S V Hodgson

5.0k total citations
46 papers, 1.8k citations indexed

About

S V Hodgson is a scholar working on Pathology and Forensic Medicine, Oncology and Genetics. According to data from OpenAlex, S V Hodgson has authored 46 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pathology and Forensic Medicine, 20 papers in Oncology and 19 papers in Genetics. Recurrent topics in S V Hodgson's work include Genetic factors in colorectal cancer (26 papers), Colorectal Cancer Screening and Detection (17 papers) and BRCA gene mutations in cancer (8 papers). S V Hodgson is often cited by papers focused on Genetic factors in colorectal cancer (26 papers), Colorectal Cancer Screening and Detection (17 papers) and BRCA gene mutations in cancer (8 papers). S V Hodgson collaborates with scholars based in United Kingdom, United States and Australia. S V Hodgson's co-authors include Ian Tomlinson, Walter F. Bodmer, R K S Phillips, S Cottrell, Kay Neale, S Whitelaw, Devendra Desai, Charis Eng, I C Talbot and Victoria Murday and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Gastroenterology.

In The Last Decade

S V Hodgson

45 papers receiving 1.7k citations

Peers

S V Hodgson

PFM

ONCOL

GENET

Julie Maynard United Kingdom

Sabine Bartnitzke Germany

Marianne Tiainen Finland

Wolfgang G. Ballhausen Germany

Chrystelle Colas France

Ettore Macrì Italy

Ian Tomlinson United Kingdom

Zimu Zheng United States

B A Gusterson United Kingdom

Debra M. Lillington United Kingdom

Julie Maynard United Kingdom

S V Hodgson

1.1k ×1.2

PFM

701 ×1.0

ONCOL

829 ×1.3

251 ×0.5

GENET

460 ×1.6

Citations per year, relative to S V Hodgson S V Hodgson (= 1×) peers Julie Maynard

Countries citing papers authored by S V Hodgson

Since Specialization

Citations

This map shows the geographic impact of S V Hodgson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by S V Hodgson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S V Hodgson more than expected).

Fields of papers citing papers by S V Hodgson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S V Hodgson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by S V Hodgson. The network helps show where S V Hodgson may publish in the future.

Co-authorship network of co-authors of S V Hodgson

This figure shows the co-authorship network connecting the top 25 collaborators of S V Hodgson. A scholar is included among the top collaborators of S V Hodgson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with S V Hodgson. S V Hodgson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Beggs, Andrew D., et al.. (2014). Expression and DNA methylation of TNF, IFNG and FOXP3 in colorectal cancer and their prognostic significance. British Journal of Cancer. 111(8). 1581–1589. 31 indexed citations

Nieuwenhuis, Marry H., C. Marleen Kets, Maureen Murphy‐Ryan, et al.. (2012). Is colorectal surveillance indicated in patients with PTEN mutations?. Colorectal Disease. 14(9). e562–6. 25 indexed citations

Jones, Angela M., Andrew D. Beggs, Luis G. Carvajal‐Carmona, et al.. (2011). TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres. Gut. 61(2). 248–254. 75 indexed citations

Johnson, Victoria, Lara Lipton, Amir Taher Eftekhar Sadat, et al.. (2005). Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families. Journal of Medical Genetics. 42(10). 756–762. 14 indexed citations

Sutton, Stephen, et al.. (2004). Anticipated reactions to genetic testing for hereditary non‐polyposis colorectal cancer susceptibility*. Clinical Genetics. 66(5). 437–444. 14 indexed citations

Tischkowitz, Marc, Neil V. Morgan, David Grimwade, et al.. (2004). Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia. Leukemia. 18(3). 420–425. 61 indexed citations

Lipton, Lara, Victoria Johnson, Peter Risby, et al.. (2004). Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic. Journal of Clinical Oncology. 22(24). 4934–4943. 84 indexed citations

Jaeger, E, K Woodford-Richens, Andrew Rowan, et al.. (2003). An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome. The American Journal of Human Genetics. 72(5). 1261–1267. 70 indexed citations

Tischkowitz, Marc, Neil V. Morgan, S V Hodgson, et al.. (2001). Mutation analysis of the Fanconi Anaemia group A, C, E, F and G genes in sporadic acute myeloid leukaemia. Journal of Medical Genetics. 38.

10.

Evans, Helen, Cathryn M. Lewis, David Robinson, et al.. (2001). Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England. British Journal of Cancer. 84(3). 435–440. 103 indexed citations

11.

Lipton, Lara, Huw Thomas, Rosalind A. Eeles, et al.. (2001). Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene?. Familial Cancer. 1(3-4). 189–195. 5 indexed citations

12.

Hodgson, S V, N E Haites, Maria A. Caligo, et al.. (2000). A survey of the current clinical facilities for the management of familial cancer in Europe: Table 1. Journal of Medical Genetics. 37(8). 605–607. 14 indexed citations

13.

Olavesen, Mark G., Jochen Hampe, Muddassar M. Mirza, et al.. (2000). Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease. Immunogenetics. 51(1). 1–7. 30 indexed citations

14.

Beck, N E, Ian Tomlinson, Tessa Homfray, et al.. (1997). Frequency of germline hereditary non-polyposis colorectal cancer gene mutations in patients with multiple or early onset colorectal adenomas. Gut. 41(2). 235–238. 17 indexed citations

15.

Whitelaw, S, I. Tomlinson, H. J. W. Thomas, et al.. (1997). Clinical and molecular features of the hereditary mixed polyposis syndrome. Gastroenterology. 112(2). 327–334. 100 indexed citations

16.

Patchett, Stephen, E M Alstead, Brian P. Saunders, S V Hodgson, & Michael J.G. Farthing. (1997). Regional proliferative patterns in the colon of patients at risk for hereditary nonpolyposis colorectal cancer. Diseases of the Colon & Rectum. 40(2). 168–171. 11 indexed citations

17.

Hodgson, S V, et al.. (1995). Two brothers with an unbalanced 8;17 translocation and infantile pyloric stenosis. Clinical Genetics. 48(6). 328–330. 13 indexed citations

18.

Nugent, Karen, et al.. (1994). Phenotypic expression in familial adenomatous polyposis: partial prediction by mutation analysis.. Gut. 35(11). 1622–1623. 95 indexed citations

19.

Muntoni, Francesco, Paola Gobbi, Caroline A. Sewry, et al.. (1994). Deletions in the 5' region of dystrophin and resulting phenotypes.. Journal of Medical Genetics. 31(11). 843–847. 66 indexed citations

20.

Hodgson, S V, et al.. (1986). A de novo X;13 translocation with abnormal phenotype.. Journal of Medical Genetics. 23(5). 477–478. 7 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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