Alexander Zimprich at Medical University Vienna - Research Interests, Publications & Academic Profile

Alexander Zimprich

Principal Investigator/Associate Prof. Dr.

Medical University of Vienna

Austria

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Research Interests

Neurology

90%

Epidemiology

20%

Neurodegenerative Disease

80%

Medical Science

80%

Genome-wide Association

30%

Hereditary Diseases

30%

Parkinson's Disease

30%

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Articles15

Identification of Pathogenic Pathways for Recurrence of Focal Segmental Glomerulosclerosis after Kidney Transplantation

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Year:

2024

Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers.

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Year:

2023

No Association of Multiple Sclerosis with <i>C9orf72</i> Hexanucleotide Repeat Size in an Austrian Cohort

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Year:

2023

Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.

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Year:

2023

Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).

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Year:

2023

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.

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Year:

2023

Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

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Year:

2023

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.

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Year:

2023

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

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Year:

2023

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

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Year:

2023

Development of a multiplexed targeted mass spectrometry assay for LRRK2-phosphorylated Rabs and Ser910/Ser935 biomarker sites.

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Year:

2021

Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.

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Year:

2020

Co-incidental C9orf72 expansion mutation-related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt-Jakob disease.

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Year:

2020

A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke.

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Year:

2020

Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families

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Year:

2020

Collaborators16

Rayjean Hung

University of Toronto

CANADA

Karen Nuytemans

Assistant Professor

University of Miami

UNITED STATES

Christiane Zweier

SWITZERLAND

Anne Joutel

INSERM

FRANCE

Pierre-Emmanuel Sugier

INSERM

FRANCE

Tao Xie

Professor

University of Chicago Medicine

UNITED STATES

David Crosiers

Professor at University of Antwerp

University of Antwerp

BELGIUM

Caroline Ran

Karolinska Institutet

SWEDEN

Tobias Zrzavy

AUSTRIA

Wolfgang Winnicki

Medical University of Vienna

AUSTRIA

Akiyoshi Nakayama

Associate Professor

National Defense Medical College

JAPAN

Esther Sammler

UNITED KINGDOM

Meike Kasten

University of Lübeck

GERMANY

Sergiu Groppa

University Medical Center of the Johannes Gutenberg University Mainz

GERMANY

Peter Wild Crea

National Institute on Aging

UNITED STATES

Christine Schneider

University Hospital Augsburg

GERMANY

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