Emotional expression visual mismatch negativity in children von Kovarski, Klara, Charpentier, Judith, Houy‐Durand, Emmanuelle, Batty, Magali, Gomot, Marie

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Loss-of-function mutations in ADCY3 cause monogenic severe obesity von Saeed, Sadia, Bonnefond, Amélie, Tamanini, Filippo, Mirza, Muhammad Usman, Manzoor, Jaida, Janjua, Qasim M., Din, Sadia M., Gaitan, Julien, Milochau, Alexandra, Durand, Emmanuelle, Vaillant, Emmanuel, Haseeb, Attiya, De Graeve, Franck, Rabearivelo, Iandry, Sand, Olivier, Queniat, Gurvan, Boutry, Raphaël, Schott, Dina A., Ayesha, Hina, Ali, Muhammad, Khan, Waqas I., Butt, Taeed A., Rinne, Tuula, Stumpel, Connie, Abderrahmani, Amar, Lang, Jochen, Arslan, Muhammad, Froguel, Philippe

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Emotional visual mismatch negativity: a joint investigation of social and non-social dimensions in adults with autism von Kovarski, Klara, Charpentier, Judith, Roux, Sylvie, Batty, Magali, Houy-Durand, Emmanuelle, Gomot, Marie

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Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene von 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

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Dynamic hydroxymethylation of deoxyribonucleic acid marks differentiation-associated enhancers von Sérandour, Aurélien A, Avner, Stéphane, Oger, Frédérik, Bizot, Maud, Percevault, Frédéric, Lucchetti-Miganeh, Céline, Palierne, Gaëlle, Gheeraert, Céline, Barloy-Hubler, Frédérique, Péron, Christine Le, Madigou, Thierry, Durand, Emmanuelle, Froguel, Philippe, Staels, Bart, Lefebvre, Philippe, Métivier, Raphaël, Eeckhoute, Jérôme, Salbert, Gilles

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Functional genetics reveals the contribution of delta opioid receptor to type 2 diabetes and beta-cell function von Meulebrouck, Sarah, Merrheim, Judith, Queniat, Gurvan, Bourouh, Cyril, Derhourhi, Mehdi, Boissel, Mathilde, Yi, Xiaoyan, Badreddine, Alaa, Boutry, Raphaël, Leloire, Audrey, Toussaint, Bénédicte, Amanzougarene, Souhila, Vaillant, Emmanuel, Durand, Emmanuelle, Loiselle, Hélène, Huyvaert, Marlène, Dechaume, Aurélie, Scherrer, Victoria, Marchetti, Piero, Balkau, Beverley, Charpentier, Guillaume, Franc, Sylvia, Marre, Michel, Roussel, Ronan, Scharfmann, Raphaël, Cnop, Miriam, Canouil, Mickaël, Baron, Morgane, Froguel, Philippe, Bonnefond, Amélie

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Epigenetic and Transcriptomic Programming of HSC Quiescence Signaling in Large for Gestational Age Neonates von Pelletier, Alexandre, Carrier, Arnaud, Zhao, Yongmei, Canouil, Mickaël, Derhourhi, Mehdi, Durand, Emmanuelle, Berberian-Ferrato, Lionel, Greally, John, Hughes, Francine, Froguel, Philippe, Bonnefond, Amélie, Delahaye, Fabien

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Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features von Bonnefond, Amélie, Raimondo, Anne, Stutzmann, Fanny, Ghoussaini, Maya, Ramachandrappa, Shwetha, Bersten, David C, Durand, Emmanuelle, Vatin, Vincent, Balkau, Beverley, Lantieri, Olivier, Raverdy, Violeta, Pattou, François, Van Hul, Wim, Van Gaal, Luc, Peet, Daniel J, Weill, Jacques, Miller, Jennifer L, Horber, Fritz, Goldstone, Anthony P, Driscoll, Daniel J, Bruning, John B, Meyre, David, Whitelaw, Murray L, Froguel, Philippe

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Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity von Vaisse, C, Clement, K, Durand, E, Hercberg, S, Guy-Grand, B, Froguel, P

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Galectin-3 modulates epithelial cell adaptation to stress at the ER-mitochondria interface von Coppin, Lucie, Jannin, Arnaud, Ait Yahya, Emilie, Thuillier, Caroline, Villenet, Céline, Tardivel, Meryem, Bongiovanni, Antonino, Gaston, Cécile, de Beco, Simon, Barois, Nicolas, van Seuningen, Isabelle, Durand, Emmanuelle, Bonnefond, Amélie, Vienne, Jean-Claude, Vamecq, Joseph, Figeac, Martin, Vincent, Audrey, Delacour, Delphine, Porchet, Nicole, Pigny, Pascal

