Charles J. Reyes

Luebeck, SH, Germany

Last Updated: 09/26/2026

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Found 11 publications

iPSC motor neurons, but not other derived cell types, capture gene expression changes in postmortem sporadic ALS motor neurons.

iPSC motor neurons, but not other derived cell types, capture gene expression changes in postmortem sporadic ALS motor neurons.

Journal: Cell reports

Published: September 27, 2022

Basal Ganglia Atrophy as a Marker for Prodromal X-Linked Dystonia-Parkinsonism.

Basal Ganglia Atrophy as a Marker for Prodromal X-Linked Dystonia-Parkinsonism.

Journal: Annals of neurology

Published: July 30, 2022

Repeat-Associated Non-AUG Translation of AGAGGG Repeats that Cause X-Linked Dystonia-Parkinsonism.

Repeat-Associated Non-AUG Translation of AGAGGG Repeats that Cause X-Linked Dystonia-Parkinsonism.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: May 01, 2022

Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in TAF1 with Nanopore Sequencing.

Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in TAF1 with Nanopore Sequencing.

Journal: Genes

Published: December 17, 2021

Prodromal X-Linked Dystonia-Parkinsonism is Characterized by a Subclinical Motor Phenotype.

Prodromal X-Linked Dystonia-Parkinsonism is Characterized by a Subclinical Motor Phenotype.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: December 16, 2021

Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing.

Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing.

Journal: Neurology. Genetics

Published: February 08, 2021

Expanding Data Collection for the MDSGene Database: X-linked Dystonia-Parkinsonism as Use Case Example.

Expanding Data Collection for the MDSGene Database: X-linked Dystonia-Parkinsonism as Use Case Example.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: December 03, 2019

DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-Parkinsonism.

DNA Methylation as a Potential Molecular Mechanism in X-linked Dystonia-Parkinsonism.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 17, 2019

A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.

A hexanucleotide repeat modifies expressivity of X-linked dystonia parkinsonism.

Journal: Annals of neurology

Published: August 16, 2018

An integrated OMICS approach unravels the elusive genetic cause of X-linked dystonia-parkinsonism.

An integrated OMICS approach unravels the elusive genetic cause of X-linked dystonia-parkinsonism.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: May 11, 2018

Matrin3 binds directly to intronic pyrimidine-rich sequences and controls alternative splicing.

Matrin3 binds directly to intronic pyrimidine-rich sequences and controls alternative splicing.

Journal: Genes to cells : devoted to molecular & cellular mechanisms

Published: January 09, 2017

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Last Updated: 09/26/2026