Christoph Hotzy

Vienna, Austria

Last Updated: 09/26/2026

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Found 13 publications

Correction: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes.

Correction: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes.

Journal: Human genomics

Published: August 27, 2023

Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes.

Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes.

Journal: Human genomics

Published: March 06, 2023

Elevated urine BMP phospholipids in LRRK2 and VPS35 mutation carriers with and without Parkinson's disease.

Elevated urine BMP phospholipids in LRRK2 and VPS35 mutation carriers with and without Parkinson's disease.

Journal: NPJ Parkinson's disease

Published: November 22, 2022

C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients.

C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients.

Journal: Neurobiology of disease

Published: June 13, 2022

Correction to: The urinary microbiome shows different bacterial genera in renal transplant recipients and non-transplant patients at time of acute kidney injury - a pilot study.

Correction to: The urinary microbiome shows different bacterial genera in renal transplant recipients and non-transplant patients at time of acute kidney injury - a pilot study.

Journal: BMC nephrology

Published: May 09, 2020

Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes.

Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes.

Journal: Journal of medical genetics

Published: October 28, 2019

The urinary microbiome shows different bacterial genera in renal transplant recipients and non-transplant patients at time of acute kidney injury - a pilot study.

The urinary microbiome shows different bacterial genera in renal transplant recipients and non-transplant patients at time of acute kidney injury - a pilot study.

Journal: BMC nephrology

Published: July 13, 2019

TPP2 mutation associated with sterile brain inflammation mimicking MS.

TPP2 mutation associated with sterile brain inflammation mimicking MS.

Journal: Neurology. Genetics

Published: March 28, 2018

The Parkinson's disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human.

The Parkinson's disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human.

Journal: The Biochemical journal

Published: March 27, 2018

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene.

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene.

Journal: European journal of neurology

Published: October 31, 2016

Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes.

Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes.

Journal: Annals of neurology

Published: December 02, 2014

No evidence for a role of rare CYP27B1 variants in Austrian multiple sclerosis patients.

No evidence for a role of rare CYP27B1 variants in Austrian multiple sclerosis patients.

Journal: Multiple sclerosis (Houndmills, Basingstoke, England)

Published: July 27, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026