| 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 | 560 | 2005 |
| 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 | 304* | 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 | 270 | 2002 |
| 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 | 212 | 2004 |
| 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 | 190 | 2004 |
| 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 | 164 | 2017 |
| 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 | 140 | 2010 |
| 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 | 130 | 2006 |
| 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 | 128 | 2007 |
| Natural and undetermined sudden death: value of post-mortem genetic investigation O Sanchez, O Campuzano, A Fernández-Falgueras, ... PLoS One 11 (12), e0167358, 2016 | 93 | 2016 |
| 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 | 79 | 2010 |
| 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 | 70 | 2014 |
| 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 | 62 | 2012 |
| 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 | 60 | 2020 |
| 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 | 60 | 2007 |
| 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 | 59 | 2017 |
| 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 | 53 | 2015 |
| 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 | 53 | 2005 |
| 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 | 51 | 2013 |
| 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 | 48 | 2019 |
