Publications & Works

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

Expanding of mutation spectrum in Muscular Dystrophies: A Turkish Cohort

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.28, no.SUPPL 1, pp.435-436, 2020 (Journal Indexed in SCI) identifier

Male infertility in Sertoli cell-only syndrome: An investigation of autosomal gene defects

INTERNATIONAL JOURNAL OF UROLOGY, vol.26, no.2, pp.292-298, 2019 (Journal Indexed in SCI) identifier identifier identifier

The effect of polymorphic metabolism enzymes on serum phenytoin level

NEUROLOGICAL SCIENCES, vol.36, no.3, pp.397-401, 2015 (Journal Indexed in SCI) identifier identifier identifier

Preliminary Findings of α -Actinin-3 Gene Distribution in Elite Turkish Wind Surfers.

Balkan journal of medical genetics : BJMG, vol.16, no.1, pp.69-72, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

Effects of ACE polymorphisms and other risk factors on the severity of coronary artery disease

GENETICS AND MOLECULAR RESEARCH, vol.12, no.4, pp.6895-6906, 2013 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Detection of Mitochondrial DNA Mutations in Nonmuscle Invasive Bladder Cancer

GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.16, no.7, pp.672-678, 2012 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

New candidate chromosomal regions for chordoma development

SURGICAL NEUROLOGY, vol.68, no.4, pp.425-430, 2007 (Journal Indexed in SCI) identifier identifier identifier

New candidate chromosomal regions for chordoma development - Commentary

SURGICAL NEUROLOGY, vol.68, no.4, pp.430, 2007 (Journal Indexed in SCI) identifier

Lack of SCN1A mutations in familial febrile seizures.

Epilepsia, vol.43, no.5, pp.559-62, 2002 (Journal Indexed in SCI Expanded) identifier identifier identifier

Detection and typing of human papillomavirus in cervical specimens of Turkish women.

European journal of gynaecological oncology, vol.18, pp.546-50, 1997 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

Articles Published in Other Journals

New Methods in Cancer Management: Liquid Biopsy Technique and Biomarkers

Türkiye Klinikleri İç Hastalıkları Dergisi, vol.5, no.2, pp.74-87, 2020 (Other Refereed National Journals) Creative Commons License Sustainable Development

Analysis of ctDNA Biomarker in Breast Cancer

International Journal of Cancer and Oncology, vol.7, no.1, pp.10-18, 2020 (Refereed Journals of Other Institutions) Creative Commons License Sustainable Development

Obeziteyle ilişkili Beslenme Alışkanlıklarının Araştırılmasında Yeni Yöntem Üç Faktörlü Beslenme Anketi

Marmara Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi, vol.5, no.3, pp.162-169, 2015 (Other Refereed National Journals)

A new method in investigation of obesity-related eating behaviors 'three-factor eating questionnaire'

CLINICAL AND EXPERIMENTAL HEALTH SCIENCES, vol.5, no.3, pp.162-169, 2015 (Journal Indexed in ESCI) Sustainable Development identifier

Tuberoz skleroz hastalığının moleküler genetiği

Türk Nöroşirürji Dergisi, vol.19, pp.50-54, 2009 (Other Refereed National Journals)

von Hippel Lindau hastalığının moleküler genetiği

Türk Nöroşirürji Dergisi, vol.19, pp.36-40, 2009 (Other Refereed National Journals)

Refereed Congress / Symposium Publications in Proceedings

CDH2 and TP53 gene expression in metastatic breast cancer patients

International Eurasian Conference on BioTechnology and BioChemistry (BioTechBioChem 2020), Ankara, Turkey, 16 - 18 December 2020, pp.20 Sustainable Development

CDH2 and TP53 gene expression in metastatic breast cancer patients

International Eurasian Conference on BioTechnology and BioChemistry (BioTechBioChem 2020), Ankara, Turkey, 16 - 18 December 2020 Sustainable Development

Metastatik meme kanseri hastalarında Bcl-3 gen ekspresyonu

14. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 20 - 22 November 2020, pp.63 Sustainable Development

Schaaf Yang sendromu

4. Ulusal Çocuk Genetik kongresi, İstanbul, Turkey, 25 - 27 September 2019

A novel intronic ATM gene mutation affecting splicing in a patient with Ataxia-Telangiectasia

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.255-256 identifier

FGF3 gene mutations related to two syndromic Congenital deafness cases: Congenital deafness with inner ear agenesis (Michel aplasia), microtia, and microdontia and Otodental dysplasia

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.893 identifier

Von Hippel Lindau Patients

13. BALKAN GENETİK KONGRESİ, Edirne, Turkey, 16 - 20 April 2019

REVERSE GENETİK İLE TANI KOYULAN NADİR BİR SPASTİK PARAPLEJİ AİLESİ

13.ULUSLARARASI KATILIMLI ULUSAL TIBBİ GENETİK ANABİLİM DALI, Turkey, 7 - 11 November 2018

Inversion Y Having Different Phenotypic Expressions at Three Brothers

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.829 identifier

BBS10 frameshift mutation in a Turkish girl with Bardet Biedl Syndrome.

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017

A Novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017

BBS10 frameshift mutation in a turkish girl with bardet biedl syndrome

The European Society of Human Genetics 2017, KOPENHAGEN, Denmark, 25 - 30 May 2017

A novel HNF1B mutation in a family with two MODY patients

The European Society of Human Genetics 2017., KOPENHAGEN, Denmark, 25 - 28 May 2017

Silver Russel Sendromlu bir olgu

12. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016

Clinical Evaluation of a MDC1A Case Carrying LAMA2 Mutation

ULUSAL TIBBİ GENETİK KONGRESİ, İZMİR ÇEŞME, Turkey, 5 - 09 October 2016

Analysis of The Molecular Markers in 49 AML Patients

European Society of Human Genetics Congress, Barcelona, Spain, 21 - 24 May 2016

46 XX SRY pozitif erkek sendromlu olgu

11. Ulusal Tıbbi Genetik Kongresi, 24-27 Eylül 2014, İstanbul, Turkey, 24 - 27 September 2014

Cytogenetic analysis and Y chromosome microdeletion results in infertile males undergoing assisted reproductive technology (ART)

European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, France, 25 - 28 May 2002, vol.10, pp.302 identifier