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Carles Ferrer-Costa
Carles Ferrer-Costa
Head of Bioinformatics at Gendiag
Verified email at gendiag.com
Title
Cited by
Cited by
Year
PMUT: a web-based tool for the annotation of pathological mutations on proteins
C Ferrer-Costa, JL Gelpí, L Zamakola, I Parraga, X De La Cruz, M Orozco
Bioinformatics 21 (14), 3176-3178, 2005
5522005
A consensus view of protein dynamics
M Rueda, C Ferrer-Costa, T Meyer, A Pérez, J Camps, A Hospital, ...
Proceedings of the National Academy of Sciences 104 (3), 796-801, 2007
296*2007
Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties
C Ferrer-Costa, M Orozco, X de la Cruz
Journal of molecular biology 315 (4), 771-786, 2002
2652002
Sequence‐based prediction of pathological mutations
C Ferrer‐Costa, M Orozco, X De La Cruz
Proteins: Structure, Function, and Bioinformatics 57 (4), 811-819, 2004
2122004
Functional and structural conservation of CBS domains from CLC chloride channels
R Estévez, M Pusch, C Ferrer‐Costa, M Orozco, TJ Jentsch
The Journal of physiology 557 (2), 363-378, 2004
1882004
Blood biomarkers for the early diagnosis of stroke: the stroke-chip study
A Bustamante, E López-Cancio, S Pich, A Penalba, D Giralt, ...
Stroke 48 (9), 2419-2425, 2017
1482017
MoDEL (Molecular Dynamics Extended Library): a database of atomistic molecular dynamics trajectories
T Meyer, M D'Abramo, M Rueda, C Ferrer-Costa, A Pérez, O Carrillo, ...
Structure 18 (11), 1399-1409, 2010
1302010
The structure of human 4F2hc ectodomain provides a model for homodimerization and electrostatic interaction with plasma membrane
J Fort, LR de la Ballina, HE Burghardt, C Ferrer-Costa, J Turnay, ...
Journal of Biological Chemistry 282 (43), 31444-31452, 2007
1232007
Essential dynamics: a tool for efficient trajectory compression and management
T Meyer, C Ferrer-Costa, A Pérez, M Rueda, A Bidon-Chanal, FJ Luque, ...
Journal of Chemical Theory and Computation 2 (2), 251-258, 2006
1232006
Natural and undetermined sudden death: value of post-mortem genetic investigation
O Sanchez, O Campuzano, A Fernández-Falgueras, ...
PLoS One 11 (12), e0167358, 2016
792016
Approaching elastic network models to molecular dynamics flexibility
L Orellana, M Rueda, C Ferrer-Costa, JR Lopez-Blanco, P Chacón, ...
Journal of Chemical Theory and Computation 6 (9), 2910-2923, 2010
772010
Post-mortem genetic analysis in juvenile cases of sudden cardiac death
O Campuzano, O Sanchez-Molero, C Allegue, M Coll, I Mademont-Soler, ...
Forensic science international 245, 30-37, 2014
642014
Ultra-deep pyrosequencing detects conserved genomic sites and quantifies linkage of drug-resistant amino acid changes in the hepatitis B virus genome
F Rodriguez-Frias, D Tabernero, J Quer, JI Esteban, I Ortega, E Domingo, ...
PloS one 7 (5), e37874, 2012
622012
Characterization of compensated mutations in terms of structural and physico-chemical properties
C Ferrer-Costa, M Orozco, X de la Cruz
Journal of Molecular Biology 365 (1), 249-256, 2007
612007
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy
I Mademont-Soler, J Mates, R Yotti, MA Espinosa, A Pérez-Serra, ...
PLoS One 12 (8), e0181465, 2017
552017
PupasView: a visual tool for selecting suitable SNPs, with putative pathological effect in genes, for genotyping purposes
L Conde, JM Vaquerizas, C Ferrer-Costa, X de la Cruz, M Orozco, ...
Nucleic acids research 33 (suppl_2), W501-W505, 2005
532005
Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
O Campuzano, G Sarquella-Brugada, A Fernandez-Falgueras, M Coll, ...
EBioMedicine 54, 2020
482020
A genetically vulnerable myocardium may predispose to myocarditis
O Campuzano, A Fernández-Falgueras, G Sarquella-Brugada, ...
Journal of the American College of Cardiology 66 (25), 2913-2914, 2015
482015
The catalytic site structural gate of adenosine deaminase allosterically modulates ligand binding to adenosine receptors
E Gracia, D Farré, A Cortés, C Ferrer‐Costa, M Orozco, J Mallol, C Lluís, ...
The FASEB Journal 27 (3), 1048-1061, 2013
482013
Short QT syndrome: a comprehensive genetic interpretation and clinical translation of rare variants
O Campuzano, A Fernandez-Falgueras, X Lemus, G Sarquella-Brugada, ...
Journal of clinical medicine 8 (7), 1035, 2019
432019
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