Associated Papers
Case Report: Decoding genetic risks of vascular parkinsonism: a case series.
Shalash A et al.
Frontiers in Genetics, 2025
Exploring the genetic and genomic connection underlying neurodegeneration with brain iron accumulation and the risk for Parkinson's disease.
Alvarez Jerez P et al.
Npj Parkinson's Disease, 2023
Molecular genetics of neuropsychiatric illness: some musings.
Janardhanan M et al.
Frontiers in Genetics, 2023
Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases.
Kolarova H et al.
Ebiomedicine, 2022
35180557 (PubMed )
Supplement: mmc3.xlsx › List1
Sequence and Structure-Based Analyses of Human Ankyrin Repeats.
Chakrabarty B et al.
Molecules (basel, Switzerland), 2022
35056738 (PubMed )
Supplement: molecules-27-00423-s001.zip › SupplementaryFileS4.xlsx › Sheet1
Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development.
Kolarikova K et al.
Frontiers in Neuroscience, 2022
Lack of Association Between PLA2G6 Genetic Variation and Parkinson's Disease: A Systematic Review.
Liu H et al.
Neuropsychiatric Disease and Treatment, 2020
Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.
Hildebrandt MR et al.
Stem Cell Reports, 2019
31813827 (PubMed )
Supplement: mmc2.xlsx › SNVs
New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background.
Bartoníková T et al.
Medicine, 2018
Genome-wide assessment of Parkinson's disease in a Southern Spanish population.
Bandrés-Ciga S et al.
Neurobiology of Aging, 2016
The PLA2G6 gene in early-onset Parkinson's disease.
Kauther KM et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2011
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