Prof. AHMET İLTER GÜNEY

Publication Network

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

Mutation Spectrum of Familial Adenomatous Polyposis Patients in Turkish Population: Identification of 3 Novel APC Mutations

Ates E. A. , ALAVANDA C. , Demir S., KEKLİKKIRAN Ç. , Attaallah W., ÖZDOĞAN O. C. , et al.

TURKISH JOURNAL OF GASTROENTEROLOGY, vol.33, no.2, pp.81-87, 2022 (Journal Indexed in SCI) Sustainable Development

Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency

TÜRKYILMAZ A., ALAVANDA C. , Ates E. A. , GEÇKİNLİ B. B. , Polat H. , GÖKCÜ M., et al.

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2022 (Journal Indexed in SCI)

A Novel ATM Gene Mutation Affecting Splicing in an Ataxia-Telangiectasia Patient

Ates E. A. , TÜRKYILMAZ A., Eltan S. B. , BARIŞ S. , GÜNEY A. İ.

MOLECULAR SYNDROMOLOGY, 2021 (Journal Indexed in SCI)

Genetic and Clinical Characterization of Patients with Maturity-Onset of Diabetes of the Young (MODY): Identification of Novel Variations

Ates E. A. , ÜSTAY Ö. , Polat H. , APAYDIN T. , ELBASAN O. , Yildirim O., et al.

BALKAN MEDICAL JOURNAL, vol.38, no.5, pp.272-277, 2021 (Journal Indexed in SCI) Sustainable Development

Secondary findings in 622 Turkish clinical exome sequencing data

Ates E. A. , TÜRKYILMAZ A., Yildirim O., ALAVANDA C. , Polat H. , Demir S., et al.

JOURNAL OF HUMAN GENETICS, 2021 (Journal Indexed in SCI)

Expanding of mutation spectrum in Muscular Dystrophies: A Turkish Cohort

ALAVANDA C. , Polat H. , Ilker A., Ates E. A. , SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , et al.

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

Characterization of BRCA Genes' Variants in Turkish Hereditary Breast and Ovarian Cancer(HBOC) Patients

Ates E. A. , ALAVANDA C. , Polat H. , TÜRKYILMAZ A., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , et al.

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.28, no.SUPPL 1, pp.935, 2020 (Journal Indexed in SCI) Sustainable Development

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

KOÇ G., Ozdemir A. A. , Girgin G., Akbal C., Kirac D., Avcilar T., et al.

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

Evaluation of mismatch repair (MMR) protein expression with correlation of germline mutation analysis for Lynch syndrome screening in endometrial cancers in Turkish women; preliminary results

Seven I. E. , Kombak F. E. , Bozkurtlar E., Yalcinkaya C., Ates E. A. , Guney A. I. , et al.

VIRCHOWS ARCHIV, vol.473, 2018 (Journal Indexed in SCI) Sustainable Development

Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder

Avcilar T., Kirac D., Ergec D., KOÇ G., ULUCAN K. , Kaya Z., et al.

ONCOLOGY LETTERS, vol.12, no.4, pp.2872-2879, 2016 (Journal Indexed in SCI) Sustainable Development

Effects of genetic factors to stent thrombosis due to clopidogrel resistance after coronary stent placement

Kirac D., Erdem A., Avcilar T., Yesilcimen K., GÜNEY A. İ. , Emre A., et al.

CELLULAR AND MOLECULAR BIOLOGY, vol.62, no.1, pp.51-55, 2016 (Journal Indexed in SCI)

Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth

Kirac D., Eraydin F., Avcilar T., Ulucan K., Ozdemir F., Guney A. I. , et al.

CELLULAR AND MOLECULAR BIOLOGY, vol.62, no.13, pp.78-84, 2016 (Journal Indexed in SCI)

The effect of polymorphic metabolic enzymes on serum phenytoin level

Özkaymakçı A., GÜLÇEBİ İDRİZ OĞLU M. , ERGEÇ D., ULUCAN K. , Uzan M., Özkara C., et al.

Neurological Sciences, 2015 (Journal Indexed in SSCI)

The effect of polymorphic metabolism enzymes on serum phenytoin level

Ozkaynakci A., Gulcebi M. I. , Ergec D., Ulucan K. , Uzan M., Ozkara C., et al.

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

The Frequency and the Effects of 21-Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients

Kirac D., GÜNEY A. İ. , Akcay T., GÜRAN T. , ULUCAN K. , Turan S. , et al.

ANNALS OF HUMAN GENETICS, vol.78, no.6, pp.399-409, 2014 (Journal Indexed in SCI)

MTHFR C677T polymorphism is associated with non syndromic cleft lip with or without palate in a Turkish population

ULUCAN K. , AKÇAY A., KIRAÇ D., Taşkın N., ERGEÇ D., Akçay T., et al.

Sylwan, 2014 (Journal Indexed in SCI Expanded)

The frequency and the effects of 21 Hydroxylase gene defects in congenital adrenal hyperplasial patients

KIRAÇ D., GÜNEY A. İ. , Akçay T., Güran t., ULUCAN K. , TURAN S. , et al.

