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  1. 2022

  2. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility (Nature Genetics, (2022), 54, 3, (232-239), 10.1038/s41588-021-01007-6)

    Barc, J., Tadros, R., Glinge, C., Chiang, D. Y., Jouni, M., Simonet, F., Jurgens, S. J., Baudic, M., Nicastro, M., Potet, F., Offerhaus, J. A., Walsh, R., Choi, S. H., Verkerk, A. O., Mizusawa, Y., Anys, S., Minois, D., Arnaud, M., Duchateau, J., Wijeyeratne, Y. D., & 138 othersMuir, A., Papadakis, M., Castelletti, S., Torchio, M., Ortuño, C. G., Lacunza, J., Giachino, D. F., Cerrato, N., Martins, R. P., Campuzano, O., van Dooren, S., Thollet, A., Kyndt, F., Mazzanti, A., Clémenty, N., Bisson, A., Corveleyn, A., Stallmeyer, B., Dittmann, S., Saenen, J., Noël, A., Honarbakhsh, S., Rudic, B., Marzak, H., Rowe, M. K., Federspiel, C., le Page, S., Placide, L., Milhem, A., Barajas-Martinez, H., Beckmann, B-M., Krapels, I. P., Steinfurt, J., Winkel, B. G., Jabbari, R., Shoemaker, M. B., Boukens, B. J., Škorić-Milosavljević, D., Bikker, H., Manevy, F., Lichtner, P., Ribasés, M., Meitinger, T., Müller-Nurasyid, M., Strauch, K., Peters, A., Schulz, H., Schwettmann, L., Leidl, R., Heier, M., Veldink, J. H., van den Berg, L. H., van Damme, P., Cusi, D., Lanzani, C., Rigade, S., Charpentier, E., Baron, E., Bonnaud, S., Lecointe, S., Donnart, A., le Marec, H., Chatel, S., Karakachoff, M., Bézieau, S., London, B., Tfelt-Hansen, J., Roden, D., Odening, K. E., Cerrone, M., Chinitz, L. A., Volders, P. G., van de Berg, M. P., Laurent, G., Faivre, L., Antzelevitch, C., Kääb, S., Arnaout, A. A., Dupuis, J-M., Pasquie, J-L., Billon, O., Roberts, J. D., Jesel, L., Borggrefe, M., Lambiase, P. D., Mansourati, J., Loeys, B., Leenhardt, A., Guicheney, P., Maury, P., Schulze-Bahr, E., Robyns, T., Breckpot, J., Babuty, D., Priori, S. G., Napolitano, C., Defaye, P., Anselme, F., KORA-Study Group, Darmon, J. P., Nantes Referral Center for inherited cardiac arrhythmia, Wiart, F., de Asmundis, C., Brugada, P., Brugada, R., Arbelo, E., Brugada, J., Mabo, P., Behar, N., Giustetto, C., Molina, M. S., Gimeno, J. R., Hasdemir, C., Schwartz, P. J., Crotti, L., McKeown, P. P., Sharma, S., Behr, E. R., Haissaguerre, M., Sacher, F., Rooryck, C., Tan, H. L., Remme, C. A., Postema, P. G., Delmar, M., Ellinor, P. T., Lubitz, S. A., Gourraud, J-B., Tanck, M. W., George, A. L., MacRae, C. A., Burridge, P. W., Dina, C., Probst, V., Wilde, A. A., Schott, J-J., Redon, R. & Bezzina, C. R., 1 May 2022, In: Nature genetics. 54, 5, p. 735 1 p.

    Research output: Contribution to journal › Comment/Letter to the editor › Academic

