Alejandro Brea‐Fernández

1.1k total citations
16 papers, 168 citations indexed

About

Alejandro Brea‐Fernández is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Alejandro Brea‐Fernández has authored 16 papers receiving a total of 168 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Alejandro Brea‐Fernández's work include Genetic factors in colorectal cancer (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Alejandro Brea‐Fernández is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Alejandro Brea‐Fernández collaborates with scholars based in Spain, United States and Saudi Arabia. Alejandro Brea‐Fernández's co-authors include Ãngel Carracedo, Clara Ruíz-Ponte, Sergi Castellvı́-Bel, Antoni Castells, Ceres Fernández–Rozadilla, Esther Pomares, Miguel Blanco, Xavier Llor, Manuel Sánchez‐Salorio and Marı́a Brión and has published in prestigious journals such as Gastroenterology, PLoS ONE and BMC Genomics.

In The Last Decade

Alejandro Brea‐Fernández

15 papers receiving 165 citations

Peers

Countries citing papers authored by Alejandro Brea‐Fernández

Since Specialization

Citations

This map shows the geographic impact of Alejandro Brea‐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 Brea‐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 Brea‐Fernández more than expected).

Fields of papers citing papers by Alejandro Brea‐Fernández

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders 2023 ·Cytogenetic and Genome Research ·Alejandro Brea‐Fernández, (unknown), (unknown), (unknown), (unknown), Carmen Gómez‐Lado, Jesús Manuel Eirís Puñal, Montse Fernández‐Prieto, Francisco Barros, Roberto J. Brea, Ãngel Carracedo	0
2	Trio-based exome sequencing reveals a high rate of the de novo variants in intellectual disability 2022 ·European Journal of Human Genetics ·Alejandro Brea‐Fernández, (unknown), Jorge Amigo, (unknown), (unknown), Montse Fernández‐Prieto, Francisco Barros, Silvia De Rubeis, Joseph D. Buxbaum, Ãngel Carracedo	13
3	Expanding the clinical and molecular spectrum of the CWC27-related spliceosomopathy 2019 ·Journal of Human Genetics ·Alejandro Brea‐Fernández, (unknown), David Dacruz-Álvarez, (unknown), Jacobo Limeres Posse, Lourdes Loidi	9
4	Novel truncating variants expand the phenotypic spectrum of KAT6B‐related disorders 2018 ·American Journal of Medical Genetics Part A ·Alejandro Brea‐Fernández, (unknown), Jesús Manuel Eirís Puñal, Francisco Barros, Ãngel Carracedo	8
5	The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer 2016 ·European Journal of Human Genetics ·Clara Esteban-Jurado, Sebastià Franch‐Expósito, Jenifer Muñoz, Teresa Ocaña, Sabela Carballal, María López‐Cerón, Míriam Cuatrecasas, María Vila-Casadesús, Juan José Lozano, (unknown), Sergi Beltrán, Alejandro Brea‐Fernández, Clara Ruíz-Ponte, Antoni Castells, Luís Bujanda, Pilar Garré, Trinidad Caldés, Joaquín Cubiella, Francesc Balaguer, Sergi Castellvı́-Bel	35
6	Candidate predisposing germline copy number variants in early onset colorectal cancer patients 2016 ·Clinical & Translational Oncology ·Alejandro Brea‐Fernández, Ceres Fernández–Rozadilla, (unknown), Daniel Azuara, M. Morell, Juan Clofent, Luisa de Castro, (unknown), M. Andreu, Xavier Bessa, Xavier Llor, Rosa M. Xicola, Rodrigo Jover, Antoni Castells, Sergi Castellvı́-Bel, Gabriel Capellá, Ãngel Carracedo, Clara Ruíz-Ponte	4
7	Pharmacogenomics of CRC treatments: putting bricks on the path to personalized medicine 2014 ·BMC Genomics ·Ceres Fernández–Rozadilla, (unknown), Mahmood Rasool, Francisco Barros, Antoni Castells, Sergi Castellvı́-Bel, Alejandro Brea‐Fernández, Clara Ruíz-Ponte, Ãngel Carracedo	5
