Ivana Dzinovic

Munich, BY, Germany

Last Updated: 09/26/2026

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Found 21 publications

Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omics.

Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omics.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 28, 2026

Trio analysis in dystonia identifies de novo KLC1 variants in a kinesinopathy with distinct motor and neurodevelopmental features.

Trio analysis in dystonia identifies de novo KLC1 variants in a kinesinopathy with distinct motor and neurodevelopmental features.

Journal: EBioMedicine
Published: March 17, 2026

CACNA1C -Related Channelopathy Presenting With Adult-Onset Combined Dystonia-Parkinsonism: A Novel Neurological Presentation.

CACNA1C -Related Channelopathy Presenting With Adult-Onset Combined Dystonia-Parkinsonism: A Novel Neurological Presentation.

Journal: American journal of medical genetics. Part A
Published: February 15, 2026

Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4.

Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: December 19, 2025

Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers Ahead.

Collaborative Genomics for Dystonia in Central and Eastern Europe: Successes Achieved, New Frontiers Ahead.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: December 03, 2025

Novel Pathogenic GCH1 Variant in Familial DOPA-Responsive Dystonia.

Novel Pathogenic GCH1 Variant in Familial DOPA-Responsive Dystonia.

Journal: Neuropediatrics
Published: November 14, 2025

Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort.

Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort.

Journal: Annals of neurology
Published: September 24, 2025

Dystonia: Insights into Mechanisms and Novel Therapeutics.

Dystonia: Insights into Mechanisms and Novel Therapeutics.

Journal: Current neurology and neuroscience reports
Published: July 18, 2025

Integrating Long-Read Nanopore Sequencing for Precision Resolution of Genomic Variants in Dystonia.

Integrating Long-Read Nanopore Sequencing for Precision Resolution of Genomic Variants in Dystonia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 11, 2025

Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase.

Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 15, 2025

De novo protein-coding gene variants in developmental stuttering.

De novo protein-coding gene variants in developmental stuttering.

Journal: Molecular psychiatry
Published: November 22, 2024

Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia.

Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia.

Journal: Brain : a journal of neurology
Published: October 04, 2024
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Last Updated: 09/26/2026