Marta Gîrdea
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
-
- Cancer Genomics and Diagnostics
Papers in
- Genetics 7
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
-
- Cancer Genomics and Diagnostics 6
- Co-authors
- Michael Brudno (7 shared papers)Sergiu Dumitriu (6 shared papers)Kym M. Boycott (3 shared papers)Dimitri J. Stavropoulos (2 shared papers)M. Stephen Meyn (2 shared papers)Sarah Bowdin (2 shared papers)Joyce So (1 shared paper)Marc Fiume (1 shared paper)
- Journals
- Human Mutation (4 papers)European Journal of Human Genetics (1 paper)Algorithms for Molecular Biology (1 paper)PLoS ONE (1 paper)Journal of Paediatrics and Child Health (1 paper)
- Partner nations
- CanadaRomaniaUnited States
In The Last Decade
Marta Gîrdea
12 papers receiving 338 citations
Peers
Comparison fields: 5 of 67
- Genetics 250
- Cancer Research 70
- Molecular Biology 177
- Aging 4
- Health Informatics 3
Countries citing papers authored by Marta Gîrdea
This map shows the geographic impact of Marta Gîrdea'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 Marta Gîrdea with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marta Gîrdea more than expected).
Fields of papers citing papers by Marta Gîrdea
This network shows the impact of papers produced by Marta Gîrdea. 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 Marta Gîrdea. The network helps show where Marta Gîrdea may publish in the future.
Co-authors
The 25 scholars most cited alongside Marta Gîrdea, 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 | 2013 | 144 | |
| 2 | 2015 | 75 | |
| 3 | 2015 | 35 | |
| 4 | 2017 | 27 | |
| 5 | 2014 | 22 | |
| 6 | 2022 | 11 | |
| 7 | 2010 | 10 | |
| 8 | 2015 | 6 | |
| 9 | 2008 | 6 | |
| 10 | 2010 | 4 | |
| 11 | 2007 | 4 | |
| 12 | Knowledge Management in a Wiki Platform via Microformats. | 2007 | 2 |
About Marta Gîrdea
Marta Gîrdea is a scholar working on Genetics, Cancer Research, Molecular Biology, Artificial Intelligence and Information Systems, having authored 12 papers that have together received 346 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Semantic Web and Ontologies (3 papers), Biomedical Text Mining and Ontologies (3 papers), RNA and protein synthesis mechanisms (2 papers), Genomics and Phylogenetic Studies (2 papers) and Machine Learning in Bioinformatics (1 paper). The work is most often cited by research in Genetics (250 citations), Cancer Research (70 citations), Molecular Biology (177 citations), Aging (4 citations) and Health Informatics (3 citations). Marta Gîrdea has collaborated with scholars based in Canada, Romania and United States. Frequent co-authors include Michael Brudno, Sergiu Dumitriu, Kym M. Boycott, Dimitri J. Stavropoulos, M. Stephen Meyn, Sarah Bowdin, Joyce So, Marc Fiume, Hanna Faghfoury and Sébastien Chénier. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Algorithms for Molecular Biology, PLoS ONE and Journal of Paediatrics and Child Health.
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.