Doris Skoric - Milosavljevic

ACS - Cardiomyopathy and Arrhythmia ACS - Pulmonary Hypertension and Critical Care Affiliatie UvA Amsterdam Reproduction & Development (AR&D) Standard PhD Candidate, Doctoral School Physician, Human Genetics Other Academic Staff, Human Genetics External PhD Candidate, Human Genetics

Specialization

Focus of research

Latest publications

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 others, Nannenberg, 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
Yield and pitfalls of ajmaline testing in the evaluation of unexplained cardiac arrest and sudden unexplained death: Single centre experience of 482 families.
Tadros, R., Nannenberg, E. A., Lieve, K. V., Skoric-Milosavljevic, D., Lahrouchi, N., Lekanne Dit Deprez, R. H., Vendrik, J., Reckman, Y. J., Postema, P. G., Amin, A. S., Bezzina, C. R., Wilde, A. A. M. & Tan, H. L., 2017, In: Journal of the American College of Cardiology Clinical Electrophysiology. 3, 12, p. 1400-1408
Research output: Contribution to journal › Article* › Academic › peer-review
Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature
Milosavljević, D., Overwater, E., Tamminga, S., de Boer, K., Elting, M. W., van Hoorn, M. E., Rinne, T., Houweling, A. C. & Milosavljevic, D., Jul 2016, In: American journal of medical genetics. Part A. 170A, 7, p. 1874-1880
Research output: Contribution to journal › Article* › Academic › peer-review
All publications

Doris Skoric - Milosavljevic

Specialization

Focus of research

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

Yield and pitfalls of ajmaline testing in the evaluation of unexplained cardiac arrest and sudden unexplained death: Single centre experience of 482 families.

Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature

Amsterdam UMC makes use of cookies