Munaza Ahmed

5.0k citations
8 papers · 1.1k indexed · 2 hit papers · h-index 5
Topics
BRCA gene mutations in cancer (6 papers)DNA Repair Mechanisms (3 papers)Genomic variations and chromosomal abnormalities (3 papers)

In The Last Decade

Munaza Ahmed

8 papers receiving 1.0k citations

Hit Papers

Truncating mutations in the Fanconi anemia J gene BRIP1 a...200620262012201920062006100200300400500

Peers

Munaza Ahmed
Comparison fields: 5 of 53
  • Genetics 734
  • Molecular Biology 636
  • Cancer Research 344
  • Pathology and Forensic Medicine 252
  • Oncology 245
Replace Anitta Tamminen with:
Anitta Tamminen Finland
Jón Þór Bergþorsson Iceland
Hannaleena Eerola Finland
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Lesley McGuffog United Kingdom
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Munaza Ahmed relative to Anitta Tamminen Finland Anitta Tamminen's profile →
Citations per field
00.5×2.6×
Anitta Tamminen · 1×
Citations per year

Countries citing papers authored by Munaza Ahmed

Since Specialization
Citations

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

Fields of papers citing papers by Munaza Ahmed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Munaza Ahmed

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

All Works

8 of 8 papers shown
#WorkIndexed citations
1 5
2 1
3 11
4 1
5 9
6 1
7
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility allelesbreakdown →
511
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Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility allelesbreakdown →
513

About Munaza Ahmed

Munaza Ahmed is a scholar working on Genetics, Physiology and Cancer Research, having authored 8 papers that have together received 1.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), DNA Repair Mechanisms (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (734 citations), Cancer Research (344 citations) and Pathology and Forensic Medicine (252 citations). Munaza Ahmed has collaborated with scholars based in United Kingdom, Australia and Denmark. Frequent co-authors include D. Gareth Evans, Patrick Kelly, Hiran Jayatilake, Sheila Seal, Anthony Renwick, Deborah J. Thompson, Bernard V. North, Douglas F. Easton, Diana Eccles and Lesley McGuffog. Their work appears in journals such as Nature Genetics, Journal of Medical Genetics and European Journal of Surgical Oncology.

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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