Karen Smith‐McCune
Impact in
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics
- Cancer-related molecular mechanisms research
- Oncology top 0.1%
- PARP inhibition in cancer therapy
Papers in
-
- Cancer Genomics and Diagnostics 36
- Epidemiology 53
- Cervical Cancer and HPV Research 50
- Co-authors
- George F. Sawaya (23 shared papers)Noel Weidner (1 shared paper)Douglas Hanahan (2 shared papers)Gordon Brent Mills (5 shared papers)Akiko Kobayashi (6 shared papers)Frank P. McCormick (1 shared paper)Miriam Kuppermann (8 shared papers)Teresa M. Darragh (11 shared papers)
- Journals
- Cell Reports (11 papers)Nature Communications (11 papers)Cell (9 papers)Nature (7 papers)American Journal of Obstetrics and Gynecology (6 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Karen Smith‐McCune
133 papers receiving 37.7k citations
Karen Smith‐McCune's Hit Papers
Peers
Comparison fields: 5 of 177
- Cancer Research 12.6k
- Oncology 9.2k
- Reproductive Medicine 2.3k
- Molecular Biology 19.5k
- Pathology and Forensic Medicine 2.9k
Countries citing papers authored by Karen Smith‐McCune
This map shows the geographic impact of Karen Smith‐McCune'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 Karen Smith‐McCune with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karen Smith‐McCune more than expected).
Fields of papers citing papers by Karen Smith‐McCune
This network shows the impact of papers produced by Karen Smith‐McCune. 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 Karen Smith‐McCune. The network helps show where Karen Smith‐McCune may publish in the future.
Co-authors
The 25 scholars most cited alongside Karen Smith‐McCune, 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 136 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Integrated genomic analyses of ovarian carcinoma Hit paper breakdown → | 2011 | 6345 |
| 2 | An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics Hit paper breakdown → | 2018 | 2602 |
| 3 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 4 | Oncogenic Signaling Pathways in The Cancer Genome Atlas Hit paper breakdown → | 2018 | 2334 |
| 5 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 6 | Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer Hit paper breakdown → | 2018 | 1720 |
| 7 | Comprehensive Characterization of Cancer Driver Genes and Mutations Hit paper breakdown → | 2018 | 1714 |
| 8 | Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation Hit paper breakdown → | 2018 | 1617 |
| 9 | Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas Hit paper breakdown → | 2018 | 810 |
| 10 | Genomic and Functional Approaches to Understanding Cancer Aneuploidy Hit paper breakdown → | 2018 | 749 |
| 11 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 12 | Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients Hit paper breakdown → | 2018 | 685 |
| 13 | Patterns of genomic loss of heterozygosity predict homologous recombination repair defects in epithelial ovarian cancer Hit paper breakdown → | 2012 | 620 |
| 14 | Pathogenic Germline Variants in 10,389 Adult Cancers Hit paper breakdown → | 2018 | 606 |
| 15 | Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines Hit paper breakdown → | 2018 | 583 |
| 16 | The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma Hit paper breakdown → | 2018 | 569 |
| 17 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 18 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 19 | A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers Hit paper breakdown → | 2018 | 456 |
| 20 | Driver Fusions and Their Implications in the Development and Treatment of Human Cancers Hit paper breakdown → | 2018 | 451 |
About Karen Smith‐McCune
Karen Smith‐McCune is a scholar working on Cancer Research, Epidemiology, Microbiology, Oncology and Molecular Biology, having authored 136 papers that have together received 38.2k indexed citations. Recurring topics across this work include Cervical Cancer and HPV Research (50 papers), Cancer Genomics and Diagnostics (36 papers), Reproductive tract infections research (14 papers), Genetic factors in colorectal cancer (12 papers), Reproductive System and Pregnancy (12 papers), RNA modifications and cancer (10 papers), Genital Health and Disease (9 papers) and RNA Research and Splicing (9 papers). The work is most often cited by research in Cancer Research (12.6k citations), Oncology (9.2k citations), Reproductive Medicine (2.3k citations), Molecular Biology (19.5k citations) and Pathology and Forensic Medicine (2.9k citations). Karen Smith‐McCune has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include George F. Sawaya, Noel Weidner, Douglas Hanahan, Gordon Brent Mills, Akiko Kobayashi, Frank P. McCormick, Miriam Kuppermann, Teresa M. Darragh, Joe W. Gray and VIVIAN K. WEINBERG. Their work appears in journals such as Cell Reports, Nature Communications, Cell, Nature and American Journal of Obstetrics and Gynecology.
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.