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Ilse Meerschaut

  • Laarbeeklaan 101

    1090 Jette

    Belgium

  • Source: Scopus
  • Calculated based on number of publications stored in Pure and citations from Scopus
20152023

Research activity per year

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Personal profile

Education/Academic qualification

AEPC Certification of basic training in Paediatric and Congenital Cardiology, Association for European Paediatric and Congenital Cardiology

Award Date: 27 Apr 2023

Doctor in de Gezondheidswetenschappen., Ghent University

Award Date: 6 Dec 2021

Master in de Specialistische geneeskunde: pediatrie., Ghent University

Award Date: 4 Jul 2019

Postgraduate – Permanent Education Course on Human Genetics., Belgian Society of Human Genetics

Award Date: 8 Jun 2018

Master of Medicine in de geneeskunde: ziekenhuisarts., Ghent University

Award Date: 21 Jun 2012

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  • 1 Similar Profiles
  • Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice

    Sheppard, S. E., Bryant, L., Wickramasekara, R. N., Vaccaro, C., Robertson, B., Hallgren, J., Hulen, J., Watson, C. J., Faundes, V., Duffourd, Y., Lee, P., Simon, M. C., de la Cruz, X., Padilla, N., Flores-Mendez, M., Akizu, N., Smiler, J., Pellegrino Da Silva, R., Li, D., March, M. & 100 others, Diaz-Rosado, A., Peixoto de Barcelos, I., Choa, Z. X., Lim, C. Y., Dubourg, C., Journel, H., Demurger, F., Mulhern, M., Akman, C., Lippa, N., Andrews, M., Baldridge, D., Constantino, J., van Haeringen, A., Snoeck-Streef, I., Chow, P., Hing, A., Graham, J. M., Au, M., Faivre, L., Shen, W., Mao, R., Palumbos, J., Viskochil, D., Gahl, W., Tifft, C., Macnamara, E., Hauser, N., Miller, R., Maffeo, J., Afenjar, A., Doummar, D., Keren, B., Arn, P., Macklin-Mantia, S., Meerschaut, I., Callewaert, B., Reis, A., Zweier, C., Brewer, C., Saggar, A., Smeland, M. F., Kumar, A., Elmslie, F., Deshpande, C., Nizon, M., Cogne, B., van Ierland, Y., Wilke, M., van Slegtenhorst, M., Koudijs, S., Chen, J. Y., Dredge, D., Pier, D., Wortmann, S., Kamsteeg, E-J., Koch, J., Haynes, D., Pollack, L., Titheradge, H., Ranguin, K., Denommé-Pichon, A-S., Weber, S., Pérez de la Fuente, R., Sánchez Del Pozo, J., Lezana Rosales, J. M., Joset, P., Steindl, K., Rauch, A., Mei, D., Mari, F., Guerrini, R., Lespinasse, J., Tran Mau-Them, F., Philippe, C., Dauriat, B., Raymond, L., Moutton, S., Cueto-González, A. M., Tan, T. Y., Mignot, C., Grotto, S., Renaldo, F., Drivas, T. G., Hennessy, L., Raper, A., Parenti, I., Kaiser, F. J., Kuechler, A., Busk, Ø. L., Islam, L., Siedlik, J. A., Henderson, L. B., Juusola, J., Person, R., Schnur, R. E., Vitobello, A., Banka, S., Bhoj, E. J. & Stessman, H. A. F., Mar 2023, In: Science Advances. 9, 10, 16 p., eade1463.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
  • Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects

    Cappuccio, G., Brunetti‐Pierri, N., Clift, P., Learn, C., Dykes, J. C., Mercer, C. L., Callewaert, B., Meerschaut, I., Spinelli, A. M., Bruno, I., Gillespie, M. J., Dorfman, A. T., Grimberg, A., Lindsay, M. E. & Lin, A. E., May 2022, In: American Journal of Medical Genetics Part A. 188, 5, p. 1384-1395 12 p.

    Research output: Contribution to journalArticlepeer-review

  • Exploring the Mutational Landscape of Isolated Congenital Heart Defects: An Exome Sequencing Study Using Cardiac DNA

    Meerschaut, I., Steyaert, W., Bové, T., François, K., Martens, T., Groote, K. D., Wilde, H. D., Mosquera, L. M., Panzer, J., Vandekerckhove, K., Moons, L., Vermassen, P., Symoens, S., Coucke, P. J., Wolf, D. D. & Callewaert, B., 7 Jul 2022, In: Genes. 13, 7, p. 1-12 12 p., 1214.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    2 Citations (Scopus)
    13 Downloads (Pure)
  • Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases

    Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., Zechi‐Ceide, R., Kokitsu‐Nakata, N. M., Kido, Y., Marlin, S., Halem, S. G., Meerschaut, I., Callewaert, B., Chung, H. Y. B., Revencu, N., Lehalle, D., petit, F., Propst, E. J., Papsin, B. C., Phillips, J. H. & 17 others, Jakobsen, L., Tanno, P. L., Thévenon, J., McGaughran, J., Gerkes, E. H., Leoni, C., Kroisel, P., Tan, T. Y., Henderson, A., Terhal, P., Basel‐Salmon, L., Alkindy, A., White, S. M., Passos‐Bueno, M. R., Pingault, V., Pontual, L. D. & Amiel, J., May 2022, In: Human Mutation. 43, 5, p. 582-594 13 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
  • A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome

    Meerschaut, I., Vergult, S., Dheedene, A., Menten, B., Groote, K. D., Wilde, H. D., Mosquera, L. M., Panzer, J., Vandekerckhove, K., Coucke, P. J., Wolf, D. D. & Callewaert, B., Jul 2021, In: Genes. 12, 7, 16 p., 1048.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    5 Citations (Scopus)