Marta Gîrdea

2.4k total citations
12 papers, 346 citations indexed

About

Marta Gîrdea is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Marta Gîrdea has authored 12 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Cancer Research and 5 papers in Molecular Biology. Recurrent topics in Marta Gîrdea's work include Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Marta Gîrdea is often cited by papers focused on Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Marta Gîrdea collaborates with scholars based in Canada, Romania and United States. Marta Gîrdea's co-authors include Michael Brudno, Sergiu Dumitriu, Kym M. Boycott, M. Stephen Meyn, Dimitri J. Stavropoulos, Sarah Bowdin, Sébastien Chénier, Peter N. Ray, Marc Fiume and Joyce So and has published in prestigious journals such as PLoS ONE, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Marta Gîrdea

12 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marta Gîrdea Canada	7	250	177	70	45	25	12	346
Sergiu Dumitriu Canada	6	214 0.9×	151 0.9×	65 0.9×	40 0.9×	21 0.8×	12	292
Amin Ardeshirdavani Belgium	7	161 0.6×	227 1.3×	58 0.8×	35 0.8×	14 0.6×	11	352
Lora Ziyabari United States	3	122 0.5×	220 1.2×	75 1.1×	21 0.5×	19 0.8×	4	350
Anne Sturcke United States	2	115 0.5×	209 1.2×	74 1.1×	20 0.4×	19 0.8×	3	327
Brendan Vaughan United Kingdom	4	183 0.7×	399 2.3×	64 0.9×	14 0.3×	27 1.1×	4	601
Zachary Zappala United States	6	244 1.0×	266 1.5×	73 1.0×	9 0.2×	15 0.6×	6	420
Nataliya Sharopova United States	3	114 0.5×	212 1.2×	77 1.1×	20 0.4×	19 0.8×	3	333
Simon White United States	9	185 0.7×	292 1.6×	93 1.3×	14 0.3×	9 0.4×	13	479
Masato Kimura United States	2	111 0.4×	205 1.2×	74 1.1×	21 0.5×	19 0.8×	2	324
Moira Lee United States	1	111 0.4×	205 1.2×	74 1.1×	20 0.4×	19 0.8×	2	321

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-authorship network of co-authors of Marta Gîrdea

This figure shows the co-authorship network connecting the top 25 collaborators of Marta Gîrdea. A scholar is included among the top collaborators of Marta Gîrdea 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 Marta Gîrdea. Marta Gîrdea is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Osmond, Matthew, Taila Hartley, Marta Gîrdea, et al.. (2022). PhenomeCentral: 7 years of rare disease matchmaking. Human Mutation. 43(6). 674–681. 11 indexed citations

Hayeems, Robin Z., Jasmin Bhawra, Kate Tsiplova, et al.. (2017). Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. European Journal of Human Genetics. 25(12). 1303–1312. 27 indexed citations

Buske, Orion J., Marta Gîrdea, Sergiu Dumitriu, et al.. (2015). PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases. Human Mutation. 36(10). 931–940. 75 indexed citations

Foong, Justin, Marta Gîrdea, James Stavropoulos, & Michael Brudno. (2015). Prioritizing Clinically Relevant Copy Number Variation from Genetic Interactions and Gene Function Data. PLoS ONE. 10(10). e0139656–e0139656. 6 indexed citations

Buske, Orion J., François Schiettecatte, Sergiu Dumitriu, et al.. (2015). The Matchmaker Exchange API: Automating Patient Matching Through the Exchange of Structured Phenotypic and Genotypic Profiles. Human Mutation. 36(10). 922–927. 35 indexed citations

Baynam, Gareth, Mark Walters, Peter Claes, et al.. (2014). Phenotyping: Targeting genotype's rich cousin for diagnosis. Journal of Paediatrics and Child Health. 51(4). 381–386. 22 indexed citations

Gîrdea, Marta, Sergiu Dumitriu, Marc Fiume, et al.. (2013). PhenoTips: Patient Phenotyping Software for Clinical and Research Use. Human Mutation. 34(8). 1057–1065. 144 indexed citations

Noé, Laurent, Marta Gîrdea, & Grégory Kucherov. (2010). Designing Efficient Spaced Seeds for SOLiD Read Mapping. HAL (Le Centre pour la Communication Scientifique Directe). 2010. 1–12. 4 indexed citations

Gîrdea, Marta, Laurent Noé, & Grégory Kucherov. (2010). Back-translation for discovering distant protein homologies in the presence of frameshift mutations. Algorithms for Molecular Biology. 5(1). 6–6. 10 indexed citations

10.

Dumitriu, Sergiu, et al.. (2008). A Competency-Oriented Modeling Approach for Personalized E-Learning Systems. 3538. 410–415. 6 indexed citations

11.

Dumitriu, Sergiu, et al.. (2007). Knowledge Management in a Wiki Platform via Microformats.. The Florida AI Research Society. 278–283. 2 indexed citations

12.

Gîrdea, Marta, et al.. (2007). A Hybrid Genetic Programming and Boosting Technique for Learning Kernel Functions from Training Data. 6. 395–402. 4 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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