Mark T. Ross
- Cancer Research top 10%
- Cancer Genomics and Diagnostics 6
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Molecular Biology top 10%
- Genomics and Chromatin Dynamics 5
- Genomics and Phylogenetic Studies 4
- RNA regulation and disease 3
- Epigenetics and DNA Methylation 3
- Pathology and Forensic Medicine top 10%
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- Chromosomal and Genetic Variations 9
- Co-authors
- David BentleyBarbara E. StrangerDaniel LeongamornlertEmmanouil T. DermitzakisF.L. LovellColette M. JohnstonZoya KingsburyVincent P. Stanton
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Mark T. Ross
35 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 97
- Cancer Research 220
- Genetics 403
- Genetics 144
- Molecular Biology 699
- Pathology and Forensic Medicine 131
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 1 | |
| 2 | 2023 | 41 | |
| 3 | 2023 | 4 | |
| 4 | 2021 | 5 | |
| 5 | 2020 | 42 | |
| 6 | Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family. | 2018 | 19 |
| 7 | 2014 | 19 | |
| 8 | 2013 | 130 | |
| 9 | 2007 | 44 | |
| 10 | 2005 | 81 | |
| 11 | 2005 | 13 | |
| 12 | 2002 | 72 | |
| 13 | 2001 | 12 | |
| 14 | 2001 | 10 | |
| 15 | 1999 | 18 | |
| 16 | 1998 | 6 | |
| 17 | 1998 | 31 | |
| 18 | 1997 | 8 | |
| 19 | 1995 | 49 | |
| 20 | 1992 | 15 |
About Mark T. Ross
Mark T. Ross is a scholar working on Genetics, Cancer Research, Molecular Biology, Hematology and Plant Science, having authored 35 papers that have together received 1.2k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (9 papers), Cancer Genomics and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomics and Chromatin Dynamics (5 papers), Genomics and Phylogenetic Studies (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), RNA regulation and disease (3 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Cancer Research (220 citations), Genetics (403 citations), Genetics (144 citations), Molecular Biology (699 citations) and Pathology and Forensic Medicine (131 citations). Mark T. Ross has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include David Bentley, Barbara E. Stranger, Daniel Leongamornlert, Emmanouil T. Dermitzakis, F.L. Lovell, Colette M. Johnston, 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 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.