Shirley V. Hodgson

9.0k total citations · 1 hit paper
59 papers, 3.9k citations indexed

About

Shirley V. Hodgson is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Shirley V. Hodgson has authored 59 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 23 papers in Pathology and Forensic Medicine and 22 papers in Genetics. Recurrent topics in Shirley V. Hodgson's work include Genetic factors in colorectal cancer (23 papers), BRCA gene mutations in cancer (15 papers) and DNA Repair Mechanisms (13 papers). Shirley V. Hodgson is often cited by papers focused on Genetic factors in colorectal cancer (23 papers), BRCA gene mutations in cancer (15 papers) and DNA Repair Mechanisms (13 papers). Shirley V. Hodgson collaborates with scholars based in United Kingdom, United States and Netherlands. Shirley V. Hodgson's co-authors include Ian Tomlinson, Lara Lipton, Oliver M. Sieber, Robin Phillips, Huw Thomas, Christopher G. Mathew, Marc Tischkowitz, Lauri A. Aaltonen, Marie-Luise Bisgaard and Karl Heinimann and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Shirley V. Hodgson

57 papers receiving 3.8k citations

Hit Papers

Multiple Colorectal Adenomas, Classic Adenomatous Polypos... 2003 2026 2010 2018 2003 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Multiple Colorectal Adenomas, Classic Adenomatous Polyposis, and Germ-Line Mutations inMYH
    2003 596 citations Oliver M. Sieber, Lara Lipton et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Shirley V. Hodgson United Kingdom 29 1.7k 1.6k 1.2k 1.2k 1.2k 59 3.9k
Maurizio Genuardi Italy 38 2.3k 1.4× 1.8k 1.1× 1.3k 1.1× 1.7k 1.5× 1.1k 1.0× 203 5.1k
Rolf H. Sijmons Netherlands 41 1.7k 1.0× 2.3k 1.5× 1.9k 1.6× 1.6k 1.4× 1.4k 1.2× 147 5.1k
Ketil Heimdal Norway 29 1.2k 0.7× 1.1k 0.7× 1.0k 0.9× 1.5k 1.3× 787 0.7× 103 3.6k
Ian Tomlinson United Kingdom 30 1.4k 0.8× 1.6k 1.0× 1.2k 1.0× 502 0.4× 918 0.8× 48 3.2k
Fiona Lalloo United Kingdom 39 1.1k 0.6× 1.6k 1.1× 1.7k 1.4× 2.4k 2.1× 1.5k 1.3× 119 5.0k
Jennifer Saam United States 19 1.9k 1.1× 2.1k 1.3× 1.8k 1.5× 1.7k 1.4× 1.3k 1.1× 45 4.6k
B. A. J. Ponder United Kingdom 30 1.6k 0.9× 775 0.5× 994 0.8× 1.4k 1.2× 733 0.6× 54 3.7k
Hilmi Özçelik Canada 34 2.3k 1.3× 636 0.4× 1.2k 1.0× 1.1k 0.9× 758 0.6× 79 3.6k
David E. Goldgar France 37 2.1k 1.2× 820 0.5× 1.1k 1.0× 3.2k 2.7× 1.1k 0.9× 72 4.9k
Nicolaus Friedrichs Germany 30 1.7k 1.0× 936 0.6× 945 0.8× 403 0.3× 595 0.5× 75 3.3k

Countries citing papers authored by Shirley V. Hodgson

Since Specialization
Citations

This map shows the geographic impact of Shirley 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 Shirley 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 Shirley V. Hodgson more than expected).

Fields of papers citing papers by Shirley V. Hodgson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shirley 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 Shirley V. Hodgson. The network helps show where Shirley V. Hodgson may publish in the future.

