Lynn Greenhalgh

6.1k total citations
11 papers, 507 citations indexed

About

Lynn Greenhalgh is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lynn Greenhalgh has authored 11 papers receiving a total of 507 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Pathology and Forensic Medicine and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lynn Greenhalgh's work include RNA modifications and cancer (2 papers), Cancer Genomics and Diagnostics (2 papers) and Genetic factors in colorectal cancer (2 papers). Lynn Greenhalgh is often cited by papers focused on RNA modifications and cancer (2 papers), Cancer Genomics and Diagnostics (2 papers) and Genetic factors in colorectal cancer (2 papers). Lynn Greenhalgh collaborates with scholars based in United Kingdom, United States and Australia. Lynn Greenhalgh's co-authors include Ruth Newbury‐Ecob, Richard Caswell, Thalia Antoniadi, Weijia Xie, Konrad Paszkiewicz, Robert Hastings, Michael N. Weedon, Maggie Williams, Sian Ellard and Judith G. Hall and has published in prestigious journals such as Journal of Clinical Oncology, The American Journal of Human Genetics and Human Reproduction.

In The Last Decade

Lynn Greenhalgh

11 papers receiving 498 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lynn Greenhalgh United Kingdom 8 226 181 87 80 62 11 507
Annick Francis Belgium 11 496 2.2× 125 0.7× 80 0.9× 106 1.3× 54 0.9× 16 800
Karine Sii-Felice France 14 418 1.8× 99 0.5× 55 0.6× 53 0.7× 102 1.6× 17 589
Fatema Alzahrani Saudi Arabia 14 430 1.9× 386 2.1× 33 0.4× 62 0.8× 55 0.9× 25 724
Raimund Fahsold Germany 14 344 1.5× 159 0.9× 85 1.0× 50 0.6× 27 0.4× 27 777
V. Ventruto Italy 17 479 2.1× 288 1.6× 37 0.4× 87 1.1× 81 1.3× 48 792
Ellen A.W. Blokland Netherlands 10 528 2.3× 165 0.9× 66 0.8× 103 1.3× 90 1.5× 11 721
R. Cinti Italy 13 280 1.2× 99 0.5× 91 1.0× 42 0.5× 51 0.8× 23 548
Laura Kerosuo United States 15 411 1.8× 90 0.5× 69 0.8× 70 0.9× 62 1.0× 27 643
Marie Trková Czechia 13 272 1.2× 145 0.8× 19 0.2× 21 0.3× 110 1.8× 33 589
Dayana Krawchuk Canada 9 623 2.8× 119 0.7× 142 1.6× 166 2.1× 33 0.5× 10 814

Countries citing papers authored by Lynn Greenhalgh

Since Specialization
Citations

This map shows the geographic impact of Lynn Greenhalgh'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 Lynn Greenhalgh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lynn Greenhalgh more than expected).

Fields of papers citing papers by Lynn Greenhalgh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lynn Greenhalgh. 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 Lynn Greenhalgh. The network helps show where Lynn Greenhalgh may publish in the future.

Co-authorship network of co-authors of Lynn Greenhalgh

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

All Works

11 of 11 papers shown
1.
Wai, Htoo A., Tessy Thomas, David J. Bunyan, et al.. (2022). A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project. Genome Medicine. 14(1). 79–79. 20 indexed citations
2.
Baynam, Gareth, Lisa Ewans, Lynn Greenhalgh, et al.. (2022). Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome. American Journal of Neuroradiology. 43(11). 1660–1666. 1 indexed citations
3.
Martin, Antony P., et al.. (2018). Mainstreaming BRCA mutation testing for ovarian cancer patients: Addressing health inequalities.. Journal of Clinical Oncology. 36(15_suppl). e18526–e18526. 1 indexed citations
4.
Campbell, Fiona, et al.. (2017). Identifying Lynch Syndrome in Women Presenting With Endometrial Carcinoma Under the Age of 50 Years. International Journal of Gynecological Cancer. 27(5). 931–937. 13 indexed citations
5.
McKay, Victoria, et al.. (2015). First report of somatic mosaicism for mutations in STK11 in four patients with Peutz–Jeghers syndrome. Familial Cancer. 15(1). 57–61. 16 indexed citations
6.
Weedon, Michael N., Robert Hastings, Richard Caswell, et al.. (2011). Exome Sequencing Identifies a DYNC1H1 Mutation in a Large Pedigree with Dominant Axonal Charcot-Marie-Tooth Disease. The American Journal of Human Genetics. 89(2). 308–312. 200 indexed citations
7.
Becker, Kristin, Oliver FitzGerald, Andrew Green, et al.. (2009). Constitutional trisomy 8 and Behçet syndrome. American Journal of Medical Genetics Part A. 149A(5). 982–986. 19 indexed citations
8.
Klopocki, Eva, Harald Schulze, Gabriele Strauß, et al.. (2007). Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome. The American Journal of Human Genetics. 80(2). 232–240. 201 indexed citations
9.
Kalidas, Kamini, Adam Shaw, Andrew H. Crosby, et al.. (2004). Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11. Journal of Human Genetics. 50(1). 21–25. 19 indexed citations
10.
Greenhalgh, Lynn & K.F. Miller. (1997). Donor insemination. Prevalence of antibodies to cytomegalovirus.. PubMed. 42(2). 111–3. 3 indexed citations
11.
Schover, Leslie R., et al.. (1994). Psychological screening and the success of donor insemination. Human Reproduction. 9(1). 176–178. 14 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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