Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Effects of thymoquinone in prevention of experimental contrast-induced nephropathy in rats.

Iranian journal of basic medical sciences, cilt.22, sa.12, ss.1432-1439, 2019 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Comparison of Different Dialysis Modalities in End-Stage Renal Disease Patients with Acute Dialysis Requirement

TURKISH NEPHROLOGY DIALYSIS AND TRANSPLANTATION JOURNAL, cilt.26, sa.3, ss.298-304, 2017 (ESCI İndekslerine Giren Dergi) Creative Commons License identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

A novel EDAR gene variant causing autosomal dominant hypohidrotic ectodermal dysplasia

V. Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Nevşehir, Türkiye, 20 - 22 Şubat 2020, cilt.31, ss.1

Familial Mediterranean fever looking into ten years’xx experience

51st European Society of Human GeneticsConference, Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.903

Molecular pathological evaluationof Alport syndrome

International Participated Erciyes Medical Genetics Days, Kayseri, Türkiye, 21 - 23 Şubat 2019

Identification and frequency of CFTR gene variants

International Participated Erciyes Medical Genetics Days, Kayseri, Türkiye, 21 - 23 Şubat 2019

Gene variants of Congenital Adrenal Hyperplasia in Anatolian population

European Biotechnology Congress 2018, Atina, Yunanistan, 26 - 28 Nisan 2018, cilt.280, ss.21 identifier

The correlation of genotype-phenotype of FMF disease and its review of statistical data

European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256 identifier

Retrospective results of 18 years prenatal diagnosis cases and its evaluation

European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256 identifier

NF1 gene variant allele frequencies comparison of Turkish population with databases

European Biotechnology Congress, Dubrovnik, Hırvatistan, 25 - 27 Mayıs 2017, cilt.256 identifier

A case of XYY male patient with micropenis

European Biotechnology Conference, Letonya, 5 - 07 Mayıs 2016, cilt.231 identifier

Lack of amplification in next generation sequencing? Check for deletions.

European Conference of Human Genetics 2016, Barselona, İspanya, 21 - 24 Mayıs 2016, cilt.24, ss.475-476

Guidelines for the evaluation of the sequence variants

Medical Genetics and Clinical Applications (with International Participation) Congress, Kayseri, Türkiye, 11 - 13 Şubat 2016, cilt.38, ss.20

A case with 49, XXXXY syndrome: rare chromosomal aneuploidies

European Biotechnology Congress 2011, İstanbul, Türkiye, 28 Eylül - 01 Ekim 2011, cilt.22, ss.106 identifier

Prenatally detected de novo 46, XX, t(2121)(p12p12) at chorionic villus sampling

European Biotechnology Congress 2011, İstanbul, Türkiye, 28 Eylül - 01 Ekim 2011, cilt.22, ss.107 identifier

A case of 46, XX, t(217)(q37.1q25) with recurrent miscarriage

European Biotechnology Congress 2011, İstanbul, Türkiye, 28 Eylül - 01 Ekim 2011, cilt.22, ss.107 identifier

Kitap & Kitap Bölümleri

Yoğun Bakım Genomiği

YOĞUN BAKIM, PROF.DR. IŞIL ÖZKOÇAK TURAN, PROF.DR. VOLKAN HANCI, Editör, AKADEMİSYEN KİTAP EVİ (LANGE), Ankara, ss.1067-1084, 2018

YENİ NESİL DİZİLEME TEKNOLOJİLERİ

GÜNCEL BİYOTEKNOLOJİ VE UYGULAMALARI, Dündar M., Bağış H., Editör, Erciyes Üniversitesi Yayınları, Kayseri, ss.371-394, 2017

Bireysel Tıp

Tıbbi Genetik ve Klinik Uygulamaları, munis dündar, Editör, mgrup matbaacılık, Kayseri, ss.1147-1162, 2016