Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Vitamin D Receptor Gene BSMI, FOKI, APAI, and TAQI Polymorphisms and the Risk of Atopic Dermatitis

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, vol.26, no.2, pp.106-110, 2016 (Journal Indexed in SCI) identifier identifier identifier

The relationship between C-reactive protein rs3091244 polymorphism and ankylosing spondylitis

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, vol.19, no.1, pp.43-48, 2016 (Journal Indexed in SCI) identifier identifier identifier

Hyperimmunoglobulin D Syndrome: Case Report

ARCHIVES OF RHEUMATOLOGY, vol.30, no.3, pp.244-246, 2015 (Journal Indexed in SCI) identifier identifier

Is the HLA B27 genotype a risc faktor for psoriatic arthritis and psoriasis vulgaris?

TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY, vol.48, no.3, pp.131-134, 2014 (Journal Indexed in SCI) identifier identifier

The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures

EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, vol.18, no.5, pp.657-660, 2014 (Journal Indexed in SCI) identifier identifier identifier

DOUBLE TRANSLOCATION: AN INTERESTING FAMILY HISTORY

BALKAN JOURNAL OF MEDICAL GENETICS, vol.16, no.1, pp.77-80, 2013 (Journal Indexed in SCI) identifier identifier identifier

Combined Germline Variations of Thrombophilic Genes Promote Genesis of Lung Cancer

ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, no.9, pp.5449-5454, 2013 (Journal Indexed in SCI) identifier identifier identifier

Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations

GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.16, no.4, pp.279-286, 2012 (Journal Indexed in SCI) identifier identifier identifier

Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas

MOLECULAR BIOLOGY REPORTS, vol.39, no.2, pp.1595-1599, 2012 (Journal Indexed in SCI) identifier identifier identifier

In Vivo Evaluation of the Genotoxic Effects of Gonadotropins on Rat Reticulocytes

CURRENT THERAPEUTIC RESEARCH-CLINICAL AND EXPERIMENTAL, vol.72, no.2, pp.60-70, 2011 (Journal Indexed in SCI) identifier identifier identifier

Iodine-131 treatment and chromosomal damage: in vivo dose-effect relationship

EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, vol.31, no.5, pp.676-684, 2004 (Journal Indexed in SCI) identifier identifier identifier

Articles Published in Other Journals

Tedaviyi Etkileyen Tarama Testleri

Türkiye Klinikleri Sağlık Bilimleri Dergisi, 2020 (Other Refereed National Journals)

Warfarin Resistance: A Case Report

EURASIAN JOURNAL OF EMERGENCY MEDICINE, vol.18, no.1, pp.61-63, 2019 (Journal Indexed in ESCI) identifier

Evaluation of the physical and biological dosimetry methods in iodine-131-treated patients

World Journal of Nuclear Medicine, vol.17, no.4, pp.253-260, 2018 (Refereed Journals of Other Institutions)

Kanser Etiyolojisinde Tetikleyici Moleküler Mekanizmalar

Turkiye Klinikleri J Med Genet-Special Topics, vol.2, no.2, pp.74-87, 2017 (Other Refereed National Journals)

Günümüzde Kanser Tanısında Kullanılan Geçerli ve Güvenilir Moleküler Tetkikler

Turkiye Klinikleri Journal of Medical Genetics-Special Topics, vol.2, no.2, pp.113-122, 2017 (Other Refereed National Journals)

Çok Parametreli ve Çoklu Bilinmeyenli Kanser

Türkiye Klinikleri Journal of Medical Genetics-Special Topics, vol.2, no.2, pp.60-68, 2017 (Other Refereed National Journals)

Kanser Etyolojisinde Tetikleyici Moleküler Mekanizmalar

Turkiye Klinikleri Journal of Medical Genetics-Special Topics, vol.2, no.2, pp.74-87, 2017 (Other Refereed National Journals)

The GJB2 gene mutation profiles in hearing impaired patients from Western Turkey, Canakkale

Biomedical Genetics and Genomics, vol.2, no.2, pp.1-5, 2017 (Refereed Journals of Other Institutions)

A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus

Biomedical Genetics and Genomics, vol.2, no.1, pp.1-3, 2017 (Refereed Journals of Other Institutions)

Hypermethylated promoter profiles for tumour suppressor APC p53 MSH6 and MGMT genes in CRC tumours

journal of biomedical research, vol.2, no.6, pp.41-47, 2016 (Refereed Journals of Other Institutions)

