Yasemin Dincer
Martinsried, BY, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 8 publications
Recessive NUP54 Variants Underlie Early-Onset Dystonia with Striatal Lesions.
Journal: Annals of neurology
Published: August 01, 2022
Recommendations for whole genome sequencing in diagnostics for rare diseases.
Journal: European journal of human genetics : EJHG
Published: December 23, 2021
Clinically relevant copy-number variants in exome sequencing data of patients with dystonia.
Journal: Parkinsonism & related disorders
Published: December 02, 2020
Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability.
Journal: Human mutation
Published: October 19, 2020
Monogenic variants in dystonia: an exome-wide sequencing study.
Journal: The Lancet. Neurology
Published: March 11, 2020
De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 04, 2019
Increased PDGFR-beta and VEGFR-2 protein levels are associated with resistance to platinum-based chemotherapy and adverse outcome of ovarian cancer patients.
Journal: Oncotarget
Published: January 27, 2017
Significance of serum c-erbB-2 oncoprotein, insulin-like growth factor-1 and vascular endothelial growth factor levels in ovarian cancer.
Journal: Bratislavske lekarske listy
Published: March 02, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026