Ina Schmitt

Bonn, NW, Germany

Last Updated: 09/26/2026

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Found 21 publications

The Alpha-Synuclein Gene (SNCA) is a Genomic Target of Methyl-CpG Binding Protein 2 (MeCP2)-Implications for Parkinson's Disease and Rett Syndrome.

The Alpha-Synuclein Gene (SNCA) is a Genomic Target of Methyl-CpG Binding Protein 2 (MeCP2)-Implications for Parkinson's Disease and Rett Syndrome.

Journal: Molecular neurobiology

Published: October 06, 2023

Increased diversity of Malassezia species on the skin of Parkinson's disease patients.

Increased diversity of Malassezia species on the skin of Parkinson's disease patients.

Journal: Frontiers in aging neuroscience

Published: August 02, 2023

High throughput compound screening in neuronal cells identifies statins as activators of ataxin 3 expression.

High throughput compound screening in neuronal cells identifies statins as activators of ataxin 3 expression.

Journal: Scientific reports

Published: June 20, 2023

Methylation of alpha-synuclein in a Sudanese cohort.

Methylation of alpha-synuclein in a Sudanese cohort.

Journal: Parkinsonism & related disorders

Published: February 01, 2022

Epigenome-Wide Analysis of DNA Methylation in Parkinson's Disease Cortex.

Epigenome-Wide Analysis of DNA Methylation in Parkinson's Disease Cortex.

Journal: Life (Basel, Switzerland)

Published: January 06, 2022

Epigenetic and gene expression changes of neuronal cells from MSA patients are pronounced in enzymes for cell metabolism and calcium-regulated protein kinases.

Epigenetic and gene expression changes of neuronal cells from MSA patients are pronounced in enzymes for cell metabolism and calcium-regulated protein kinases.

Journal: Acta neuropathologica

Published: June 17, 2021

Activators of alpha synuclein expression identified by reporter cell line-based high throughput drug screen.

Activators of alpha synuclein expression identified by reporter cell line-based high throughput drug screen.

Journal: Scientific reports

Published: May 20, 2021

Common genetic variants associated with Parkinson's disease display widespread signature of epigenetic plasticity.

Common genetic variants associated with Parkinson's disease display widespread signature of epigenetic plasticity.

Journal: Scientific reports

Published: May 03, 2019

DNA methylation alterations in iPSC- and hESC-derived neurons: potential implications for neurological disease modeling.

DNA methylation alterations in iPSC- and hESC-derived neurons: potential implications for neurological disease modeling.

Journal: Clinical epigenetics

Published: August 31, 2017

DNA methylation of DLG4 and GJA-1 of human hippocampus and prefrontal cortex in major depression is unchanged in comparison to healthy individuals.

DNA methylation of DLG4 and GJA-1 of human hippocampus and prefrontal cortex in major depression is unchanged in comparison to healthy individuals.

Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia

Published: February 15, 2017

DNA methylation of imprinted loci of autosomal chromosomes and IGF2 is not affected in Parkinson's disease patients' peripheral blood mononuclear cells.

DNA methylation of imprinted loci of autosomal chromosomes and IGF2 is not affected in Parkinson's disease patients' peripheral blood mononuclear cells.

Journal: Neurological research

Published: January 14, 2017

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.

Journal: Brain : a journal of neurology

Published: October 21, 2016

Showing 1-12 of 21

Last Updated: 09/26/2026