Marta Gîrdea

2.4k citations
13 papers · 377 · h-index 7

Impact in

  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Cancer Genomics and Diagnostics

Papers in

    • Genomics and Rare Diseases 7
    • Genomic variations and chromosomal abnormalities 4
    • Cancer Genomics and Diagnostics 6

Marta Gîrdea

13 papers receiving 368 citations

Peers

Marta Gîrdea
Comparison fields: 5 of 62
  • Genetics 256
  • Cancer Research 67
  • Molecular Biology 158
  • Aging 4
  • Health Informatics 3
Replace Sergiu Dumitriu with:
Sergiu Dumitriu Canada
Orion J. Buske Canada
Mafalda Dias United States
Christine Mundlos Germany
Joshua C. Gilbert United States
Nataliya Sharopova United States
Bruno Urbero France
Zachary Zappala United States
Ivan Limongelli Italy
Lora Ziyabari United States
Marta Gîrdea relative to Sergiu Dumitriu Canada Sergiu Dumitriu's profile →
Citations per field
00.5×1.5×
Sergiu Dumitriu · 1×
Citations per year

Countries citing papers authored by Marta Gîrdea

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Marta Gîrdea Line = papers co-authored together Marta Gîrdea links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 2013156
2 201581
3 201536
4 201729
5 201425
6 201012
7 202211
8 20156
9 20086
10 20104
11 20074
12 20074
13
Knowledge Management in a Wiki Platform via Microformats.
20073

About Marta Gîrdea

Marta Gîrdea is a scholar working on Genetics, Cancer Research, Artificial Intelligence, Molecular Biology and Information Systems, having authored 13 papers that have together received 377 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (6 papers), Semantic Web and Ontologies (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Biomedical Text Mining and Ontologies (3 papers), Service-Oriented Architecture and Web Services (2 papers), Wikis in Education and Collaboration (1 paper) and Metaheuristic Optimization Algorithms Research (1 paper). The work is most often cited by research in Genetics (256 citations), Cancer Research (67 citations), Molecular Biology (158 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, Marc Fiume, Hanna Faghfoury, Joyce So 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.

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