Mark T. Ross
Impact in
- Genetics top 0.1%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 23
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetic Associations and Epidemiology 5
- Genetic Mapping and Diversity in Plants and Animals 4
-
- Cancer Genomics and Diagnostics 7
- Co-authors
- David Bentley (9 shared papers)Zoya Kingsbury (6 shared papers)Colette M. Johnston (1 shared paper)Barbara E. Stranger (1 shared paper)Frances L. Lovell (1 shared paper)Emmanouil T. Dermitzakis (1 shared paper)Daniel A. Leongamornlert (1 shared paper)Jennifer Becq (5 shared papers)
- Journals
- Genomics (10 papers)Nature Genetics (7 papers)Blood (5 papers)Nature (5 papers)Genome Medicine (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Mark T. Ross
56 papers receiving 30.3k citations
Mark T. Ross's Hit Papers
Peers
Comparison fields: 5 of 204
- Genetics 8.4k
- Cancer Research 3k
- Molecular Biology 12.1k
- Plant Science 4.1k
- Oncology 1.3k
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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Initial sequencing and analysis of the human genome Hit paper breakdown → | 2001 | 17743 |
| 2 | A second generation human haplotype map of over 3.1 million SNPs Hit paper breakdown → | 2007 | 3536 |
| 3 | Accurate whole human genome sequencing using reversible terminator chemistry Hit paper breakdown → | 2008 | 2737 |
| 4 | A comprehensive catalogue of somatic mutations from a human cancer genome Hit paper breakdown → | 2009 | 1344 |
| 5 | The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes Hit paper breakdown → | 2016 | 1342 |
| 6 | The DNA sequence of the human X chromosome Hit paper breakdown → | 2005 | 855 |
| 7 | BAP1 loss defines a new class of renal cell carcinoma Hit paper breakdown → | 2012 | 790 |
| 8 | 1998 | 645 | |
| 9 | 2003 | 260 | |
| 10 | 2012 | 256 | |
| 11 | 2015 | 234 | |
| 12 | 2013 | 190 | |
| 13 | 2012 | 162 | |
| 14 | 2020 | 157 | |
| 15 | 2013 | 147 | |
| 16 | 2018 | 134 | |
| 17 | 2008 | 118 | |
| 18 | 2005 | 87 | |
| 19 | 2002 | 75 | |
| 20 | 2014 | 68 |
About Mark T. Ross
Mark T. Ross is a scholar working on Genetics, Cancer Research, Molecular Biology, Genetics and Hematology, having authored 57 papers that have together received 31.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Cancer Genomics and Diagnostics (7 papers), Genetic Associations and Epidemiology (5 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers), Genomics and Phylogenetic Studies (4 papers), Acute Lymphoblastic Leukemia research (4 papers) and Retinal Development and Disorders (3 papers). The work is most often cited by research in Genetics (8.4k citations), Cancer Research (3k citations), Molecular Biology (12.1k citations), Plant Science (4.1k citations) and Oncology (1.3k citations). Mark T. Ross has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include David Bentley, Zoya Kingsbury, Colette M. Johnston, Barbara E. Stranger, Frances L. Lovell, Emmanouil T. Dermitzakis, Daniel A. Leongamornlert, Jennifer Becq, David J. McBride and Vincent P. Stanton. Their work appears in journals such as Genomics, Nature Genetics, Blood, Nature and Genome Medicine.
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.