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Researcher
Sascha Vermeer
- Disciplines:Genetics, Clinical genetics and molecular diagnostics
Affiliations
- Department of Human Genetics (Department)
Member
From19 Mar 2020 → Today
Publications
1 - 8 of 8
- Case Report: An Unusual Course of Angiosarcoma After Lung Transplantation(2022)
Authors: Lucienne Michaux, Isabelle Vanden Bempt, Sascha Vermeer, Patrick Schöffski, Birgit Weynand, Raphael Sciot, Laurens Ceulemans, Geert Verleden, Dirk Van Raemdonck, Lieven Dupont, et al.
Number of pages: 7 - Genetics in primary congenital glaucoma: Implications in disease management and counseling(2021)
Authors: Catherine Cassiman, Sascha Vermeer, Ingele Casteels
Number of pages: 8 - RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvement(2021)
Authors: Sien Van Daele, Sascha Vermeer, Hilde Van Esch, Kristl Claeys, Philip Van Damme
Pages: 345 - 349Number of pages: 5 - Diagnostic yield of testing for RFC1 repeat expansions in patients with unexplained adult-onset cerebellar ataxia(2020)
Authors: Sien Van Daele, Sascha Vermeer, Philip Van Damme, Kristl Claeys, Wim Vandenberghe
Pages: 1233 - 1234Number of pages: 2 - The Characteristic Eye Movement Disorder of RFC1-Linked CANVAS(2020)
Authors: Joke Terryn, Sascha Vermeer, Wim Vandenberghe
Pages: 230 - 231Number of pages: 2 - Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers(2019)
Authors: J van Gaalen, RPPWM Maas, EF Ippel, MW Elting, KY van Spaendonck-Zwarts, Sascha Vermeer, C Verschuuren-Bemelmans, D Timmann, Bart P van de Warrenburg
Pages: 427 - 433Number of pages: 7 - Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling(2015)
Authors: Hilde Van Esch, Sascha Vermeer
Pages: 343 - 352Number of pages: 10 - IRF6 screening of syndromic and a priori non-syndromic cleft lip and palatet patients: Identification of a new type of minor VWS sign(2010)
Authors: Koenraad Devriendt, Sascha Vermeer
Pages: 67 - 74