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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. / Bezzina, Connie; Barc, Julien; Mizusawa, Yuka; Remme, Carol Ann; Gourraud, Jean-Baptiste; Simonet, Floriane; Verkerk, Arie O; Schwartz, Peter J; Crotti, Lia; Dagradi, Federica; Guicheney, Pascale; Fressart, Véronique; Leenhardt, Antoine; Antzelevitch, Charles; Bartkowiak, Susan; Borggrefe, Martin; Schimpf, Rainer; Schulze-Bahr, Eric; Zumhagen, Sven; Behr, Elijah R; Bastiaenen, Rachel; Tfelt-Hansen, Jacob; Olesen, Morten Salling; Kääb, Stefan; Beckmann, Britt M; Weeke, Peter; Watanabe, Hiroshi; Endo, Naoto; Minamino, Tohru; Horie, Minoru; Ohno, Seiko; Hasegawa, Kanae; Makita, Naomasa; Nogami, Akihiko; Shimizu, Wataru; Aiba, Takeshi; Froguel, Philippe; Balkau, Beverley; Lantieri, Olivier; Torchio, Margherita; Wiese, Cornelia; Weber, David; Wolswinkel, Rianne; Coronel, Ruben; Boukens, Bas J; Bézieau, Stéphane; Charpentier, Eric; Chatel, Stéphanie; Despres, Aurore; Gros, Françoise; Kyndt, Florence; Lecointe, Simon; Lindenbaum, Pierre; Portero, Vincent; Violleau, Jade; Gessler, Manfred; Tan, Hanno L; Roden, Dan M; Christoffels, Vincent M; Le Marec, Hervé; Wilde, Arthur A; Probst, Vincent; Schott, Jean-Jacques; Dina, Christian; Redon, Richard.
I:
Nature Genetics, Bind 45, Nr. 9, 2013, s. 1044-1049.
Publikation: Bidrag til tidsskrift › Letter › Forskning › fagfællebedømt
Harvard
Bezzina, C, Barc, J, Mizusawa, Y, Remme, CA, Gourraud, J-B, Simonet, F, Verkerk, AO, Schwartz, PJ, Crotti, L, Dagradi, F, Guicheney, P, Fressart, V, Leenhardt, A, Antzelevitch, C, Bartkowiak, S, Borggrefe, M, Schimpf, R, Schulze-Bahr, E, Zumhagen, S, Behr, ER, Bastiaenen, R, Tfelt-Hansen, J
, Olesen, MS, Kääb, S, Beckmann, BM, Weeke, P, Watanabe, H, Endo, N, Minamino, T, Horie, M, Ohno, S, Hasegawa, K, Makita, N, Nogami, A, Shimizu, W, Aiba, T, Froguel, P, Balkau, B, Lantieri, O, Torchio, M, Wiese, C, Weber, D, Wolswinkel, R, Coronel, R, Boukens, BJ, Bézieau, S, Charpentier, E, Chatel, S, Despres, A, Gros, F, Kyndt, F, Lecointe, S, Lindenbaum, P, Portero, V, Violleau, J, Gessler, M, Tan, HL, Roden, DM, Christoffels, VM, Le Marec, H, Wilde, AA, Probst, V, Schott, J-J, Dina, C & Redon, R 2013, '
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death',
Nature Genetics, bind 45, nr. 9, s. 1044-1049.
https://doi.org/10.1038/ng.2712APA
Bezzina, C., Barc, J., Mizusawa, Y., Remme, C. A., Gourraud, J-B., Simonet, F., Verkerk, A. O., Schwartz, P. J., Crotti, L., Dagradi, F., Guicheney, P., Fressart, V., Leenhardt, A., Antzelevitch, C., Bartkowiak, S., Borggrefe, M., Schimpf, R., Schulze-Bahr, E., Zumhagen, S., ... Redon, R. (2013).
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Nature Genetics,
45(9), 1044-1049.
https://doi.org/10.1038/ng.2712Vancouver
Bezzina C, Barc J, Mizusawa Y, Remme CA, Gourraud J-B, Simonet F o.a.
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Nature Genetics. 2013;45(9):1044-1049.
https://doi.org/10.1038/ng.2712Author
Bezzina, Connie ; Barc, Julien ; Mizusawa, Yuka ; Remme, Carol Ann ; Gourraud, Jean-Baptiste ; Simonet, Floriane ; Verkerk, Arie O ; Schwartz, Peter J ; Crotti, Lia ; Dagradi, Federica ; Guicheney, Pascale ; Fressart, Véronique ; Leenhardt, Antoine ; Antzelevitch, Charles ; Bartkowiak, Susan ; Borggrefe, Martin ; Schimpf, Rainer ; Schulze-Bahr, Eric ; Zumhagen, Sven ; Behr, Elijah R ; Bastiaenen, Rachel ; Tfelt-Hansen, Jacob ; Olesen, Morten Salling ; Kääb, Stefan ; Beckmann, Britt M ; Weeke, Peter ; Watanabe, Hiroshi ; Endo, Naoto ; Minamino, Tohru ; Horie, Minoru ; Ohno, Seiko ; Hasegawa, Kanae ; Makita, Naomasa ; Nogami, Akihiko ; Shimizu, Wataru ; Aiba, Takeshi ; Froguel, Philippe ; Balkau, Beverley ; Lantieri, Olivier ; Torchio, Margherita ; Wiese, Cornelia ; Weber, David ; Wolswinkel, Rianne ; Coronel, Ruben ; Boukens, Bas J ; Bézieau, Stéphane ; Charpentier, Eric ; Chatel, Stéphanie ; Despres, Aurore ; Gros, Françoise ; Kyndt, Florence ; Lecointe, Simon ; Lindenbaum, Pierre ; Portero, Vincent ; Violleau, Jade ; Gessler, Manfred ; Tan, Hanno L ; Roden, Dan M ; Christoffels, Vincent M ; Le Marec, Hervé ; Wilde, Arthur A ; Probst, Vincent ; Schott, Jean-Jacques ; Dina, Christian ; Redon, Richard. / Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. I: Nature Genetics. 2013 ; Bind 45, Nr. 9. s. 1044-1049.
