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Dive into the research topics where Liselot van der Laan is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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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
Open AccessFile19 Downloads (Pure) -
Multi-omics investigation of thyroid development and dysfunction in down syndrome
Lauffer, P., Zwaveling-Soonawala, N., Li Yim, A. Y. F., van der Laan, L., van Zelderen-Bhola, S., Venema, A. M., Mul, A. N., Bugiani, M., Siteur-van Rijnstra, E., Gunst, Q. D., van den Hoff, M. J. B., de Bakker, B. S., Boelen, A., Henneman, P. & van Trotsenburg, A. S. P., 23 Feb 2026, In: Human molecular genetics. 35, 4, ddag005.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile10 Downloads (Pure) -
A rare triplication of 16p11.2: Unravelling the genomic complexity and review of the literature
van der Laan, L., Kleinendorst, L., Haagmans, M. A., Roquas, L., van der Smagt, J. J., Koop, K., Henneman, P. & van Haelst, M. M., 1 Jun 2025, In: European journal of medical genetics. 75, 105013.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile26 Downloads (Pure) -
ARID2-related disorder: further delineation of the clinical phenotype of 27 novel individuals and description of an epigenetic signature
Houdayer, C., Rooney, K., van der Laan, L., Bris, C. L., Alders, M., Bahr, A., Barcia, G., Battault, C., Begemann, A., Bonneau, D., Bonnevalle, A., Boughalem, A., Bourges, A., Bournez, M., Bruel, A.-L., Buhas, D., Carallis, F., Cogné, B., Cormier-Daire, V. & Delanne, J. & 47 others, , Nov 2025, In: European journal of human genetics. 33, 11, p. 1422-1431 10 p., 100075.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile27 Downloads (Pure) -
AUTS2-related syndrome: Insights from a large European cohort
Loberti, L., Adamo, L., Antolini, E., Casamassima, G., Destrèe, A., Brunetti-Pierri, N., Genevieve, D., Christophe, P., Coubes, C., van Esch, H., Herget, T., Kortüm, F., Lisfeld, J., Möllring, A. C., Zenker, M., Levy, J., Perrin, L., Tabet, A.-C., Maruani, A. & Sorlin, A. & 55 others, , 1 Jun 2025, In: Genetics in medicine. 27, 6, 101375.Research output: Contribution to journal › Article › Academic › peer-review
Open AccessFile32 Downloads (Pure)