Edmund Cheesman

Germline Mutations in <i>SUFU</i> Cause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated With <i>PTCH1</i> Mutations

Miriam J. Smith, Christian Beetz, Simon G. Williams et al. · Journal of Clinical Oncology · 2014 · 294 citations

Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course

Annika K. Wefers, Damian Stichel, Daniel Schrimpf et al. · Acta Neuropathologica · 2019 · 128 citations · Full text

Glioma, Tumor Heterogeneity, Recurrent Gene Fusions +10

Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>

C.J. Duncan, Benjamin Thompson, Rui Chen et al. · Science Immunology · 2019 · 108 citations · Full text

Increased Risk for Malignancies in 131 Affected CTLA4 Mutation Carriers

David Egg, Charlotte Schwab, Annemarie Gabrysch et al. · Frontiers in Immunology · 2018 · 99 citations · Full text

Frequent Derepression of the Mesenchymal Transcription Factor Gene FOXC1 in Acute Myeloid Leukemia

Tim D.D. Somerville, Daniel H. Wiseman, Gary J. Spencer et al. · Cancer Cell · 2015 · 72 citations · Full text

Hematological Malignancy, Chromatin, Transcriptional Regulation +9