| hnRNPDL phase separation is regulated by alternative splicing and disease-causing mutations accelerate its aggregation C Batlle, P Yang, M Coughlin, J Messing, M Pesarrodona, E Szulc, ... Cell reports 30 (4), 1117-1128. e5, 2020 | 60 | 2020 |
| Amyloids or prions? That is the question R Sabate, F Rousseau, J Schymkowitz, C Batlle, S Ventura Prion 9 (3), 200-206, 2015 | 50 | 2015 |
| Characterization of amyloid cores in prion domains R Sant’Anna, MR Fernández, C Batlle, S Navarro, NS De Groot, L Serpell, ... Scientific reports 6 (1), 34274, 2016 | 48 | 2016 |
| Insight into the specificity and severity of pathogenic mechanisms associated with missense mutations through experimental and structural perturbation analyses E Medina-Carmona, I Betancor-Fernández, J Santos, N Mesa-Torres, ... Human Molecular Genetics 28 (1), 1-15, 2019 | 29 | 2019 |
| Characterization of soft amyloid cores in human prion-like proteins C Batlle, NS De Groot, V Iglesias, S Navarro, S Ventura Scientific reports 7 (1), 12134, 2017 | 28 | 2017 |
| AMYCO: evaluation of mutational impact on prion-like proteins aggregation propensity V Iglesias, O Conchillo-Sole, C Batlle, S Ventura BMC bioinformatics 20, 1-5, 2019 | 25 | 2019 |
| Prion-like proteins and their computational identification in proteomes C Batlle, V Iglesias, S Navarro, S Ventura Expert review of proteomics 14 (4), 335-350, 2017 | 25 | 2017 |
| Rational optimization of a transcription factor activation domain inhibitor S Basu, P Martínez-Cristóbal, M Frigolé-Vivas, M Pesarrodona, M Lewis, ... Nature Structural & Molecular Biology 30 (12), 1958-1969, 2023 | 14 | 2023 |
| Amyloid cores in prion domains: Key regulators for prion conformational conversion MR Fernández, C Batlle, M Gil-García, S Ventura Prion 11 (1), 31-39, 2017 | 14 | 2017 |
| MED15 prion-like domain forms a coiled-coil responsible for its amyloid conversion and propagation C Batlle, I Calvo, V Iglesias, C J. Lynch, M Gil-Garcia, M Serrano, ... Communications Biology 4 (1), 414, 2021 | 11 | 2021 |
| Perfecting prediction of mutational impact on the aggregation propensity of the ALS‐associated hn RNPA 2 prion‐like protein C Batlle, MR Fernández, V Iglesias, S Ventura FEBS letters 591 (13), 1966-1971, 2017 | 10 | 2017 |
| Prion-like domain disease-causing mutations and misregulation of alternative splicing relevance in limb-girdle muscular dystrophy (LGMD) 1G C Batlle, S Ventura Neural Regeneration Research 15 (12), 2239-2240, 2020 | 8 | 2020 |
| Androgen receptor condensates as drug targets S Basu, P Martínez-Cristóbal, M Pesarrodona, M Frigolé-Vivas, E Szulc, ... BioRxiv, 2022.08. 18.504385, 2022 | 4 | 2022 |
| Los alumnos portugueses en la Real Academia de Bellas Artes de San Fernando desde su fundación hasta principios del siglo XIX: Consideraciones biográficas y estadísticas C Mongay Batlle, G Avinyó, I Rega Castro Éditions Baywolf, 2014 | 1 | 2014 |
| Xavier Gosé, paradigma de la construcció de patrimoni cultural a la ciutat de Lleida CM Batlle ARTS, 32-35, 2014 | 1 | 2014 |
| Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants D Natera‐de Benito, J Olival, C Garcia‐Cabau, C Jou, M Roldan, ... Annals of Clinical and Translational Neurology 10 (3), 408-425, 2023 | | 2023 |
| P. 152 The novel ANXA11 variant p. Asp40Ile in a childhood-onset oculopharyngeal muscular dystrophy shows the pathogenic relevance of Asp40 in ANXA11 disorders D Natera-de Benito, J Olival, C Garcia-Cabau, A Codina, M Roldan, ... Neuromuscular Disorders 32, S109, 2022 | | 2022 |
| Role of alternative splicing in phase separation and pathogenic aggregation C Batlle, JP Taylor, S Ventura EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS 50 (SUPPL 1), 90-90, 2021 | | 2021 |
| 病毒样相关疾病的致病突变和可变剪接相关性的调控异常 C Batlle, S Ventura 中国神经再生研究 (英文版) 15 (12), 2239, 2020 | | 2020 |
| Persistencia de la Época Moderna. Una revisión del mundo académico de las Bellas Artes en el Madrid de los siglos XVIII y XIX CM Batlle Universitat de Lleida, 2017 | | 2017 |
