A new indicator in coronary artery diseases

by Nihan Erginel Ünaltuna
Published 2020-09-01

Negative results in screening for possible new sequence variations on ATP-binding cassette transporter A1 gene in Turkish adults with metabolic syndrome

by Neslihan Çoban, Altan Onat, Filiz Geyik, Nihan Erginel-ünaltuna
Published 2014-09-01

Investigating the role of ceramide metabolism-associated CERS5 (LASS5) gene in atherosclerosis pathogenesis in endothelial cells

by Neslihan Çoban, Filiz Güçlü Geyik, Özlem Yıldırım, Nihan Erginel Ünaltuna
Published 2017-03-01

Macrophage migration inhibitory factor (MIF) gene -173 G>C polymorphism and its relationship to coronary artery disease and type 2 diabetes

by Neslihan Çoban, Aycan Fahri Erkan, Berkay Ekici, Maide Kaşit, Nihan Erginel Ünaltuna, Eren Vurgun
Published 2019-01-01

ACSL4 gen polimorfizminin (rs7886473) metabolik sendrom ve lipid düzeyleri üzerine etkisi

by Eren VURGUN, İrem Yağmur DİKER, Neslihan ÇOBAN, Filiz GEYİK, Gamze GÜVEN, Nihan ERGİNEL ÜNALTUNA
Published 2018-12-01

The association of serum clusterin levels and Clusterin rs11136000 polymorphisms with Alzheimer disease in a Turkish cohort

by Gamze Guven, Ebru Ozer, Basar Bilgic, Hasmet Hanagasi, Hakan Gurvit, Ebba Lohmann, Nihan Erginel-Unaltuna
Published 2020-01-01

Association of APOA5-1131T>C polymorphism with obesity in coronary artery disease

by Neslihan Çoban, Aybike Sena Özuynuk, Aycan Fahri Erkan, Berkay Ekici, Maide Kaşit, Nihan Erginel Ünaltuna
Published 2020-07-01

Association between PSEN1 p.E318G Variant and APOE Polymorphism and Alzheimer Disease in Turkish Patients

by Gamze Güven, Haşmet Hanağası, Ebba Lohmann, Nihan Erginel Ünaltuna, Rukiye Aslan, Çağla Dönmez, Başar Bilgiç
Published 2021-06-01

Sex-specific associations of TCF7L2 variants with fasting glucose, type 2 diabetes and coronary heart disease among Turkish adults

by Ayşe Berna Yüzbaşıoğulları, Evrim Kömürcü-bayrak, Altan Onat, Gunay Can, Nina Mononen, Reijo Laaksonen, Mika Kähönen, Terho Lehtimäki, Nihan Erginel-ünaltuna
Published 2020-10-01

Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients.

by Gamze Guven, Ebba Lohmann, Jose Bras, J Raphael Gibbs, Hakan Gurvit, Basar Bilgic, Hasmet Hanagasi, Patrizia Rizzu, Peter Heutink, Murat Emre, Nihan Erginel-Unaltuna, Walter Just, John Hardy, Andrew Singleton, Rita Guerreiro
Published 2016-01-01