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Liselot Laan, van der
  • 224
    Citations
20222026

Research activity per year

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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, Abdul-Khaliq, H., Dähnert, I., Bu’Lock, F., Loughna, S., Brook, J. D., Mital, S., Russell, R. B., Pickardt, T., Bauer, U., Kramer, H.-H., Uebing, A., Henneman, P., Sadikovic, B., Postma, A. & Hitz, M.-P., 1 Dec 2026, In: Genome medicine. 18, 1, 2.

    Research output: Contribution to journalArticleAcademicpeer-review

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  • 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 journalArticleAcademicpeer-review

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    10 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 journalArticleAcademicpeer-review

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    26 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, Demaret, T., Denommé-Pichon, A.-S., Désir, J., Dubourg, C., Fradin, M. L., Geneviève, D., Goel, H., Goldenberg, A., Gripp, K. W., Guichet, A., Guimier, A., Jacquinet, A., Keren, B., Legoff, L., Levy, M. A., McConkey, H., Mendelsohn, B. A., Mignot, C., Milon, V., Nizon, M., Oneda, B., Pasquier, L., Patat, O., Philippe, C., Procaccio, V., Procopio, R., Prouteau, C., Rambaud, T., Rauch, A., Relator, R., Rondeau, S., Santen, G. W. E., Schleit, J., Sorlin, A., Steindl, K., Tedder, M., Tessarech, M., Mau-Them, F. T., Trost, D., van der Sluijs, P. J., Vincent, M., Whalen, S., Thauvin-Robinet, C., Isidor, B., Sadikovic, B., Vitobello, A. & Colin, E., Nov 2025, In: European journal of human genetics. 33, 11, p. 1422-1431 10 p., 100075.

    Research output: Contribution to journalArticleAcademicpeer-review

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    27 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, Stieber, D., Herissant, L., Dahan, K., Sinibaldi, L., Capolino, R., Dentici, M. L., Dallapiccola, B., Novelli, A., Garavelli, L., Caraffi, S. G., Piatelli, G., Valenzuela, I., Digilio, M. C., Caumes, R., Knopp, C., Chwiałkowska, K., Jezela-Stanek, A., Kwasniewski, M., Korotko, U., Gorzałczyńska, E., Canitano, R., Grosso, S., Rahikkala, E., Mattern, L., Elbracht, M., Zuffardi, O., Caputo, V., Toschi, B., Beunders, G., Leeuwen, L., Elting, M. W., van der Laan, L., Broekema, M. F., Groffen, A. J., van de Kamp, J. M., van Haelst, M. M., Alders, M., Mauro, S. P., de Razza, F., Varvara, D., Kick, J., Gaspar, H., Braun, D., Lausberg, E., Maier, A., Ruault, V., Genesio, R., Tartaglia, M., Tita, R., Bruttini, M., Longo, I., Baldassarri, M., Mencarelli, M. A., Renieri, A. & Pinto, A. M., 1 Jun 2025, In: Genetics in medicine. 27, 6, 101375.

    Research output: Contribution to journalArticleAcademicpeer-review

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    32 Downloads (Pure)