Ágnes Baross
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Cancer Genomics and Diagnostics
Papers in
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- DNA Repair Mechanisms 2
- Genomics and Phylogenetic Studies 1
- RNA and protein synthesis mechanisms 1
- Molecular Biology Techniques and Applications 1
- Genetics 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Marco A. Marra (4 shared papers)Patrice Eydoux (2 shared papers)Sylvie Langlois (2 shared papers)Jan M. Friedman (2 shared papers)Allen Delaney (2 shared papers)Helen V. Firth (1 shared paper)Farah Zahir (1 shared paper)Howard Martin (1 shared paper)
- Journals
- Journal of Medical Genetics (1 paper)BMC Bioinformatics (1 paper)Genes Chromosomes and Cancer (1 paper)Genome Research (1 paper)Oncogene (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Ágnes Baross
5 papers receiving 151 citations
Peers
Comparison fields: 5 of 34
- Genetics 90
- Cancer Research 21
- Molecular Biology 90
- Genetics 8
- Cognitive Neuroscience 14
Countries citing papers authored by Ágnes Baross
This map shows the geographic impact of Ágnes Baross'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 Ágnes Baross with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ágnes Baross more than expected).
Fields of papers citing papers by Ágnes Baross
This network shows the impact of papers produced by Ágnes Baross. 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 Ágnes Baross. The network helps show where Ágnes Baross may publish in the future.
Co-authors
The 25 scholars most cited alongside Ágnes Baross, 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 | 2007 | 63 | |
| 2 | 2007 | 43 | |
| 3 | 2004 | 21 | |
| 4 | 2002 | 17 | |
| 5 | 2004 | 11 |
About Ágnes Baross
Ágnes Baross is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Physiology and Biotechnology, having authored 5 papers that have together received 155 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Phylogenetic Studies (1 paper), RNA and protein synthesis mechanisms (1 paper), Cancer Genomics and Diagnostics (1 paper), Telomeres, Telomerase, and Senescence (1 paper), Genetic factors in colorectal cancer (1 paper) and Molecular Biology Techniques and Applications (1 paper). The work is most often cited by research in Genetics (90 citations), Cancer Research (21 citations), Molecular Biology (90 citations), Genetics (8 citations) and Cognitive Neuroscience (14 citations). Ágnes Baross has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Marco A. Marra, Patrice Eydoux, Sylvie Langlois, Jan M. Friedman, Allen Delaney, Helen V. Firth, Farah Zahir, Howard Martin, Lionel Willatt and William T. Gibson. Their work appears in journals such as Journal of Medical Genetics, BMC Bioinformatics, Genes Chromosomes and Cancer, Genome Research and Oncogene.
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.