| MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function E Minones-Moyano, S Porta, G Escaramís, R Rabionet, S Iraola, ... Human molecular genetics 20 (15), 3067-3078, 2011 | 577 | 2011 |
| A myriad of miRNA variants in control and Huntington’s disease brain regions detected by massively parallel sequencing E Martí, L Pantano, M Banez-Coronel, F Llorens, E Minones-Moyano, ... Nucleic acids research 38 (20), 7219-7235, 2010 | 354 | 2010 |
| Patient-derived frontotemporal lobar degeneration brain extracts induce formation and spreading of TDP-43 pathology in vivo S Porta, Y Xu, CR Restrepo, LK Kwong, B Zhang, HJ Brown, EB Lee, ... Nature communications 9 (1), 4220, 2018 | 235 | 2018 |
| Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration EB Lee, S Porta, G Michael Baer, Y Xu, ER Suh, LK Kwong, L Elman, ... Acta neuropathologica 134, 65-78, 2017 | 232 | 2017 |
| A pathogenic mechanism in Huntington's disease involves small CAG-repeated RNAs with neurotoxic activity M Bañez-Coronel, S Porta, B Kagerbauer, E Mateu-Huertas, L Pantano, ... PLoS genetics 8 (2), e1002481, 2012 | 217 | 2012 |
| Increased striatal adenosine A2A receptor levels is an early event in Parkinson’s disease-related pathology and it is potentially regulated by miR-34b I Villar-Menéndez, S Porta, SP Buira, T Pereira-Veiga, S Díaz-Sánchez, ... Neurobiology of disease 69, 206-214, 2014 | 129 | 2014 |
| Neuronal hemoglobin is reduced in Alzheimer's disease, argyrophilic grain disease, Parkinson's disease, and dementia with Lewy bodies I Ferrer, A Gómez, M Carmona, G Huesa, S Porta, M Riera-Codina, ... Journal of Alzheimer's Disease 23 (3), 537-550, 2011 | 121 | 2011 |
| Autosomal dominant VCP hypomorph mutation impairs disaggregation of PHF-tau NF Darwich, JM Phan, B Kim, ER Suh, JD Papatriantafyllou, L Changolkar, ... Science 370 (6519), eaay8826, 2020 | 115 | 2020 |
| RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: a potential pathogenic process in neurodegeneration S Porta, SA Serra, M Huch, MA Valverde, F Llorens, X Estivill, ML Arbones, ... Human Molecular Genetics 16 (9), 1039-1050, 2007 | 111 | 2007 |
| Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory KR Martin, A Corlett, D Dubach, T Mustafa, HA Coleman, HC Parkington, ... Human Molecular Genetics 21 (13), 3025-3041, 2012 | 98 | 2012 |
| DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease DJ Keating, D Dubach, MP Zanin, Y Yu, K Martin, YF Zhao, C Chen, ... Human molecular genetics 17 (7), 1020-1030, 2008 | 98 | 2008 |
| TDP-43 promotes neurodegeneration by impairing chromatin remodeling A Berson, A Sartoris, R Nativio, V Van Deerlin, JB Toledo, S Porta, S Liu, ... Current Biology 27 (23), 3579-3590. e6, 2017 | 87 | 2017 |
| Limbic-predominant age-related TDP-43 encephalopathy differs from frontotemporal lobar degeneration JL Robinson, S Porta, FG Garrett, P Zhang, SX Xie, ER Suh, ... Brain 143 (9), 2844-2857, 2020 | 63 | 2020 |
| Upregulation of a small vault RNA (svtRNA2-1a) is an early event in Parkinson disease and induces neuronal dysfunction E Miñones-Moyano, MR Friedländer, J Pallares, B Kagerbauer, S Porta, ... RNA biology 10 (7), 1093-1106, 2013 | 59 | 2013 |
| Differential expression of members of the RCAN family of calcineurin regulators suggests selective functions for these proteins in the brain S Porta, E Martí, S De La Luna, ML Arbonés European Journal of Neuroscience 26 (5), 1213-1226, 2007 | 51 | 2007 |
| Aberrant activation of non-coding RNA targets of transcriptional elongation complexes contributes to TDP-43 toxicity CY Chung, A Berson, JR Kennerdell, A Sartoris, T Unger, S Porta, HJ Kim, ... Nature communications 9 (1), 4406, 2018 | 43 | 2018 |
| Drosha Inclusions Are New Components of Dipeptide-Repeat Protein Aggregates in FTLD-TDP and ALS C9orf72 Expansion Cases S Porta, LK Kwong, JQ Trojanowski, VMY Lee Journal of Neuropathology & Experimental Neurology 74 (4), 380-387, 2015 | 43 | 2015 |
| Distinct brain‐derived TDP‐43 strains from FTLD‐TDP subtypes induce diverse morphological TDP‐43 aggregates and spreading patterns in vitro and in vivo S Porta, Y Xu, T Lehr, B Zhang, E Meymand, M Olufemi, A Stieber, EB Lee, ... Neuropathology and applied neurobiology 47 (7), 1033-1049, 2021 | 41 | 2021 |
| Seeding the aggregation of TDP-43 requires post-fibrillization proteolytic cleavage ST Kumar, S Nazarov, S Porta, N Maharjan, U Cendrowska, M Kabani, ... Nature Neuroscience 26 (6), 983-996, 2023 | 39 | 2023 |
| Distinct characteristics of limbic-predominant age-related TDP-43 encephalopathy in Lewy body disease MT Uemura, JL Robinson, KAQ Cousins, TF Tropea, DC Kargilis, ... Acta neuropathologica 143 (1), 15-31, 2022 | 39 | 2022 |
