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A fragile balance: FMR1 expression levelsOOSTRA, Ben A; WILLEMSEN, Rob.Human molecular genetics (Print). 2003, Vol 12, pp R249-R257, issn 0964-6906, NS2Article

Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's diseaseBONIFATI, Vincenzo; OOSTRA, Ben A; HEUTINK, Peter et al.Journal of molecular medicine (Berlin. Print). 2004, Vol 82, Num 3, pp 163-174, issn 0946-2716, 12 p.Article

Rgs4 mRNA expression is decreased in the brain of Fmr1 knockout mouseTERVONEN, Topi; AKERMAN, Karl; OOSTRA, Ben A et al.Molecular brain research. 2005, Vol 133, Num 1, pp 162-165, issn 0169-328X, 4 p.Article

Chasing genes in Alzheimer's and Parkinson's diseaseBERTOLI-AVELLA, Aida M; OOSTRA, Ben A; HEUTINK, Peter et al.Human genetics. 2004, Vol 114, Num 5, pp 413-438, issn 0340-6717, 26 p.Article

FMRP detection assay for the diagnosis of the fragile X syndromeWILLEMSEN, Rob; OOSTRA, Ben A.American journal of medical genetics. 2000, Vol 97, Num 3, pp 183-188, issn 0148-7299Article

Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindredBREEDVELD, Guido J; FABBRINI, Giovanni; OOSTRA, Ben A et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 4, pp 417-423, issn 1364-6745, 7 p.Article

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatmentsTABOLACCI, Elisabetta; PIETROBONO, Roberta; MOSCATO, Umberto et al.European journal of human genetics. 2005, Vol 13, Num 5, pp 641-648, issn 1018-4813, 8 p.Article

Sculpting the brain - : The role of FMRP in synaptic plasticityREIS, Surya A; OOSTRA, Ben A; WILLEMSEN, Rob et al.The molecular basis of fragile X syndrome. 2005, pp 145-169, isbn 81-7736-257-7, 1Vol, 25 p.Book Chapter

Homozygous PINK1 C-terminus mutation causing early-onset parkinsonismROHE, Christan F; MONTAGNA, Pasquale; BREEDVELD, Guido et al.Annals of neurology. 2004, Vol 56, Num 3, pp 427-431, issn 0364-5134, 5 p.Article

Timing of the absence of FMR1 expression in full mutation chorionic villiWILLEMSEN, Rob; BONTEKOE, Carola J. M; SEVERIJNEN, Lies-Anne et al.Human genetics. 2002, Vol 110, Num 6, pp 601-605, issn 0340-6717Article

A Genome-Wide Association Study of Depressive SymptomsHEK, Karin; DEMIRKAN, Ayse; YONGMEI LIU et al.Biological psychiatry (1969). 2013, Vol 73, Num 7, pp 667-678, issn 0006-3223, 12 p.Article

Plasma phosphatidylcholine and sphingomyelin concentrations are associated with depression and anxiety symptoms in a Dutch family-based lipidomics studyDEMIRKAN, Ayşe; ISAACS, Aaron; SCHMITZ, Gerd et al.Journal of psychiatric research. 2013, Vol 47, Num 3, pp 357-362, issn 0022-3956, 6 p.Article

NPHP4 Variants Are Associated With Pleiotropic Heart MalformationsFRENCH, Vanessa M; DE LAAR, Ingrid M. B. H. Van; BREEDVELD, Guido et al.Circulation research. 2012, Vol 110, Num 12, pp 1564-1574, issn 0009-7330, 11 p.Article

Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individualsHEID, Iris M; HENNEMAN, Peter; TIMPSON, Nicholas J et al.Atherosclerosis. 2010, Vol 208, Num 2, pp 412-420, issn 0021-9150, 9 p.Article

Shared genetic factors in the co-occurrence of symptoms of depression and cardiovascular risk factorsLOPEZ-LEON, Sandra; AULCHENKO, Yurii S; TIEMEIER, Henning et al.Journal of affective disorders. 2010, Vol 122, Num 3, pp 247-252, issn 0165-0327, 6 p.Article

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosisAULCHENKO, Yurii S; HOPPENBROUWERS, Ilse A; GOOSSENS, Dirk et al.Nature genetics. 2008, Vol 40, Num 12, pp 1402-1403, issn 1061-4036, 2 p.Article

Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenesMUSUMECI, Sebastiano A; CALABRESE, Giuseppe; CATANIA, Maria Vincenza et al.Experimental neurology (Print). 2007, Vol 203, Num 1, pp 233-240, issn 0014-4886, 8 p.Article

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's diseaseDI FONZO, Alessio; ROHE, Christan F; GOLDWURM, Stefano et al.Lancet (British edition). 2005, Vol 365, Num 9457, pp 412-415, issn 0140-6736, 4 p.Article

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's diseaseMARTINEZ, Maria; BRICE, Alexis; HARDY, John et al.American journal of medical genetics. 2005, Vol 136B, Num 1, pp 72-74, issn 0148-7299, 3 p.Article

Novel parkin mutations detected in patients with early-onset Parkinson's diseaseGIROUD-BENITEZ, José L; AKYOL, Ali; STOCCHI, Fabrizio et al.Movement disorders. 2005, Vol 20, Num 4, pp 424-431, issn 0885-3185, 8 p.Article

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismBONIFATI, Vincenzo; RIZZU, Patrizia; VAN DONGEN, Jeroen W et al.Science (Washington, D.C.). 2003, Vol 299, Num 5604, pp 256-259, issn 0036-8075, 4 p.Article

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisNJAJOU, Omer T; VAESSEN, Norbert; VAN DUIJN, Cornelia M et al.Nature genetics. 2001, Vol 28, Num 3, pp 213-214, issn 1061-4036Article

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