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 | 549 | 2011 |
Human microRNAs miR-22, miR-138-2, miR-148a, and miR-488 are associated with panic disorder and regulate several anxiety candidate genes and related pathways M Muiños-Gimeno, Y Espinosa-Parrilla, M Guidi, B Kagerbauer, T Sipilä, ... Biological psychiatry 69 (6), 526-533, 2011 | 235 | 2011 |
Protein S deficiency: a database of mutations–summary of the first update S Gandrille, D Borgel, N Sala, Y Espinosa-Parrilla, R Simmonds, ... Thrombosis and haemostasis 84 (11), 918-918, 2000 | 170 | 2000 |
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures J Amiel, Y Espinosa-Parrilla, J Steffann, P Gosset, A Pelet, M Prieur, ... The American Journal of Human Genetics 69 (6), 1370-1377, 2001 | 133 | 2001 |
Allele variants in functional MicroRNA target sites of the neurotrophin‐3 receptor gene (NTRK3) as susceptibility factors for anxiety disorders M Muiños‐Gimeno, M Guidi, B Kagerbauer, R Martín‐Santos, R Navinés, ... Human mutation 30 (7), 1062-1071, 2009 | 111 | 2009 |
Overexpression of miR-128 specifically inhibits the truncated isoform of NTRK3 and upregulates BCL2 in SH-SY5Y neuroblastoma cells M Guidi, M Muiños-Gimeno, B Kagerbauer, E Martí, X Estivill, ... BMC molecular biology 11, 1-17, 2010 | 99 | 2010 |
Mutations of the RET gene in isolated and syndromic Hirschsprung’s disease in human disclose major and modifier alleles at a single locus LÏ de Pontual, A Pelet, D Trochet, F Jaubert, Y Espinosa-Parrilla, ... Journal of medical genetics 43 (5), 419-423, 2006 | 61 | 2006 |
Genetic association of gastric cancer with miRNA clusters including the cancer‐related genes MIR29, MIR25, MIR93 and MIR106: Results from the EPIC … Y Espinosa‐Parrilla, X Muñoz, C Bonet, N Garcia, A Vencesla, ... International journal of cancer 135 (9), 2065-2076, 2014 | 59 | 2014 |
Expression of the SMADIP1 gene during early human development Y Espinosa-Parrilla, J Amiel, J Augé, F Encha-Razavi, A Munnich, ... Mechanisms of development 114 (1-2), 187-191, 2002 | 46 | 2002 |
Decoding the role of platelets and related microRNAs in aging and neurodegenerative disorders Y Espinosa-Parrilla, C Gonzalez-Billault, E Fuentes, I Palomo, M Alarcón Frontiers in Aging Neuroscience 11, 151, 2019 | 45 | 2019 |
Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease M Muiños-Gimeno, M Montfort, M Bayés, X Estivill, Y Espinosa-Parrilla European Journal of Human Genetics 18 (2), 218-226, 2010 | 45 | 2010 |
A founder effect at the EPCAM locus in congenital tufting enteropathy in the Arabic Gulf J Salomon, Y Espinosa-Parrilla, O Goulet, P Guigue, D Canioni, ... European journal of medical genetics 54 (3), 319-322, 2011 | 44 | 2011 |
Ancient genomes in South Patagonia reveal population movements associated with technological shifts and geography N Nakatsuka, P Luisi, JMB Motti, M Salemme, F Santiago, ... Nature Communications 11 (1), 3868, 2020 | 42 | 2020 |
Protein S secretion differences of missense mutants account for phenotypic heterogeneity Y Espinosa-Parrilla, T Yamazaki, N Sala, B Dahlbäck, PG de Frutos Blood, The Journal of the American Society of Hematology 95 (1), 173-179, 2000 | 42 | 2000 |
Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency Y Espinosa‐Parrilla, M Morell, JC Souto, I Tirado, J Fontcuberta, X Estivill, ... Human mutation 14 (1), 30-39, 1999 | 38 | 1999 |
An ancestral miR-1304 allele present in Neanderthals regulates genes involved in enamel formation and could explain dental differences with modern humans M Lopez-Valenzuela, O Ramírez, A Rosas, S García-Vargas, ... Molecular Biology and Evolution 29 (7), 1797-1806, 2012 | 37 | 2012 |
Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Protein S deficiency: a … S Gandrille, D Borgel, N Sala, Y Espinosa-Parrilla, R Simmonds, ... Thromb Haemost 84 (5), 918, 2000 | 35 | 2000 |
Natural bioactive compounds as protectors of mitochondrial dysfunction in cardiovascular diseases and aging D Arauna, M Furrianca, Y Espinosa-Parrilla, E Fuentes, M Alarcón, ... Molecules 24 (23), 4259, 2019 | 34 | 2019 |
Absence of Linkage Between Type III Protein S Deficiency and the PROS1 and C4BP Genes in Families Carrying the Protein S Heerlen Allele Y Espinosa-Parrilla, M Morell, JC Souto, M Borrell, D Heine-Suñer, ... Blood, The Journal of the American Society of Hematology 89 (8), 2799-2806, 1997 | 32 | 1997 |
Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors Y Espinosa-Parrilla, G Navarro, M Morell, E Abella, X Estivill, N Sala Thrombosis and haemostasis 83 (01), 102-106, 2000 | 29 | 2000 |