Articles
48
All (48)
SCI-E, SSCI, AHCI (32)
SCI-E, SSCI, AHCI, ESCI (39)
ESCI (7)
Scopus (40)
TRDizin (10)
Other Publications (6)
21. [Association of APOA5-1131T>C polymorphism with obesity in coronary artery disease].
Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir
, vol.48, no.5, pp.461-471, 2020 (ESCI, Scopus, TRDizin)
27. Evaluation of Dystrophin Gene Deletion Patterns in a Large Duchene/Becker Msuscular Dystrophy Patient Sample; 17 Years Experience from one Turkish Diagnostic Center
Deneysel Tıp Dergisi
, vol.7, no.14, pp.50-61, 2017 (Peer-Reviewed Journal)
31. Investigating the role of ceramide metabolism-associated CERS5 (LASS5) gene in atherosclerosis pathogenesis in endothelial cells
TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY
, vol.45, no.2, pp.118-125, 2017 (ESCI, Scopus, TRDizin)
33. KORONER ARTER HASTALIĞI OLMAYAN VE STATİN İLE TEDAVİ EDİLEN BIREYLERDE AMPK YOLAĞINDAYENI BIR ADAYMODÜLATÖR OLARAK MICRORNA-625-5P
Deneysel Tıp Araştırma Enstitüsü Dergisi
, vol.6, no.11, pp.11-20, 2016 (Peer-Reviewed Journal)
36. Kardiyomiyopatiye Neden Olna Kardiyak Troponin T Gne Mutasyonlarının Araştırılması
Deneysel Tıp Araştırma Enstitüsü Dergisi
, vol.4, no.10, pp.17-24, 2016 (Peer-Reviewed Journal)
39. Low "quotient" Lp(a) Concentration Mediates Autoimmune Activation and Independently Predicts Cardiometabolic Risk
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
, vol.123, no.1, pp.11-18, 2015 (SCI-Expanded, Scopus)
40. 15 Yıllık Huntington Hastalığı Test Sonuçları ve Literatürdeki HH Test Kılavuzları
Deneysel Tıp Araştırma Enstitüsü Dergisi
, vol.5, no.10, pp.10-16, 2015 (Peer-Reviewed Journal)
42. Ateroskleroz Gelişiminde Genetik Faktörlerin Rolü.
Deneysel Tıp Araştırma Enstitüsü Dergisi
, vol.4, no.7, pp.3-12, 2014 (Peer-Reviewed Journal)
48. The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks.
Clinica chimica acta; international journal of clinical chemistry
, vol.383, pp.110-5, 2007 (SCI-Expanded, Scopus)
Papers Presented at Peer-Reviewed Scientific Conferences
71
1. Investigation of genetic variations in ion channel genes in chronic thromboembolic pulmonary hypertension patients
European Society of Cardiology Congress 2025, Spain, 29 August - 01 September 2025, (Summary Text)
2. ABCA3 and NOTCH1 mRNA Expressions Differ in Chronic Thromboembolic Pulmonary Hypertension Patients with Rare Missense Variants
European Human Genetics Conference 2025, Italy, 24 - 27 May 2025, (Summary Text)
3. TTN Varyantları ile Birliktelik Gösteren Multifaktöriyel Kronik Tromboembolik Pulmoner Hipertansiyon: Olgu Sunumu
Kardiyolojide Nadir Hastalıklar; Genetikten Tedaviye Yeni Ufuklar Sempozyumu, İzmir, Turkey, 28 February - 01 March 2025, (Summary Text)
4. Alfa Talasemi ile İlişkili Pulmoner Hipertansiyon, Bir Olgu Sunumu
Kardiyolojide Nadir Hastalıklar; Genetikten Tedaviye Yeni Ufuklar Sempozyumu, İzmir, Turkey, 28 February - 01 March 2025, (Summary Text)
5. Examining ferroptosis indicators in the neuroblastoma cell line
