Barbara C. Godthelp

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Marieke Levitus, Quinten Waisfisz, Barbara C. Godthelp et al. · Nature Genetics · 2005 · 430 citations · Full text

Dna Helicase Brip1, Genetic Disorder, Natural Sciences +6

Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

Petra van der Lelij, Krystyńa Chrzańowska, Barbara C. Godthelp et al. · The American Journal of Human Genetics · 2010 · 270 citations · Full text

Mendelian Disorder, Warsaw Breakage Syndrome, Genetic Disorder +9

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability

Barbara C. Godthelp · Nucleic Acids Research · 2002 · 145 citations · Full text

Genetics, Genomic Mechanism, Molecular Biology +17

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

Thiyam Ramsing Singh, Sietske T. Bakker, Sheba Agarwal et al. · Blood · 2009 · 135 citations · Full text

Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair

Mischa G. Vrouwe, Elhaam Elghalbzouri-Maghrani, Matty Meijers et al. · Human Molecular Genetics · 2007 · 105 citations · Full text