9qh liği Molar Gebelik için bir risk faktörü mü

Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, pp.14-15, 2016 (Refereed Journals of Other Institutions)

9qh liği Molar Gebelik İçin Bir Risk Faktörü mü

Jinekoloji - Obstetrik ve Neonatoloji Tıp Dergisi, 2016 (Other Refereed National Journals)

Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population

INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE, vol.4, no.2, pp.120-127, 2015 (Journal Indexed in ESCI) identifier identifier

Tiroid Kanserinde Moleküler Etyolojik Faktörler Derleme

Cumhuriyet Journal Medical, vol.36, pp.128-146, 2014 (Other Refereed National Journals)

Refereed Congress / Symposium Publications in Proceedings

A novel variant for SQSTM1 gene in a patient with frontotemporal dementia.

European Biotechnology Congress 2020, Prag, Czech Republic, 24 September 2020

A Rare Chromosomal Aneuploidy That Diagnosed With Array CGH And MLPA Validation : Trisomy 4 in a fetus

V.International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Turkey, 20 February 2020

BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.156-1156

A unique keratosis pattern in a case of epidermolytic hyperkeratosis: Report of a case in 46,XX,9qh karyotype”

2nd International Dermatology and Cosmetology Congress (INDERCOS 2017), İstanbul, Turkey, 15 - 18 March 2017

The possible association of some thrombophilic gene polymorphisms with deep vein thrombosis and pulmonary thromboembolism

XII. Ulusal Tıbbi Genetik Kongrresi. Official Journal of Turkish Society of medical Genetics, İzmir, Turkey, 5 - 09 October 2016

UGT1A1 GENE MUTATIONS MAY CAUSE MYCOPHENOLATE MOFETIL INDUCED LEUCOPENIA AFTER RENAL TRANSPLANTATION A CASE REPORT

Gevher Nesibe Tıp Günleri 2016 ve Tıbbi Genetik ve Klinik Uygulamaları Kongresi, Kayseri, Turkey, 11 - 13 February 2016

The RFLP profiles at BRAF V600E mutations in thyroid FNAB nodules

European Biotechnology Congress, Bucharest, Romania, 7 - 09 May 2015, vol.208 identifier

Short stature and other clinical findings of a case with karyotype 46 XYdel Y q11 2 12 mar

. Abstracts of the 1th Eurepean Cytogenetics Conference, Turkey, 22 June 1997 - 25 March 2015

P06 205 Evaluation of CYP2C9 and CYP2D6 gene polymorphisms in thyroid cancer

European Human Genetics Conference. Nürnberg-GERMANY 23-26 June 2012, 23 - 26 June 2012, vol.20, pp.198

6 P76 Increased T allele frequency in MTHFR C677T gene in thyroid carcinoma

8th European Cytogenetic Conference, 02-05 July 2011, Porto, Portugal, 2 - 05 July 2011, vol.19, pp.175

Adelosan İdiyopatik Skolyozda MATN 1 ve LCT C13910T Gen Polimorfizmi

23.Ulusal Fiziksel Tıp ve Rehabilitasyon Kongresi. Türk Fiz Rehab Derg 2011:57 Özel Sayı;1-334.p-146, Turkey, 11 - 15 May 2011

PS 68 Acut effect of I 131 treatment on chromosomes

Annual Congress of the European Association of Nuclear Medicine, 25-29 Aug 2001, NAPOLİ, Italy, 25 - 29 August 2001, vol.28, pp.1092

Popülasyonda sentromer polimorfizmi

Atatürk Üniversitesi X. Ulusal Biyoloji kongresi, Turkey, 18 - 20 July 1990

Kangal köpeklerinde Canis familiaris kromozomal araştırmalar

IX. Ulusal Biyoloji Kongresi, Turkey, 21 - 23 September 1988

Books & Book Chapters

Biyoteknoloji esasları ve tıbbi genetikte yeni uygulama alanları

in: Tıbbi Genetik ve Klinik Uygulamaları, Munis DÜNDAR, Editor, MG GRUP MATBAACILIK, KAYSERİ 2016;syf 935- 958, Kayseri, pp.539-556, 2016

Kardiyovasküler sistem hastalıklarına genetik yaklaşım

in: Tıbbi Genetik ve Klinik Uygulamaları, Munis DÜNDAR, Editor, MG GRUP MATBAACILIK, Kayseri, pp.935-958, 2016

Kardiyovasküler Hastalıkların Genetiği

in: Tıbbi Genetik ve Klinik Uygulamaları, Munis Dündar, Editor, Erciyes Üniversitesi, 2016