Edmund Cheesman - Concepedia

Concepedia

Author

Edmund Cheesman

Royal Manchester Children's Hospital ORCID

Also Known As

A Dashwood, Cheesman E, E Cheesman, E. Cheesman, Edmund Cheesman

57

Publications

1.1K

Citations

15

H-Index

30

Concepts

All Affiliations

Royal Manchester Children's Hospital University of Manchester Royal Devon & Exeter NHS Foundation Trust University of Exeter Manchester University NHS Foundation Trust

EC

About

Edmund Cheesman is an author at Royal Manchester Children's Hospital specializing in medicine, pathology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	275
2	Cell Biology	3	3	229
3	Diabetes	1	1	29
4	Immunology	1	1	29
5	Molecular Genetics	1	1	29

Edmund Cheesman

×

19

Publications

1.1K

Citations

15

H-Index

	Year	Citations
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, Journal of Clinical Oncology	2014	294
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, Acta Neuropathologica GliomaTumor HeterogeneityRecurrent Gene FusionsMalignant DiseaseDistinct Tumour Entity	2019	128
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, Science Immunology	2019	108
Increased Risk for Malignancies in 131 Affected CTLA4 Mutation Carriers David Egg, Charlotte Schwab, Annemarie Gabrysch, Frontiers in Immunology	2018	99
Frequent Derepression of the Mesenchymal Transcription Factor Gene FOXC1 in Acute Myeloid Leukemia Tim D.D. Somerville, Daniel H. Wiseman, Gary J. Spencer, Cancer Cell Hematological MalignancyChromatinTranscriptional RegulationGeneticsAcute Myeloid Leukemia	2015	72
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism Matthew N. Wakeling, Nick Owens, Jessica R. Hopkinson, Nature Genetics	2022	57
Intracranial Angiomatoid Fibrous Histiocytoma with EWSR1-CREB Family Fusions: A Report of 2 Pediatric Cases Athanasios Konstantinidis, Edmund Cheesman, James O’Sullivan, World Neurosurgery Pediatric CasesEwsr1-creb Family FusionsPathology	2019	45
Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease Bing Han, Melanie Newbould, Gauri Batra, American Journal of Clinical Pathology	2016	41
Papillary craniopharyngioma in a 4-year-old girl with BRAF V600E mutation: a case report and review of the literature Roisin Borrill, Edmund Cheesman, Stavros Stivaros, Child s Nervous System	2018	40
Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinism Jayne Houghton, Indraneel Banerjee, Guftar Shaikh, The Journal of Pathology Clinical Research Genetic CausesGeneticsImmunologyPathologyMolecular Genetics	2019	29

Page 1