Sanne Alsters

DR.

20122020

Research output per year

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Research Output

Non-sustained ventricular tachycardias, conduction disorders and an impaired left ventricular ejection fraction in a 32-year-old woman

Alsters, S., Polyukhovych, Y., Bikker, H., Wong, L. & Houweling, A. C., Feb 2020, In : Netherlands Heart Journal. 28, 5, p. 295-296 2 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation

Alsters, S., Wong, L., Peferoen, L., Niessen, H. W. M., Bikker, H., Elting, M. W. & Houweling, A. C., 1 May 2019, In : Netherlands Heart Journal. 27, 5, p. 282-283 2 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Mutation update for the SATB2 gene

Zarate, Y. A., Bosanko, K. A., Caffrey, A. R., Bernstein, J. A., Martin, D. M., Williams, M. S., Berry-Kravis, E. M., Mark, P. R., Manning, M. A., Bhambhani, V., Vargas, M., Seeley, A. H., Estrada-Veras, J. I., van Dooren, M. F., Schwab, M., Vanderver, A., Melis, D., Alsadah, A., Sadler, L., Van Esch, H. & 28 others, Callewaert, B., Oostra, A., Maclean, J., Dentici, M. L., Orlando, V., Lipson, M., Sparagana, S. P., Maarup, T. J., Alsters, S. I. M., Brautbar, A., Kovitch, E., Naidu, S., Lees, M., Smith, D. M., Turner, L., Raggio, V., Spangenberg, L., Garcia-Miñaúr, S., Roeder, E. R., Littlejohn, R. O., Grange, D., Pfotenhauer, J., Jones, M. C., Balasubramanian, M., Martinez-Monseny, A., Blok, L. S., Gavrilova, R. & Fish, J. L., 1 Jan 2019, In : Human Mutation. 40, 8, p. 1013-1029 17 p.

Research output: Contribution to journalArticleAcademicpeer-review

Genetische obesitas: NIEUWE DIAGNOSTISCHE MOGELIJKHEDEN

Translated title of the contribution: Genetic obesity: New diagnostic optionsDe Vries, T. I., Alsters, S. I. M., Kleinendorst, L., Van Haaften, G., Van Der Zwaag, B. & Van Haelst, M. M., 2017, In : Nederlands Tijdschrift voor Geneeskunde. 161, 19, D688.

Research output: Contribution to journalArticleProfessional

Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic Hypogonadism

Alsters, S. I. M., Goldstone, A. P., Buxton, J. L., Zekavati, A., Sosinsky, A., Yiorkas, A. M., Holder, S., Klaber, R. E., Bridges, N., van Haelst, M. M., le Roux, C. W., Walley, A. J., Walters, R. G., Mueller, M. & Blakemore, A. I. F., 2015, In : PLoS ONE. 10, 6, p. e0131417

Research output: Contribution to journalArticleAcademicpeer-review