Annekatrin Wernstedt

The NF1 Gene Contains Hotspots for L1 Endonuclease-Dependent De Novo Insertion

Katharina Wimmer, Tom Callens, Annekatrin Wernstedt et al. · PLoS Genetics · 2011 · 107 citations · Full text

Multiple pilomatricomas with somatic <i>CTNNB1</i> mutations in children with constitutive mismatch repair deficiency

Magdalena Chmara, Annekatrin Wernstedt, Bartosz Wasąg et al. · Genes Chromosomes and Cancer · 2013 · 51 citations

Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome

Annette F. Baas, Michael T. Gabbett, Milan Rimac et al. · European Journal of Human Genetics · 2012 · 49 citations · Full text

Gray Matter Heterotopia, Corpus Callosum, Neuropathology

Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient with a constitutional PMS2 deficiency

Peter Vasovčák, Anna Křepelová, Mirco Menigatti et al. · DNA repair · 2012 · 39 citations · Full text

AG‐exclusion zone revisited: Lessons to learn from 91 intronic NF1 3′ splice site mutations outside the canonical AG‐dinucleotides

Katharina Wimmer, Esther Schamschula, Annekatrin Wernstedt et al. · Human Mutation · 2020 · 32 citations · Full text