SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
Genome wide genotyping for the characterization of disease locus in a family with an uncharacterized neurometabolic disease
Annual Symposium of the Society for the Study of Inborn Error of Metabolism, İstanbul, Türkiye, 31 Ağustos - 03 Eylül 2010, cilt.33, ss.173
Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene
European Human Genetics Conference, Amsterdam, Hollanda, 28 - 31 Mayıs 2011, ss.11
Identification of a novel insertion mutation in PCCA gene of a Turkish propionic acidemia patient
9. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 05 Aralık 2010, cilt.78, ss.125
Structural analysis of three novel missense mutations in the Mut gene of methylmalonic acidemia patients
9. Uluslararası Katılımlı Tıbbi Genetik Kongresi, İstanbul, Türkiye, 1 - 05 Aralık 2010, cilt.78, ss.125
Characterization of fahasecin a powerful bacteriocin isolated from wine flora In addition to control of MF in wines the ihibition of important pathogens is provided
Central European Symposium on Industrial Microbiology and Microbial Ecology, MALINSKA, Hırvatistan, 22 - 25 Eylül 2010
Homozigotluk haritalaması ve ekzon dizileme yöntemi ile infantile onset spinocerebellar ataxi IOSCA ya neden olan C10orf2 gen mutasyonunun saptanması
Uluslararası Katılımlı 11. Metabolik Hastalıklar ve Beslenme Kongresi, ÇESME/İZMİR, Türkiye, 14 - 16 Nisan 2011
Molecular and structural analysis of six nonsense mutations in mut methylmalonic acidemia patients including two novel nonsense mutations
Annual Symposium of the Society for the Study of Inborn Error of Metabolism, İstanbul, Türkiye, 31 Ağustos - 03 Eylül 2010, cilt.33, ss.177
Galactosemia in a Turkish population with a high prevalence of Q188R mutation
Annual Symposium of the Society for the Study of Inborn Error of Metabolism, İstanbul, Türkiye, 31 Ağustos - 03 Eylül 2010, cilt.33, ss.66
Molecular analysis of homocystinuria in Turkish patients
Annual Symposium of the Society for the Study of Inborn Error of Metabolism, İstanbul, Türkiye, 31 Ağustos - 03 Eylül 2010, cilt.33, ss.35
Association of polyneuropathy mental retardation sensorineural hearing loss 6th nerve palsy convulsions and oral dyskinesia a propable new neurometabolic disorder
Annual Symposium of the Society for the Study of Inborn Error of Metabolism, İstanbul, Türkiye, 31 Ağustos - 03 Eylül 2010, cilt.33, ss.178
Leuconostoc mesenteroides subsp cremoris tarafından üretilen bir bakteriyosinin tanımlanması
15. Ulusal Biyoteknoloji Kongresi, Antalya, Türkiye, 28 - 31 Ekim 2007, ss.21
Leuconostoc mesenteroides subsp cremoris tarafından üretilen bir bakteriyosinin saflaştırılması
15. Ulusal Biyoteknoloji Kongresi, Antalya, Türkiye, 28 - 31 Ekim 2007, ss.51