Ben A. Oostra
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genetic Associations and Epidemiology, Autism Spectrum Disorder Research, Epigenetics and DNA Methylation, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Biological, clinical and population relevance of 95 loci for blood lipids(2010)3,661 cited
- → Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17(1998)3,499 cited
- → Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome(1991)3,494 cited
- → Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox(1991)2,092 cited
- → Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits(1997)1,035 cited
- → Identification of seven loci affecting mean telomere length and their association with disease(2013)955 cited
- → Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts(2008)859 cited
- → New loci associated with kidney function and chronic kidney disease(2010)802 cited
- → Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior(2010)692 cited
- → A point mutation in the FMR-1 gene associated with fragile X mental retardation(1993)619 cited