Associated Papers
Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.
Kukkle PL et al.
Advanced Biology, 2022
Spinocerebellar ataxia type 23 (SCA23): a review.
Wu F et al.
Journal of Neurology, 2021
Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562.
Zhou B et al.
Genome Research, 2019
30737237 (PubMed )
Supplement: supp_gr.234948.118_Supplemental_Table_S6.xlsx › SNVs
NCI-60 whole exome sequencing and pharmacological CellMiner analyses.
Reinhold WC et al.
Plos One, 2014
25032700 (PubMed )
Supplement: pone.0101670.s001.xlsx › Supplementary_Table_1
Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases.
Jezierska J et al.
Journal of Neurology, 2013
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