57th European Society of Human Genetics (ESHG) Conference, Berlin, Germany, 1 - 04 June 2024, pp.1197-1198, (Summary Text)
6. Gene polymorphisms of angiopoietin-like protein 8 and plasminogen activator inhibitor-1 as potential effector of CAD
57th European Society of Human Genetics (ESHG) Conference, Berlin, Germany, 1 - 04 June 2024, pp.1001, (Summary Text)
7. Genetic variants in EDN1 and PAI-1 and their role in coronary artery disease susceptibility and clinical outcomes
40. Ulusal Kardiyoloji Kongresi, Antalya, Turkey, 6 - 10 November 2024, pp.80, (Summary Text)
9. EXPRESSION LEVEL OF CERAMIDE SYNTHASE 5 (CERS5) GENE IN THE EPICARDIAL ADIPOSE TISSUE OF CORONARY ARTERY DISEASE PATIENTS
92nd European Atherosclerosis Society Congress, Lyon, France, 26 - 29 May 2024, pp.39, (Summary Text)
10. ERASTIN-INDUCED FERROPTOSIS ALTERS GENE EXPRESSION LEVELS OF SREBF2 AND SLC25A1 IN MACROPHAGES
92nd European Atherosclerosis Society Congress, Lyon, France, 26 - 29 May 2024, pp.10, (Summary Text)
11. The combined effects of ANGPTL8 (rs2278426), APOC1 (rs11568822), and APOA5 (rs662799) polymorphisms on CAD risk factors
9th International Congress of Molecular Medicine, 18 - 20 December 2023, pp.12, (Summary Text)
12. AMPK alpha-1 and TNFA gene expression levels are associated with myocardial infarction markers
9th International Congress of Molecular Medicine, 18 - 20 December 2023, pp.18, (Summary Text)
13. HEPG2 Hücre Hattında Ferroptoz ile İlişkili Genlerin Ekspresyon Değişimlerinin İncelenmesi
18.Tıbbi Biyoloji ve Genetik Kongresi, Ankara, Turkey, 26 - 29 October 2023, pp.26, (Summary Text)
14. Anjiyopoietin Benzeri Protein 8 Rs2278426’nın Minör Alleli Koroner Arter Hastalığı ve Tip 2 Diyabetes Mellitus Patoloji Mekanizmalarını Etkiler
18. Tıbbi Biyoloji ve Genetik Kongresi, Ankara, Turkey, 26 - 29 October 2023, pp.29, (Summary Text)
16. Coronary artery disease severity scores and lipid levels are associated with ANRIL polymorphisms in female patients
38th National Cardiology Congress,, Antalya, Turkey, 10 - 13 November 2022, vol.26, pp.24, (Summary Text)
18. The lipid ratios and lipid levels are associated with the combination of NOS3 and APOE gene polymorphisms in coronary artery disease
37th Turkish Cardiology Congress With International Participation, Antalya, Turkey, 18 - 21 November 2021, vol.25, pp.50, (Summary Text)
23. miR-130b and miR- 18a correlated with stenosis and lipid levels in CAD patients
36.Uluslararası Katılımlı Türk Kardiyoloji Kongresi, 3 - 06 December 2020, vol.24, pp.95, (Summary Text)
26. ANRIL Gen Varyantlarının Ateroskleroz Yaygınlığı ve Ciddiyeti İle İlişkileri
14. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Ankara, Turkey, 20 - 22 November 2020, pp.23, (Summary Text)
28. The role RORalpha target genes in postmortem advanced atherosclerotic plaques and patients with CAD
7th INTERNATIONAL CONGRESS of THE MOLECULAR BIOLOGY ASSOCIATION of TURKEY, İstanbul, Turkey, 27 - 29 September 2019, pp.124, (Summary Text)