Annals Of Human Genetics, 2014 (Journal Indexed in SCI Expanded)

Effect of alpha-actinin-3 gene on trained and untrained Turkish middle-school children's sprinting performance: a pilot study

Ulucan K., Bayyurt G. M. , KONUK M., GÜNEY A. İ.

BIOLOGICAL RHYTHM RESEARCH, vol.45, no.4, pp.509-514, 2014 (Journal Indexed in SCI)

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

Ulucan K., Gole S., Altindas N., Guney A. İ.

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

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

Guney A. I. , Ergec D., Kirac D., Ozturhan H., Caner M., Koc G., et al.

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

Transforming growth factor-beta 3 intron 5 polymorphism as a screening marker for non-syndromic cleft lip with or without cleft palate

Ulucan K. , Bayraktar N., Parmaksiz E., Akcay A., GÜNEY A. İ.

MOLECULAR MEDICINE REPORTS, vol.6, no.6, pp.1465-1467, 2012 (Journal Indexed in SCI)

Detection of Mitochondrial DNA Mutations in Nonmuscle Invasive Bladder Cancer

GÜNEY A. İ. , Ergec D. S. , Tavukcu H. H. , Koc G., Kirac D., ULUCAN K. , et al.

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

Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients

Guney A. I. , Javadova D., Kirac D., Ulucan K., Koc G., Ergec D., et al.

GENETICS AND MOLECULAR RESEARCH, vol.11, no.2, pp.1039-1048, 2012 (Journal Indexed in SCI)

Multifactor dimensionality reduction analysis of MTHFR, PAI-1, ACE, PON1, and eNOS gene polymorphisms in patients with early onset coronary artery disease

Agirbasli M., Guney A. I. , Ozturhan H. S. , Agirbasli D., Ulucan K., Sevinc D., et al.

EUROPEAN JOURNAL OF CARDIOVASCULAR PREVENTION & REHABILITATION, vol.18, no.6, pp.803-809, 2011 (Journal Indexed in SCI)

reduction analysis of MTHFR PAI1 ACE PON1 and eNOS gene polymorphisms in patients with early onset coronary artery disease

Agirbasli M., GÜNEY A. İ. , Özturhan M., ULUCAN K. , Agirbasli D., ERGEÇ D., et al.

European Jpurnal of preventive cardiology, vol.18, pp.803-809, 2011 (Journal Indexed in SCI Expanded)

Genetic diagnosis in infertile men with numerical and constitutional sperm abnormalities

Cinar C., Yazici C., Ergunsu S., Beyazyurek C., Javadova D., Saglam Y., et al.

GENETIC TESTING, vol.12, no.2, pp.195-202, 2008 (Journal Indexed in SCI)

New candidate chromosomal regions for chordoma development

Bayrakli F. , Guney I. , Kilic T., Ozek M., Pamir M. N.

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

New candidate chromosomal regions for chordoma development - Commentary

Liau L. M.

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

Autosomal recessive idiopathic epilepsy in an inbred family from Turkey: identification of a putative locus on chromosome 9q32-33.

Baykan B., Madia F., Bebek N., Gianotti S., Guney A. İ. , Cine N., et al.

Epilepsia, vol.45, no.5, pp.479-87, 2004 (Journal Indexed in SCI Expanded)

Lack of SCN1A mutations in familial febrile seizures.

Malacarne M., Madia F., Gennaro E., Vacca D., Guney I. , Buono S., et al.

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

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

Güney A. İ. , Ince U., Küllü S., Pekin S., Cirakoğlu B.

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

Articles Published in Other Journals

Expression of NF-κB Regulators (BCL-3, NFKB1, NFKB2) in Metastatic Breast Cancer Patients

FEJZULLAHU A., AKIN TELLİ T., PEKER EYÜBOĞLU İ. , YUMUK P. F. , GÜNEY A. İ.

Cancer Science & Research, vol.4, no.2, pp.1-9, 2021 (Refereed Journals of Other Institutions)

New Methods in Cancer Management: Liquid Biopsy Technique and Biomarkers

Fejzullahu A., Güney A. İ.

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

Analysis of ctDNA Biomarker in Breast Cancer

Fejzullahu A., Güney A. İ.

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

Obeziteyle ilişkili Beslenme Alışkanlıklarının Araştırılmasında Yeni Yöntem Üç Faktörlü Beslenme Anketi

KIRAÇ D., KASPAR E. Ç. , AVCILAR T., ÇAKIR Ö. K. , ULUCAN K. , KURTEL H. , et al.

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

Obeziteyle İlişkili Beslenme Alışkanlıklarının Araştırılmasında Yeni Bir Yöntem“Üç Faktörlü Beslenme Anketi”

Kıraç D., Kaspar E. Ç. , Avcılar t., KASIMAY ÇAKIR Ö. , ULUCAN K. , KURTEL H. , et al.

