Rosalina M.L. van Spaendonk

Clinical spectrum of 4H leukodystrophy caused by <i>POLR3A</i> and <i>POLR3B</i> mutations

Nicole I. Wolf, Adeline Vanderver, Rosalina M.L. van Spaendonk et al. · Neurology · 2014 · 203 citations · Full text

Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus

Gea Beunders, Els Voorhoeve, Christelle Golzio et al. · The American Journal of Human Genetics · 2013 · 185 citations · Full text

Exonic Deletions, Developmental Biology, Molecular Neuroscience +7

The selectable marker human dihydrofolate reductase enables sequential genetic manipulation of the Plasmodium berghei genome

Tania F. de Koning‐Ward, David A. Fidock, Vandana Thathy et al. · Molecular and Biochemical Parasitology · 2000 · 91 citations

Genetics, Malaria, Sequential Genetic Manipulation +11

Genetic subtyping of Fanconi anemia by comprehensive mutation screening

Najim Ameziane, Abdellatif Errami, France Léveillé et al. · Human Mutation · 2007 · 86 citations

Genetics, Immunology, Pathology +16

Functional Equivalence of Structurally Distinct Ribosomes in the Malaria Parasite, Plasmodium berghei

Rosalina M.L. van Spaendonk, Jai Ramesar, Auke van Wigcheren et al. · Journal of Biological Chemistry · 2001 · 81 citations · Full text