Co-authorship network of co-authors of Shirley V. Hodgson

This figure shows the co-authorship network connecting the top 25 collaborators of Shirley V. Hodgson. A scholar is included among the top collaborators of Shirley 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 Shirley V. Hodgson. Shirley V. Hodgson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
El, Carla van, Martina C. Cornel, Pascal Borry, et al.. (2013). Whole-genome sequencing in health care. European Journal of Human Genetics. 21(6). 580–584. 256 indexed citations
2.
Church, David N., Sarah Briggs, Claire Palles, et al.. (2013). DNA polymerase ɛ and δ exonuclease domain mutations in endometrial cancer. Human Molecular Genetics. 22(14). 2820–2828. 262 indexed citations
3.
Nieuwenhuis, Marry H., C. Marleen Kets, Maureen Murphy‐Ryan, et al.. (2013). Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome. Familial Cancer. 13(1). 57–63. 91 indexed citations
4.
Beggs, Andrew D., Angela Jones, Neil A. Shepherd, et al.. (2013). Loss of Expression and Promoter Methylation of SLIT2 Are Associated with Sessile Serrated Adenoma Formation. PLoS Genetics. 9(5). e1003488–e1003488. 16 indexed citations
5.
El, Carla van, Martina C. Cornel, Pascal Borry, et al.. (2013). Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.. PubMed. 21 Suppl 1. S1–5. 270 indexed citations
6.
Beggs, Andrew D., et al.. (2012). Whole‐genome methylation analysis of benign and malignant colorectal tumours. The Journal of Pathology. 229(5). 697–704. 66 indexed citations
7.
Farrell, Michael, David J. Hughes, Ian Berry, et al.. (2012). Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome. Familial Cancer. 11(3). 509–518. 3 indexed citations
8.
Pollard, Patrick J., Mona El‐Bahrawy, Richard Poulsom, et al.. (2006). Expression of HIF-1α, HIF-2α (EPAS1), and Their Target Genes in Paraganglioma and Pheochromocytoma with VHL and SDH Mutations. The Journal of Clinical Endocrinology & Metabolism. 91(11). 4593–4598. 109 indexed citations
9.
Hodgson, Shirley V., Patrick J. Morrison, & Melita Irving. (2004). Breast cancer genetics: Unsolved questions and open perspectives in an expanding clinical practice. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 129C(1). 56–64. 14 indexed citations
10.
Halford, Sarah, Andrew Rowan, Lara Lipton, et al.. (2003). Germline Mutations but Not Somatic Changes at the MYH Locus Contribute to the Pathogenesis of Unselected Colorectal Cancers. American Journal Of Pathology. 162(5). 1545–1548. 102 indexed citations
11.
12.
Tischkowitz, Marc, Najim Ameziane, Quinten Waisfisz, et al.. (2003). Bi‐allelic silencing of the Fanconi anaemia gene FANCF in acute myeloid leukaemia. British Journal of Haematology. 123(3). 469–471. 48 indexed citations
13.
Morrison, Patrick J., Shirley V. Hodgson, & Neva E. Haites. (2002). Familial Breast and Ovarian Cancer: Genetics, Screening and Management. 97(3). 551–64. 6 indexed citations
14.
Thiselton, Dawn L., Ilaria Zito, Catherine Plant, et al.. (2000). Novel frameshift mutations in theRP2 gene and polymorphic variants. Human Mutation. 15(6). 580–580. 21 indexed citations
15.
Hodgson, Shirley V.. (1998). The genetics of learning disabilities. Developmental Medicine & Child Neurology. 40(2). 137–140. 4 indexed citations
16.
Ogilvie, Caroline Mackie, et al.. (1998). Deletion of chromosome 3q proximal region gives rise to a variable phenotype. Clinical Genetics. 53(3). 220–222. 24 indexed citations
17.
Johnson, Neil, Tim Lancaster, Alice Fuller, & Shirley V. Hodgson. (1995). The prevalence of a family history of cancer in general practice. Family Practice. 12(3). 287–289. 37 indexed citations
18.
MacGeoch, C., Diana M. Barnes, Julia A. Newton, et al.. (1993). p53 Protein Detected By Immunohistochemical Staining is Not Always Mutant. Disease Markers. 11(5-6). 239–250. 45 indexed citations
19.
Spigelman, Allan D., Shirley V. Hodgson, & J P S Thomson. (1992). Management of familial adenomatous polyposis. Baillière s Clinical Gastroenterology. 6(1). 75–94. 2 indexed citations
20.
Hodgson, Shirley V., Brian Neville, Richard W. Jones, Claudine Fear, & Martin Bobrow. (1985). Two cases of X/autosome translocation in females with incontinentia pigmenti. Human Genetics. 71(3). 231–234. 66 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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