Johannes van de Nes
Ruhr University Bochum(DE)
Publications by Year
Research Areas
Ocular Oncology and Treatments, Glioma Diagnosis and Treatment, Epigenetics and DNA Methylation, Neurofibromatosis and Schwannoma Cases, Genetic Syndromes and Imprinting
Most-Cited Works
- → Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3(2013)524 cited
- → Genetic and clinico-pathologic analysis of metastatic uveal melanoma(2013)91 cited
- → Targeted next generation sequencing reveals unique mutation profile of primary melanocytic tumors of the central nervous system(2016)81 cited
- → Imaging of adult astrocytic brain tumours with 7 T MRI: preliminary results(2009)56 cited
- → New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome(2017)44 cited
- → Absence of TERT promoter mutations in primary melanocytic tumours of the central nervous system(2014)23 cited
- → The C15orf2 gene in the Prader–Willi syndrome region is subject to genomic imprinting and positive selection(2009)23 cited
- → A broad spectrum of posterior reversible encephalopathy syndrome - a case series with clinical and paraclinical characterisation, and histopathological findings(2021)15 cited
- → Methylation analysis of SST and SSTR4 promoters in the neocortex of Alzheimer's disease patients(2014)12 cited
- → Diagnosing a Primary Leptomeningeal Melanoma by Gene Mutation Signature(2016)9 cited