SA Narod

2.0k citations
18 papers · 1.1k · h-index 13

Impact in

  • Genetics top 2%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Nutrition, Genetics, and Disease
    • Ovarian cancer diagnosis and treatment

Papers in

    • BRCA gene mutations in cancer 15
    • Genomic variations and chromosomal abnormalities 4
    • Estrogen and related hormone effects 1
    • Cancer Genomics and Diagnostics 4
    • Breast Cancer Treatment Studies 2

SA Narod

18 papers receiving 1.0k citations

Peers

SA Narod
Comparison fields: 5 of 49
  • Genetics 797
  • Reproductive Medicine 155
  • Cancer Research 218
  • Pathology and Forensic Medicine 188
  • Oncology 188
Replace Susan Randall Armel with:
Susan Randall Armel Canada
M. Daly United States
Monica Barile Italy
Barbara Weber United States
Aletta Poll Canada
DF Easton United Kingdom
M Llacuachaqui Canada
Steven A. Narod Canada
D. G. Crüger Denmark
Bert van Geel Netherlands
SA Narod relative to Susan Randall Armel Canada Susan Randall Armel's profile →
Citations per field
00.5×1.5×
Susan Randall Armel · 1×
Citations per year

Countries citing papers authored by SA Narod

Since Specialization
Citations

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

Fields of papers citing papers by SA Narod

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

18 of 18 papers shown
#Work
1 1999323
2 2002276
3 2004120
4 201563
5 200757
6 200848
7 201044
8 200228
9 200927
10 201126
11 201021
12 200021
13 201312
14 201110
15 20117
16 20136
17 20124
18
Familial and hormonal risk factors for papillary serous uterine cancer.
20024

About SA Narod

SA Narod is a scholar working on Genetics, Cancer Research, Molecular Biology, Public Health, Environmental and Occupational Health and Pathology and Forensic Medicine, having authored 18 papers that have together received 1.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (15 papers), DNA Repair Mechanisms (4 papers), Cancer Genomics and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Patient Dignity and Privacy (2 papers), Breast Cancer Treatment Studies (2 papers), Estrogen and related hormone effects (1 paper) and Selenium in Biological Systems (1 paper). The work is most often cited by research in Genetics (797 citations), Reproductive Medicine (155 citations), Cancer Research (218 citations), Pathology and Forensic Medicine (188 citations) and Oncology (188 citations). SA Narod has collaborated with scholars based in Canada, United States and Poland. Frequent co-authors include Alexander Liede, William D. Foulkes, Jan Lubiński, Cezary Cybulski, Nancy Hamel, Martin Klein, Lisa Di Prospero, Elizabeth Warner, Joanne Honeyford and Diane Allingham‐Hawkins. Their work appears in journals such as Clinical Genetics, JNCI Journal of the National Cancer Institute, Breast Cancer Research and Treatment, Cancer Research and Prostate Cancer and Prostatic Diseases.

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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