Sokhna Haissatou Diaw

Discordant Monozygotic Parkinson Disease Twins: Role of Mitochondrial Integrity

I. König, K. Lohmann, P. Urban, 2020, Annals of neurology.

Emerging role of a systems biology approach to elucidate factors of reduced penetrance: transcriptional changes in THAP1-linked dystonia as an example

H. Busch, K. Lohmann, A. Münchau, 2022, Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V.

Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated Neurodegeneration

K. Lohmann, S. Zittel, A. Rakovic, 2022, International journal of molecular sciences.

Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's disease.

K. Lohmann, C. Klein, P. Seibler, 2019, Stem cell research.

Linking Huntington's Disease and X‐linked Dystonia Parkinsonism on the Molecular Level

K. Lohmann, Sokhna Haissatou Diaw, 2020, Movement disorders : official journal of the Movement Disorder Society.

The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant

B. Peterlin, A. Münchau, A. Maver, 2023, Genes.

Not to Miss: Intronic Variants, Treatment, and Review of the Phenotypic Spectrum in VPS13D-Related Disorder

N. Brüggemann, K. Lohmann, S. Efthymiou, 2023, International journal of molecular sciences.

Characterization of the pathogenic α-Synuclein Variant V15A in Parkinson´s disease

K. Lohmann, M. Borsche, Marija Dulovic-Mahlow, 2023, NPJ Parkinson's disease.

DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery.

K. Lohmann, S. Zittel, A. Grünewald, 2024, Neurogenetics.