Projects per year
Personal profile
Research interests
- Arrhythmias
- Cardiomyopathy
- Electrophysiology
- Genetics
- Sudden death
Specialisation
External positions
Consultant, Cydan
consultant, LQTtherapeutics
Fingerprint
- 1 Similar Profiles
Collaborations and top research areas from the last five years
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RYR2-targeted Gene Therapies for Treating Catecholaminergic Polymorphic Ventricular Tachycardia
Roberts, J. D. J. D. (Principal investigator), Chen, S. R. W. S. R. W. (CoPI), Gollob, M. H. M. H. (CoPI), Healey, J. S. J. S. (CoPI), Krahn, A. D. A. D. (CoPI), Paré, G. G. (CoPI), Sanatani, S. S. (CoPI), Tadros, R. R. (CoPI) & Wilde, A. A. M. (CoPI)
Institute of Circulatory and Respiratory Health
01/10/2022 → 30/09/2027
Project: Research
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SILENCELQTS- SGK1 inhibition as a novel therapeutic approach in Long QT syndrome
Odening, K. K. (Principal investigator), Vidal, M. M. (CoPI), Gepstein, L. L. (CoPI), Wilde, A. A. M. (CoPI) & Wilde, A. A. M. A. A. M. (CoPI)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
01/12/2021 → 30/11/2024
Project: Research
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Flecainide Therapy Reduces Exercise-Induced Ventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
van der Werf, C., Kannankeril, P. J., Sacher, F., Krahn, A. D., Viskin, S., Leenhardt, A., Shimizu, W., Sumitomo, N., Fish, F. A., Bhuiyan, Z. A., Willems, A. R., van der Veen, M. J., Watanabe, H., Laborderie, J., Haïssaguerre, M., Knollmann, B. C. & Wilde, A. A. M., 2011, In: Journal of the American College of Cardiology. 57, 22, p. 2244-2254Research output: Contribution to journal › Editorial › Academic › peer-review
345 Citations (Scopus) -
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Bezzina, C. R., 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. & Behr, E. R. & 45 others, , 2013, In: Nature genetics. 45, 9, p. 1044-1049Research output: Contribution to journal › Article › Academic › peer-review
453 Citations (Scopus) -
HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013
Priori, S. G., Wilde, A. A., Horie, M., Cho, Y., Behr, E. R., Berul, C., Blom, N., Brugada, J., Chiang, C.-E., Huikuri, H., Kannankeril, P., Krahn, A., Leenhardt, A., Moss, A., Schwartz, P. J., Shimizu, W., Tomaselli, G. & Tracy, C., 2013, In: Heart rhythm. 10, 12, p. 1932-1963Research output: Contribution to journal › Article › Academic › peer-review
1517 Citations (Scopus) -
Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience
Hofman, N., Tan, H. L., Alders, M., Kolder, I., de Haij, S., Mannens, M. M. A. M., Lombardi, M. P., Lekanne Deprez, R. H., van Langen, I. & Wilde, A. A. M., 2013, In: Circulation. 128, 14, p. 1513-1521Research output: Contribution to journal › Article › Academic › peer-review
124 Citations (Scopus) -
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study
Wilde, A. A. M., Moss, A. J., Kaufman, E. S., Shimizu, W., Peterson, D. R., Benhorin, J., Lopes, C., Towbin, J. A., Spazzolini, C., Crotti, L., Zareba, W., Goldenberg, I., Kanters, J. K., Robinson, J. L., Qi, M., Hofman, N., Tester, D. J., Bezzina, C. R., Alders, M. & Aiba, T. & 7 others, , 2016, In: Circulation. 134, 12, p. 872-882Research output: Contribution to journal › Article › Academic › peer-review
155 Citations (Scopus)
Prizes
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1st Windland Smith Rice Cardiovasc. Genomics Visiting Professor.
Wilde, A. A. M. (Recipient), 2018
Prize: Honorary award › Academic
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Distinguished Scientist Award, Heart Rhythm Society
Wilde, A. A. M. (Recipient), 2012
Prize: Honorary award › Academic
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