Associated Papers
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Marianski K et al.
Human Genetics, 2025
41442065 (PubMed )
Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
Large-scale genetic characterization of Parkinson's disease in the African and African admixed populations.
Akçimen F et al.
Brain : a Journal of Neurology, 2025
41058593 (PubMed )
Supplement: awaf379_supplementary_data.zip › brain-2025-00177-File011.xlsx › SupplementaryTable4
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?
Senkevich K et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
38853950 (PubMed )
Supplement: media-1.xlsx › S_table_4.SYNJ1_AMP_PD_and_UKBB
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