Martin Paucar

Karolinska Institutet

Sweden

Research Interests

Explore related searches

Professors in Sweden

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (10)

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Collaborators (6)

Per Svenningsson

King’s College London

UNITED KINGDOM

View details

Zhongbo Chen

UNITED KINGDOM

View details

Vasco Sousa

Karolinska Institutet

SWEDEN

View details

Anna Lindstrand

Professor

Karolinska Institutet

SWEDEN

View details

Ann Nordgren

Professor

University of Gothenburg

SWEDEN

View details

Arianna Tucci

Clinical Reader in Genomic Medicine

Queen Mary University of London

UNITED KINGDOM

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Martin Paucar

Research Interests

Explore related searches

Contact this professor

Articles (10)

An X-Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene.

Acute Vestibular Syndrome Unmasking an RFC1 -Spectrum Disorder

Repeat Variants, Biomarkers, and Molecular Signatures in Parkinson’s Disease: ATXN2, ATXN3, CACNA1A, PRNP, TBP, C9ORF72, TOMM40, APOE, and POLG—A Swedish Perspective

ATP1A3 dysfunction causes motor hyperexcitability and afterhyperpolarization loss in a dystonia model.

The <scp><i>ZFHX3</i> GGC</scp> Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs.

Comment to: “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”

Phenotypic variability in a large kindred with spastic paraplegia associated with a novel REEP1 variant.

Novel findings in a Swedish primary familial brain calcification cohort.

Cerebrospinal fluid glial fibrillary acidic protein, in contrast to amyloid beta protein, is associated with disease symptoms in Huntington's disease.

Collaborators (6)

Per Svenningsson

Zhongbo Chen

Vasco Sousa

Anna Lindstrand

Ann Nordgren

Arianna Tucci

Make your next move.