Yasemin Dincer

Recommendations for whole genome sequencing in diagnostics for rare diseases

N. de Leeuw, J. Belmont, J. Clayton-Smith, 2022, European Journal of Human Genetics.

Clinical, neuroimaging, and molecular spectrum of TECPR2‐associated hereditary sensory and autonomic neuropathy with intellectual disability

A. Pagnamenta, J. Lupski, J. Meiler, 2020, medRxiv.

Multiple Integration and Data Annotation Study (MIDAS): improving next-generation sequencing data analysis by genotype-phenotype correlations

H. Klein, V. Mall, S. Eck, 2018 .

Monogenic variants in dystonia: an exome-wide sequencing study

W. Chung, J. Volkmann, T. Strom, 2020, The Lancet Neurology.

De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy

G. B. Schaefer, J. Winkelmann, K. Clark, 2020, Genetics in Medicine.

Clinically relevant copy-number variants in exome sequencing data of patients with dystonia.

T. Strom, R. Jech, B. Haslinger, 2021, Parkinsonism & related disorders.

Recessive NUP54 Variants Underlie Early‐Onset Dystonia with Striatal Lesions

H. Prokisch, J. Winkelmann, V. Mall, 2022, Annals of neurology.

Increased PDGFR-beta and VEGFR-2 protein levels are associated with resistance to platinum-based chemotherapy and adverse outcome of ovarian cancer patients.

A. Hapfelmeier, K. Becker, S. Gündisch, 2017, Oncotarget.