcher, David, De Graeve, Franck, Lecoeur, Cécile, Sand, Olivier, Vaxillaire, Martine, Froguel, Philippe
Publicado em 2012

Insulin Gene Mutations Resulting in Early-Onset Diabetes: Marked Differences in Clinical Presentation, Metabolic Status, and Pathogenic Effect Through Endoplasmic Reticulum Retenti...

Por Meur, Gargi, Simon, Albane, Harun, Nasret, Virally, Marie, Dechaume, Aurélie, Bonnefond, Amélie, Fetita, Sabrina, Tarasov, Andrei I., Guillausseau, Pierre-Jean, Boesgaard, Trine Welløv, Pedersen, Oluf, Hansen, Torben, Polak, Michel, Gautier, Jean-François, Froguel, Philippe, Rutter, Guy A., Vaxillaire, Martine
Publicado em 2010

Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach

Por Bonnefond, Amélie, Yengo, Loïc, Dechaume, Aurélie, Canouil, Mickaël, Castelain, Maxime, Roger, Estelle, Allegaert, Frédéric, Caiazzo, Robert, Raverdy, Violeta, Pigeyre, Marie, Arredouani, Abdelilah, Borys, Jean-Michel, Lévy-Marchal, Claire, Weill, Jacques, Roussel, Ronan, Balkau, Beverley, Marre, Michel, Pattou, François, Brousseau, Thierry, Froguel, Philippe
Publicado no BMC Med (2017)

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

What Is the Contribution of Two Genetic Variants Regulating VEGF Levels to Type 2 Diabetes Risk and to Microvascular Complications?

Por Bonnefond, Amélie, Saulnier, Pierre-Jean, Stathopoulou, Maria G., Grarup, Niels, Ndiaye, Ndeye Coumba, Roussel, Ronan, Nezhad, Mohsen Azimi, Dechaume, Aurélie, Lantieri, Olivier, Hercberg, Serge, Lauritzen, Torsten, Balkau, Beverley, El-Sayed Moustafa, Julia S., Hansen, Torben, Pedersen, Oluf, Froguel, Philippe, Charpentier, Guillaume, Marre, Michel, Hadjadj, Samy, Visvikis-Siest, Sophie
Publicado em 2013

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

A Genome-Wide Association Study Identifies rs2000999 as a Strong Genetic Determinant of Circulating Haptoglobin Levels

Por Froguel, Philippe, Ndiaye, Ndeye Coumba, Bonnefond, Amélie, Bouatia-Naji, Nabila, Dechaume, Aurélie, Siest, Gérard, Herbeth, Bernard, Falchi, Mario, Bottolo, Leonardo, Guéant-Rodriguez, Rosa-Maria, Lecoeur, Cécile, Langlois, Michel R., Labrune, Yann, Ruokonen, Aimo, El Shamieh, Said, Stathopoulou, Maria G., Morandi, Anita, Maffeis, Claudio, Meyre, David, Delanghe, Joris R., Jacobson, Peter, Sjöström, Lars, Carlsson, Lena M. S., Walley, Andrew, Elliott, Paul, Jarvelin, Marjo-Riita, Dedoussis, George V., Visvikis-Siest, Sophie
Publicado em 2012