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Novel LEPR mutations in obese Pakistani children identified by PCR‐based enrichment and next generation sequencing von Saeed, Sadia, Bonnefond, Amélie, Manzoor, Jaida, Philippe, Julien, Durand, Emmanuelle, Arshad, Mohsin, Sand, Olivier, Butt, Taeed A, Falchi, Mario, Arslan, Muhammad, Froguel, Philippe

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Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome von Bonnefond, Amélie, Durand, Emmanuelle, Sand, Olivier, De Graeve, Franck, Gallina, Sophie, Busiah, Kanetee, Lobbens, Stéphane, Simon, Albane, Bellanné-Chantelot, Christine, Létourneau, Louis, Scharfmann, Raphael, Delplanque, Jérôme, Sladek, Robert, Polak, Michel, Vaxillaire, Martine, Froguel, Philippe

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Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis von Le Collen, Lauriane, Delemer, Brigitte, Spodenkiewicz, Marta, Cornillet Lefebvre, Pascale, Durand, Emmanuelle, Vaillant, Emmanuel, Badreddine, Alaa, Derhourhi, Mehdi, Mouhoub, Tarik Ait, Jouret, Guillaume, Juttet, Pauline, Souchon, Pierre François, Vaxillaire, Martine, Froguel, Philippe, Bonnefond, Amélie, Doco Fenzy, Martine

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Expression and functional assessment of candidate type 2 diabetes susceptibility genes identify four new genes contributing to human insulin secretion von Ndiaye, Fatou K, Ortalli, Ana, Canouil, Mickaël, Huyvaert, Marlène, Salazar-Cardozo, Clara, Lecoeur, Cécile, Verbanck, Marie, Pawlowski, Valérie, Boutry, Raphaël, Durand, Emmanuelle, Rabearivelo, Iandry, Sand, Olivier, Marselli, Lorella, Kerr-Conte, Julie, Chandra, Vikash, Scharfmann, Raphaël, Poulain-Godefroy, Odile, Marchetti, Piero, Pattou, François, Abderrahmani, Amar, Froguel, Philippe, Bonnefond, Amélie

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Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value von Cauchi, Stéphane, Meyre, David, Durand, Emmanuelle, Proença, Christine, Marre, Michel, Hadjadj, Samy, Choquet, Hélène, De Graeve, Franck, Gaget, Stefan, Allegaert, Frederic, Delplanque, Jérôme, Permutt, Marshall Alan, Wasson, Jon, Blech, Ilana, Charpentier, Guillaume, Balkau, Beverley, Vergnaud, Anne-Claire, Czernichow, Sébastien, Patsch, Wolfgang, Chikri, Mohamed, Glaser, Benjamin, Sladek, Robert, Froguel, Philippe

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Combined effects of MC4R and FTO common genetic variants on obesity in European general populations von Cauchi, Stéphane, Stutzmann, Fanny, Cavalcanti-Proença, Christine, Durand, Emmanuelle, Pouta, Anneli, Hartikainen, Anna-Liisa, Marre, Michel, Vol, Sylviane, Tammelin, Tuija, Laitinen, Jaana, Gonzalez-Izquierdo, Arturo, Blakemore, Alexandra IF, Elliott, Paul, Meyre, David, Balkau, Beverley, Järvelin, Marjo-Riitta, Froguel, Philippe

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Glucose Regulates m6A Methylation of RNA in Pancreatic Islets von Bornaque, Florine, Delannoy, Clément Philippe, Courty, Emilie, Rabhi, Nabil, Carney, Charlène, Rolland, Laure, Moreno, Maeva, Gromada, Xavier, Bourouh, Cyril, Petit, Pauline, Durand, Emmanuelle, Pattou, François, Kerr-Conte, Julie, Froguel, Philippe, Bonnefond, Amélie, Oger, Frédérik, Annicotte, Jean-Sébastien

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

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Knocking Down CDKN2A in 3D hiPSC-Derived Brown Adipose Progenitors Potentiates Differentiation, Oxidative Metabolism and Browning Process von Kahoul, Yasmina, Yao, Xi, Oger, Frédérik, Moreno, Maeva, Amanzougarene, Souhila, Derhourhi, Mehdi, Durand, Emmanuelle, Boutry, Raphael, Bonnefond, Amélie, Froguel, Philippe, Dani, Christian, Annicotte, Jean-Sébastien, Breton, Christophe

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NMR Measure of Translational Diffusion and Fractal Dimension. Application to Molecular Mass Measurement von Augé, Sophie, Schmit, Pierre-Olivier, Crutchfield, Christopher A, Islam, Mohammad T, Harris, Douglas J, Durand, Emmanuelle, Clemancey, Martin, Quoineaud, Anne-Agathe, Lancelin, Jean-Marc, Prigent, Yann, Taulelle, Francis, Delsuc, Marc-André

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