Edwin Reyniers

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 · 619 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

David A. Koolen, Lisenka E.L.M. Vissers, Rolph Pfundt et al. · Nature Genetics · 2006 · 466 citations

Genetic Disorder, Genetics, Common Inversion Polymorphism +9

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 · 303 citations

Spermatogenesis, Infertility, Developmental Biology +14

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome

Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer et al. · European Journal of Medical Genetics · 2009 · 215 citations

Developmental Biology, Genetic Disorder, Genetics +7

Mildly impaired water maze performance in maleFmr1 knockout mice

Rudi D’Hooge, Guy Nagels, F. Franck et al. · Neuroscience · 1997 · 208 citations

Knockout Mouse, Behavioral Neuroscience, Physiology +3