Nisha Pradhan
Impact in
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
Papers in
-
- Lymphoma Diagnosis and Treatment 2
- Genetics 2
- Chronic Lymphocytic Leukemia Research 2
- BRCA gene mutations in cancer 2
- Genetic Associations and Epidemiology 2
- Co-authors
- Allan Clark (1 shared paper)Thomas Hummel (1 shared paper)Duncan Boak (1 shared paper)Carl Martin Philpott (1 shared paper)Robert A. Meguid (4 shared papers)William G. Henderson (4 shared papers)Michael R. Bronsert (4 shared papers)Adam R. Dyas (3 shared papers)
- Journals
- Genetic Epidemiology (2 papers)Human Mutation (2 papers)Patient Safety in Surgery (1 paper)JAMA Oncology (1 paper)JNCI Journal of the National Cancer Institute (1 paper)
- Partner nations
- United StatesUnited KingdomPoland
In The Last Decade
Nisha Pradhan
17 papers receiving 1.0k citations
Nisha Pradhan's Hit Papers
Peers
Comparison fields: 5 of 69
- Cancer Research 235
- Genetics 438
- Sensory Systems 48
- Pathology and Forensic Medicine 162
- Oncology 170
Countries citing papers authored by Nisha Pradhan
This map shows the geographic impact of Nisha Pradhan'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 Nisha Pradhan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nisha Pradhan more than expected).
Fields of papers citing papers by Nisha Pradhan
This network shows the impact of papers produced by Nisha Pradhan. 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 Nisha Pradhan. The network helps show where Nisha Pradhan may publish in the future.
Co-authors
The 25 scholars most cited alongside Nisha Pradhan, 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 | Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing Hit paper breakdown → | 2017 | 397 |
| 2 | 2018 | 242 | |
| 3 | 2018 | 142 | |
| 4 | 2019 | 49 | |
| 5 | 2019 | 32 | |
| 6 | 2020 | 31 | |
| 7 | 2018 | 30 | |
| 8 | 2019 | 30 | |
| 9 | 2017 | 23 | |
| 10 | 2019 | 16 | |
| 11 | 2018 | 15 | |
| 12 | 2019 | 15 | |
| 13 | 2022 | 11 | |
| 14 | 2019 | 7 | |
| 15 | 2021 | 4 | |
| 16 | 2021 | 2 | |
| 17 | 2023 | 1 | |
| 18 | 2020 | 0 |
About Nisha Pradhan
Nisha Pradhan is a scholar working on Pathology and Forensic Medicine, Genetics, Cardiology and Cardiovascular Medicine, Oncology and Genetics, having authored 18 papers that have together received 1.0k indexed citations. Recurring topics across this work include Cardiac, Anesthesia and Surgical Outcomes (3 papers), Lymphoma Diagnosis and Treatment (2 papers), Chronic Lymphocytic Leukemia Research (2 papers), BRCA gene mutations in cancer (2 papers), Renal cell carcinoma treatment (2 papers), Genetic Associations and Epidemiology (2 papers), CRISPR and Genetic Engineering (1 paper) and Olfactory and Sensory Function Studies (1 paper). The work is most often cited by research in Cancer Research (235 citations), Genetics (438 citations), Sensory Systems (48 citations), Pathology and Forensic Medicine (162 citations) and Oncology (170 citations). Nisha Pradhan has collaborated with scholars based in United States, United Kingdom and Poland. Frequent co-authors include Allan Clark, Thomas Hummel, Duncan Boak, Carl Martin Philpott, Robert A. Meguid, William G. Henderson, Michael R. Bronsert, Adam R. Dyas, Alicia C. Staley and Kevin A. Clauson. Their work appears in journals such as Genetic Epidemiology, Human Mutation, Patient Safety in Surgery, JAMA Oncology and JNCI Journal of the National Cancer Institute.
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.