Nagehan Ersoy Tunalı

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease

Silke Metzger, Peter Bauer, Juergen Tomiuk et al. · Neurogenetics · 2005 · 47 citations · Full text

Genetic Disorder, Genetics, Human Polymorphism +7

A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: Functional analysis of the mutant protein

Nagehan Ersoy Tunalı, C Marobbio, Necip Ozan Tiryakioğlu et al. · Molecular Genetics and Metabolism · 2014 · 27 citations · Full text

Engineering, Genetics, Pathology +16

Association of the BsmI, ApaI, TaqI, Tru9I and FokI Polymorphisms of the Vitamin D Receptor Gene with Nephrolithiasis in the Turkish Population.

Ömer Onur Çakır, Emre Demir, Kutluhan Incekara et al. · PubMed · 2016 · 23 citations

miR-132-3p, miR-106b-5p, and miR-19b-3p Are Associated with Brain-Derived Neurotrophic Factor Production and Clinical Activity in Multiple Sclerosis: A Pilot Study

Fatma Sağır, Nagehan Ersoy Tunalı, Temel Tombul et al. · Genetic Testing and Molecular Biomarkers · 2021 · 23 citations

Association of AKR1C3 Polymorphisms with Bladder Cancer.

Necip Ozan Tiryakioğlu, Nagehan Ersoy Tunalı · PubMed · 2016 · 13 citations