Gordon Glendon

500 citations
8 papers · 256 · h-index 6

Impact in

  • Genetics top 10%
    • BRCA gene mutations in cancer
    • Global Cancer Incidence and Screening
    • Cancer Risks and Factors
    • Cancer survivorship and care

Papers in

Gordon Glendon

8 papers receiving 246 citations

Peers

Gordon Glendon
Comparison fields: 5 of 40
  • Genetics 165
  • Oncology 64
  • Pediatrics, Perinatology and Child Health 42
  • Reproductive Medicine 16
  • Cancer Research 19
Replace Danielle Hanna with:
Danielle Hanna Canada
Mary E. Velthuizen Netherlands
Robin Lee United States
Sherry Grumet United States
F Chabal France
Joyce Seldon United States
Anna von Wachenfeldt Sweden
Amanda Brandt United States
Kirsten F. L. Douma Netherlands
Patti M. Wilcox United States
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Citations per field
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Citations per year

Countries citing papers authored by Gordon Glendon

Since Specialization
Citations

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

Fields of papers citing papers by Gordon Glendon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gordon Glendon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gordon Glendon Line = papers co-authored together Gordon Glendon links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1 199975
2 200948
3 200045
4 200036
5 200230
6 199818
7 20222
8 20002

About Gordon Glendon

Gordon Glendon is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Sociology and Political Science, Reproductive Medicine and Pathology and Forensic Medicine, having authored 8 papers that have together received 256 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (7 papers), Childhood Cancer Survivors' Quality of Life (1 paper), Genetic factors in colorectal cancer (1 paper), Prenatal Screening and Diagnostics (1 paper), Reproductive Health and Technologies (1 paper), Global Cancer Incidence and Screening (1 paper), Family Support in Illness (1 paper) and Ovarian cancer diagnosis and treatment (1 paper). The work is most often cited by research in Genetics (165 citations), Oncology (64 citations), Pediatrics, Perinatology and Child Health (42 citations), Reproductive Medicine (16 citations) and Cancer Research (19 citations). Gordon Glendon has collaborated with scholars based in Canada, United States and Australia. Frequent co-authors include Kelly‐Anne Phillips, Julia A. Knight, Jonathan Hunter, Mary Jane Esplen, Noreen Stuckless, Alexander Liede, Kate Butler, Brenda B. Toner, Wendy S. Meschino and Irene L. Andrulis. Their work appears in journals such as Psycho-Oncology, The Journal of Pediatrics, Clinical Genetics, The Canadian Journal of Psychiatry and New England Journal of Medicine.

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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