Lieve Vits

A point mutation in the FMR-1 gene associated with fragile X mental retardation

Kristel De Boulle, Annemieke J.M.H. Verkerk, Edwin Reyniers et al. · Nature Genetics · 1993 · 621 citations

Life Sciences, Genetics, Molecular Genetics +16

The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm

Edwin Reyniers, Lieve Vits, Kristel De Boulle et al. · Nature Genetics · 1993 · 304 citations

Life Sciences, Genetics, Molecular Genetics +14

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Gert Jansen, Patrick J. Willems, M. Coerwinkel et al. · PubMed · 1994 · 163 citations

Life Sciences, Genetics, Molecular Genetics +15

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM

Lieve Vits, Guy Van Camp, Paul Coucke et al. · Nature Genetics · 1994 · 154 citations

Life Sciences, Genetics, Molecular Genetics +10

Genotype-phenotype correlation in L1 associated diseases.

Eric Fransen, Guy Van Camp, Rudi D’Hooge et al. · Journal of Medical Genetics · 1998 · 113 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17