Merel van Maarle

20072019
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Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2007 2019

Implementing NIPT as part of a national prenatal screening program: The Dutch TRIDENT studies

Weiss, M. M., Galjaard, R. H., Sistermans, E. A., Bax, C. J., Bekker, M. N., de Die-Smulders, C. E. M., Feenstra, I., Hoffer, M. J. V., den Hollander, N. S., Knapen, M. F. C. M., van Langen, I. M., Lichtenbelt, K. D., Lombardi, P. M., van Maarle, M. C., van der Meij, K. R. M., Pieters, M. J., Schuring-Blom, G. H., Sikkel, E., Stevens, S. J., Suijkerbuijk, R. F. & 4 othersvan der Ven, A. J. E. M., Van Opstal, D., Henneman, L. & Macville, M. V., Jul 2019, In : European Journal of Human Genetics. 27, p. 823-824

Research output: Contribution to journalMeeting AbstractAcademic

TRIDENT-2: National Implementation of Genome-Wide Non-Invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands

van der Meij, K. R. M., Sistermans, E. A., Macville, M. V. E., Stevens, S. J. C., Bax, C. J., Bekker, M. N., Bilardo, C. M., Boon, E. M. J., Boter, M., Diderich, K. E. M., de Die-Smulders, C. E. M., Duin, L. K., Faas, B. H. W., Feenstra, I., Haak, M. C., Hoffer, M. J. V., den Hollander, N. S., Hollink, I. H. I. M., Jehee, F. S., Knapen, M. F. C. M. & 21 othersKooper, A. J. A., van Langen, I. M., Lichtenbelt, K. D., Linskens, I. H., van Maarle, M. C., Oepkes, D., Pieters, M. J., Schuring-Blom, G. H., Sikkel, E., Sikkema-Raddatz, B., Smeets, D. F. C. M., Srebniak, M. I., Suijkerbuijk, R. F., Tan-Sindhunata, G. M., van der Ven, A. J. E. M., van Zelderen-Bhola, S. L., Henneman, L., Galjaard, R-J. H., Van Opstal, D., Weiss, M. M. & Dutch NIPT Consortium, 5 Dec 2019, In : American journal of human genetics. 105

Research output: Contribution to journalArticleAcademicpeer-review

Genetically isolated populations: Implications for genetic care

Matthijssen, I. B., 2018, 242 p.

Research output: ThesisResearch external, graduation externalAcademic

Implementing NIPT as part of a national prenatal screening program: The Dutch TRIDENT studies

Galjaard, R-J., Henneman, L., Macville, M., Bax, C., Bekker, M., De Die-Smulders, C., Feenstra, I., Hoffer, M., Den Hollander, N., Van Langen, I., Lichtenbelt, K., Lombardi, P., Van Maarle, M., Van Der Meij, K., Pieters, M., Schuring-Blom, H., Sikkel, E., Stevens, S., Suijkerbuijk, R., Van Der Ven, J. & 3 othersVan Opstal, D., Weiss, J. & Sistermans, E., 2018, In : Prenatal Diagnosis. 38

Research output: Contribution to journalMeeting AbstractAcademic

RARS2 mutations: Is pontocerebellar hypoplasia type 6 a mitochondrial encephalopathy?

van Dijk, T., van Ruissen, F., Jaeger, B., Rodenburg, R. J., Tamminga, S., van Maarle, M., Baas, F., Wolf, N. I. & Poll-The, B. T., 2017, JIMD Reports. Springer, Vol. 33. p. 87-92 (JIMD Reports).

Research output: Chapter in Book/Report/Conference proceedingChapterAcademicpeer-review