Mark A. Pershouse
Impact in
- Genetics top 2%
- Glioma Diagnosis and Treatment
- Cancer Research top 5%
Papers in
-
- Genomics and Chromatin Dynamics 5
- RNA modifications and cancer 4
- RNA Research and Splicing 3
- Ubiquitin and proteasome pathways 3
- Peroxisome Proliferator-Activated Receptors 2
- Co-authors
- Peter A. Steck (11 shared papers)W.K. Alfred Yung (7 shared papers)Huai Lin (4 shared papers)Azra Hadi Ligon (5 shared papers)Lauren A. Langford (3 shared papers)Samar A. Jasser (3 shared papers)Cheryl Anne Frye (1 shared paper)Sean V. Tavtigian (1 shared paper)
- Journals
- Genes Chromosomes and Cancer (3 papers)Oncogene (3 papers)Progress in community health partnerships (2 papers)Inhalation Toxicology (2 papers)Genomics (2 papers)
- Partner nations
- United StatesChinaRussia
In The Last Decade
Mark A. Pershouse
32 papers receiving 3.5k citations
Mark A. Pershouse's Hit Papers
Peers
Comparison fields: 5 of 103
- Genetics 479
- Cancer Research 521
- Molecular Biology 2.6k
- Pathology and Forensic Medicine 451
- Oncology 648
Countries citing papers authored by Mark A. Pershouse
This map shows the geographic impact of Mark A. Pershouse'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 Mark A. Pershouse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark A. Pershouse more than expected).
Fields of papers citing papers by Mark A. Pershouse
This network shows the impact of papers produced by Mark A. Pershouse. 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 Mark A. Pershouse. The network helps show where Mark A. Pershouse may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark A. Pershouse, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers Hit paper breakdown → | 1997 | 2380 |
| 2 | MMAC1/PTEN mutations in primary tumor specimens and tumor cell lines. | 1997 | 407 |
| 3 | 1988 | 128 | |
| 4 | Allelic deletion analyses of MMAC/PTEN and DMBT1 loci in gliomas: relationship to prognostic significance. | 1998 | 84 |
| 5 | 1995 | 79 | |
| 6 | 1997 | 71 | |
| 7 | Analysis of the functional role of chromosome 10 loss in human glioblastomas. | 1993 | 68 |
| 8 | 1985 | 67 | |
| 9 | 2013 | 56 | |
| 10 | 2005 | 52 | |
| 11 | 1999 | 50 | |
| 12 | 2005 | 32 | |
| 13 | 2016 | 21 | |
| 14 | 1992 | 17 | |
| 15 | 1996 | 17 | |
| 16 | 2006 | 16 | |
| 17 | 2016 | 14 | |
| 18 | 2008 | 12 | |
| 19 | Flow cytometric applications in cytopathology. | 1988 | 11 |
| 20 | 1997 | 9 |
About Mark A. Pershouse
Mark A. Pershouse is a scholar working on Molecular Biology, Cancer Research, Cell Biology, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine, having authored 34 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (5 papers), Occupational and environmental lung diseases (5 papers), Microtubule and mitosis dynamics (4 papers), RNA modifications and cancer (4 papers), Chromosomal and Genetic Variations (3 papers), RNA Research and Splicing (3 papers), Ubiquitin and proteasome pathways (3 papers) and Peroxisome Proliferator-Activated Receptors (2 papers). The work is most often cited by research in Genetics (479 citations), Cancer Research (521 citations), Molecular Biology (2.6k citations), Pathology and Forensic Medicine (451 citations) and Oncology (648 citations). Mark A. Pershouse has collaborated with scholars based in United States, China and Russia. Frequent co-authors include Peter A. Steck, W.K. Alfred Yung, Huai Lin, Azra Hadi Ligon, Lauren A. Langford, Samar A. Jasser, Cheryl Anne Frye, Sean V. Tavtigian, Thomas Hattier and Rong Hua Hu. Their work appears in journals such as Genes Chromosomes and Cancer, Oncogene, Progress in community health partnerships, Inhalation Toxicology and Genomics.
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.