Konrad Oexle

Munich, BY, Germany

Last Updated: 09/26/2026

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Found 72 publications

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

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

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.

Journal: Nature genetics
Published: June 24, 2025

Beyond volume: Unraveling the genetics of human brain geometry.

Beyond volume: Unraveling the genetics of human brain geometry.

Journal: Science advances
Published: June 13, 2025

Can we predict sleep health based on brain features? A large-scale machine learning study using the UK Biobank.

Can we predict sleep health based on brain features? A large-scale machine learning study using the UK Biobank.

Journal: Brain communications
Published: June 10, 2025

Corrigendum to "Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders" [Parkinson. Relat. Disord. (2025) 133 107319].

Corrigendum to "Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders" [Parkinson. Relat. Disord. (2025) 133 107319].

Journal: Parkinsonism & related disorders
Published: March 22, 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

Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders.

Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders.

Journal: Translational psychiatry
Published: November 05, 2024

Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders.

Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders.

Journal: Parkinsonism & related disorders
Published: October 09, 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

Are there two disjunct episignatures for KMT2B-related disease?

Are there two disjunct episignatures for KMT2B-related disease?

Journal: Brain communications
Published: September 19, 2024

RLS-associated MEIS transcription factors control distinct processes in human neural stem cells.

RLS-associated MEIS transcription factors control distinct processes in human neural stem cells.

Journal: Scientific reports
Published: June 24, 2024
Showing 1-12 of 72

Last Updated: 09/26/2026