| Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016 | 414 | 2016 |
| 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 N Oksala, M Levula, N Airla, M Pelto-Huikko, RM Ortiz, O Järvinen, ... Annals of medicine 41 (4), 279-290, 2009 | 104 | 2009 |
| A new F‐box protein 7 gene mutation causing typical Parkinson's disease E Lohmann, AS Coquel, A Honoré, H Gurvit, H Hanagasi, M Emre, ... Movement Disorders 30 (8), 1130-1133, 2015 | 76 | 2015 |
| Prevalence of Prader–Willi syndrome among infants with hypotonia B Tuysuz, N Kartal, T Erener-Ercan, F Guclu-Geyik, M Vural, Y Perk, ... The Journal of pediatrics 164 (5), 1064-1067, 2014 | 50 | 2014 |
| Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients N Çine, AC Hatemi, N Erginel‐Unaltuna Clinical genetics 61 (1), 66-70, 2002 | 49 | 2002 |
| Endothelial function and endothelial nitric oxide synthase intron 4a/b polymorphism in primary hyperparathyroidism A Ekmekci, N Abaci, NC Ozbey, A Agayev, N Aksakal, H Oflaz, ... Journal of endocrinological investigation 32, 611-616, 2009 | 48 | 2009 |
| Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients E Lohmann, RJ Guerreiro, N Erginel-Unaltuna, N Gurunlian, B Bilgic, ... Neurobiology of aging 33 (8), 1850. e17-1850. e27, 2012 | 46 | 2012 |
| Ventricular pre‐excitation and cardiac hypertrophy mimicking hypertrophic cardiomyopathy in a Turkish family with a novel PRKAG2 mutation F Bayrak, E Komurcu‐Bayrak, B Mutlu, G Kahveci, Y Basaran, ... European journal of heart failure 8 (7), 712-715, 2006 | 46 | 2006 |
| Gender-modulated impact of apolipoprotein A5 gene (APOA5) −1131T>C and c.56C>G polymorphisms on lipids, dyslipidemia and metabolic syndrome in Turkish … E Komurcu-Bayrak, A Onat, M Poda, SE Humphries, J Palmen, F Guclu, ... Clinical chemistry and laboratory medicine 46 (6), 778-784, 2008 | 45 | 2008 |
| Association of C-reactive protein (CRP) gene allelic variants with serum CRP levels and hypertension in Turkish adults E Komurcu-Bayrak, N Erginel-Unaltuna, A Onat, B Ozsait, C Eklund, ... Atherosclerosis 206 (2), 474-479, 2009 | 43 | 2009 |
| Distribution of the M129V polymorphism of the prion protein gene in a Turkish population suggests a high risk for Creutzfeldt-Jakob disease N Erginel-Unaltuna, K Peoc'h, E Komurcu, TT Acuner, H Issever, ... European Journal of Human Genetics 9 (12), 965-968, 2001 | 41 | 2001 |
| The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks E Komurcu-Bayrak, A Onat, M Poda, SE Humphries, J Acharya, ... Clinica chimica acta 383 (1-2), 110-115, 2007 | 39 | 2007 |
| French Parkinson’s Disease Genetics Study (PDG), International Parkinson’s Disease Genomics Consortium (IPDGC). 2016. Loss of VPS13C Function in Autosomal-Recessive … S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... Am J Hum Genet 98, 500-513, 0 | 37 | |
| HPCA confirmed as a genetic cause of DYT2‐like dystonia phenotype B Atasu, H Hanagasi, B Bilgic, M Pak, N Erginel‐Unaltuna, AK Hauser, ... Movement Disorders 33 (8), 1354-1358, 2018 | 36 | 2018 |
| Risk of obesity and metabolic syndrome associated with FTO gene variants discloses clinically relevant gender difference among Turks F Guclu-Geyik, A Onat, AB Yuzbasıogulları, N Coban, G Can, T Lehtimäki, ... Molecular biology reports 43, 485-494, 2016 | 31 | 2016 |
| Clinical variability in ataxia–telangiectasia E Lohmann, S Krüger, AK Hauser, H Hanagasi, G Guven, ... Journal of neurology 262, 1724-1727, 2015 | 31 | 2015 |
| Low “quotient” Lp (a) concentration mediates autoimmune activation and independently predicts cardiometabolic risk A Onat, N Çoban, G Can, M Yüksel, A Karagöz, H Yüksel, E Ademoğlu, ... Experimental and Clinical Endocrinology & Diabetes, 11-18, 2014 | 29 | 2014 |
| Van Der Woude syndrome: variable penetrance of a novel mutation (p. Arg 84Gly) of the IRF6 gene in a Turkish family D Turhani, D Thurnher, K Yerit, K Sinko, G Wittwer, WL Adeyemo, K Frei, ... International journal of molecular medicine 15 (2), 247-251, 2005 | 29 | 2005 |
| Sex-and obesity-specific association of aromatase (CYP19A1) gene variant with apolipoprotein B and hypertension N Coban, A Onat, F Guclu-Geyik, G Can, N Erginel-Unaltuna Archives of medical research 46 (7), 564-571, 2015 | 28 | 2015 |
| Oxidative stress-mediated (sex-specific) loss of protection against type-2 diabetes by macrophage migration inhibitory factor (MIF)−173G/C polymorphism N Coban, A Onat, O Yildirim, G Can, N Erginel-Unaltuna Clinica Chimica Acta 438, 1-6, 2015 | 28 | 2015 |
