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Nederlands Tijdschrift Voor Geneeskunde|March 28, 2001
[From gene to disease; fragile X-syndrome: hereditary mental retardation due to a developmental gene]L B de Vries, B A OostraClinical Genetics|June 10, 2011
CGG repeat in the FMR1 gene: size mattersR Willemsen, J Levenga, B A OostraJournal of Molecular Medicine (Berlin, Germany)|January 9, 2004
Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's diseaseVincenzo Bonifati, Ben A Oostra, Peter HeutinkCellular and Molecular Life Sciences : CMLS|July 9, 2004
Unraveling the pathogenesis of Parkinson's disease--the contribution of monogenic formsV Bonifati, B A Oostra, P HeutinkCurrent Neurology and Neuroscience Reports|September 1, 2005
FXTAS: a progressive neurologic syndrome associated with Fragile X premutationRob Willemsen, Edwin Mientjes, Ben A OostraThe Journal of Laryngology and Otology|August 12, 2009
Assessment of obstruction level and selection of patients for obstructive sleep apnoea surgery: an evidence-based approachC Georgalas, G Garas, E Hadjihannas, et al.Microscopy Research and Technique|July 12, 2002
Fragile X syndrome, the Fragile X related proteins, and animal modelsAndré T Hoogeveen, Rob Willemsen, Ben A OostraArchives of Disease in Childhood. Fetal and Neonatal Edition|October 19, 1999
Neonatal focal temporal lobe or atrial wall haemorrhagic infarctionP Govaert, K Smets, E Matthys, et al.Molecular Medicine Today|April 27, 2000
Fragile X syndrome at the turn of the centuryR F Kooy, R Willemsen, B 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 OostraPageof 51