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Discovery of a DNA methylation episignature for Weiss-Kruszka syndrome
McConkey, H., van der Laan, L., Ghosh, S., Kleinendorst, L., Levy, M. A., Rzasa, J., van Hagen, J. M., Waisfisz, Q., Schulz, H. L., Heller, C., Huhn, K., Obermaier, C. D., Platzer, K., Jamra, R. A., Marinakis, N., Veltra, D., Kosma, K., Sofocleous, C., Henneman, P. & Sadikovic, B. & 1 others, , 1 Dec 2026, In: Human Genetics. 145, 1, 63.Research output: Contribution to Journal › Article › Academic › peer-review
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DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects
Dombrowsky, G., van der Laan, L., Silva, A., Breckpot, J., Audain, E., Wilsdon, A., Levy, M. A., Vos, N., Mannens, M., Wang, J., Jain, A., Lesurf, R., Winlaw, D., Bezzina, C. R., Thomas, M. A., Caliebe, A., Klaassen, S., Berger, F., Dittrich, S. & Stiller, B. & 15 others, , 1 Dec 2026, In: Genome Medicine. 18, 1, 2.Research output: Contribution to Journal › Article › Academic › peer-review
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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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