Constanze Walldorf

Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC

Monika Morak, Hans Konrad Schackert, Nils Rahner et al. · European Journal of Human Genetics · 2008 · 124 citations

Medicine, Genetics, Molecular Genetics +10

DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation

Hartmut Engels, Antje Brockschmidt, Alexander Hoischen et al. · Neurology · 2007 · 94 citations

Life Sciences, Genetics, Molecular Genetics +17

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1

Stefan Krüger, Miriam Kinzel, Constanze Walldorf et al. · European Journal of Human Genetics · 2007 · 89 citations · Full text

Life Sciences, Hematology, Oncology +14

Coexisting somatic promoter hypermethylation and pathogenic <i>MLH1</i> germline mutation in Lynch syndrome

Nils Rahner, Nicolaus Friedrichs, Verena Steinke et al. · The Journal of Pathology · 2007 · 75 citations

Life Sciences, Genetics, Oncology +17

Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation

Christian H Brenk, Eva‐Christina Prott, Detlef Trost et al. · European Journal of Human Genetics · 2006 · 49 citations

Life Sciences, Genetics, Molecular Genetics +12