Shirley V. Hodgson - Concepedia

Author

Shirley V. Hodgson

Also Known As

Bernard, Loris, S V Hodgson, Shirley Hodgson, Shirley V Hodgson, Shirley V hodgson, Shirley V. Hodgson, Shirley Victoria Hodgson

136

Publications

Citations

H-Index

Concepts

All Affiliations

Guy's Hospital St George's, University of London Cancer Research UK St Mark's Hospital St George's Hospital

About

Shirley V. Hodgson is an author at Guy's Hospital specializing in medicine, pathology, and cancer research.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	23	3.9K
2	Health Sciences	1	1	47
3	Law	1	1	44
4	Natural Sciences	1	1	16
5	Nursing	1	1	49

Shirley V. Hodgson

Publications

8.7K

Citations

H-Index

Page 1

	Year	Citations
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial John Burn, Anne‐Marie Gerdes, Finlay Macrae, The Lancet Long-term EffectOncologyCancer EpidemiologyCancer RiskMedicine	2011	940
Multiple Colorectal Adenomas, Classic Adenomatous Polyposis, and Germ-Line Mutations in<i>MYH</i> Oliver M. Sieber, Lara Lipton, Michael Crabtree, New England Journal of Medicine	2003	859
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts Hans F. A. Vasen, Ignacio Blanco, Katja Aktan–Collan, Gut	2013	722
Disruption of the Fanconi anemia–BRCA pathway in cisplatin-sensitive ovarian tumors Toshiyasu Taniguchi, Marc Tischkowitz, Najim Ameziane, Nature Medicine Tumor BiologyOncologyMedicineCancer Cell BiologyGynecology	2003	540
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial John Burn, Harsh Sheth, Faye Elliott, The Lancet	2020	385
Whole-genome sequencing in health care Carla van El, Martina C. Cornel, Pascal Borry, European Journal of Human Genetics SequencingNext-generation SequencingGenomicsMedicineBioinformatics	2013	374
DNA polymerase ɛ and δ exonuclease domain mutations in endometrial cancer David N. Church, Sarah Briggs, Claire Palles, Human Molecular Genetics	2013	358
Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. Carla van El, Martina C. Cornel, Pascal Borry, PubMed Whole-genome SequencingSequencingMedicineGeneticsNext-generation Sequencing	2013	356
Tumor risks and genotypeâphenotypeâproteotype analysis in 358 patients with germline mutations in<i>SDHB</i>and<i>SDHD</i> Christopher J. Ricketts, Julia Forman, Eleanor Rattenberry, Human Mutation	2009	336
Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes* Xiaoping Zhou, K Woodford-Richens, Rainer Lehtonen, The American Journal of Human Genetics Genetic DisorderGeneticsPathogenesisPathologyJuvenile Polyposis Syndrome	2001	257

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