Alejandro Brea‐Fernández

Author

Fundación Pública Galega de Medicina Xenómica ORCID

Also Known As

A Brea-Fernández, A Brea‐Fernández, A J Brea-Fernandez, A. Brea-Fernandez, A. Brea-Fernández, A. J. Brea-Fernandez, A.J. Brea‐Fernández, Alejandro Brea, Alejandro Brea-Fernandez, Alejandro Brea-Fernández

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Fundación Pública Galega de Medicina Xenómica Centre for Biomedical Network Research on Rare Diseases Universidade de Santiago de Compostela Universitat de Barcelona Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas

About

Alejandro Brea‐Fernández is an author at Fundación Pública Galega de Medicina Xenómica specializing in medicine, pathology, and cancer research.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	514
2	Public Health	1	1	215
3	Cell Biology	1	1	15
4	Epidemiology	1	1	215
5	Molecular Biology	1	1	33

Alejandro Brea‐Fernández

Publications

Citations

H-Index

Page 1

	Year	Citations
Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation María Rodríguez–Soler, Lucía Pérez–Carbonell, Carla Guarinós, Gastroenterology EpidemiologySomatic VariantCancer PathologyCancer RiskGenetic Disorder	2013	215
Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer Lucía Pérez–Carbonell, Clara Ruíz-Ponte, Carla Guarinós, Gut	2011	187
Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer Ruta Sahasrabudhe, Paul C. Lott, Mábel Bohórquez, Gastroenterology Genome InstabilitySomatic VariantGastrointestinal OncologyGeneticsPathology	2016	126
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia Darius Ebrahimi‐Fakhari, Julian Teinert, Robert Behne, Brain	2019	74
Single Nucleotide Polymorphisms in the Wnt and BMP Pathways and Colorectal Cancer Risk in a Spanish Cohort Ceres Fernández–Rozadilla, Luisa de Castro, Juan Clofent, PLoS ONE	2010	73
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer Clara Esteban-Jurado, Sebastià Franch‐Expósito, Jenifer Muñoz, European Journal of Human Genetics Fanconi AnemiaGenome InstabilityOncogenic AgentMedicineGenetics	2016	53
Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration Ceres Fernández–Rozadilla, Jean‐Baptiste Cazier, Vı́ctor Moreno, The Pharmacogenomics Journal Genome-wide Association StudyOncologyChemoprevention StrategyMedicineColorectal Cancer	2012	51
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12 Ceres Fernández–Rozadilla, Jean‐Baptiste Cazier, Ian Tomlinson, BMC Genomics	2013	40
Prevalence of<i>MLH1</i>constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer Adela Castillejo, Eva Hernández‐Illán, María Rodríguez–Soler, Journal of Medical Genetics	2015	37
Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa Alejandro Brea‐Fernández, Esther Pomares, Marı́a Brión, British Journal of Ophthalmology	2008	35

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