Alejandro Moles‐Fernández

932 total citations
11 papers, 183 citations indexed

About

Alejandro Moles‐Fernández is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Alejandro Moles‐Fernández has authored 11 papers receiving a total of 183 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Alejandro Moles‐Fernández's work include BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (4 papers) and DNA Repair Mechanisms (4 papers). Alejandro Moles‐Fernández is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (4 papers) and DNA Repair Mechanisms (4 papers). Alejandro Moles‐Fernández collaborates with scholars based in Spain, Palestinian Territory and Sweden. Alejandro Moles‐Fernández's co-authors include Orland Dı́ez, Sara Gutiérrez‐Enríquez, Judith Balmañà, Gemma Montalban, Sandra Bonache, Estela Carrasco, Adrià López‐Fernández, Neda Stjepanovic, Vanessa Bach and Neus Gadea and has published in prestigious journals such as Clinical Chemistry, Journal of Medical Genetics and Breast Cancer Research and Treatment.

In The Last Decade

Alejandro Moles‐Fernández

11 papers receiving 181 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alejandro Moles‐Fernández Spain 7 134 96 45 34 24 11 183
Gemma Montalban Spain 8 149 1.1× 121 1.3× 45 1.0× 44 1.3× 41 1.7× 11 208
Daniel S. Marchuk United States 4 62 0.5× 90 0.9× 54 1.2× 37 1.1× 18 0.8× 5 144
Eva Tornero Spain 8 142 1.1× 177 1.8× 93 2.1× 56 1.6× 39 1.6× 15 254
Martina Zimovjanová Czechia 7 49 0.4× 85 0.9× 36 0.8× 19 0.6× 41 1.7× 16 127
Jamie Allen United Kingdom 8 96 0.7× 101 1.1× 49 1.1× 31 0.9× 31 1.3× 13 162
Sami Belhadj Spain 8 79 0.6× 53 0.6× 46 1.0× 70 2.1× 51 2.1× 8 157
Paula Rofes Spain 6 65 0.5× 52 0.5× 35 0.8× 48 1.4× 30 1.3× 11 118
Wendy A. van Zelst-Stams Netherlands 5 87 0.6× 53 0.6× 58 1.3× 72 2.1× 45 1.9× 5 168
Richard W. Park United States 4 88 0.7× 66 0.7× 80 1.8× 21 0.6× 18 0.8× 5 161
Pasquelena De Nittis Italy 5 88 0.7× 38 0.4× 20 0.4× 24 0.7× 28 1.2× 7 135

Countries citing papers authored by Alejandro Moles‐Fernández

Since Specialization
Citations

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

Fields of papers citing papers by Alejandro Moles‐Fernández

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alejandro Moles‐Fernández. 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 Alejandro Moles‐Fernández. The network helps show where Alejandro Moles‐Fernández may publish in the future.

Co-authorship network of co-authors of Alejandro Moles‐Fernández

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

All Works

11 of 11 papers shown
1.
Papakonstantinou, Andri, Adrià López‐Fernández, Judit Matito, et al.. (2025). Identifying germline pathogenic variants in breast cancer using tumor sequencing. The Breast. 81. 104439–104439. 1 indexed citations
2.
Padilla, Natàlia, Alejandro Moles‐Fernández, Lídia Feliubadaló, et al.. (2023). A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical Analysis. Journal of Molecular Diagnostics. 26(1). 17–28. 3 indexed citations
3.
Montalban, Gemma, Sandra Bonache, Vanessa Bach, et al.. (2021). BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary breast/ovarian cancer patients. Cancer Genetics. 258-259. 10–17. 5 indexed citations
4.
5.
Feliubadaló, Lídia, Alejandro Moles‐Fernández, Marta Santamariña, et al.. (2020). A Collaborative Effort to Define Classification Criteria forATMVariants in Hereditary Cancer Patients. Clinical Chemistry. 67(3). 518–533. 15 indexed citations
6.
Montalban, Gemma, Sandra Bonache, Alejandro Moles‐Fernández, et al.. (2019). Incorporation of semi‐quantitative analysis of splicing alterations for the clinical interpretation of variants inBRCA1andBRCA2genes. Human Mutation. 40(12). 2296–2317. 9 indexed citations
7.
Padilla, Natàlia, Alejandro Moles‐Fernández, Gemma Montalban, et al.. (2019). BRCA1 ‐ and BRCA2 ‐specific in silico tools for variant interpretation in the CAGI 5 ENIGMA challenge. Human Mutation. 40(9). 1593–1611. 8 indexed citations
8.
Bonache, Sandra, Alejandro Moles‐Fernández, Gemma Montalban, et al.. (2018). Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of Cancer Research and Clinical Oncology. 144(12). 2495–2513. 49 indexed citations
9.
Moles‐Fernández, Alejandro, Gemma Montalban, Sandra Bonache, et al.. (2018). Computational Tools for Splicing Defect Prediction in Breast/Ovarian Cancer Genes: How Efficient Are They at Predicting RNA Alterations?. Frontiers in Genetics. 9. 366–366. 46 indexed citations
10.
Montalban, Gemma, Sandra Bonache, Alejandro Moles‐Fernández, et al.. (2018). Alternative transcript imbalance underlying breast cancer susceptibility in a family carrying PALB2 c.3201+5G>T. Breast Cancer Research and Treatment. 174(2). 543–550. 4 indexed citations
11.
Montalban, Gemma, Sandra Bonache, Alejandro Moles‐Fernández, et al.. (2018). Screening of BRCA1/2 deep intronic regions by targeted gene sequencing identifies the first germline BRCA1 variant causing pseudoexon activation in a patient with breast/ovarian cancer. Journal of Medical Genetics. 56(2). 63–74. 24 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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