Semanti Mukherjee
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Genetics top 2%
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Myeloproliferative Neoplasms: Diagnosis and Treatment
Papers in
- Genetics 18
- Genetic Associations and Epidemiology 9
- BRCA gene mutations in cancer 6
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 4
-
- Cancer Genomics and Diagnostics 6
- Co-authors
- Samir Kumar Maji (8 shared papers)Robert J. Klein (7 shared papers)Ajay Singh Sawner (5 shared papers)Kenneth Offit (8 shared papers)Manisha Poudyal (5 shared papers)Laxmikant G. Gadhe (6 shared papers)Pradeep Kadu (5 shared papers)Arunima Sakunthala (4 shared papers)
- Journals
- Journal of Clinical Oncology (5 papers)JCO Precision Oncology (4 papers)Nature Communications (4 papers)Clinical Cancer Research (3 papers)Nature Genetics (3 papers)
- Partner nations
- United StatesIndiaUnited Kingdom
In The Last Decade
Semanti Mukherjee
53 papers receiving 4.4k citations
Semanti Mukherjee's Hit Papers
Peers
Comparison fields: 5 of 139
- Cancer Research 687
- Genetics 1.1k
- Pathology and Forensic Medicine 661
- Genetics 291
- Oncology 706
Countries citing papers authored by Semanti Mukherjee
This map shows the geographic impact of Semanti Mukherjee'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 Semanti Mukherjee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Semanti Mukherjee more than expected).
Fields of papers citing papers by Semanti Mukherjee
This network shows the impact of papers produced by Semanti Mukherjee. 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 Semanti Mukherjee. The network helps show where Semanti Mukherjee may publish in the future.
Co-authors
The 25 scholars most cited alongside Semanti Mukherjee, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease Hit paper breakdown → | 2018 | 674 |
| 2 | Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer Hit paper breakdown → | 2018 | 484 |
| 3 | 2016 | 414 | |
| 4 | 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 |
| 5 | 2009 | 302 | |
| 6 | 2018 | 186 | |
| 7 | 2013 | 170 | |
| 8 | 2018 | 142 | |
| 9 | 2014 | 135 | |
| 10 | 2021 | 117 | |
| 11 | 2023 | 107 | |
| 12 | 2020 | 93 | |
| 13 | 2022 | 93 | |
| 14 | 2013 | 90 | |
| 15 | 1994 | 83 | |
| 16 | 2021 | 80 | |
| 17 | 2020 | 79 | |
| 18 | 2019 | 75 | |
| 19 | 2018 | 70 | |
| 20 | 2020 | 64 |
About Semanti Mukherjee
Semanti Mukherjee is a scholar working on Genetics, Cancer Research, Neurology, Molecular Biology and Oncology, having authored 54 papers that have together received 4.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (9 papers), Cancer Genomics and Diagnostics (6 papers), BRCA gene mutations in cancer (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers), RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). The work is most often cited by research in Cancer Research (687 citations), Genetics (1.1k citations), Pathology and Forensic Medicine (661 citations), Genetics (291 citations) and Oncology (706 citations). Semanti Mukherjee has collaborated with scholars based in United States, India and United Kingdom. Frequent co-authors include Samir Kumar Maji, Robert J. Klein, Ajay Singh Sawner, Kenneth Offit, Manisha Poudyal, Laxmikant G. Gadhe, Pradeep Kadu, Arunima Sakunthala, Adam Joel Bass and Hagop Kantarjian. Their work appears in journals such as Journal of Clinical Oncology, JCO Precision Oncology, Nature Communications, Clinical Cancer Research and Nature Genetics.
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.