Annemieke J.M.H. Verkerk

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe et al. · Cell · 1991 · 3.5K citations

Life Sciences, Genetics, Molecular Genetics +12

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

Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

Joseph Borg, Petros Papadopoulos, Marianthi Georgitsi et al. · Nature Genetics · 2010 · 377 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

Coleta Verheij, Cathy Bakker, Esther de Graaff et al. · Nature · 1993 · 340 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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