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
- Co-authors
- Harriet A. Druker (2 shared papers)Uri Tabori (2 shared papers)David M. Malkin (2 shared papers)Jodi Lees (1 shared paper)Aletta Poll (4 shared papers)Kelly A. Metcalfe (4 shared papers)Marcia Llacuachaqui (3 shared papers)Steven Alexander Narod (3 shared papers)
- Journals
- Genetics in Medicine (1 paper)Cancer Research (1 paper)British Journal of Cancer (1 paper)Clinical Genetics (1 paper)Fertility and Sterility (1 paper)
- Partner nations
- CanadaUnited StatesFrance
In The Last Decade
Sonia Nanda
8 papers receiving 519 citations
Peers
Comparison fields: 5 of 41
- Genetics 268
- Cancer Research 98
- Oncology 147
- Aging 9
- Reproductive Medicine 37
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 | 163 | |
| 2 | 2007 | 123 | |
| 3 | 2012 | 68 | |
| 4 | 2010 | 47 | |
| 5 | 2016 | 43 | |
| 6 | 2015 | 41 | |
| 7 | 2013 | 33 | |
| 8 | 2014 | 16 | |
| 9 | 2021 | 0 |
About Sonia Nanda
Sonia Nanda is a scholar working on Genetics, General Dentistry, Periodontics, Oncology and Reproductive Medicine, having authored 9 papers that have together received 534 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Cancer-related Molecular Pathways (2 papers), Cancer Genomics and Diagnostics (1 paper), Ovarian cancer diagnosis and treatment (1 paper), Nutrition, Genetics, and Disease (1 paper), DNA Repair Mechanisms (1 paper), Dental Health and Care Utilization (1 paper) and Ethics in Clinical Research (1 paper). The work is most often cited by research in Genetics (268 citations), Cancer Research (98 citations), Oncology (147 citations), Aging (9 citations) and Reproductive Medicine (37 citations). Sonia Nanda has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Harriet A. Druker, Uri Tabori, David M. Malkin, Jodi Lees, Aletta Poll, Kelly A. Metcalfe, Marcia Llacuachaqui, Steven Alexander Narod, Małgorzata Pieńkowska and Stephen W. Scherer. Their work appears in journals such as Genetics in Medicine, Cancer Research, British Journal of Cancer, Clinical Genetics and Fertility and Sterility.
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.