Marta Pineda

8.3k total citations
85 papers, 2.5k citations indexed

About

Marta Pineda is a scholar working on Pathology and Forensic Medicine, Cancer Research and Molecular Biology. According to data from OpenAlex, Marta Pineda has authored 85 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Pathology and Forensic Medicine, 48 papers in Cancer Research and 30 papers in Molecular Biology. Recurrent topics in Marta Pineda's work include Genetic factors in colorectal cancer (50 papers), Cancer Genomics and Diagnostics (47 papers) and Genomics and Rare Diseases (19 papers). Marta Pineda is often cited by papers focused on Genetic factors in colorectal cancer (50 papers), Cancer Genomics and Diagnostics (47 papers) and Genomics and Rare Diseases (19 papers). Marta Pineda collaborates with scholars based in Spain, United States and Germany. Marta Pineda's co-authors include Manuel Palacı́n, António Zorzano, Raúl Estévez, David Torrents, Gabriel Capellá, Esperanza Fernández, Jorge Lloberas, Conxi Lázaro, Lídia Feliubadaló and Joan Brunet and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Marta Pineda

81 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta Pineda Spain 22 1.0k 904 763 559 543 85 2.5k
Pattama Wiriyasermkul Japan 21 721 0.7× 556 0.6× 186 0.2× 197 0.4× 94 0.2× 36 1.5k
Manju Swaroop United States 27 1.5k 1.4× 159 0.2× 78 0.1× 320 0.6× 127 0.2× 42 2.6k
Joshua L. Deignan United States 18 685 0.7× 90 0.1× 151 0.2× 60 0.1× 289 0.5× 32 1.6k
Ryuichi Ohgaki Japan 22 798 0.8× 558 0.6× 49 0.1× 209 0.4× 106 0.2× 45 1.4k
Steven M. Harrison United States 22 1.5k 1.4× 41 0.0× 317 0.4× 103 0.2× 443 0.8× 52 3.2k
Youfeng Yang United States 30 2.7k 2.5× 138 0.2× 80 0.1× 318 0.6× 1.6k 3.0× 64 3.8k
Norman L. Lehman United States 30 1.1k 1.0× 48 0.1× 186 0.2× 487 0.9× 285 0.5× 73 2.4k
Xiliang Zha China 26 1.1k 1.1× 109 0.1× 105 0.1× 273 0.5× 292 0.5× 78 1.8k
Annora Thoeng Australia 16 1.3k 1.2× 319 0.4× 33 0.0× 153 0.3× 508 0.9× 18 1.8k
Hiroki Sawa Japan 21 821 0.8× 118 0.1× 92 0.1× 292 0.5× 177 0.3× 57 1.5k

Countries citing papers authored by Marta Pineda

Since Specialization
Citations

This map shows the geographic impact of Marta Pineda'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 Pineda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marta Pineda more than expected).

Fields of papers citing papers by Marta Pineda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marta Pineda. 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 Pineda. The network helps show where Marta Pineda may publish in the future.

