Associated Papers
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease.
Saini P et al.
Neurobiology of Aging, 2021
The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.
Illés A et al.
Frontiers in Genetics, 2019
DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.
Gagliardi M et al.
Parkinsonism & Related Disorders, 2018
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.
Ross JP et al.
Neurobiology of Aging, 2016
DNAJC13 genetic variants in parkinsonism.
Gustavsson EK et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2015
Parkinson's disease, genetic variability and the Faroe Islands.
Petersen MS et al.
Parkinsonism & Related Disorders, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A0A6-01A.domain
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1013.391
Genetic Identification in Early Onset Parkinsonism among Norwegian Patients.
Gustavsson EK et al.
Movement Disorders Clinical Practice, 0
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