Sonia Nanda
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 5
- BRCA gene mutations in cancer 4
- Nutrition, Genetics, and Disease 1
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- DNA Repair Mechanisms 1
- Epigenetics and DNA Methylation 1
- Co-authors
- Harriet Druker (2 shared papers)David Malkin (2 shared papers)Uri Tabori (2 shared papers)Aletta Poll (4 shared papers)Jodi Lees (1 shared paper)Kelly Metcalfe (4 shared papers)M Llacuachaqui (3 shared papers)Steven A. Narod (3 shared papers)
- Journals
- Clinical Genetics (1 paper)Breast Cancer Research and Treatment (1 paper)Proceedings of the National Academy of Sciences (1 paper)Cancer Research (1 paper)British Journal of Cancer (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Sonia Nanda
7 papers receiving 420 citations
Peers
Comparison fields: 5 of 39
- Genetics 219
- Cancer Research 83
- Aging 9
- Oncology 123
- Pathology and Forensic Medicine 40
Countries citing papers authored by Sonia Nanda
This map shows the geographic impact of Sonia Nanda'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 Sonia Nanda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sonia Nanda more than expected).
Fields of papers citing papers by Sonia Nanda
This network shows the impact of papers produced by Sonia Nanda. 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 Sonia Nanda. The network helps show where Sonia Nanda may publish in the future.
Co-authors
The 25 scholars most cited alongside Sonia Nanda, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 135 | |
| 2 | 2007 | 107 | |
| 3 | 2012 | 62 | |
| 4 | 2010 | 47 | |
| 5 | 2016 | 38 | |
| 6 | 2013 | 27 | |
| 7 | 2014 | 11 | |
| 8 | 2021 | 0 |
About Sonia Nanda
Sonia Nanda is a scholar working on Genetics, Molecular Biology, Oncology, General Dentistry and Periodontics, having authored 8 papers that have together received 427 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Cancer-related Molecular Pathways (2 papers), DNA Repair Mechanisms (1 paper), Epigenetics and DNA Methylation (1 paper), Cancer Genomics and Diagnostics (1 paper), Dental Research and COVID-19 (1 paper), Telomeres, Telomerase, and Senescence (1 paper) and Nutrition, Genetics, and Disease (1 paper). The work is most often cited by research in Genetics (219 citations), Cancer Research (83 citations), Aging (9 citations), Oncology (123 citations) and Pathology and Forensic Medicine (40 citations). Sonia Nanda has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Harriet Druker, David Malkin, Uri Tabori, Aletta Poll, Jodi Lees, Kelly Metcalfe, M Llacuachaqui, Steven A. Narod, Ana Novokmet and Adam Shlien. Their work appears in journals such as Clinical Genetics, Breast Cancer Research and Treatment, Proceedings of the National Academy of Sciences, Cancer Research and British Journal of Cancer.
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.