Randi Koll

Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E

Eva Klopocki, Bianca P. Hennig, Katarina Dathe et al. · The American Journal of Human Genetics · 2010 · 144 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

The genomic and transcriptional landscape of primary central nervous system lymphoma

Josefine Radke, Naveed Ishaque, Randi Koll et al. · Nature Communications · 2022 · 140 citations · Full text

Life Sciences, Molecular Biology, Oncology +17

Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis

Eva Klopocki, Silke B. Lohan, Francesco Brancati et al. · The American Journal of Human Genetics · 2010 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Predictive MGMT status in a homogeneous cohort of IDH wildtype glioblastoma patients

Josefine Radke, Arend Koch, Fabienne Pritsch et al. · Acta Neuropathologica Communications · 2019 · 97 citations · Full text

Medicine, Cancer Biology, Oncology +17

Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4

Pablo Villavicencio‐Lorini, Eva Klopocki, Marc Trimborn et al. · European Journal of Human Genetics · 2012 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8