Mark T. Ross

42.5k total citations
35 papers, 1.2k citations indexed

About

Mark T. Ross is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Mark T. Ross has authored 35 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 17 papers in Genetics and 9 papers in Plant Science. Recurrent topics in Mark T. Ross's work include Chromosomal and Genetic Variations (9 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Mark T. Ross is often cited by papers focused on Chromosomal and Genetic Variations (9 papers), Cancer Genomics and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Mark T. Ross collaborates with scholars based in United Kingdom, United States and Germany. Mark T. Ross's 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 and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Mark T. Ross

35 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Mark T. Ross United Kingdom	17	699	403	220	197	144	35	1.2k
Gregory B. Peters Australia	21	773 1.1×	420 1.0×	120 0.5×	116 0.6×	61 0.4×	33	1.3k
Thomas J. Vasicek United States	14	1.9k 2.7×	381 0.9×	162 0.7×	121 0.6×	105 0.7×	17	2.3k
Karl Hackmann Germany	19	739 1.1×	614 1.5×	97 0.4×	66 0.3×	128 0.9×	54	1.3k
Sabina Solinas‐Toldo Germany	12	786 1.1×	963 2.4×	369 1.7×	373 1.9×	95 0.7×	24	1.6k
Ivo Renkens Netherlands	15	894 1.3×	524 1.3×	306 1.4×	251 1.3×	46 0.3×	21	1.3k
Chieh-Ju C. Tang Taiwan	8	960 1.4×	551 1.4×	64 0.3×	351 1.8×	82 0.6×	12	1.4k
Roland Green United States	18	1.9k 2.8×	372 0.9×	252 1.1×	296 1.5×	54 0.4×	21	2.3k
Mitchell L. Leibowitz United States	8	1.0k 1.4×	425 1.1×	226 1.0×	252 1.3×	65 0.5×	9	1.3k
Susan Pfeifer‐Ohlsson Sweden	16	1.1k 1.5×	519 1.3×	122 0.6×	94 0.5×	60 0.4×	23	1.6k
Raymond A. Poot Netherlands	23	2.4k 3.4×	531 1.3×	209 0.9×	190 1.0×	80 0.6×	34	2.7k

Countries citing papers authored by Mark T. Ross

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Mark T. Ross

This figure shows the co-authorship network connecting the top 25 collaborators of Mark T. Ross. A scholar is included among the top collaborators of Mark T. Ross based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mark T. Ross. Mark T. Ross is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Berri, Stefano, John F. Peden, Claire Fielding, et al.. (2025). A dedicated caller for DUX4 rearrangements from whole-genome sequencing data. BMC Medical Genomics. 18(1). 24–24. 1 indexed citations

Ryan, Sarra, John F. Peden, Zoya Kingsbury, et al.. (2023). Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia. Leukemia. 37(3). 518–528. 41 indexed citations

McBride, David J., Claire Fielding, Alexandra Vatsiou, et al.. (2023). Whole-Genome Sequencing Can Identify Clinically Relevant Variants from a Single Sub-Punch of a Dried Blood Spot Specimen. International Journal of Neonatal Screening. 9(3). 52–52. 4 indexed citations

He, Miao, Zoya Kingsbury, Jennifer Becq, et al.. (2021). Clinical-grade whole-genome sequencing and 3′ transcriptome analysis of colorectal cancer patients. Genome Medicine. 13(1). 33–33. 5 indexed citations

Lau, Edmund, Fairleigh Reeves, Ken Chow, et al.. (2020). Detection of ctDNA in plasma of patients with clinically localised prostate cancer is associated with rapid disease progression. Genome Medicine. 12(1). 72–72. 42 indexed citations

Ross, Mark T., David Bentley, Margarida Mendes Lopes, et al.. (2018). Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family.. PubMed. 24. 407–413. 19 indexed citations

Guilhamon, Paul, Lee M Butcher, Nadège Presneau, et al.. (2014). Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics. Genome Medicine. 6(12). 116–116. 19 indexed citations

Guilhamon, Paul, Malihe Eskandarpour, Dina Halai, et al.. (2013). Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2. Nature Communications. 4(1). 2166–2166. 130 indexed citations

Shevchenko, Alexander I., Eugeny A. Elisaphenko, Siobhan Whitehead, et al.. (2007). Genes flanking Xist in mouse and human are separated on the X chromosome in American marsupials. Chromosome Research. 15(2). 127–36. 44 indexed citations

10.

Woodward, Karen, Maria Cundall, Karen Sperle, et al.. (2005). Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination. The American Journal of Human Genetics. 77(6). 966–987. 81 indexed citations

11.

Koina, Edda, Matthew J. Wakefield, Christine M. Distèche, et al.. (2005). Isolation, X location and activity of the marsupial homologue of SLC16A2, an XIST-flanking gene in eutherian mammals. Chromosome Research. 13(7). 687–698. 13 indexed citations

12.

Thiselton, Dawn L., Jennifer McDowall, Oliver Brandau, et al.. (2002). An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders. Genomics. 79(4). 560–572. 72 indexed citations

13.

Braybrook, Claire, Gareth R. Howell, Alfreð Árnason, et al.. (2001). Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region. Human Genetics. 108(6). 537–545. 12 indexed citations

14.

Evans, Kathryn L., Stéphanie Le Hellard, Stewart W. Morris, et al.. (2001). A 6.9-Mb High-Resolution BAC/PAC Contig of Human 4p15.3–p16.1, a Candidate Region for Bipolar Affective Disorder. Genomics. 71(3). 315–323. 10 indexed citations

15.

Walpole, Susannah M., Eve L. Bingham, Jillian Durham, et al.. (1999). Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22. Genomics. 55(3). 275–283. 18 indexed citations

16.

Brandau, Oliver, Gerald Nyakatura, Kerry Baldwin Jedele, et al.. (1998). UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2. European Journal of Human Genetics. 6(5). 459–466. 6 indexed citations

17.

Vosse, Esther van de, Susannah M. Walpole, Anthony Cahn, et al.. (1998). Characterization ofSCML1,a New Gene in Xp22, with Homology to Developmental Polycomb Genes. Genomics. 49(1). 96–102. 31 indexed citations

18.

Walpole, Susannah M., Gareth R. Howell, David Bentley, et al.. (1997). High-Resolution Physical Map of the X-linked Retinoschisis Interval in Xp22. Genomics. 44(3). 300–308. 8 indexed citations

19.

Meindl, Alfons, Maria Raquel Santos Carvalho, Klaus M. Herrmann, et al.. (1995). A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa. Human Molecular Genetics. 4(12). 2339–2346. 49 indexed citations

20.

Ross, Mark T., Dean Nižetić, Catherine Nguyen, et al.. (1992). Selection of a human chromosome 21 enriched YAC sub–library using a chromosome–specific composite probe. Nature Genetics. 1(4). 284–290. 15 indexed citations

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.

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