Co-authorship network of co-authors of Marta Pineda

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

All Works

20 of 20 papers shown
1.
Rofes, Paula, Mireia Menéndez, Àlex Teulé, et al.. (2025). TP53 germline testing and hereditary cancer: how somatic events and clinical criteria affect variant detection rate. Genome Medicine. 17(1). 3–3. 1 indexed citations
2.
Carballal, Sabela, Francesc Balaguer, Luís Bujanda, et al.. (2024). Use of multi-gene panels in patients at high risk of hereditary digestive cancer: Position statement of AEG, SEOM, AEGH and IMPaCT-GENÓMICA consortium. Gastroenterología y Hepatología (English Edition). 47(3). 293–318.
3.
Costas, Laura, Francisco M. Peinado, José-Manuel Molina-Molina, et al.. (2024). Total Effective Xenoestrogen Burden in Serum Samples and Risk of Endometrial Cancer in the Spanish Screenwide Case–Control Study. Environmental Health Perspectives. 132(2). 27012–27012. 3 indexed citations
4.
Guerrini‐Rousseau, Léa, Richard Gallon, Marta Pineda, et al.. (2024). Report of the sixth meeting of the European Consortium ‘Care for CMMRD’ (C4CMMRD), Paris, France, November 16th 2022. Familial Cancer. 23(4). 447–457. 3 indexed citations
5.
Carballal, Sabela, Francesc Balaguer, Luís Bujanda, et al.. (2023). Uso de paneles de genes en pacientes con alto riesgo de cáncer digestivo hereditario: documento de posicionamiento de la AEG, SEOM, AEGH y consorcio IMPaCT-GENÓMICA. Gastroenterología y Hepatología. 47(3). 293–318. 1 indexed citations
6.
Klinkhammer, Hannah, Núria Bonifaci, Isabel Spier, et al.. (2023). Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome. Journal of Medical Genetics. 60(11). 1044–1051. 2 indexed citations
7.
Costas, Laura, Paula Peremiquel‐Trillas, José Manuel Martínez, et al.. (2023). Evaluation of Somatic Mutations in Urine Samples as a Noninvasive Method for the Detection and Molecular Classification of Endometrial Cancer. Clinical Cancer Research. 29(18). 3681–3690. 2 indexed citations
8.
Cajal, Teresa Ramón y, Marta Pineda, Elena Aguirre, et al.. (2023). SEOM clinical guideline on heritable TP53-related cancer syndrome (2022). Clinical & Translational Oncology. 25(9). 2627–2633. 4 indexed citations
9.
Beisvåg, Vidar, Elizabeth Holliday, Joan Brunet, et al.. (2023). MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome. Scientific Reports. 13(1). 18783–18783. 3 indexed citations
10.
Costas, Laura, Yolanda Benavente, Paula Peremiquel‐Trillas, et al.. (2022). Night work, chronotype and risk of endometrial cancer in the Screenwide case–control study. Occupational and Environmental Medicine. 79(9). 624–627. 11 indexed citations
11.
Peremiquel‐Trillas, Paula, Laia Alemany, Alberto Ameijide, et al.. (2022). Predicting Ovarian-Cancer Burden in Catalonia by 2030: An Age–Period–Cohort Modelling. International Journal of Environmental Research and Public Health. 19(3). 1404–1404. 7 indexed citations
12.
Navarro, Matilde, Àlex Teulé, Ares Solanes, et al.. (2021). Correction: Dueñas et al. Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 2020, 12, 3419. Cancers. 13(13). 3104–3104. 1 indexed citations
13.
Valle, Jesús Del, Elisabeth Castellanos, Lídia Feliubadaló, et al.. (2021). CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools. Bioinformatics. 37(22). 4227–4229. 2 indexed citations
14.
Vidal, August, Raquel Ibáñez, Paula Peremiquel‐Trillas, et al.. (2021). Sensitivity of cervical cytology in endometrial cancer detection in a tertiary hospital in Spain. Cancer Medicine. 10(19). 6762–6766. 5 indexed citations
15.
Valle, Jesús Del, Lídia Feliubadaló, Marta Pineda, et al.. (2020). Screening of CNVs using NGS data improves mutation detection yield and decreases costs in genetic testing for hereditary cancer. Journal of Medical Genetics. 59(1). 75–78. 6 indexed citations
16.
Terradas, Mariona, Pilar Mur, Sami Belhadj, et al.. (2020). TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut. 70(6). 1139–1146. 11 indexed citations
17.
Stradella, Agostina, Jesús Del Valle, Paula Rofes, et al.. (2020). ERCC3, a new ovarian cancer susceptibility gene?. European Journal of Cancer. 141. 1–8. 9 indexed citations
18.
Valle, Jesús Del, Elisabeth Castellanos, Lídia Feliubadaló, et al.. (2020). Evaluation of CNV detection tools for NGS panel data in genetic diagnostics. European Journal of Human Genetics. 28(12). 1645–1655. 76 indexed citations
19.
Navarro, Matilde, Àlex Teulé, Ares Solanes, et al.. (2020). Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers. 12(11). 3419–3419. 12 indexed citations
20.
Pérez‐Cabornero, Lucía, Mar Infante, Eladio A. Velasco, et al.. (2011). Characterization of New Founder Alu-Mediated Rearrangements in MSH2 Gene Associated with a Lynch Syndrome Phenotype. Cancer Prevention Research. 4(10). 1546–1555. 15 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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