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Fingerprint Dive into the research topics where Matteo Pedrazzini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

The genetics underlying acquired long QT syndrome: Impact for genetic screening

Itoh, H., Crotti, L., Aiba, T., Spazzolini, C., Denjoy, I., Fressart, V., Hayashi, K., Nakajima, T., Ohno, S., Makiyama, T., Wu, J., Hasegawa, K., Mastantuono, E., Dagradi, F., Pedrazzini, M., Yamagishi, M., Berthet, M., Murakami, Y., Shimizu, W., Guicheney, P. & 2 others, Schwartz, P. J. & Horie, M., May 7 2016, In : European Heart Journal. 37, 18, p. 1456-1464 9 p.

Research output: Contribution to journalArticle

  • The genetics underlying acquired long QT syndrome: Impact for genetic screening

    Itoh, H., Crotti, L., Aiba, T., Spazzolini, C., Denjoy, I., Fressart, V., Hayashi, K., Nakajima, T., Ohno, S., Makiyama, T., Wu, J., Hasegawa, K., Mastantuono, E., Dagradi, F., Pedrazzini, M., Yamagishi, M., Berthet, M., Murakami, Y., Shimizu, W., Guicheney, P. & 2 others, Schwartz, P. J. & Horie, M., May 7 2016, In : European Heart Journal. 37, 18, p. 1456-1464 9 p.

    Research output: Contribution to journalArticle

  • JAK2 exon 14 skipping in patients with primary myelofibrosis: A minor splice variant modulated by the JAK2-V617F allele burden

    Catarsi, P., Rosti, V., Morreale, G., Poletto, V., Villani, L., Bertorelli, R., Pedrazzini, M., Zorzetto, M. & Barosi, G., Jan 24 2015, In : PLoS One. 10, 1, e0116636.

    Research output: Contribution to journalArticle

  • Calmodulin mutations associated with recurrent cardiac arrest in infants

    Crotti, L., Johnson, C. N., Graf, E., De Ferrari, G. M., Cuneo, B. F., Ovadia, M., Papagiannis, J., Feldkamp, M. D., Rathi, S. G., Kunic, J. D., Pedrazzini, M., Wieland, T., Lichtner, P., Beckmann, B. M., Clark, T., Shaffer, C., Benson, D. W., Kääb, S., Meitinger, T., Strom, T. M. & 3 others, Chazin, W. J., Schwartz, P. J. & George, A. L., Mar 5 2013, In : Circulation. 127, 9, p. 1009-1017 9 p.

    Research output: Contribution to journalArticle

  • Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome

    Duchatelet, S., Crotti, L., Peat, R. A., Denjoy, I., Itoh, H., Berthet, M., Ohno, S., Fressart, V., Monti, M. C., Crocamo, C., Pedrazzini, M., Dagradi, F., Vicentini, A., Klug, D., Brink, P. A., Goosen, A., Swan, H., Toivonen, L., Lahtinen, A. M., Kontula, K. & 6 others, Shimizu, W., Horie, M., George, A. L., Trégouët, D. A., Guicheney, P. & Schwartz, P. J., Aug 2013, In : Circulation: Cardiovascular Genetics. 6, 4, p. 354-361 8 p.

    Research output: Contribution to journalArticle