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Episignature-based modelled first-tier diagnostic approach in the Dutch Caribbean: advancing equal care through epigenetic classification
van der Laan, L., Luijckx, A., Lo-A-Njoe, S., Ecury-Goossen, G. M., Falix, F. A., Faries, S., Manshande, M. E., Philippi, P. A. E. A. C., van der Plas, E. M., Veenhuis, H. D., Rafael-Croes, L., Mannens, M. M. A. M., Sadikovic, B., Henneman, P., Alders, M. & van Haelst, M. M., 20 May 2026, In: Frontiers in Genetics. 17, p. 1803993 1 p.Research output: Contribution to Journal › Article › Academic › peer-review
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Fatal persistent pulmonary hypertension as part of 3q11.1-q21.3 deletion syndrome?
Lo A Njoe, S. M., van der Laan, L., Postma, A. V., van Doorn, A., Ecury-Goossen, G. M. & van Haelst, M. M., 5 Dec 2025, In: Medical Reports.Research output: Contribution to Journal › Article › Academic › peer-review
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GMDS Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly
Lo-A-Njoe, S. M., Verberne, E. A., van der Veken, L. T., Arends, E., van Tintelen, J. P., Postma, A. V. & van Haelst, M. M., 1 Sept 2023, In: Cardiogenetics. 13, 3, p. 106-112Research output: Contribution to Journal › Article › Academic › peer-review
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