The complex genetic basis of fibromuscular dysplasia, a systemic arteriopathy associated with multiple forms of cardiovascular disease

por Georges, Adrien, Bouatia-Naji, Nabila
Publicado 2022

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

por Perrocheau, Maëlle, Kiando, Soto Romuald, Vernerey, Déwi, Dina, Christian, Galan, Pilar, Hagege, Albert, Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado 2015

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

por 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
Publicado 2007

Genetic mechanisms underlying arrhythmogenic mitral valve prolapse: Current and future perspectives

por Levy, Sydney, Sharaf Dabbagh, Ghaith, Giudicessi, John R., Haqqani, Haris, Khanji, Mohammed Y., Obeng-Gyimah, Edmond, Betts, Megan N., Ricci, Fabrizio, Asatryan, Babken, Bouatia-Naji, Nabila, Nazarian, Saman, Chahal, C. Anwar A.
Publicado 2023

Genetics and pathophysiology of mitral valve prolapse

por Delwarde, Constance, Capoulade, Romain, Mérot, Jean, Le Scouarnec, Solena, Bouatia-Naji, Nabila, Yu, Mengyao, Huttin, Olivier, Selton-Suty, Christine, Sellal, Jean-Marc, Piriou, Nicolas, Schott, Jean-Jacques, Dina, Christian, Le Tourneau, Thierry
Publicado 2023

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

por 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.
Publicado 2010

Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease

por Yu, Mengyao, Tcheandjieu, Catherine, Georges, Adrien, Xiao, Ke, Tejeda, Helio, Dina, Christian, Le Tourneau, Thierry, Fiterau, Madalina, Judy, Renae, Tsao, Noah L., Amgalan, Dulguun, Munger, Chad J., Engreitz, Jesse M., Damrauer, Scott M., Bouatia-Naji, Nabila, Priest, James R.
Publicado 2022

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

por 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.
Publicado 2011

Research Opportunities in the Treatment of Mitral Valve Prolapse

por Delling, Francesca N., Noseworthy, Peter A., Adams, David H., Basso, Cristina, Borger, Michael, Bouatia-Naji, Nabila, Elmariah, Sammy, Evans, Frank, Gerstenfeld, Edward, Hung, Judy, Tourneau, Thierry Le, Lewis, John, Miller, Marc A., Norris, Russell A., Padala, Muralidhar, Perazzolo-Marra, Martina, Shah, Dipan J., Weinsaft, Jonathan W., Enriquez-Sarano, Maurice, Levine, Robert A.
Publicado 2022

Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

por Bakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M.
Publicado 2023

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

por 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
Publicado 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

por 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.
Publicado 2010

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...

por 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
Publicado 2009

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

por 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
Publicado 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 2012

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

por 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
Publicado 2020

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

por 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
Publicado 2016

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

por 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
Publicado 2011

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

por 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
Publicado 2015

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

por 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
Publicado 2020