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Microscopy Research and Technique|July 12, 2002
Fragile X syndrome, the Fragile X related proteins, and animal modelsAndré T Hoogeveen, Rob Willemsen, Ben A OostraBioessays : News and Reviews in Molecular, Cellular and Developmental Biology|January 21, 2009
Microsatellite repeat instability and neurological diseaseJudith R Brouwer, Rob Willemsen, Ben A OostraJournal of Molecular Histology|July 6, 2006
Isolation of mouse neuritic mRNAsSurya A Reis, Ben A Oostra, Rob WillemsenBrain Research. Molecular Brain Research|January 22, 2005
Rgs4 mRNA expression is decreased in the brain of Fmr1 knockout mouseTopi Tervonen, Karl Akerman, Ben A Oostra, et al.Human Genetics|March 5, 2004
Chasing genes in Alzheimer's and Parkinson's diseaseAida M Bertoli-Avella, Ben A Oostra, Peter HeutinkEuropean Journal of Ophthalmology|March 19, 2024
Inherited retinal dystrophies and orphan designations in the European UnionJane Moseley, Tim Leest, Kristina Larsson, et al.Mental Retardation and Developmental Disabilities Research Reviews|March 3, 2004
The fragile X syndrome: from molecular genetics to neurobiologyRob Willemsen, Ben A Oostra, Gary J Bassell, et al.Human Genetics|July 11, 2002
Timing of the absence of FMR1 expression in full mutation chorionic villiRob Willemsen, Carola J M Bontekoe, Lies-Anne Severijnen, et al.Trends in Molecular Medicine|September 25, 2010
Potential therapeutic interventions for fragile X syndromeJosien Levenga, Femke M S de Vrij, Ben A Oostra, et al.Neurogenetics|May 4, 2010
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindredGuido J Breedveld, Giovanni Fabbrini, Ben A Oostra, et al.Pageof 31