Mark T. Ross
Impact in
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
Papers in
-
- Genomics and Chromatin Dynamics 5
- Genomics and Phylogenetic Studies 4
- Genetics 17
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Animal Genetics and Reproduction 3
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- David Bentley (9 shared papers)Emmanouil T. Dermitzakis (1 shared paper)Colette M. Johnston (1 shared paper)F.L. Lovell (1 shared paper)Daniel Leongamornlert (1 shared paper)Barbara E. Stranger (1 shared paper)Zoya Kingsbury (6 shared papers)Vincent P. Stanton (1 shared paper)
- Journals
- Genomics (9 papers)Genome Medicine (3 papers)Blood (2 papers)Chromosome Research (2 papers)Mammalian Genome (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Mark T. Ross
35 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 93
- Cancer Research 208
- Genetics 397
- Genetics 137
- Molecular Biology 667
- Pathology and Forensic Medicine 119
Countries citing papers authored by Mark T. Ross
This map shows the geographic impact of Mark T. Ross'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 T. Ross with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark T. Ross more than expected).
Fields of papers citing papers by Mark T. Ross
This network shows the impact of papers produced by Mark T. Ross. 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 T. Ross. The network helps show where Mark T. Ross may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark T. Ross, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 220 | |
| 2 | 2013 | 133 | |
| 3 | 2008 | 118 | |
| 4 | 2005 | 82 | |
| 5 | 2002 | 73 | |
| 6 | 2005 | 69 | |
| 7 | 1999 | 66 | |
| 8 | 2007 | 51 | |
| 9 | 1995 | 51 | |
| 10 | 2020 | 45 | |
| 11 | 2023 | 44 | |
| 12 | 1998 | 31 | |
| 13 | 1990 | 24 | |
| 14 | 2006 | 20 | |
| 15 | 2014 | 19 | |
| 16 | 1999 | 18 | |
| 17 | Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family. | 2018 | 18 |
| 18 | 2001 | 17 | |
| 19 | 1992 | 15 | |
| 20 | 1994 | 15 |
About Mark T. Ross
Mark T. Ross is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Hematology, having authored 35 papers that have together received 1.2k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomics and Chromatin Dynamics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Phylogenetic Studies (4 papers), Cancer Genomics and Diagnostics (3 papers), Animal Genetics and Reproduction (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Cancer Research (208 citations), Genetics (397 citations), Genetics (137 citations), Molecular Biology (667 citations) and Pathology and Forensic Medicine (119 citations). Mark T. Ross has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include David Bentley, Emmanouil T. Dermitzakis, Colette M. Johnston, F.L. Lovell, Daniel Leongamornlert, Barbara E. Stranger, Zoya Kingsbury, Vincent P. Stanton, John D. McPherson and Alfons Meindl. Their work appears in journals such as Genomics, Genome Medicine, Blood, Chromosome Research and Mammalian Genome.
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.