Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse

di Perrocheau, Maëlle, Kiando, Soto Romuald, Vernerey, Déwi, Dina, Christian, Galan, Pilar, Hagege, Albert, Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Pubblicato in J Cardiovasc Dev Dis (2015)

Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity

di Bouatia-Naji, Nabila, Vatin, Vincent, Lecoeur, Cécile, Heude, Barbara, Proença, Christine, Veslot, Jacques, Jouret, Béatrice, Tichet, Jean, Charpentier, Guillaume, Marre, Michel, Balkau, Beverley, Froguel, Philippe, Meyre, David
Pubblicazione 2007

Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci

di Kyryachenko, Sergiy, Georges, Adrien, Yu, Mengyao, Barrandou, Takiy, Guo, Lilong, Bruneval, Patrick, Rubio, Tony, Gronwald, Judith, Baraki, Hassina, Kutschka, Ingo, Aras, Kedar K., Efimov, Igor R., Norris, Russel A., Voigt, Niels, Bouatia-Naji, Nabila
Pubblicato in Circ Res (2021)

Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways

di Soranzo, Nicole, Sanna, Serena, Wheeler, Eleanor, Gieger, Christian, Radke, Dörte, Dupuis, Josée, Bouatia-Naji, Nabila, Langenberg, Claudia, Prokopenko, Inga, Stolerman, Elliot, Sandhu, Manjinder S., Heeney, Matthew M., Devaney, Joseph M., Reilly, Muredach P., Ricketts, Sally L.
Pubblicazione 2010

GWAS-driven Gene-set Analyses, Genetic and Functional Follow-up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse

di Yu, Mengyao, Georges, Adrien, Tucker, Nathan R., Kyryachenko, Sergiy, Toomer, Katelyn, Schott, Jean-Jacques, Delling, Francesca N., Fernandez-Friera, Leticia, Solis, Jorge, Ellinor, Patrick T., Levine, Robert A., Slaugenhaupt, Susan A., Hagège, Albert A., Dina, Christian, Jeunemaitre, Xavier, Milan, David J., Norris, Russell A., Bouatia-Naji, Nabila
Pubblicato in Circ Genom Precis Med (2019)

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

di Meyre, David, Bouatia-Naji, Nabila, Tounian, Agnès, Samson, Chantal, Lecoeur, Cécile, Vatin, Vincent, Ghoussaini, Maya, Wachter, Christophe, Hercberg, Serge, Charpentier, Guillaume, Patsch, Wolfgang, Pattou, François, Charles, Marie-Aline, Tounian, Patrick, Clément, Karine, Jouret, Béatrice, Weill, Jacques, Maddux, Betty A., Goldfine, Ira D., Walley, Andrew, Boutin, Philippe, Dina, Christian, Froguel, Philippe
Pubblicazione 2005

Genetic Polymorphisms in the Hypothalamic Pathway in Relation to Subsequent Weight Change – The DiOGenes Study

di Du, Huaidong, Vimaleswaran, Karani S., Ängquist, Lars, Hansen, Rikke D., van der A, Daphne L., Holst, Claus, Tjønneland, Anne, Overvad, Kim, Jakobsen, Marianne Uhre, Boeing, Heiner, Meidtner, Karina, Palli, Domenico, Masala, Giovanna, Bouatia-Naji, Nabila, Saris, Wim H. M., Feskens, Edith J. M., J.Wareham, Nicolas, Sørensen, Thorkild I. A., Loos, Ruth J. F.
Pubblicazione 2011

Genetic Variant in HK1 Is Associated With a Proanemic State and A1C but Not Other Glycemic Control–Related Traits

di Bonnefond, Amélie, Vaxillaire, Martine, Labrune, Yann, Lecoeur, Cécile, Chèvre, Jean-Claude, Bouatia-Naji, Nabila, Cauchi, Stéphane, Balkau, Beverley, Marre, Michel, Tichet, Jean, Riveline, Jean-Pierre, Hadjadj, Samy, Gallois, Yves, Czernichow, Sébastien, Hercberg, Serge, Kaakinen, Marika, Wiesner, Susanne, Charpentier, Guillaume, Lévy-Marchal, Claire, Elliott, Paul, Jarvelin, Marjo-Riitta, Horber, Fritz, Dina, Christian, Pedersen, Oluf, Sladek, Robert, Meyre, David, Froguel, Philippe
Pubblicazione 2009

