Esther Darder

1.8k total citations
18 papers, 369 citations indexed

About

Esther Darder is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Esther Darder has authored 18 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Oncology. Recurrent topics in Esther Darder's work include BRCA gene mutations in cancer (13 papers), DNA Repair Mechanisms (4 papers) and Genetic factors in colorectal cancer (4 papers). Esther Darder is often cited by papers focused on BRCA gene mutations in cancer (13 papers), DNA Repair Mechanisms (4 papers) and Genetic factors in colorectal cancer (4 papers). Esther Darder collaborates with scholars based in Spain, Palestinian Territory and Canada. Esther Darder's co-authors include Joan Brunet, Conxi Lázaro, Ignacio Blanco, Judith Balmañà, Gabriel Capellá, Àngela Velasco, Neus Gadea, Fernando Bellido, Marta Pineda and Tirso Pons and has published in prestigious journals such as Journal of Clinical Oncology, Human Reproduction and European Journal of Cancer.

In The Last Decade

Esther Darder

14 papers receiving 365 citations

Peers

Esther Darder

GENET

PFM

ONCOL

Joanne Honeyford Canada

Julie Erlichman United States

Wendy A.G. van Zelst–Stams Netherlands

Jacquelyn Powers United States

Sara Pirzadeh‐Miller United States

Talia Donenberg United States

Anne‐Bine Skytte Denmark

Sonia Nanda Canada

Kristin B. Niendorf United States

Eli Marie Grindedal Norway

Joanne Honeyford Canada

Esther Darder

340 ×1.9

GENET

83 ×0.5

PFM

113 ×0.9

62 ×0.6

ONCOL

104 ×1.0

Citations per year, relative to Esther Darder Esther Darder (= 1×) peers Joanne Honeyford

Countries citing papers authored by Esther Darder

Since Specialization

Citations

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

Fields of papers citing papers by Esther Darder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Darder

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

All Works

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18 of 18 papers shown

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

Salvador, L., Jesús Del Valle, Anne‐Sophie Chong, et al.. (2025). DICER1 in pediatric and adult cancer predisposition populations: Prevalence, phenotypes, and mosaicism. Genetics in Medicine. 27(5). 101385–101385.

López‐Fernández, Adrià, et al.. (2025). Exploring communication preferences for disclosing breast cancer risk in women with a family history. Journal of Genetic Counseling. 34(5). e70114–e70114.

López‐Fernández, Adrià, Guillermo Villacampa, Mónica Salinas, et al.. (2023). Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result. Journal of Genetic Counseling. 32(4). 778–787. 3 indexed citations

Pardo, Marta, Esther Darder, Anna Carbó, et al.. (2023). Risk of endometrial cancer after RRSO in BRCA 1/2 carriers: a multicentre cohort study. Clinical & Translational Oncology. 26(4). 1033–1037.

Barretina-Ginesta, Maria-Pilar, Marta Pardo, L. M. Cardenas, et al.. (2023). Clinical features of long-term survivors with advanced high-grade serous ovarian cancer.. Journal of Clinical Oncology. 41(16_suppl). e17575–e17575. 1 indexed citations

López‐Fernández, Adrià, Guillermo Villacampa, Èlia Grau, et al.. (2021). Patients’ and professionals’ perspective of non-in-person visits in hereditary cancer: predictors and impact of the COVID-19 pandemic. Genetics in Medicine. 23(8). 1450–1457. 4 indexed citations

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

Bellido, Fernando, Marta Pineda, Gemma Aiza, et al.. (2015). POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance. Genetics in Medicine. 18(4). 325–332. 175 indexed citations

10.

Sumalla, Enric C., et al.. (2015). Adaptación cultural y validación de la versión española de la Escala de Autoconcepto en BRCA en mujeres portadoras con alto riesgo de cáncer de mama y ovario hereditario. Medicina Clínica. 146(4). 148–154.

11.

Gadea, Neus, Joan Brunet, Teresa Ramón y Cajal, et al.. (2012). What factors may influence psychological well being at three months and one year post BRCA genetic result disclosure?. The Breast. 21(6). 755–760. 32 indexed citations

12.

Fernández‐Rodríguez, Juana, Francisco Quiles, Ignacio Blanco, et al.. (2012). Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families. BMC Cancer. 12(1). 84–84. 12 indexed citations

13.

Valle, Jesús Del, Olga Campos, Àngela Velasco, et al.. (2011). Identification of a new complex rearrangement affecting exon 20 of BRCA1. Breast Cancer Research and Treatment. 130(1). 341–344. 2 indexed citations

14.

Graña, Begoña, Laura Fachal, Esther Darder, et al.. (2011). Germline ATM mutational analysis in BRCA1/BRCA2 negative hereditary breast cancer families by MALDI-TOF mass spectrometry. Breast Cancer Research and Treatment. 128(2). 573–579. 7 indexed citations

15.

Valle, Jesús Del, Lídia Feliubadaló, Marga Nadal, et al.. (2009). Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes. Breast Cancer Research and Treatment. 122(3). 733–743. 28 indexed citations

16.

Sanz, Judit, Teresa Ramón y Cajal, Esther Darder, et al.. (2009). Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain. Familial Cancer. 9(3). 297–304. 34 indexed citations

17.

Balmañà, Judith, et al.. (2009). Opinion about reproductive decision making among individuals undergoing BRCA1/2 genetic testing in a multicentre Spanish cohort. Human Reproduction. 24(7). 1772–1772. 2 indexed citations

18.

Balmañà, Judith, Begoña Graña, Esther Darder, et al.. (2008). Opinion about reproductive decision making among individuals undergoing BRCA1/2 genetic testing in a multicentre Spanish cohort. Human Reproduction. 24(4). 1000–1006. 59 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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