A. T. Hoogeveen

Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.

Alessandra d’Azzo, A. T. Hoogeveen, Arnold Reuser et al. · Proceedings of the National Academy of Sciences · 1982 · 364 citations · Full text

Normal Human Fibroblasts, Glycobiology, Mature 64,000-Dalton Form +16

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

Fragile X Syndrome, Mendelian Disorder, Fmr-1 Gene Product +12

Characterization and localization of the Huntington disease gene product

A. T. Hoogeveen, Rob Willemsen, Nicolle Meyer et al. · Human Molecular Genetics · 1993 · 203 citations

Genetics, Immunology, Molecular Biology +16

Immunocytochemical and Biochemical Characterization of FMRP, FXR1P, and FXR2P in the Mouse

Cathy Bakker, Yolanda de Diego‐Otero, Carola Bontekoe et al. · Experimental Cell Research · 2000 · 193 citations

Inflammation, Knockout Mouse, Biochemical Characterization +10

Normal phenotype in two brothers with a full FMR1 mutation

H. J. M. Smeets, Anne Smits, Coleta Verheij et al. · Human Molecular Genetics · 1995 · 178 citations

Epigenetic Change, Genetics, Pathology +17