Genetic and Functional Assessment of the Role of the rs13431652-A and rs573225-A Alleles in the G6PC2 Promoter That Are Strongly Associated With Elevated Fasting Glucose Levels

di Bouatia-Naji, Nabila, Bonnefond, Amélie, Baerenwald, Devin A., Marchand, Marion, Bugliani, Marco, Marchetti, Piero, Pattou, François, Printz, Richard L., Flemming, Brian P., Umunakwe, Obi C., Conley, Nicholas L., Vaxillaire, Martine, Lantieri, Olivier, Balkau, Beverley, Marre, Michel, Lévy-Marchal, Claire, Elliott, Paul, Jarvelin, Marjo-Riitta, Meyre, David, Dina, Christian, Oeser, James K., Froguel, Philippe, O'Brien, Richard M.
Pubblicazione 2010

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

di 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
Pubblicazione 2012

A plasma proteogenomic signature for fibromuscular dysplasia

di Olin, Jeffrey W, Di Narzo, Antonio F, d’Escamard, Valentina, Kadian-Dodov, Daniella, Cheng, Haoxiang, Georges, Adrien, King, Annette, Thomas, Allison, Barwari, Temo, Michelis, Katherine C, Bouchareb, Rihab, Bander, Emir, Anyanwu, Anelechi, Stelzer, Paul, Filsoufi, Farzan, Florman, Sander, Civelek, Mete, Debette, Stephanie, Jeunemaitre, Xavier, Björkegren, Johan L M, Mayr, Manuel, Bouatia-Naji, Nabila, Hao, Ke, Kovacic, Jason C
Pubblicato in Cardiovasc Res (2020)

G-allele of Intronic rs10830963 in MTNR1B Confers Increased Risk of Impaired Fasting Glycemia and Type 2 Diabetes Through an Impaired Glucose-Stimulated Insulin Release: Studies In...

di Sparsø, Thomas, Bonnefond, Amélie, Andersson, Ehm, Bouatia-Naji, Nabila, Holmkvist, Johan, Wegner, Lise, Grarup, Niels, Gjesing, Anette P., Banasik, Karina, Cavalcanti-Proença, Christine, Marchand, Marion, Vaxillaire, Martine, Charpentier, Guillaume, Jarvelin, Marjo-Riitta, Tichet, Jean, Balkau, Beverley, Marre, Michel, Lévy-Marchal, Claire, Færch, Kristine, Borch-Johnsen, Knut, Jørgensen, Torben, Madsbad, Sten, Poulsen, Pernille, Vaag, Allan, Dina, Christian, Hansen, Torben, Pedersen, Oluf, Froguel, Philippe
Pubblicazione 2009

Dietary Factors Impact on the Association between CTSS Variants and Obesity Related Traits

di Hooton, Henri, Ängquist, Lars, Holst, Claus, Hager, Jorg, Rousseau, Francis, Hansen, Rikke D., Tjønneland, Anne, Roswall, Nina, van der A, Daphne L., Overvad, Kim, Jakobsen, Marianne Uhre, Boeing, Heiner, Meidtner, Karina, Palli, Domenico, Masala, Giovanna, Bouatia-Naji, Nabila, Saris, Wim H. M., Feskens, Edith J. M., Wareham, Nicolas J., Vimaleswaran, Karani S., Langin, Dominique, Loos, Ruth J. F., Sørensen, Thorkild I. A., Clément, Karine
Pubblicazione 2012

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

di 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
Pubblicazione 2012

Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing

di Carss, Keren J., Baranowska, Anna A., Armisen, Javier, Webb, Tom R., Hamby, Stephen E., Premawardhana, Diluka, Al-Hussaini, Abtehale, Wood, Alice, Wang, Quanli, Deevi, Sri V. V., Vitsios, Dimitrios, Lewis, Samuel H., Kotecha, Deevia, Bouatia-Naji, Nabila, Hesselson, Stephanie, Iismaa, Siiri E., Tarr, Ingrid, McGrath-Cadell, Lucy, Muller, David W., Dunwoodie, Sally L., Fatkin, Diane, Graham, Robert M., Giannoulatou, Eleni, Samani, Nilesh J., Petrovski, Slavé, Haefliger, Carolina, Adlam, David
Pubblicato in Circ Genom Precis Med (2020)

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance

di Kiando, Soto Romuald, Tucker, Nathan R., Castro-Vega, Luis-Jaime, Katz, Alexander, D’Escamard, Valentina, Tréard, Cyrielle, Fraher, Daniel, Albuisson, Juliette, Kadian-Dodov, Daniella, Ye, Zi, Austin, Erin, Yang, Min-Lee, Hunker, Kristina, Barlassina, Cristina, Cusi, Daniele, Galan, Pilar, Empana, Jean-Philippe, Jouven, Xavier, Gimenez-Roqueplo, Anne-Paule, Bruneval, Patrick, Hyun Kim, Esther Soo, Olin, Jeffrey W., Gornik, Heather L., Azizi, Michel, Plouin, Pierre-François, Ellinor, Patrick T., Kullo, Iftikhar J., Milan, David J., Ganesh, Santhi K., Boutouyrie, Pierre, Kovacic, Jason C., Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Pubblicato in PLoS Genet (2016)

