Afig Berdelı

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Saskia F. Heeringa, Gil Chernin, Moumita Chaki et al. · Journal of Clinical Investigation · 2011 · 400 citations · Full text

Medicine, Genetics, Molecular Genetics +17

The G894T polymorphism on endothelial nitric oxide synthase gene is associated with premature coronary artery disease in a Turkish population

Sırrı F. Cam, Cevad Şekuri, İstemihan Tengiz et al. · Thrombosis Research · 2005 · 65 citations

Medicine, Cardiology, Genetics +14

NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome

Afig Berdelı, Önder Yavaşcan, Erkin Serdaroğlu et al. · Pediatric Nephrology · 2007 · 63 citations

Medicine, Genetics, Molecular Genetics +12

Renin-angiotensin system gene polymorphisms and premature coronary heart disease

Cevad Şekuri, Fethi Sırrı Çam, Ertuğrul Ercan et al. · Journal of the Renin-Angiotensin-Aldosterone System · 2005 · 62 citations · Full text

Medicine, Cardiology, Genetics +15

Differential expression of inflammasome regulatory transcripts in periodontal disease

Kübra Aral, Eynar Berdeli, Paul R. Cooper et al. · Journal of Periodontology · 2019 · 62 citations · Full text

Dentistry, Oral Biology, Periodontology +17