  3. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

    Barc, J., Tadros, R., Glinge, C., Chiang, D. Y., Jouni, M., Simonet, F., Jurgens, S. J., Baudic, M., Nicastro, M., Potet, F., Offerhaus, J. A., Walsh, R., Choi, S. H., Verkerk, A. O., Mizusawa, Y., Anys, S., Minois, D., Arnaud, M., Duchateau, J., Wijeyeratne, Y. D., & 128 othersMuir, A., Papadakis, M., Castelletti, S., Torchio, M., Ortuño, C. G., Lacunza, J., Giachino, D. F., Cerrato, N., Martins, R. P., Campuzano, O., van Dooren, S., Thollet, A., Kyndt, F., Mazzanti, A., Clémenty, N., Bisson, A., Corveleyn, A., Stallmeyer, B., Dittmann, S., Saenen, J., Noël, A., Honarbakhsh, S., Rudic, B., Marzak, H., Rowe, M. K., Federspiel, C., le Page, S., Placide, L., Milhem, A., Barajas-Martinez, H., Beckmann, B-M., Krapels, I. P., Steinfurt, J., Winkel, B. G., Jabbari, R., Shoemaker, M. B., Boukens, B. J., Škorić-Milosavljević, D., Bikker, H., Manevy, F. C., Lichtner, P., Ribasés, M., Meitinger, T., Müller-Nurasyid, M., Veldink, J. H., van den Berg, L. H., van Damme, P., Cusi, D., Lanzani, C., Rigade, S., Charpentier, E., Baron, E., Bonnaud, S., Lecointe, S., Donnart, A., le Marec, H., Chatel, S., Karakachoff, M., Bézieau, S., London, B., Tfelt-Hansen, J., Roden, D., Odening, K. E., Cerrone, M., Chinitz, L. A., Volders, P. G., van de Berg, M. P., Laurent, G., Faivre, L., Antzelevitch, C., Kääb, S., Arnaout, A. A., Dupuis, J-M., Pasquie, J-L., Billon, O., Roberts, J. D., Jesel, L., Borggrefe, M., Lambiase, P. D., Mansourati, J., Loeys, B., Leenhardt, A., Guicheney, P., Maury, P., Schulze-Bahr, E., Robyns, T., Breckpot, J., Babuty, D., Priori, S. G., Napolitano, C., de Asmundis, C., Brugada, P., Brugada, R., Arbelo, E., Brugada, J., Mabo, P., Behar, N., Giustetto, C., Molina, M. S., Gimeno, J. R., Hasdemir, C., Schwartz, P. J., Crotti, L., McKeown, P. P., Sharma, S., Behr, E. R., Haissaguerre, M., Sacher, F., Rooryck, C., Tan, H. L., Remme, C. A., Postema, P. G., Delmar, M., Ellinor, P. T., Lubitz, S. A., Gourraud, J-B., Tanck, M. W., KORA-Study Group, George, A. L., Nantes Referral Center for inherited cardiac arrhythmia, MacRae, C. A., Burridge, P. W., Dina, C., Probst, V., Wilde, A. A., Schott, J-J., Redon, R. & Bezzina, C. R., 1 Mar 2022, In: Nature genetics. 54, 3, p. 232-239 8 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  4. An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

    Peltenburg, P. J., Kallas, D., Bos, J. M., Lieve, K. V. V., Franciosi, S., Roston, T. M., Denjoy, I., Sorensen, K. B., Ohno, S., Roses-Noguer, F., Aiba, T., Maltret, A., LaPage, M. J., Atallah, J., Giudicessi, J. R., Clur, S-A. B., Blom, N. A., Tanck, M., Extramiana, F., Kato, K., & 31 othersBarc, J., Borggrefe, M., Behr, E. R., Sarquella-Brugada, G., Tfelt-Hansen, J., Zorio, E., Swan, H., Kammeraad, J. A. E., Krahn, A. D., Davis, A., Sacher, F., Schwartz, P. J., Roberts, J. D., Skinner, J. R., van den Berg, M. P., Kannankeril, P. J., Drago, F., Robyns, T., Haugaa, K., Tavacova, T., Semsarian, C., Till, J., Probst, V., Brugada, R., Shimizu, W., Horie, M., Leenhardt, A., Ackerman, M. J., Sanatani, S., van der Werf, C. & Wilde, A. A. M., 1 Feb 2022, In: Circulation. 145, 5, p. 333-344 12 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  5. 2021

  6. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

    Walsh, R., Lahrouchi, N., Tadros, R., Kyndt, F., Glinge, C., Postema, P. G., Amin, A. S., Nannenberg, E. A., Ware, J. S., Whiffin, N., Mazzarotto, F., Škorić-Milosavljević, D., Krijger, C., Arbelo, E., Babuty, D., Barajas-Martinez, H., Beckmann, B. M., Bézieau, S., Bos, J. M., Breckpot, J., & 31 othersCampuzano, O., Castelletti, S., Celen, C., Clauss, S., Corveleyn, A., Crotti, L., Dagradi, F., de Asmundis, C., Denjoy, I., Dittmann, S., Ellinor, P. T., Ortuño, C. G., Giustetto, C., Gourraud, J-B., Hazeki, D., Horie, M., Ishikawa, T., Itoh, H., Kaneko, Y., Kanters, J. R. K., Kimoto, H., Kotta, M-C., Krapels, I. P. C., Kurabayashi, M., Lazarte, J., Leenhardt, A., Loeys, B. L., Robyns, T., Nantes Referral Center for inherited cardiac arrhythmia, Barc, J. & Bezzina, C. R., Jan 2021, In: Genetics in medicine. 23, 1, p. 47-58 12 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  7. 2020

