Susen Winkler

Ratzeburger Allee 160
Luebeck, SH 23538, Germany

Last Updated: 09/26/2026

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Found 9 publications

Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only.

Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only.

Journal: Journal of neurology

Published: August 10, 2014

Altered glycosylation of complexed native IgG molecules is associated with disease activity of systemic lupus erythematosus.

Altered glycosylation of complexed native IgG molecules is associated with disease activity of systemic lupus erythematosus.

Journal: Lupus

Published: July 16, 2014

The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease.

The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease.

Journal: Journal of neurology

Published: December 17, 2013

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 16, 2013

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.

Journal: Journal of neurology

Published: July 18, 2013

A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotyping.

A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotyping.

Journal: JAMA neurology

Published: May 24, 2013

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.

Journal: Annals of neurology

Published: September 19, 2012

Genetic risk factors in Parkinson's disease: single gene effects and interactions of genotypes.

Genetic risk factors in Parkinson's disease: single gene effects and interactions of genotypes.

Journal: Journal of neurology

Published: July 13, 2012

Autoantibodies against galectin-2 peptides as biomarkers for the antiphospholipid syndrome.

Autoantibodies against galectin-2 peptides as biomarkers for the antiphospholipid syndrome.

Journal: Lupus

Published: May 29, 2012

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Last Updated: 09/26/2026