Associated Papers
Elucidate biomarkers and the molecular pathways associated with genetic variants that contribute to the etiology of Parkinson's disease.
Nguyen HD
Acta Neurologica Belgica, 2025
A Next-Generation Sequencing Study in a Cohort of Sicilian Patients with Parkinson's Disease.
Salemi M et al.
Biomedicines, 2023
Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes.
Cereda M et al.
Nature Communications, 2016
27377421 (PubMed )
Supplement: ncomms12072-s6.xlsx › Supplementary_Data_5
Identification of Parkinson's disease candidate genes using CAESAR and screening of MAPT and SNCAIP in South African Parkinson's disease patients.
Keyser RJ et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2011
Genetic association study of synphilin-1 in idiopathic Parkinson's disease.
Myhre R et al.
Bmc Medical Genetics, 2008
Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.
Marx FP et al.
Human Molecular Genetics, 2003
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