  8. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    Lahrouchi, N., Tadros, R., Crotti, L., Mizusawa, Y., Postema, P. G., Beekman, L., Walsh, R., Hasegawa, K., Barc, J., Ernsting, M., Turkowski, K. L., Mazzanti, A., Beckmann, B. M., Shimamoto, K., Diamant, U-B., Wijeyeratne, Y. D., Kucho, Y., Robyns, T., Ishikawa, T., Arbelo, E., & 86 othersChristiansen, M., Winbo, A., Jabbari, R., Lubitz, S. A., Steinfurt, J., Rudic, B., Loeys, B., Shoemaker, M. B., Weeke, P. E., Pfeiffer, R., Davies, B., Andorin, A., Hofman, N., Dagradi, F., Pedrazzini, M., Tester, D. J., Bos, J. M., Sarquella-Brugada, G., Campuzano, Ó., Platonov, P. G., Stallmeyer, B., Zumhagen, S., Nannenberg, E. A., Veldink, J. H., van den Berg, L. H., Al-Chalabi, A., Shaw, C. E., Shaw, P. J., Morrison, K. E., Andersen, P. M., Müller-Nurasyid, M., Cusi, D., Barlassina, C., Galan, P., Lathrop, M., Munter, M., Werge, T., Ribasés, M., Aung, T., Khor, C. C., Ozaki, M., Lichtner, P., Meitinger, T., van Tintelen, J. P., Hoedemaekers, Y., Denjoy, I., Leenhardt, A., Napolitano, C., Shimizu, W., Schott, J-J., Gourraud, J-B., Makiyama, T., Ohno, S., Itoh, H., Krahn, A. D., Antzelevitch, C., Roden, D. M., Saenen, J., Borggrefe, M., Odening, K. E., Ellinor, P. T., Tfelt-Hansen, J., Skinner, J. R., van den Berg, M. P., Olesen, M. S., Brugada, J., Brugada, R., Makita, N., Breckpot, J., Yoshinaga, M., Behr, E. R., Rydberg, A., Aiba, T., Kääb, S., Priori, S. G., Guicheney, P., Tan, H. L., Newton-Cheh, C., Ackerman, M. J., Schwartz, P. J., Schulze-Bahr, E., Probst, V., Horie, M., Wilde, A. A., Tanck, M. W. T. & Bezzina, C. R., 28 Jul 2020, In: Circulation. 142, 4, p. 324-338 15 p.

    Research output: Contribution to journal › Article › Academic › peer-review

  9. Scn5a mutation type and a genetic risk score associate variably with brugada syndrome phenotype in scn5a families

    Wijeyeratne, Y. D., Tanck, M. W., Mizusawa, Y., Batchvarov, V., Barc, J., Crotti, L., Bos, J. M., Tester, D. J., Muir, A., Veltmann, C., Ohno, S., Page, S. P., Galvin, J., Tadros, R., Muggenthaler, M., Raju, H., Denjoy, I., Schott, J-J., Gourraud, J-B., Skoric-Milosavljevic, D., & 25 othersNannenberg, E. A., Redon, R., Papadakis, M., Kyndt, F., Dagradi, F., Castelletti, S., Torchio, M., Meitinger, T., Lichtner, P., Ishikawa, T., Wilde, A. A. M., Takahashi, K., Sharma, S., Roden, D. M., Borggrefe, M. M., McKeown, P. P., Shimizu, W., Horie, M., Makita, N., Aiba, T., Ackerman, M. J., Schwartz, P. J., Probst, V., Bezzina, C. R. & Behr, E. R., 2020, In: Circulation: Genomic and Precision Medicine. p. 599-608 10 p., 002911.

    Research output: Contribution to journal › Article › Academic › peer-review

  10. 2019

  11. GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum

    Škorić-Milosavljević, D., Tjong, F. V. Y., Barc, J., Backx, A. P. C. M., Clur, S-A. B., van Spaendonck-Zwarts, K., Oostra, R-J., Lahrouchi, N., Beekman, L., Bökenkamp, R., Barge-Schaapveld, D. Q. C. M., Mulder, B. J., Lodder, E. M., Bezzina, C. R. & Postma, A. V., 2019, In: American journal of medical genetics. Part A. 179, 9, p. 1836-1845

    Research output: Contribution to journal › Article › Academic › peer-review

  12. 2017

  13. The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity

    Veerman, C. C., Podliesna, S., Tadros, R., Lodder, E. M., Mengarelli, I., de Jonge, B., Beekman, L., Barc, J., Wilders, R., Wilde, A. A., Boukens, B. J., Coronel, R., Verkerk, A., Remme, C. A. & Bezzina, C. R., 2017, In: Circulation research. 121, 5, p. 537-548

    Research output: Contribution to journal › Article › Academic › peer-review

  14. 2016

  15. hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities

    Veerman, C. C., Mengarelli, I., Guan, K., Stauske, M., Barc, J., Tan, H. L., Wilde, A. A. M., Verkerk, A. O. & Bezzina, C. R., 2016, In: Scientific reports. 6, p. 30967

    Research output: Contribution to journal › Article › Academic › peer-review

  16. Sudden Cardiac Arrest and Rare Genetic Variants in the Community

    Milano, A., Blom, M. T., Lodder, E. M., van Hoeijen, D. A., Barc, J., Koopmann, T. T., Bardai, A., Beekman, L., Lichtner, P., van den Berg, M. P., Wilde, A. A. M., Bezzina, C. R. & Tan, H. L., 2016, In: Circulation. Cardiovascular genetics. 9, 2, p. 147-153

    Research output: Contribution to journal › Article › Academic › peer-review

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ID: 116641