Association of Genetic Loci With Glucose Levels in Childhood and Adolescence: A Meta-Analysis of Over 6,000 Children

di Barker, Adam, Sharp, Stephen J., Timpson, Nicholas J., Bouatia-Naji, Nabila, Warrington, Nicole M., Kanoni, Stavroula, Beilin, Lawrence J., Brage, Soren, Deloukas, Panos, Evans, David M., Grontved, Anders, Hassanali, Neelam, Lawlor, Deborah A., Lecoeur, Cecile, Loos, Ruth J.F., Lye, Stephen J., McCarthy, Mark I., Mori, Trevor A., Ndiaye, Ndeye Coumba, Newnham, John P., Ntalla, Ioanna, Pennell, Craig E., St Pourcain, Beate, Prokopenko, Inga, Ring, Susan M., Sattar, Naveed, Visvikis-Siest, Sophie, Dedoussis, George V., Palmer, Lyle J., Froguel, Philippe, Smith, George Davey, Ekelund, Ulf, Wareham, Nicholas J., Langenberg, Claudia
Pubblicazione 2011

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

di Dina, Christian, Bouatia-Naji, Nabila, Tucker, Nathan, Delling, Francesca N., Toomer, Katelynn, Durst, Ronen, Perrocheau, Maelle, Fernandez-Friera, Leticia, Solis, Jorge, Le Tourneau, Thierry, Chen, Ming-Huei, Probst, Vincent, Bosse, Yohan, Pibarot, Philippe, Zelenika, Diana, Lathrop, Mark, Hercberg, Serge, Roussel, Ronan, Benjamin, Emelia J., Bonnet, Fabrice, Su Hao, LO, Dolmatova, Elena, Simonet, Floriane, Lecointe, Simon, Kyndt, Florence, Redon, Richard, Le Marec, Hervé, Froguel, Philippe, Ellinor, Patrick T., Vasan, Ramachandran S., Bruneval, Patrick, Norris, Russell A., Milan, David J., Slaugenhaupt, Susan A., Levine, Robert A., Schott, Jean-Jacques, Hagege, Albert A., Jeunemaitre, Xavier
Pubblicato in Nat Genet (2015)

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

di Georges, Adrien, Albuisson, Juliette, Berrandou, Takiy, Dupré, Délia, Lorthioir, Aurélien, D’Escamard, Valentina, Di Narzo, Antonio F, Kadian-Dodov, Daniella, Olin, Jeffrey W, Warchol-Celinska, Ewa, Prejbisz, Aleksander, Januszewicz, Andrzej, Bruneval, Patrick, Baranowska, Anna A, Webb, Tom R, Hamby, Stephen E, Samani, Nilesh J, Adlam, David, Fendrikova-Mahlay, Natalia, Hazen, Stanley, Wang, Yu, Yang, Min-Lee, Hunker, Kristina, Combaret, Nicolas, Motreff, Pascal, Chédid, Antoine, Fiquet, Béatrice, Plouin, Pierre-François, Mousseaux, Elie, Azarine, Arshid, Amar, Laurence, Azizi, Michel, Gornik, Heather L, Ganesh, Santhi K, Kovacic, Jason C, Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Pubblicato in Cardiovasc Res (2020)

Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits

di Billings, Liana K., Hsu, Yi-Hsiang, Ackerman, Rachel J., Dupuis, Josée, Voight, Benjamin F., Rasmussen-Torvik, Laura J., Hercberg, Serge, Lathrop, Mark, Barnes, Daniel, Langenberg, Claudia, Hui, Jennie, Fu, Mao, Bouatia-Naji, Nabila, Lecoeur, Cecile, An, Ping, Magnusson, Patrik K., Surakka, Ida, Ripatti, Samuli, Christiansen, Lene, Dalgård, Christine, Folkersen, Lasse, Grundberg, Elin, Eriksson, Per, Kaprio, Jaakko, Ohm Kyvik, Kirsten, Pedersen, Nancy L., Borecki, Ingrid B., Province, Michael A., Balkau, Beverley, Froguel, Philippe, Shuldiner, Alan R., Palmer, Lyle J., Wareham, Nick, Meneton, Pierre, Johnson, Toby, Pankow, James S., Karasik, David, Meigs, James B., Kiel, Douglas P., Florez, Jose C.
Pubblicazione 2012