Clin Exp Health Sci, vol.5, pp.162-169, 2015 (Other Refereed National Journals)

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

Kirac D., KASPAR E. Ç. , Avcilar T., Cakir Ö. , ULUCAN K. , KURTEL H. , et al.

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

Tuberoz skleroz hastalığının moleküler genetiği

BAYRAKLI F. , ÇANKAYA T., bayraklı ş., BAYRİ Y. , GÜNEY A. İ.

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

von Hippel Lindau hastalığının moleküler genetiği

BAYRAKLI F. , ÇANKAYA T., BAYRİ Y. , GÜNEY A. İ.

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

Genetic alterations of androgen receptor gene and p53 by fluorescence in situ hybridization and immunodetection of bcl-2 in prostatic intraepithelial neoplasia and carcinoma

KAYA H. , GÜNEY A. İ. , ÇELİKEL Ç. , küllü s.

Marmara Medical Journal, vol.14, no.1, pp.207-212, 2001 (Other Refereed National Journals)

Refereed Congress / Symposium Publications in Proceedings

CDH2 and TP53 gene expression in metastatic breast cancer patients

Fejzullahu A., Akın Telli T., Peker Eyüboğlu İ., Yumuk P. F. , Güney A. İ.

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

FEJZULLAHU A., AKIN TELLİ T., PEKER EYÜBOĞLU İ. , YUMUK P. F. , GÜNEY A. İ.

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

Bcl-3 gene expression in metastatic breast cancer patients

Fejzullahu A., Akın Telli T., Peker Eyüboğlu İ., Yumuk P. F. , Güney A. İ.

39th World Cancer Conference, Rome, Italy, 25 - 26 November 2020, pp.7 Sustainable Development

Metastatik meme kanseri hastalarında Bcl-3 gen ekspresyonu

Fejzullahu A., Akın Telli T., Peker Eyüboğlu İ., Yumuk P. F. , Güney A. İ.

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

Bcl-3 gene expression in metastatic breast cancer patients

FEJZULLAHU A., AKIN TELLİ T., PEKER EYÜBOĞLU İ. , YUMUK P. F. , GÜNEY A. İ.

world cancer 2020, Belek, Turkey, 25 - 26 November 2020 Sustainable Development

Molecular Analysis of Familial Adenomatous Polyposis Patients in Turkish Population: Two Novel APC Mutations, Two Recurrent MUTYH Mutations and Phenotype-Genotype Relationship

Gültepe P., Arslan Ateş E., Yıldırım Ö., Güney A. İ.

16. Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2019, pp.44

Nadir bir iskelet displazisi: Piknodizostoz tanısı alan iki kız kardeş

ALAVANDA C. , GEÇKİNLİ B. B. , ARSLAN ATEŞ E., POLAT H. , SÖYLEMEZ M. A. , GÜNEY A. İ. , et al.

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

Schaaf Yang sendromu

Alavanda C. , Arslan Ateş E., Polat H. , Geçkinli B. B. , Söylemez M. A. , Güney A. İ. , et al.

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

Ates E. A. , Turkyilmaz A., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , ATA P. , ARMAN A. , et al.

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

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

Turkyilmaz A., GEÇKİNLİ B. B. , Ates E. A. , SÖYLEMEZ M. A. , GÜNEY A. İ. , ATA P. , et al.

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

Investigations of CYP2C19 polymorphisms which effect clopidogrel resistance and development of stent thromposis in stent implanted CAD patients

KIRAÇ D., AVCILAR T., Erdem A., Yeşilçimen K., GÜNEY A. İ. , ULUCAN K. , et al.

ESHG Congress 2015, 6 - 09 June 2015

Distribution of angiotensin I converting enzyme insertion deletion and actinin 3 codon 577 polymorphisms in Turkish male soccer players

ULUCAN K. , Sercan C., BIYIKLI T., KIRAÇ D., GÜNEY A. İ.

ESHG Congress 2015, 6 - 09 June 2015

Autosomal gene defects investigation of male infertility in germ cell aplasia cases

KOÇ G., Özdemir A., Girgin G., Avcılar T., KIRAÇ D., ULUCAN K. , et al.

ESHG Congress 2015, 6 - 09 June 2015

The Role of TGFΒ3 and Methylenetetrahydrofolate Reductase Polymorphisms in the Development of Non-Syndromic Cleft Lip with or without Cleft Palate

ERSOY B., ULUCAN K. , CELEBILER O., GUNEY A. İ.

1st International Congress of Turkish CelftLip and Palate Society, 28 - 30 November 2014, pp.36

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

Guney A. İ. , Biricik A., Tetik E., Berkil H., Kahraman S.

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

Detection of Human Papillomavirus HPV DNA in Testicular Tissues by using In Situ Hybridization ISH and Hybrid Capture

GÜNEY A. İ. , MOUGIN C., SİLİ U. , MADOZ L., KÜLLÜ S., ÇIRAKOĞLU B., et al.

9th Symposium De Biologie Clinique Des Cancers, Strasbourg, France, 28 - 31 October 1996

Publications & Works

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

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings