Sean Jurgens

Standard PhD Candidate, ACS - Heart Failure & Arrhythmias Affiliatie UvA MD-PhD, Cardiology Standard PhD Candidate, Doctoral School MD-PhD, Experimental Cardiology

Specialization

Focus of research

Latest publications

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
Baudic, M., Murata, H., Bosada, F. M., Melo, U. S., Aizawa, T., Lindenbaum, P., van der Maarel, L. E., Guedon, A., Baron, E., Fremy, E., Foucal, A., Ishikawa, T., Ushinohama, H., Jurgens, S. J., Choi, S. H., Kyndt, F., le Scouarnec, S., Wakker, V., Thollet, A., Rajalu, A., & 24 othersTakaki, T., Ohno, S., Shimizu, W., Horie, M., Kimura, T., Ellinor, P. T., Petit, F., Dulac, Y., Bru, P., Boland, A., Deleuze, J-F., Redon, R., le Marec, H., le Tourneau, T., Gourraud, J-B., Yoshida, Y., Makita, N., Vieyres, C., Makiyama, T., Mundlos, S., Christoffels, V. M., Probst, V., Schott, J-J. & Barc, J., 1 Dec 2024, In: Nature communications. 15, 1, 3380.
Research output: Contribution to journal › Article › Academic › peer-review
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank
Ryu, J., Rämö, J. T., Jurgens, S. J., Niiranen, T., Sanna-Cherchi, S., Bauer, K. A., Haj, A., Choi, S. H., Palotie, A., Daly, M., Ellinor, P. T. & FinnGen, 6 Jun 2024, In: Blood. 143, 23, p. 2425-2432 8 p.
Research output: Contribution to journal › Article › Academic › peer-review
A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population
Mauleekoonphairoj, J., Tongsima, S., Khongphatthanayothin, A., Jurgens, S. J., Zimmerman, D. S., Sutjaporn, B., Wandee, P., Bezzina, C. R., Nademanee, K. & Poovorawan, Y., 1 Dec 2023, In: Scientific reports. 13, 1, 12360.
Research output: Contribution to journal › Article › Academic › peer-review
All publications

Sean Jurgens

Specialization

Focus of research

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population

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