Charles Cochran
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
-
- Genomics and Chromatin Dynamics 3
- Genetics, Bioinformatics, and Biomedical Research 1
- Viral Infectious Diseases and Gene Expression in Insects 1
- Pluripotent Stem Cells Research 1
- Genetics 6
- BRCA gene mutations in cancer 4
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Roger W. Wiseman (13 shared papers)P. Andrew Futreal (5 shared papers)Peter Söderkvist (3 shared papers)J. Dirk Iglehart (3 shared papers)Jeffrey R. Marks (2 shared papers)J. Carl Barrett (3 shared papers)Eric S. Lander (2 shared papers)William F. Dietrich (2 shared papers)
- Journals
- Human Molecular Genetics (2 papers)Environmental Health Perspectives (2 papers)Genomics (2 papers)Molecular Carcinogenesis (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesSwedenCanada
In The Last Decade
Charles Cochran
14 papers receiving 833 citations
Peers
Comparison fields: 5 of 68
- Genetics 401
- Cancer Research 197
- Oncology 270
- Molecular Biology 587
- Pathology and Forensic Medicine 153
Countries citing papers authored by Charles Cochran
This map shows the geographic impact of Charles Cochran'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 Charles Cochran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles Cochran more than expected).
Fields of papers citing papers by Charles Cochran
This network shows the impact of papers produced by Charles Cochran. 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 Charles Cochran. The network helps show where Charles Cochran may publish in the future.
Co-authors
The 25 scholars most cited alongside Charles Cochran, 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 | 1996 | 280 | |
| 2 | Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms. | 1992 | 168 |
| 3 | Allelotype analysis of mouse lung carcinomas reveals frequent allelic losses on chromosome 4 and an association between allelic imbalances on chromosome 6 and K-ras activation. | 1994 | 86 |
| 4 | 1994 | 67 | |
| 5 | 1994 | 51 | |
| 6 | 1994 | 49 | |
| 7 | 1994 | 36 | |
| 8 | 1995 | 35 | |
| 9 | Allelotype analysis of 2',3'-dideoxycytidine- and 1,3-butadiene-induced lymphomas in B6C3F1 mice. | 1996 | 28 |
| 10 | 2010 | 17 | |
| 11 | 1991 | 13 | |
| 12 | Mutation analysis of the THRA1 gene in breast cancer: deletion/fusion of the gene to a novel sequence on 17q in the BT474 cell line. | 1994 | 12 |
| 13 | 1994 | 10 | |
| 14 | 1991 | 6 |
About Charles Cochran
Charles Cochran is a scholar working on Molecular Biology, Genetics, Oncology, Cancer Research and Pulmonary and Respiratory Medicine, having authored 14 papers that have together received 858 indexed citations. Recurring topics across this work include Cancer-related Molecular Pathways (4 papers), BRCA gene mutations in cancer (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Chromatin Dynamics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics, Bioinformatics, and Biomedical Research (1 paper), Viral Infectious Diseases and Gene Expression in Insects (1 paper) and Pluripotent Stem Cells Research (1 paper). The work is most often cited by research in Genetics (401 citations), Cancer Research (197 citations), Oncology (270 citations), Molecular Biology (587 citations) and Pathology and Forensic Medicine (153 citations). Charles Cochran has collaborated with scholars based in United States, Sweden and Canada. Frequent co-authors include Roger W. Wiseman, P. Andrew Futreal, Peter Söderkvist, J. Dirk Iglehart, Jeffrey R. Marks, J. Carl Barrett, Eric S. Lander, William F. Dietrich, Rifat Hamoudi and Johnathan M. Lancaster. Their work appears in journals such as Human Molecular Genetics, Environmental Health Perspectives, Genomics, Molecular Carcinogenesis 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.