Gea Beunders

DR.

Affiliatie UvA Medical Specialist, Human Genetics Medical Specialist, Human Genetics

Specialization

Focus of research

clinical genetics

genetics of neurodevelopemental problems

Latest publications

DLG4-related synaptopathy: a new rare brain disorder: a new rare brain disorder
Rodríguez-Palmero, A., Boerrigter, M. M., Gómez-Andrés, D., Aldinger, K. A., Marcos-Alcalde, Í., Popp, B., Everman, D. B., Lovgren, A. K., Arpin, S., Bahrambeigi, V., Beunders, G., Bisgaard, A.-M., Bjerregaard, V. A., Bruel, A.-L., Challman, T. D., Cogné, B., Coubes, C., de Man, S. A., Denommé-Pichon, A.-S. & Dye, T. J. & 66 others, Elmslie, F., Feuk, L., García-Miñaúr, S., Gertler, T., Giorgio, E., Gruchy, N., Haack, T. B., Haldeman-Englert, C. R., Haukanes, B. I., Hoyer, J., Hurst, A. C. E., Isidor, B., Soller, M. J., Kushary, S., Kvarnung, M., Landau, Y. E., Leppig, K. A., Lindstrand, A., Kleinendorst, L., MacKenzie, A., Mandrile, G., Mendelsohn, B. A., Moghadasi, S., Morton, J. E., Moutton, S., Müller, A. J., O’Leary, M., Pacio-Míguez, M., Palomares-Bralo, M., Parikh, S., Pfundt, R., Pode-Shakked, B., Rauch, A., Repnikova, E., Revah-Politi, A., Ross, M. J., Ruivenkamp, C. A. L., Sarrazin, E., Savatt, J. M., Schlüter, A., Schönewolf-Greulich, B., Shad, Z., Shaw-Smith, C., Shieh, J. T., Shohat, M., Spranger, S., Thiese, H., Mau-Them, F. T., van Bon, B., van de Burgt, I., van de Laar, I. M. B. H., van Drie, E., van Haelst, M. M., van Ravenswaaij-Arts, C. M., Verdura, E., Vitobello, A., Waldmüller, S., Whiting, S., Zweier, C., Prada, C. E., de Vries, B. B. A., Dobyns, W. B., Reiter, S. F., Gómez-Puertas, P., Pujol, A. & Tümer, Z., May 2021, In: Genetics in medicine. 23, 5, p. 888-899 12 p.
Research output: Contribution to journal › Article* › Academic › peer-review
Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives: Feasibility and parental perspectives
Beunders, G., Dekker, M., Haver, O., Meijers-Heijboer, H. J. & Henneman, L., Apr 2018, In: European journal of medical genetics. 61, 4, p. 213-218
Research output: Contribution to journal › Article* › Academic › peer-review
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
Beunders, G., Voorhoeve, E., Golzio, C., Pardo, L. M., Rosenfeld, J. A., Talkowski, M. E., Simonic, I., Lionel, A. C., Vergult, S., Pyatt, R. E., Van De Kamp, J., Nieuwint, A., Weiss, M. M., Rizzu, P., Verwer, L. E. N. I., Van Spaendonk, R. M. L., Shen, Y., Wu, B. L., Yu, T. & Yu, Y. & 43 others, Chiang, C., Gusella, J. F., Lindgren, A. M., Morton, C. C., Van Binsbergen, E., Bulk, S., Van Rossem, E., Vanakker, O., Armstrong, R., Park, S. M., Greenhalgh, L., Maye, U., Neill, N. J., Abbott, K. M., Sell, S., Ladda, R., Farber, D. M., Bader, P. I., Cushing, T., Drautz, J. M., Konczal, L., Nash, P., De Los Reyes, E., Carter, M. T., Hopkins, E., Marshall, C. R., Osborne, L. R., Gripp, K. W., Thrush, D. L., Hashimoto, S., Gastier-Foster, J. M., Astbury, C., Ylstra, B., Meijers-Heijboer, H., Posthuma, D., Menten, B., Mortier, G., Scherer, S. W., Eichler, E. E., Girirajan, S., Katsanis, N., Groffen, A. J. & Sistermans, E. A., 7 Feb 2013, In: American journal of human genetics. 92, 2, p. 210-220 11 p.
Research output: Contribution to journal › Article* › Academic › peer-review
All publications

Gea Beunders

Specialization

Focus of research

DLG4-related synaptopathy: a new rare brain disorder: a new rare brain disorder

Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives: Feasibility and parental perspectives

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus

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