AFSU Avesis
AFSU Avesis
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Yayınlar & Eserler
SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler 20
Could Aneurysm and Atherosclerosis-Associated MicroRNAs (miR 24-1-5p, miR 34a-5p, miR 126-5p, miR 143-5p, miR 145-5p) Also Be Associated with Coronary Artery Ectasia?
Correction to: Investigating changes in β‑adrenergic gene expression (ADRB1 and ADRB2) in Takotsubo (stress) cardiomyopathy syndrome; a pilot study (Molecular Biology Reports, (2021), 48, 12, (7893-7900), 10.1007/s11033-021-06816-w)
Evaluation of Congenital and Chromosomal Anomalies Mortality in Turkey by Joinpoint Regression Analysis
Investigating changes in β-adrenergic gene expression (ADRB1 and ADRB2) in Takotsubo (stress) cardiomyopathy syndrome; a pilot study
A Novel PTCH1 Frameshift Mutation Leading to First Case of Gorlin-Goltz Syndrome with Bilateral Pneumothorax
TUTGUN ONRAT SERAP, DOĞAN NURHAN (2021). Evaluation of Congenital and Chromosomal Anomalies Mortality in Turkey by Joinpoint Regression Analysis. Global Journal of Epidemiology and Public Health, 6, 51- 57., Doi: 10.12974/2313-0946.2021.06.01.4
Global Journal of Epidemiology and Public Health, Cilt: 6, 2021 (ESCI)
An interesting case: 30-year-old male patient with myotonic dystrophy typeI has got normal CTG repeats sequence in the DMPK gene, but it does not comply with its clinical features
Analysis of thrombophilic gene mutations in coronary artery ectasia Koroner arter ektazisinde trombofilik gen mutasyon analizi
The genetic determination of the differentiation between ischemic dilated cardiomyopathy and idiopathic dilated cardiomyopathy
Prevalence of myocardial infarction polymorphisms in Afyonkarahisar, Western Turkey
46,XX, der(15),t(Y;15)(q12;p11) karyotype in an azoospermic male
Genetic and environmental factors in human osteoporosis.
Alterations of copy number of methylation pattern in mismatch repair genes by methylation specific-multiplex ligation-dependent probe amplification in cases of colon cancer
A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders
Incidence of neural tube defects in Afyonkarahisar, Western Turkey
Fluorescence in situ hybridization analysis with subtelomere specific probes (12pter-15qter) showed no differences in deletion patterns between normotensive and essential hypertension.
A cytogenetics study of Hydrodroma despiciens Müller 1776 Acari Hydrachnellae Hydrodromidae
Comment on the paper by Meuschel-Wehner et al.: Inner ear dysplasia in sporadic lacrimo-auriculo-dento-digital syndrome
LADD syndrome with QT prolongation LADD-Syndrom mit QT-verlängerung
Lacrimo auriculo dento digital syndrome with QT proglongation
Diğer Dergilerde Yayınlanan Makaleler 15
TUTGUN ONRAT SERAP, Keleş Yağmur, Aydın Saliha, Etiler Rana, Aktaş Zeynep (2022). Ten-year experience retrospective in investigation of the frequency of sex chromosome aneuploidies diagnosed in a reference medical center in Türkiye. International Journal of Community Medicine and Public Health
International Journal of Community Medicine and Public Health, Cilt: 9, Sayı: 10, 2022
A Rare De Novo Reciprocal Translocation 46,XX,rec(7;13)(p22;q32) Karyotype
Evaluation of ctg repeat numbers, genotype and clinical findings in myotonic dystrophy patients: A single center experience-case series Miyotonik distrofi hastalarının ctg tekrar sayıları ile genotip ve klinik bulguların değerlendirilmesi: Tek merkez deneyimi-olgu serisi
A Rare De Novo Robertsonian Translocation 45,XX, rob (13;13) (q10; q10) Karyotype Carrying in a Normal Woman; But Recurrent Abortions
“Investigation of Repeat Numbers (CAG, CTG, CGG, GAA, GCC) and Variable Expression of Our Patients with Trinucleotide Repeat Disease in Afyonkarahisar
ELMAS MUHSİN,TUTGUN ONRAT SERAP,YILDIRIM ÜMİT CAN,DEMİRBAŞ HAYRİ (2020). Evaluation of Genotype and Clinical Findings with CAG Repeat Numbers of Patients with Huntington's Disease: Single Center Experience. Turkiye Klinikleri Journal of Internal Medicine, 5(3), 112-119., Doi: 10.5336/intermed.2020-74379
Turkiye Klinikleri Journal of Internal Medicine, Cilt: 5, Sayı: 3, 2020
The effects of genetic polymorphisms and Diabetes Mellitus on the development of peripheral arterial disease
Thrombophilic Gene Mutation Analysis of Carotid Artery Disease Western TURKEY
BARLAK SEZGİN,ONRAT ERSEL,TUTGUN ONRAT SERAP,DOĞAN İSMET,DEMİRBAŞ HAYRİ,ÖZER GÖKASLAN ÇİĞDEM,YALIM ZAFER,AVŞAR ALAETTİN (2018). Thrombophilic Gene Mutation Analysis of Carotid Artery Disease Western TURKEY. International Journal of Recent Scientific Research, 9(12), 29885-29890.
International Journal of Recent Scientific Research, Cilt: 9, Sayı: 12, 2018 (Scopus)
Plasminogen Activator Inhibitor 1 PAI 1 4G 5G Allele Polymorphisms and NIDDM Non Insulin Dependent Diabetes Mellitus Risk Factor for Early Onset Myocardial Infarction
Umbilical hernia hypertelorism sensorineural deafness may be Donnai Barrow syndrome A case report
P53 Intronic Variant G13964C Analyses in Cases with Colon Cancer
Turkish Journal of Cancer, Cilt: 39, Sayı: 2, 2009
Frequency of TP53 codon72 polymorphism in cases with colon cancer
Turkish Journal of Cancer, Cilt: 39, Sayı: 1, 2009
Biyoteknoloji Genetiği Değiştirilmiş Organizmalar GDO ve Biyogüvenlik BIOTECHNOLOGY GENETICALLY MODIFIED ORGANISMS GMOs BIOSAFETY
Sendrom Dergisi, Cilt: 18, Sayı: 4, 2006
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar 1
The effect of hereditary thrombophilia on the formation of carotid artery disease: a pilot study
5th Dubrovnik Cardiology Highlights, Hırvatistan, 19 - 22 Ekim 2017