Bibtex
@article{4a76ea98b3274d51a71c291521bf3ba9,
title = "Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death",
author = "Connie Bezzina and Julien Barc and Yuka Mizusawa and Remme, {Carol Ann} and Jean-Baptiste Gourraud and Floriane Simonet and Verkerk, {Arie O} and Schwartz, {Peter J} and Lia Crotti and Federica Dagradi and Pascale Guicheney and V{\'e}ronique Fressart and Antoine Leenhardt and Charles Antzelevitch and Susan Bartkowiak and Martin Borggrefe and Rainer Schimpf and Eric Schulze-Bahr and Sven Zumhagen and Behr, {Elijah R} and Rachel Bastiaenen and Jacob Tfelt-Hansen and Olesen, {Morten Salling} and Stefan K{\"a}{\"a}b and Beckmann, {Britt M} and Peter Weeke and Hiroshi Watanabe and Naoto Endo and Tohru Minamino and Minoru Horie and Seiko Ohno and Kanae Hasegawa and Naomasa Makita and Akihiko Nogami and Wataru Shimizu and Takeshi Aiba and Philippe Froguel and Beverley Balkau and Olivier Lantieri and Margherita Torchio and Cornelia Wiese and David Weber and Rianne Wolswinkel and Ruben Coronel and Boukens, {Bas J} and St{\'e}phane B{\'e}zieau and Eric Charpentier and St{\'e}phanie Chatel and Aurore Despres and Fran{\c c}oise Gros and Florence Kyndt and Simon Lecointe and Pierre Lindenbaum and Vincent Portero and Jade Violleau and Manfred Gessler and Tan, {Hanno L} and Roden, {Dan M} and Christoffels, {Vincent M} and {Le Marec}, Herv{\'e} and Wilde, {Arthur A} and Vincent Probst and Jean-Jacques Schott and Christian Dina and Richard Redon",
year = "2013",
doi = "10.1038/ng.2712",
language = "English",
volume = "45",
pages = "1044--1049",
journal = "Nature Genetics",
issn = "1061-4036",
publisher = "nature publishing group",
number = "9",
}
RIS
TY - JOUR
T1 - Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
AU - Bezzina, Connie
AU - Barc, Julien
AU - Mizusawa, Yuka
AU - Remme, Carol Ann
AU - Gourraud, Jean-Baptiste
AU - Simonet, Floriane
AU - Verkerk, Arie O
AU - Schwartz, Peter J
AU - Crotti, Lia
AU - Dagradi, Federica
AU - Guicheney, Pascale
AU - Fressart, Véronique
AU - Leenhardt, Antoine
AU - Antzelevitch, Charles
AU - Bartkowiak, Susan
AU - Borggrefe, Martin
AU - Schimpf, Rainer
AU - Schulze-Bahr, Eric
AU - Zumhagen, Sven
AU - Behr, Elijah R
AU - Bastiaenen, Rachel
AU - Tfelt-Hansen, Jacob
AU - Olesen, Morten Salling
AU - Kääb, Stefan
AU - Beckmann, Britt M
AU - Weeke, Peter
AU - Watanabe, Hiroshi
AU - Endo, Naoto
AU - Minamino, Tohru
AU - Horie, Minoru
AU - Ohno, Seiko
AU - Hasegawa, Kanae
AU - Makita, Naomasa
AU - Nogami, Akihiko
AU - Shimizu, Wataru
AU - Aiba, Takeshi
AU - Froguel, Philippe
AU - Balkau, Beverley
AU - Lantieri, Olivier
AU - Torchio, Margherita
AU - Wiese, Cornelia
AU - Weber, David
AU - Wolswinkel, Rianne
AU - Coronel, Ruben
AU - Boukens, Bas J
AU - Bézieau, Stéphane
AU - Charpentier, Eric
AU - Chatel, Stéphanie
AU - Despres, Aurore
AU - Gros, Françoise
AU - Kyndt, Florence
AU - Lecointe, Simon
AU - Lindenbaum, Pierre
AU - Portero, Vincent
AU - Violleau, Jade
AU - Gessler, Manfred
AU - Tan, Hanno L
AU - Roden, Dan M
AU - Christoffels, Vincent M
AU - Le Marec, Hervé
AU - Wilde, Arthur A
AU - Probst, Vincent
AU - Schott, Jean-Jacques
AU - Dina, Christian
AU - Redon, Richard
PY - 2013
Y1 - 2013
U2 - 10.1038/ng.2712
DO - 10.1038/ng.2712
M3 - Letter
C2 - 23872634
VL - 45
SP - 1044
EP - 1049
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
IS - 9
ER -
