Associated Papers
Bridging pleiotropic mechanisms in leprosy type-1 reactions and neurodegenerative diseases.
Fava VM et al.
Scientific Reports, 2025
PSEN2 Thr421Met Mutation in a Patient with Early Onset Alzheimer's Disease.
Yang Y et al.
International Journal of Molecular Sciences, 2022
Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.
Cukier HN et al.
Npj Parkinson's Disease, 2022
A Pathogenic Presenilin-1 Val96Phe Mutation from a Malaysian Family.
Bagyinszky E et al.
Brain Sciences, 2021
Early-onset Alzheimer's disease patient with prion (PRNP) p.Val180Ile mutation.
Bagyinszky E et al.
Neuropsychiatric Disease and Treatment, 2019
Mutational Profiles Reveal an Aberrant TGF-β-CEA Regulated Pathway in Colon Adenomas.
Chen J et al.
Plos One, 2016
Meta-analyses of seven GIGYF2 polymorphisms with Parkinson's disease.
Dai D et al.
Biomedical Reports, 2014
Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease.
Wang L et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 2011
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population.
Meeus B et al.
Neurobiology of Aging, 2011
No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients.
Li L et al.
Neuroscience Letters, 2010
The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese population.
Cao L et al.
Parkinsonism & Related Disorders, 2010
GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.
Di Fonzo A et al.
Parkinsonism & Related Disorders, 2009
Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.
Tan EK et al.
Human Genetics, 2009
Variation in GIGYF2 is not associated with Parkinson disease.
Nichols WC et al.
Neurology, 2009
GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients.
Guo Y et al.
Neuroscience Letters, 2009
Lack of replication of association between GIGYF2 variants and Parkinson disease.
Bras J et al.
Human Molecular Genetics, 2009
Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease.
Lautier C et al.
American Journal of Human Genetics, 2008