HEY2 , A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL
Podliesna, S, Verkerk, A.O, Wolswinkel, R, Beekman, L, Barc, J, Gessler, M, Christoffels, V.M, Wilde, A.A, Remme, C.A, Bezzina, C.R
Published in Heart rhythm (01.11.2014)
Published in Heart rhythm (01.11.2014)
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Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death
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Published in Heart rhythm (01.11.2013)
Published in Heart rhythm (01.11.2013)
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Characterization of ketolactia in dairy cows during early lactation
Kowalski, Z.M., Sabatowicz, M., Barć, J., Jagusiak, W., Młocek, W., Van Saun, R.J., Dechow, C.D.
Published in Journal of dairy science (01.12.2021)
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Canola meal or soybean meal as protein source and the effect of microencapsulated sodium butyrate supplementation in calf starter mixture. II. Development of the gastrointestinal tract
Burakowska, K., Penner, G.B., Flaga, J., Przybyło, M., Barć, J., Wojciechowska-Puchałka, J., Wojtysiak, D., Kowalski, Z.M., Górka, P.
Published in Journal of dairy science (01.06.2021)
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G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome
Amarouch, M, Barc, J, Béziau, D, Kyndt, F, Le Marec, H, Babuty, D, Probst, V, Schott, J.-J, Baro, I
Published in Archives of cardiovascular diseases (2009)
Published in Archives of cardiovascular diseases (2009)
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G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome
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
Published in Archives of cardiovascular diseases (2009)
Published in Archives of cardiovascular diseases (2009)
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Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome
Makita, N, Ishikawa, T, Masuda, T, Hachiya, T, Dina, C, Simonet, F, Tank, M W T, Wilde, A A, Redon, R, Bezzina, C R, Tanaka, T, Barc, J, Okada, Y, Schott, J J
Published in European heart journal (09.11.2023)
Published in European heart journal (09.11.2023)
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Modeling familial sinus node dysfunction with a large intergenic deletion between PITX2 and ANK2 using iPS cell-derived sinoatrial nodal-like cardiomyocytes
Aizawa, T, Makiyama, T, Murata, H, Takaki, T, Baudic, M, Gao, J, Imamura, T, Ohno, S, Yoshida, Y, Shimizu, W, Makita, N, Barc, J, Schott, J J, Horie, M, Kimura, T
Published in European heart journal (09.11.2023)
Published in European heart journal (09.11.2023)
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Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation
Baudic, M, Murata, H, Bosada, F M, Souto Melo, U, Aizawa, T, Guedon, A, Lindenbaum, P, Gourraud, J B, Makita, N, Mundlos, S, Christoffels, V M, Makiyama, T, Probst, V, Schott, J J, Barc, J
Published in European heart journal (03.10.2022)
Published in European heart journal (03.10.2022)
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GENECHOC study: genetic markers of arrhythmic risk in heart failure
Anys, S, Rigade, S, Baron, E, Lecointe, S, Guyomarch, B, Klug, D, Babuty, D, Mansourati, J, Bordachar, P, Mabo, P, Thollet, A, Dina, C, Schott, J.J, Barc, J, Probst, V
Published in European heart journal (01.11.2020)
Published in European heart journal (01.11.2020)
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Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25
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
Published in European heart journal (01.11.2020)
Published in European heart journal (01.11.2020)
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Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome
Barc, J, Trados, R, Glinge, C, Simonet, F, Chiang, D, Jouni, M, Jurgens, S, The Brugada Syndrome Genetic Consortium, B.R.S, Tanck, M, Dina, C, Probst, V, Wilde, A, Redon, R, Schott, J.J, Bezzina, C
Published in European heart journal (01.11.2020)
Published in European heart journal (01.11.2020)
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Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder
Baudic, M., Murata, H., Bosada, F., Souto Melo, U., Aizawa, T., Guedon, A., Lindenbaum, P., Gourraud, J.-B., Makita, N., Mundlos, S., Christoffels, V.M., Makiyama, T., Probst, V., Schott, J.-J., Barc, J.
Published in Archives of Cardiovascular Diseases Supplements (01.01.2023)
Published in Archives of Cardiovascular Diseases Supplements (01.01.2023)
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Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy
Goudal, A., Karakachoff, M., Lindenbaum, P., Baron, E., Bonnaud, S., Kyndt, F., Bourcereau, E., Thollet, A., Redon, R., Bézieau, S., Schott, J.J., Probst, V., Barc, J.
Published in Archives of Cardiovascular Diseases Supplements (01.10.2020)
Published in Archives of Cardiovascular Diseases Supplements (01.10.2020)
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Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction
Le Guillou, X., Lindenbaum, P., Baron, E., Thollet, A., Kyndt, F., Le Marec, H., Probst, V., Schott, J.J., Gourraud, J.B., Barc, J.
Published in Archives of Cardiovascular Diseases Supplements (01.10.2020)
Published in Archives of Cardiovascular Diseases Supplements (01.10.2020)
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2014-A-31-CES - HEY2, A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL
Podliesna, S., Verkerk, A.O., Wolswinkel, R., Beekman, L., Barc, J., Gessler, M., Christoffels, V.M., Wilde, A.A., Remme, C.A., Bezzina, C.R.
Published in Heart rhythm (01.11.2014)
Published in Heart rhythm (01.11.2014)
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A mutation in CALM1 encoding calmodulin causes sudden cardiac death in childhood and adolescence
Marsman, R. F., Barc, J. G., Beekman, L., Bhuijan, Z. A., Wilde, A. A. M., Bezzina, C. R.
Published in European heart journal (02.08.2013)
Published in European heart journal (02.08.2013)
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P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder
Barc, J G, Marsman, RF, Le Scouarnec, S, Mizusawa, Y, Lindenbaum, P, Carter, N, Redon, R, Wilde, AAM, Mckeown, P, Bezzina, CR
Published in Cardiovascular research (15.07.2014)
Published in Cardiovascular research (15.07.2014)
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Genechoc Study Genetic markers of arrhythmic risk in heart failure
Anys, S., Baron, E., Lecointe, S., Guyomarch, B., Klug, D., Babuty, D., Jesel, L., Dupuis, J.M., Defaye, P., Maury, P., Pasquie, J.L., Le Franc, P., Anselme, F., Boveda, S., Olivier, A., Thollet, A., Dina, C., Schott, J.J., Barc, J., Probst, V.
Published in Archives of Cardiovascular Diseases Supplements (01.10.2020)
Published in Archives of Cardiovascular Diseases Supplements (01.10.2020)
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