Alexander Zimprich

Principal Investigator/Associate Prof. Dr.

Medical University of Vienna

Austria

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Articles (15)

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.

Article Link

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

Collaborators (21)

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

Elisabeth Stögmann

Deputy Head of the general outpatient clinic

Medical University of Vienna

AUSTRIA

Caroline Ran

Karolinska Institutet

SWEDEN

Megan Roy-Puckelwartz

Northwestern University

UNITED STATES

David O'Connell

Associate Professor

Dublin City University

IRELAND

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

Kishore R. Kumar

University of Sydney

AUSTRALIA

Karl Mechtler

Head of Facility

Research Institute of Molecular Pathology

AUSTRIA

Alexander Zimprich

Research Interests

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Contact this professor

Articles (15)

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

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

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

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

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

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

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)

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

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

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

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

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

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

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

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

Collaborators (21)

Rayjean Hung

Karen Nuytemans

Christiane Zweier

Anne Joutel

Pierre-Emmanuel Sugier

Tao Xie

David Crosiers

Elisabeth Stögmann

Caroline Ran

Megan Roy-Puckelwartz

David O'Connell

Tobias Zrzavy

Wolfgang Winnicki

Akiyoshi Nakayama

Esther Sammler

Meike Kasten

Sergiu Groppa

Peter Wild Crea

Christine Schneider

Kishore R. Kumar

Karl Mechtler

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