Sonia Moreno
St. 64 No. 51-31, 050010
Medellin, ANT, Colombia
Medellin, ANT, Colombia
Last Updated: 09/26/2026
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Found 26 publications
Genotype-phenotype association study conducted on LARGE-PD reveals novel loci associated with Parkinson's Disease.
Journal: medRxiv : the preprint server for health sciences
Published: August 12, 2025
Differences and contributors to global cognitive performance in the underrepresented Latinx Parkinson's disease population.
Journal: The Clinical neuropsychologist
Published: January 18, 2025
Primary lateral sclerosis associated with PSEN1 Pro284Leu variant in a Colombian family: Clinical and neuropathological features.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: April 15, 2024
Sex differences in the diagnosis latency of Parkinson's disease in Latin America.
Journal: Parkinsonism & related disorders
Published: February 13, 2024
Parkinson's Disease Gene Screening in Familial Cases from Central and South America.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 11, 2024
Genetic modifiers of cognitive decline in PSEN1 E280A Alzheimer's disease.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: March 28, 2023
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson Disease.
Journal: medRxiv : the preprint server for health sciences
Published: February 13, 2023
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 01, 2023
Correction to: Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Journal: Molecular neurobiology
Published: May 18, 2022
Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort.
Journal: Parkinsonism & related disorders
Published: March 25, 2022
Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Journal: Molecular neurobiology
Published: November 05, 2021
A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects.
Journal: Genome medicine
Published: July 31, 2021
Last Updated: 09/26/2026