Veronica McCabe
Impact in
- Cancer Research top 5%
- Cancer-related molecular mechanisms research
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Animal Genetics and Reproduction
Papers in
- Genetics 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Animal Genetics and Reproduction 3
- Genetics and Neurodevelopmental Disorders 2
- Genomics and Rare Diseases 1
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- Ubiquitin and proteasome pathways 2
- Genomics and Chromatin Dynamics 2
- Epigenetics and DNA Methylation 1
- Co-authors
- Neil Brockdorff (5 shared papers)Penny Cooper (3 shared papers)Alan Ashworth (2 shared papers)Graham F. Kay (2 shared papers)Dominic P. Norris (2 shared papers)Sohaila Rastan (2 shared papers)Sally Swift (1 shared paper)Dipika V. Patel (1 shared paper)
- Journals
- Mammalian Genome (1 paper)Neuron (1 paper)Nature (1 paper)Genomics (1 paper)Proceedings of the National Academy of Sciences (1 paper)
- Partner nations
- United KingdomCanadaAustralia
In The Last Decade
Veronica McCabe
8 papers receiving 1.6k citations
Veronica McCabe's Hit Papers
Peers
Comparison fields: 5 of 70
- Cancer Research 480
- Genetics 811
- Molecular Biology 1.3k
- Developmental Neuroscience 28
- Endocrinology 33
Countries citing papers authored by Veronica McCabe
This map shows the geographic impact of Veronica McCabe'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 Veronica McCabe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Veronica McCabe more than expected).
Fields of papers citing papers by Veronica McCabe
This network shows the impact of papers produced by Veronica McCabe. 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 Veronica McCabe. The network helps show where Veronica McCabe may publish in the future.
Co-authors
The 25 scholars most cited alongside Veronica McCabe, 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 | The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus Hit paper breakdown → | 1992 | 861 |
| 2 | Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome Hit paper breakdown → | 1991 | 541 |
| 3 | 2002 | 150 | |
| 4 | 1999 | 60 | |
| 5 | 1999 | 12 | |
| 6 | 1993 | 12 | |
| 7 | 2021 | 2 | |
| 8 | 1994 | 1 |
About Veronica McCabe
Veronica McCabe is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Immunology and Pediatrics, Perinatology and Child Health, having authored 8 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Animal Genetics and Reproduction (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Ubiquitin and proteasome pathways (2 papers), Genomics and Chromatin Dynamics (2 papers), Genomics and Rare Diseases (1 paper), Galectins and Cancer Biology (1 paper) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Cancer Research (480 citations), Genetics (811 citations), Molecular Biology (1.3k citations), Developmental Neuroscience (28 citations) and Endocrinology (33 citations). Veronica McCabe has collaborated with scholars based in United Kingdom, Canada and Australia. Frequent co-authors include Neil Brockdorff, Penny Cooper, Alan Ashworth, Graham F. Kay, Dominic P. Norris, Sohaila Rastan, Sally Swift, Dipika V. Patel, Sandy M. Smith and Guy Tear. Their work appears in journals such as Mammalian Genome, Neuron, Nature, Genomics and Proceedings of the National Academy of Sciences.
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.