Paul O’Donnell - Concepedia

Author

Paul O’Donnell

Also Known As

Dr. Paul O’Donnell, P J O'Donnell, P O'Donnell, P. O'Donnell, P. O’Donnell, P.J. O'DONNELL, P.J. O'Donnell, P.J. O'donnell, P.J. O’DONNELL, PT O'Donnell

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

University College London Royal National Orthopaedic Hospital Royal National Orthopaedic Hospital NHS Trust Stanmore College CRUK Lung Cancer Centre of Excellence

About

Paul O’Donnell is an author at University College London specializing in medicine, pathology, and surgical pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	25	2.6K
2	Health Sciences	3	3	55
3	Anatomy	2	2	73
4	Engineering	1	1	109
5	Natural Sciences	1	1	213

Paul O’Donnell

Publications

Citations

H-Index

Page 1

	Year	Citations
<i>IDH1</i> and <i>IDH2</i> mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours Maria Fernanda Amary, Krisztian Bacsi, Francesca Maggiani, The Journal of Pathology Cartilaginous TumoursGeneticsPathologyGliomaTumor Biology	2011	966
Brachyury Expression in Extra-axial Skeletal and Soft Tissue Chordomas: A Marker that Distinguishes Chordoma From Mixed Tumor/Myoepithelioma/Parachordoma in Soft Tissue Roberto Tirabosco, D. Chas Mangham, Andrew E. Rosenberg, The American Journal of Surgical Pathology Surgical OncologySoft Tissue ChordomasTumoral PathologyMedicineSurgical Pathology	2008	244
H3F3A (Histone 3.3) G34W Immunohistochemistry Fernanda Amary, Fitim Berisha, Hongtao Ye, The American Journal of Surgical Pathology Epigenetic ChangeMolecular BiologyPathologyEpigeneticsTumor Biology	2017	213
MRI characteristics of lipoma and atypical lipomatous tumor/well-differentiated liposarcoma: retrospective comparison with histology and MDM2 gene amplification Mélanie Brisson, Takeshi Kashima, David Delaney, Skeletal Radiology Tumoral PathologyRetrospective ComparisonMri CharacteristicsMedicineSurgical Pathology	2012	139
The H3F3 K36M mutant antibody is a sensitive and specific marker for the diagnosis of chondroblastoma Maria Fernanda Amary, Fitim Berisha, Rafael Mozela, Histopathology	2016	134
A sensitive mutation‐specific screening technique for <i>GNAS1</i> mutations in cases of fibrous dysplasia: the first report of a codon 227 mutation in bone Bernadine Idowu, Mudher Al‐Adnani, Paul O’Donnell, Histopathology	2007	115
A Simple Automated Instrument for DNA Extraction in Forensic Casework IT Fitch, Paul O’Donnell Journal of Forensic Sciences EngineeringSample TreatmentDna AnalysisMolecular BiologyInformation Forensics	2005	109
Detection of β-Catenin Mutations in Paraffin-embedded Sporadic Desmoid-type Fibromatosis by Mutation-specific Restriction Enzyme Digestion (MSRED): an Ancillary Diagnostic Tool Maria Fernanda Amary, Patrick Pauwels, Els V. Meulemans, The American Journal of Surgical Pathology FibrosisMolecular Diagnostic TechniquesSomatic VariantGenetic DisorderMedicine	2007	106
Synovial chondromatosis and soft tissue chondroma: extraosseous cartilaginous tumor defined by FN1 gene rearrangement Fernanda Amary, Luis Pérez-Casanova, Hongtao Ye, Modern Pathology Soft Tissue ChondromaCartilage DegenerationPathologyExtraosseous Cartilaginous TumorMedicine	2019	100
GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma David Delaney, Tim C. Diss, Nadège Presneau, Modern Pathology Somatic VariantIntramuscular MyxomaMedicinePathologyGnas1 Mutations	2009	88

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