Nejat Akar

Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

Mustafa Tekin, Burcu Öztürk Hişmi, Suat Fítöz et al. · The American Journal of Human Genetics · 2007 · 112 citations · Full text

Medicine, Genetics, Otolaryngology +16

Effect Of Metylenetetrahydrofolate Reductase 677 C-T, 1298 A-C, and 1317 T-C on Factor V 1691 Mutation in Turkish Deep Vein Thrombosis Patients

Nejat Akar, Ece Akar, Remin Akçay et al. · Thrombosis Research · 2000 · 67 citations

Medicine, Genetics, Molecular Genetics +16

Evidence for single origins of 35delG and delE120 mutations in the <i>GJB2</i> gene in Anatolia

Mustafa Tekin, G Boğoçlu, S. T. Arican et al. · Clinical Genetics · 2004 · 52 citations

Life Sciences, Genetics, Molecular Genetics +16

Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction

Sadi Güuleçl, Ömer Aras, Ece Akar et al. · Clinical Cardiology · 2001 · 43 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Endothelial Nitric Oxide Synthase Intron 4, 27 bp Repeat Polymorphism in Turkish Patients with Deep Vein Thrombosis and Cerebrovascular Accidents

Nejat Akar, Ece Akar, Şükrü Cin et al. · Thrombosis Research · 1999 · 27 citations

Medicine, Internal Medicine, Molecular Genetics +16