Associated Papers
Whole-Exome Sequencing Revealed New Candidate Genes for Human Dilated Cardiomyopathy.
D'Agostino Y et al.
Diagnostics (basel, Switzerland), 2022
36292100 (PubMed )
Supplement: diagnostics-12-02411-s001.zip › Supplementary_table_S3.xlsx › Foglio1
Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome-Where Are We?
Levy AM et al.
Genes, 2021
34573303 (PubMed )
Supplement: genes-12-01321-s001.zip › genes-1240846-supplementary.pdf
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.
Ross JP et al.
Neurobiology of Aging, 2016
Genome-wide assessment of Parkinson's disease in a Southern Spanish population.
Bandrés-Ciga S et al.
Neurobiology of Aging, 2016
Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.
Sun N et al.
Frontiers in Psychiatry, 2016
J protein mutations and resulting proteostasis collapse.
Koutras C et al.
Frontiers in Cellular Neuroscience, 2014
Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD.
Guo Y et al.
Neuroscience Letters, 2012
The use of next-generation sequencing in movement disorders.
Krebs CE et al.
Frontiers in Genetics, 2012
Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder.
Sundaram SK et al.
Annals of Neurology, 2011
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