Nihan Erginel‐Ünaltuna

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Suzanne Lesage, Valérie Drouet, Elisa Majounie et al. · The American Journal of Human Genetics · 2016 · 447 citations · Full text

Life Sciences, Cell Biology, Neuroscience +16

ADAM-9, ADAM-15, and ADAM-17 are upregulated in macrophages in advanced human atherosclerotic plaques in aorta and carotid and femoral arteries—Tampere vascular study

Niku Oksala, Mari Levula, Nina Airla et al. · Annals of Medicine · 2009 · 83 citations · Full text

Life Sciences, Cardiology, Molecular Biology +13

A new F‐box protein 7 gene mutation causing typical Parkinson's disease

Ebba Lohmann, Anne‐Sophie Coquel, Aurélie Honoré et al. · Movement Disorders · 2015 · 66 citations

Life Sciences, Genetics, Molecular Genetics +15

Gene polymorphisms of endothelial nitric oxide synthase enzyme associated with pulmonary hypertension in patients with COPD

Pınar Yildiz, Hüseyin Oflaz, Naci Çine et al. · Respiratory Medicine · 2003 · 52 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Endothelial Dysfunction in Patients with Asthma: The Role of Polymorphisms of ACE and Endothelial NOS Genes

Pınar Yildiz, Hüseyin Oflaz, Naci Çine et al. · Journal of Asthma · 2004 · 50 citations

Life Sciences, Genetics, Internal Medicine +12