8	High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families 2013 ·Clinical Genetics ·Alejandro Brea‐Fernández, José Cameselle‐Teijeiro, Cristina Alenda, Ceres Fernández–Rozadilla, Joaquín Cubiella, Joan Clofent, (unknown), Urbano Anido, Montserrat Milà, Francesc Balaguer, Antoni Castells, Sergi Castellvı́-Bel, Rodrigo Jover, Ãngel Carracedo, Clara Ruíz-Ponte	6
9	Seeking genetic susceptibility variants for colorectal cancer: the EPICOLON consortium experience 2012 ·Mutagenesis ·Sergi Castellvı́-Bel, Clara Ruíz-Ponte, Ceres Fernández–Rozadilla, Anna Abulí, Jenifer Muñoz, Xavier Bessa, Alejandro Brea‐Fernández, Matteo Dal Ferro, María D. Giraldez, Rosa M. Xicola, Xavier Llor, Rodrigo Jover, J. M. Piqué, M. Andreu, Antoni Castells, Ãngel Carracedo	7
10	Vaginal Tubulovillous Adenoma 2012 ·International Journal of Gynecological Pathology ·(unknown), Ihab Abdulkader, (unknown), (unknown), Alejandro Brea‐Fernández, (unknown), Clara Ruíz-Ponte, José Cameselle‐Teijeiro	6
11	An Update of In Silico Tools for the Prediction of Pathogenesis in Missense Variants 2011 ·Current Bioinformatics ·Alejandro Brea‐Fernández, (unknown), Ceres Fernández–Rozadilla, Ana Blanco, Laura Fachal, Marta Santamariña, Ana Vega, Alejandro Pazos, Ãngel Carracedo, Clara Ruíz-Ponte	2
12	Comparison Between Universal Immunohistochemistry for Mismatch Repair Proteins Versus Revised Bethesda Guidelines in the Detection of Patients With Lynch Syndrome 2011 ·Gastroenterology ·Lucía Pérez–Carbonell, Carla Guarinós, (unknown), Cristina Sánchez–Fortún, (unknown), Clara Ruíz-Ponte, Adela Castillejo, Alejandro Brea‐Fernández, Ãngel Carracedo, Víctor Manuel Barberá, Estefanía Rojas, Luís Bujanda, Joan Clofent, Montserrat Andreu, Xavier Llor, Antoni Castells, José Luís Soto, Rodrigo Jover	4
13	Single Nucleotide Polymorphisms in the Wnt and BMP Pathways and Colorectal Cancer Risk in a Spanish Cohort 2010 ·PLoS ONE ·Ceres Fernández–Rozadilla, Luisa de Castro, Juan Clofent, Alejandro Brea‐Fernández, Xavier Bessa, Anna Abulí, Montserrat Andreu, Rodrigo Jover, Rosa M. Xicola, Xavier Llor, Antoni Castells, Sergi Castellvı́-Bel, Ãngel Carracedo, Clara Ruíz-Ponte	35
14	Colorectal Cancer Susceptibility Quantitative Trait Loci in Mice as a Novel Approach to Detect Low-Penetrance Variants in Humans: A Two-Stage Case-Control Study 2010 ·Cancer Epidemiology Biomarkers & Prevention ·Ceres Fernández–Rozadilla, Rosa Tarrı́o, Juan Clofent, Luisa de Castro, Alejandro Brea‐Fernández, Xavier Bessa, Anna Abulí, Montserrat Andreu, Rodrigo Jover, Rosa M. Xicola, Xavier Llor, Antoni Castells, Sergi Castellvı́-Bel, Ãngel Carracedo, Clara Ruíz-Ponte	5
15	S1993 Comparison Between Routine Immunohistochemistry for Mismatch Repair Proteins Versus Revised Bethesda Guidelines in the Diagnosis of Lynch Syndrome in a Non-Selected Population of Colorectal Cancer Patients 2010 ·Gastroenterology ·Lucía Pérez–Carbonell, Clara Ruíz-Ponte, Xavier Bessa, José Luís Soto, Adela Castillejo, Víctor Manuel Barberá, Alejandro Brea‐Fernández, Laura Sempere, Cristina Sánchez–Fortún, Sergi Castellvı́-Bel, Francesc Balaguer, Rosa M. Xicola, Xavier Llor, Anna Abulí, Montserrat Andreu, Cristina Alenda, Artemio Payá, Ãngel Carracedo, Antoni Castells, Rodrigo Jover	1
16	Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa 2008 ·British Journal of Ophthalmology ·Alejandro Brea‐Fernández, Esther Pomares, Marı́a Brión, Gemma Marfany, Miguel Blanco, Manuel Sánchez‐Salorio, Roser Gonzàlez‐Duarte, Ãngel Carracedo	28

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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