Sonja Scholz

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National Institute of Neurological Disorders and Stroke

United States

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Recent Grants

Grant: Open

Genomic characterization of multiple system atrophy and dementia with Lewy bodies

Open Date: 2022-01-01

Close Date: 2026-12-31

Grant: Close

Genetic characterization of atypical parkinsonism

Open Date: 2016-01-01

Close Date: 2019-01-01

Articles (20)

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2022

Collaborators (16)

Benjamin H. Mullish

UNITED KINGDOM

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Ece Bayram

Assistant Professor

University of Colorado Anschutz Medical Campus

UNITED STATES

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Sharan Srinivasan

University of Michigan

UNITED STATES

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John Quinn

Professor

University of Liverpool

UNITED KINGDOM

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Caroline Jonson

University of California, San Francisco

UNITED STATES

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Gary Ho

Assistant Professor

Harvard Medical School

UNITED STATES

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Suvankar Pal

University of Edinburgh

UNITED KINGDOM

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Sarah Gagliano Taliun

Associate Professor/Professeure sous octroi agrégée

Université de Montréal

CANADA

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Sara Bandrés Ciga

Senior Staff Scientist | Head Training & Outreach

Centre for Addiction and Mental Health

UNITED STATES

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Maria Landqvist Waldö

Lund University

SWEDEN

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Steve Gentleman

Professor of Neuropathology

Imperial College London

UNITED KINGDOM

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daniel blackburn

University of Sheffield

UNITED KINGDOM

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Oliver Bandmann

UNITED KINGDOM

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Eric Yu

McGill University

CANADA

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Thomas Foltynie

University College London

UNITED KINGDOM

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Karri Kaivola

University of Helsinki

FINLAND

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Sonja Scholz

Research Interests

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Recent Grants

Articles (20)

Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk loci

Differential methylation analysis in neuropathologically confirmed dementia with Lewy bodies

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis.

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.

Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome

Multimodal assessment of mitochondrial function in Parkinson's disease

Detection of mosaic and population-level structural variants with Sniffles2

HLA in isolated REM sleep behavior disorder and Lewy body dementia

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation.

Cognitive determinants of decisional capacity in neurodegenerative disorders

A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease

A case of familial frontotemporal dementia caused by a progranulin gene mutation.

Precision diagnosis and staging of TDP-43 proteinopathies: harnessing the power of artificial intelligence

Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population

Regional genetic correlations highlight relationships between neurodegenerative disease loci and the immune system.

Large-scale rare variant burden testing in Parkinson's disease.

Author Correction: Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases

Clinical Trial-Ready Patient Cohorts for Multiple System Atrophy: Coupling Biospecimen and iPSC Banking to Longitudinal Deep-Phenotyping

Correction to: Clinical trial-ready patient cohorts for multiple system atrophy: coupling biospecimen and iPSC banking to longitudinal deep-phenotyping (The Cerebellum, (2022), 10.1007/s12311-022-01471-8)

Collaborators (16)

Benjamin H. Mullish

Ece Bayram

Sharan Srinivasan

John Quinn

Caroline Jonson

Gary Ho

Suvankar Pal

Sarah Gagliano Taliun

Sara Bandrés Ciga

Maria Landqvist Waldö

Steve Gentleman

daniel blackburn

Oliver Bandmann

Eric Yu

Thomas Foltynie

Karri Kaivola

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