Elison Sarapura‐Castro

X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson Disease

T. Thornton, F. Lopera, T. O’Connor, 2023, medRxiv.

Genome‐Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients

T. Thornton, A. Horimoto, F. Lopera, 2020, medRxiv.

Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families

S. Capellari, Piero Parchi, M. Cornejo-Olivas, 2021, Clinical Neurology and Neurosurgery.

Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients

M. Synofzik, W. Marques, O. Barsottini, 2022, Movement disorders : official journal of the Movement Disorder Society.

Characterizing the Genetic Architecture of Parkinson's Disease in Latinos

T. Thornton, A. Horimoto, F. Lopera, 2020, medRxiv.

Novel Compound Heterozygous Mutation c.3955_3958dup and c.5825C>T in the ATM Gene: Clinical Evidence of Ataxia-Telangiectasia and Cancer in a Peruvian Family

M. Cornejo-Olivas, Andrea Rivera-Valdivia, Yasser Sullcahuamán-Allende, 2021, Molecular Syndromology.

Juvenile‐Onset Huntington's Disease in Peru: A Case Series of 32 Patients

P. Mazzetti, D. Rabinowitz, Anastasia Vishnevetsky, 2022, Movement disorders clinical practice.

Machado Joseph-Disease Is Rare in the Peruvian Population.

M. Saraiva-Pereira, L. Jardim, P. Mazzetti, 2022, Cerebellum.