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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.

  • 12 Similar Profiles
Long QT Syndrome Medicine & Life Sciences
Mutation Medicine & Life Sciences
Sudden Infant Death Medicine & Life Sciences
Genetic Testing Medicine & Life Sciences
Alleles Medicine & Life Sciences
Sodium Channels Medicine & Life Sciences
Genes Medicine & Life Sciences
Cardiac Arrhythmias Medicine & Life Sciences

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Research Output 2005 2016

  • 1577 Citations
  • 11 h-Index
  • 22 Article

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

Long QT Syndrome
Genetic Testing
Mutation
Torsades de Pointes
Inborn Genetic Diseases
54 Citations (Scopus)

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

Long QT Syndrome
Genetic Testing
Mutation
Torsades de Pointes
Inborn Genetic Diseases
2 Citations (Scopus)

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

Primary Myelofibrosis
exons
Exons
Protein Isoforms
Alleles
179 Citations (Scopus)

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

Calmodulin
Heart Arrest
Mutation
Exome
Calcium
39 Citations (Scopus)

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

Long QT Syndrome
Mutation
Sudden Death
Adrenergic Agents
Italy