Deborah Ford

18.5k citations
92 papers · 6.4k · 2 hit papers · h-index 31

Impact in

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

Papers in

    • BRCA gene mutations in cancer 18
    • Genomic variations and chromosomal abnormalities 7
    • HIV/AIDS Research and Interventions 17
    • HIV/AIDS drug development and treatment 8

Deborah Ford

89 papers receiving 6.0k citations

Deborah Ford's Hit Papers

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. 1995 · 1.3k citations
1.3k0+11+22Years since publication4008001.2k

Peers

Deborah Ford
Comparison fields: 5 of 144
  • Genetics 3.1k
  • Cancer Research 936
  • Reproductive Medicine 533
  • Pathology and Forensic Medicine 972
  • Oncology 1.1k
Replace Mark H. Greene with:
Mark H. Greene United States
Klaus Friese Germany
C. M. Steel United Kingdom
J Dausset France
Any Cheung Hong Kong
Eric F. Morand Australia
Jayne S. Danska Canada
Mark S. Anderson United States
Barbara Williamson United States
Diane Provencher Canada
Deborah Ford relative to Mark H. Greene United States Mark H. Greene's profile →
Citations per field
00.5×1.5×
Mark H. Greene · 1×
Citations per year

Countries citing papers authored by Deborah Ford

Since Specialization
Citations

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

Fields of papers citing papers by Deborah Ford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 92 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.
Hit paper breakdown →
19951301
2
Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.
Hit paper breakdown →
19931045
3 1992357
4 1997295
5
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium.
1995220
6 1995216
7
Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.
1995200
8 1995194
9 2007183
10 1995153
11 2008146
12 1995125
13 1994123
14 1996108
15
Inherited susceptibility to breast cancer.
1993108
16 2010102
17 197799
18 199698
19
The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study Collaborators.
200097
20 199583

About Deborah Ford

Deborah Ford is a scholar working on Genetics, Infectious Diseases, Molecular Biology, Pathology and Forensic Medicine and Epidemiology, having authored 92 papers that have together received 6.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (18 papers), HIV/AIDS Research and Interventions (17 papers), Genetic factors in colorectal cancer (11 papers), HIV/AIDS drug development and treatment (8 papers), Genomic variations and chromosomal abnormalities (7 papers), DNA Repair Mechanisms (6 papers), Menopause: Health Impacts and Treatments (5 papers) and Cancer Genomics and Diagnostics (4 papers). The work is most often cited by research in Genetics (3.1k citations), Cancer Research (936 citations), Reproductive Medicine (533 citations), Pathology and Forensic Medicine (972 citations) and Oncology (1.1k citations). Deborah Ford has collaborated with scholars based in United Kingdom, United States and Zimbabwe. Frequent co-authors include Douglas F. Easton, D. Timothy Bishop, Gillian P. Crockford, Julian Peto, Richard Wooster, Judith M. Bliss, Anthony J. Swerdlow, Michael R. Stratton, Peter A. Daly and Ross McManus. Their work appears in journals such as Laboratory Animals, International Journal of Cancer, PLoS ONE, Nature Genetics and International Journal of Epidemiology.

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.

Explore authors with similar magnitude of impact