Ver Investigador - - Prisma - Unidad de Bibliometría

Maria Teresa Periñan Tocino

Tipo Año Título Fuente
Corrección2023 Author Correction: Peripheral inflammatory immune response differs among sporadic and familial Parkinson’s disease (npj Parkinson's Disease, (2023), 9, 1, (12), 10.1038/s41531-023-00457-5) NPJ PARKINSONS DISEASE
Artículo2023 Homocysteine levels, genetic background, and cognitive impairment in Parkinson’s disease JOURNAL OF NEUROLOGY
Nota2023 Implications of DNA methylation in Lewy body pathology MOVEMENT DISORDERS
Artículo2023 Mendelian randomisation confirms the role of Y-chromosome loss in Alzheimer’s disease aetiopathogenesis in men INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Artículo2023 Peripheral inflammatory immune response differs among sporadic and familial Parkinson’s disease NPJ PARKINSONS DISEASE
Artículo2023 The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data NPJ PARKINSONS DISEASE
Artículo2022 Early downregulation of hsa-miR-144-3p in serum from drug-naïve Parkinson’s disease patients SCIENTIFIC REPORTS
Artículo2022 Effect modification between genes and environment, and Parkinson's disease risk. Annals of neurology
Nota2022 Increased stroke risk in patients with Parkinson's disease with LRRK2 mutations MOVEMENT DISORDERS
Artículo2022 Intermediate and Expanded HTT Alleles and the Risk for alpha-Synucleinopathies MOVEMENT DISORDERS
Artículo2022 Metabolite and lipoprotein profiles reveal sex-related oxidative stress imbalance in de novo drug-naive Parkinson’s disease patients NPJ PARKINSONS DISEASE
Letter2022 Reply to: “Increased stroke risk in patients with Parkinson's disease with LRRK2 mutations” MOVEMENT DISORDERS
Editorial2022 The glycoprotein GPNMB: a secret ingredient for understanding Parkinson's disease etiology? MOVEMENT DISORDERS
Artículo2022 Transcriptomic analysis reveals an association of FCGBP with Parkinson’s disease NPJ PARKINSONS DISEASE
Revisión2021 A geroscience approach for Parkinson's disease: conceptual framework and design of PROPAG-AGEING project MECHANISMS OF AGEING AND DEVELOPMENT
Artículo2021 Association of PICALM with cognitive impairment in Parkinson's disease MOVEMENT DISORDERS
Artículo2021 Common variants in Alzheimer's disease and risk stratification by polygenic risk scores NATURE COMMUNICATIONS
Artículo2021 Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome NATURE COMMUNICATIONS
Artículo2021 Genomic characterization of host factors related to SARS-CoV-2 infection in people with dementia and control populations: the GR@ACE/DEGESCO study Journal of personalized medicine
Artículo2021 Heterogeneity of prodromal Parkinson symptoms in siblings of Parkinson disease patients NPJ PARKINSONS DISEASE
Artículo2021 Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage NATURE COMMUNICATIONS
Artículo2021 Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets JAMA NEUROLOGY
Artículo2021 Identification of sixteen novel candidate genes for late onset Parkinson's disease Molecular Neurodegeneration
Artículo2021 Integrating genetic and clinical data to predict impulse control disorders in Parkinson's disease EUROPEAN JOURNAL OF NEUROLOGY
Artículo2021 Investigation of autosomal genetic sex differences in Parkinson's disease Annals of neurology
Artículo2021 Long runs of homozygosity are associated with Alzheimer’s disease TRANSLATIONAL PSYCHIATRY
Artículo2021 Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review EUROPEAN JOURNAL OF NEUROLOGY
Artículo2021 Serum lipid profile among sporadic and familial forms of Parkinson's disease NPJ PARKINSONS DISEASE
Artículo2021 The role of RHOT1 and RHOT2 genetic variation on Parkinson disease risk and onset NEUROBIOLOGY OF AGING
Artículo2020 Analysis of p.Tyr307Asn variant in the LRP10 gene in Parkinson's disease in southern Spain NEUROBIOLOGY OF AGING
Artículo2020 Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders BRAIN
Artículo2020 Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease JOURNAL OF MEDICAL GENETICS
Artículo2020 Penetrance of Parkinson's disease in LRRK2 p.G2019S carriers is modified by a polygenic risk score MOVEMENT DISORDERS
Artículo2020 Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information NATURE COMMUNICATIONS
Artículo2020 The Parkinson's disease genome-wide association study locus browser MOVEMENT DISORDERS
Artículo2019 A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population Neuroscience Letters
Artículo2019 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: the GR@ACE project Alzheimer's & Dementia
Artículo2019 Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies LANCET NEUROLOGY
Artículo2019 Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset NPJ PARKINSONS DISEASE
Artículo2019 Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability NPJ PARKINSONS DISEASE
Artículo2019 SNCA and mTOR pathway single nucleotide polymorphisms interact to modulate the age at onset of Parkinson's disease MOVEMENT DISORDERS
Artículo2019 The genetic architecture of parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight MOVEMENT DISORDERS
Letter2018 LRP10 in α-synucleinopathies LANCET NEUROLOGY
Artículo2018 TMEM230 in Parkinson's disease in a southern Spanish population PLOS ONE

Este investigador no ha dirigido/tutorizado tesis

Proyectos de Investigación

Fecha de inicio Fecha de fin Rol Denominación Agencia financiadora
01/01/2022 31/05/2023 Contratado Estudio de los genes implicados en las distonías aisladas mediante secuenciación dirigida (US-1381391) Consejería de Economía, Conocimiento, Empresas y Universidad (Autonómico)
El investigador no tiene ningún resultado de investigación asociado