Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics von Le Scouarnec, S, Gribble, S M

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GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME von Portero, V, Le Scouarnec, S, Es-Salah-Lamoureux, Z, Burel, S, Gourraud, J, Bonnaud, S, Lindenbaum, P, Simonet, F, Violleau, J, Sandoval-Tortosa, J, Scott, C, Chatel, S, Loussouarn, G, O’Hara, T, Mabo, P, Dina, C, Le Marec, H, Schott, J, Probst, V, Baró, I, Marionneau, C, Charpentier, F, Redon, R

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Sudden Cardiac Arrest Associated with Early Repolarization von Haïssaguerre, Michel, Derval, Nicolas, Sacher, Frederic, Jesel, Laurence, Deisenhofer, Isabel, de Roy, Luc, Pasquié, Jean-Luc, Nogami, Akihiko, Babuty, Dominique, Yli-Mayry, Sinikka, De Chillou, Christian, Scanu, Patrice, Mabo, Philippe, Matsuo, Seiichiro, Probst, Vincent, Le Scouarnec, Solena, Defaye, Pascal, Schlaepfer, Juerg, Rostock, Thomas, Lacroix, Dominique, Lamaison, Dominique, Lavergne, Thomas, Aizawa, Yoshifusa, Englund, Anders, Anselme, Frederic, O'Neill, Mark, Hocini, Meleze, Lim, Kang Teng, Knecht, Sebastien, Veenhuyzen, George D, Bordachar, Pierre, Chauvin, Michel, Jais, Pierre, Coureau, Gaelle, Chene, Genevieve, Klein, George J, Clémenty, Jacques

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P6490Paradoxycal restricted motion in diastole is a frequent finding in mitral valve prolapse/dystrophy patients von Le Tourneau, T, Cueff, C, Piriou, N, Capoulade, R, Le Scouarnec, S, Merot, J, Schott, J J

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P2864A novel mechanism of sinus node dysfunction: intergenic deletion between PITX2 and ANK2 disrupts chromatin structure in pacemaker cell differentiation von Murata, H, Lindenbaum, P, Le Scouarnec, S, Baron, E, Rajalu, A, Kyndt, F, Deleuze, J F, Le Marec, H, Probst, V, Shimizu, W, Redon, R, Schott, J J

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Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25 von Baudic, M, Murata, H, Le Scouarnec, S, Foucal, A, Lindenbaum, P, Ishikawa, T, Si-Tayeb, K, Gaborit, N, Makita, N, Makiyama, T, Shimizu, W, Vieyres, C, Probst, V, Schott, J.J, Barc, J

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P756 Paradoxycal restricted motion in diastole associated to mitral valve prolapse/dystrophy: a frequent finding von Le Tourneau, T, Cueff, C, Marrec, M, Piriou, N, Capoulade, R, Le Scouarnec, S, Merot, J, Schott, J J

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G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome von Barc, J, Probst, V, Wilde, A.A.M, Sacher, F, Babuty, D, Mabo, P, Mansourati, J, Le Scouarnec, S, Kyndt, F, Guicheney, P, Albuisson, J, Meregalli, P.-G, Le Marec, H, Tan, H.-L, Schott, J.-J

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Fine-scale human genetic structure in Western France von Karakachoff, Matilde, Duforet-Frebourg, Nicolas, Simonet, Floriane, Le Scouarnec, Solena, Pellen, Nadine, Lecointe, Simon, Charpentier, Eric, Gros, Françoise, Cauchi, Stéphane, Froguel, Philippe, Copin, Nane, Le Tourneau, Thierry, Probst, Vincent, Le Marec, Hervé, Molinaro, Sabrina, Balkau, Beverley, Redon, Richard, Schott, Jean-Jacques, Blum, Michael Gb, Dina, Christian

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Paradoxycal restricted motion in diastole is a frequent finding in mitral valve prolapse/dystrophy patients von Cueff, C., Piriou, N., Capoulade, R., Merot, J., Le Scouarnec, S., Schott, J.J., Le Tourneau, T.

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226A Rad GTPase variant related to Brugada syndrome von Belbachir, N., Portero, V., Gaborit, N., Guilluy, C., Marionneau, C., Probst, V., Dina, C., Baro, I., Jessel-Morel, L., Redon, R., Schott, JJ, Charpentier, F., Le Scouarnec, S.

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P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder von Barc, J G, Marsman, RF, Le Scouarnec, S, Mizusawa, Y, Lindenbaum, P, Carter, N, Redon, R, Wilde, AAM, Mckeown, P, Bezzina, CR

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Familial aggregation of calcific aortic valve stenosis in the western part of France von PROBST, Vincent, LE SCOUARNEC, Solena, LEGENDRE, Antoine, JOUSSEAUME, Valérie, JAAFAR, Philippe, NGUYEN, Jean-Michel, CHAVENTRE, André, LE MAREC, Hervé, SCHOTT, Jean-Jacques

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Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder von Barc, J. G., Marsman, R. F., Le Scouarnec, S., Mizusawa, Y., Postma, A. V., Carter, N., Redon, R., Wilde, A. A. M., Mckeown, P., Bezzina, C. R.

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Phenotypic and genotypic approach of a large family with early onset tricuspid aortic valve sclerosis-stenosis: A multimodality evaluation von Guimbretiere, G., Le Scouarnec, S., Rigade, S., Boureau, A.S., Cueff, C., Capoulade, R., Dina, C., Mérot, J., Schott, J.J., Le Tourneau, T.

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RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome von Belbachir, N., Portero, V., Gourraud, J.B., Jesel, L., Guilluy, C., Gaborit, N., Girardeau, A., Bonnaud, S., Pattier, S., Scott, C., Burel, S., Gaignerie, A., Genin, E., Deleuze, J.F., Dina, C., Schott, J.J., Probst, V., Redon, R., Charpentier, F., Le Scouarnec, S.

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2014-A-33-CES - GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROME von Portero, V., Le Scouarnec, S., Es-Salah-Lamoureux, Z., Burel, S., Gourraud, J., Bonnaud, S., Lindenbaum, P., Simonet, F., Violleau, J., Sandoval-Tortosa, J., Scott, C., Chatel, S., Loussouarn, G., O’Hara, T., Mabo, P., Dina, C., Le Marec, H., Schott, J., Probst, V., Baró, I., Marionneau, C., Charpentier, F., Redon, R.

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Familial Agregation of Calcific Aortic valve Stenosis in the Western part of France von Probst, V., Scouarnec S., Le, Legendre, A., Jousseaume, V., Jaafar, P., J.-P., Nguyen, Chaventré, A., Marec H., Le, J.-J., Schott

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Memory Effect in Thermoresponsive Proline‐based Polymers von Badreldin, Mostafa, Le Scouarnec, Rosanna, Lecommandoux, Sebastien, Harrisson, Simon, Bonduelle, Colin

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Quicker ADC : Unlocking the Hidden Potential of Product Quantization With SIMD von Andre, Fabien, Kermarrec, Anne-Marie, Le Scouarnec, Nicolas

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