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About the author251A4E.N.M.M. von Scheibler, M. Kuijf, T.J. de Koning, J.R. Zinkstok, A. Muller, T.A.M.J. van Amelsvoort, A.M. van Eeghen, H.J.G. Boot. Parkinsonism in individuals with rare genetic neurodevelopmental disorders: A systematic review. Poster presentation at the Society of the Study of Behavioral Phenotypes conference, 2021.Emma N.M.M. von Scheibler, Josine C.C. Widdershoven, Denise C.P.B.M. van Barneveld, Nina Schröder, Agnies M. van Eeghen, Thérèse A.M.J. van Amelsvoort, Erik Boot. Age-related high-frequency hearing loss in adults with microdeletion 22q11.2. Oral presentation; 6th IASSIDD Europe congress 2021, Amsterdam, the Netherlands. Emma N.M.M. von Scheibler, Emy S. van der Valk Bouman, Tos T.J.M. Berendschot, Noël J.C. Bauer, Levinus A. Bok, Pit B.J. Vermeltfoort, Thérèse A.M.J. van Amelsvoort, Agnies M. van Eeghen, Michiel Houben, Erik Boot, Michelle B. van Egmond. Ocular findings in 142 individuals with 22q11.2 deletion syndrome. Oral presentation; 6th IASSIDD Europe congress 2021, Amsterdam, Netherlands. GrantsLes and Robbie Fountain bursary award by the Society of the Study of Behavioral Phenotypes (SSBP) to attend the international SSBP conference in Oslo, 2022.Mobility grant by the European Graduate School of Neuroscience for a one-month research and clinical internship at the Department of Human Genetics, University Hospital Leuven, Belgium.