Diana Eccles

36.9k citations
141 papers · 7.3k · 3 hit papers · h-index 44

Impact in

  • Genetics top 0.2%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Cancer Genomics and Diagnostics
    • Breast Cancer Treatment Studies

Papers in

    • BRCA gene mutations in cancer 63
    • Genomic variations and chromosomal abnormalities 9
    • Genetic Associations and Epidemiology 8
    • DNA Repair Mechanisms 15

Diana Eccles

136 papers receiving 7.0k citations

Diana Eccles's Hit Papers

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles 2006 · 541 citations
5410+6+13Years since publication200400600

Peers

Diana Eccles
Comparison fields: 5 of 135
  • Genetics 3.4k
  • Cancer Research 1.6k
  • Pathology and Forensic Medicine 1.6k
  • Oncology 1.8k
  • Reproductive Medicine 307
Replace Deborah J. Thompson with:
Deborah J. Thompson United Kingdom
Lisa Cannon‐Albright United States
Marc Tischkowitz United Kingdom
Georgia Chenevix‐Trench Australia
Rolf H. Sijmons Netherlands
Marc S. Greenblatt United States
Gail E. Tomlinson United States
David E. Goldgar France
Noralane M. Lindor United States
Gillian Mitchell Australia
Diana Eccles relative to Deborah J. Thompson United Kingdom Deborah J. Thompson's profile →
Citations per field
00.5×1.7×
Deborah J. Thompson · 1×
Citations per year

Countries citing papers authored by Diana Eccles

Since Specialization
Citations

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

Fields of papers citing papers by Diana Eccles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Diana Eccles, 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 Diana Eccles Line = papers co-authored together Diana Eccles links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 141 papers — load more, or switch the sort, to bring in the rest.

#Work
1
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
Hit paper breakdown →
2006729
2
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
Hit paper breakdown →
2006545
3
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
Hit paper breakdown →
2006541
4 2003332
5 1993219
6 2013184
7 2004173
8 2004170
9 2011167
10
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.
1996158
11
p53 mutation is a common genetic event in ovarian carcinoma.
1993158
12 2013153
13 2006149
14 2008148
15 2011109
16 1998106
17 2009103
18 200699
19 200398
20 200295

About Diana Eccles

Diana Eccles is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Oncology and Cancer Research, having authored 141 papers that have together received 7.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (63 papers), Genetic factors in colorectal cancer (32 papers), Cancer Genomics and Diagnostics (17 papers), DNA Repair Mechanisms (15 papers), Genomic variations and chromosomal abnormalities (9 papers), Ovarian cancer diagnosis and treatment (8 papers), Genetic Associations and Epidemiology (8 papers) and Cancer-related Molecular Pathways (7 papers). The work is most often cited by research in Genetics (3.4k citations), Cancer Research (1.6k citations), Pathology and Forensic Medicine (1.6k citations), Oncology (1.8k citations) and Reproductive Medicine (307 citations). Diana Eccles has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include D. Gareth Evans, Douglas F. Easton, Nazneen Rahman, Sheila Seal, Michael R. Stratton, Rita Barfoot, Anthony Renwick, Hiran Jayatilake, Lesley McGuffog and Deborah J. Thompson. Their work appears in journals such as British Journal of Cancer, Journal of Medical Genetics, Disease Markers, Cancer Research and Nature Genetics.

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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