29. Hsa-miR-584-5p as a novel candidate biomarker in Turkish men with coronary artery disease.
Uluslararası Katılımlı 35. Türk Kardiyoloji Kongresi, Antalya, Turkey, 2 - 06 October 2019, pp.3-4, (Summary Text)
30. The effect of APOA5 -1131T>C polymorphism on plasma lipid levels in Turkish coronary artery disease patients
7th International Congress of Molecular Medicine, İstanbul, Turkey, 5 - 07 September 2019, pp.131, (Summary Text)
34. Role of miR-18a and miR-584 on AMPK Pathway in Endothelial Cells
13 th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, pp.103, (Summary Text)
35. Silencing of CERS5 (Ceramide synthase 5) alters the protein and gene expression of atherosclerosis related genes in endothelial cells
13. Tıbbi Genetik Kongresi,, Muğla, Turkey, 7 - 11 November 2018, pp.185, (Full Text)
36. Genetic risk factors for coronary artery disease that are specific to Turkish population
Turkish Cardiology Congress 2018, Antalya, Turkey, 19 October 2018 - 22 October 2019, pp.113, (Summary Text)
38. Berberinin AMP-aktive edilmiş protein kinaz yolağında bulunan seçilmiş genlerin ekspresyon düzeylerine etkisi
XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 29 October 2017, pp.12, (Summary Text)
39. AMP-Aktive edilmiş Protein Kinazın (AMPK) Aktivatörü-AICAR kullanımının AMPK yolağındaki genler üzerine etkisi
XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 29 October 2017, pp.27, (Summary Text)
40. miRNA Aracili Gen Regulasyonunda PTEN Geninin 3'UTR Bölgesindeki Dizi Varyantlarinin Rolü
Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 21 October 2017, pp.1, (Full Text)
41. Investigation of the association between ITLN1 gene A326T polymorphism and in subjects with type 2 diabetes mellitus and obese: In the TARF study.
American Society of Human Genetics Congress, Orlando, United States Of America, 17 - 21 October 2017, pp.2, (Full Text)
42. The effects of missense mutations causing PRKAG2 cardiomyopathy on expression levels of selected genes involved in AMPK pathway.
American Society of Human Genetics Congress, Orlando, United States Of America, 17 - 21 October 2017, pp.1, (Full Text)
43. Investigation of microRNA expression in coronary artery disease.
American Society of Human Genetics Congress, Orlando, United States Of America, 17 - 21 October 2017, pp.3, (Full Text)
45. The Role of CYP19A1, ESR1 and MIF Genes Polymorphıms On The Angıographıc Severıty and The Extent of Atherosclerotıc Coronary Artery Dısease.
85th The European Atherosclerosis Society (EAS) Congress, PRAG, Czech Republic, 23 - 26 April 2017, vol.263, pp.3120, (Summary Text)
48. Plasma levels of miR 19a miR 26a and miR 584 are associated with severity of coronary artery disease in Turkish Men.
The American Society of Human Genetics Conference 2016, Vancouver, Canada, 17 - 21 October 2016, (Full Text)
49. Deletion and duplication patterns of dystophin gene in Turkish DuchenneBecker muscular dystrophy patients.
European Human Genetics Conference 2016,, Barcelona, Spain, 20 - 24 May 2016, pp.7, (Full Text)
50. MicroRNA-625-5p as a novel candidate modulator of AMPK pathway in statin-treated individuals without coronary artery disease
European Human Genetics Conference 2016, Barcelona, Spain, 20 - 24 May 2016, pp.6, (Full Text)
51. Role of ceramide synthase 5 gene (LASS/CERS5) in molecular pathogenesis of atherosclerosis
ESHG 2015, Glasgow, England, 6 - 09 June 2015, pp.123, (Summary Text)
52. 14 Yıllık Huntington Hastalığı Genetik Tanı Sonuçlarının Değerlendirilmesi
6. DETAE Günleri, Turkey, 24 November 2014, (Summary Text)
53. Macrophage migration inhibitory factor (MIF) gene polymorphism tends to predict type-2 diabetes risk in Turkish men, not women: implications
30. Uluslararası Katılımlı Ulusal Kardiyoloji Kongresi, Antalya, Turkey, 23 - 26 October 2014, pp.111, (Summary Text)
54. Simvastatin affects ABCA1 expression and cholesterol efflux in THP-1 macrophages by a ROR-Alpha-dependent pathway.
European Human Genetics Conference, Milan, Italy, 31 May - 03 June 2014, pp.102, (Full Text)
55. FTO gene rs1421085 polymorphism is associated with obesity and metabolic syndrome in the Turkish adults
European Human Genetics Conference 2014, Milano, Italy, 31 May - 03 June 2014, (Full Text)
59. Inhibitory Effect of SR1001 on ROR-Alpha Activity Requires Intracellular Cholesterol
European Human Genetics Conference, Paris, France, 8 - 11 July 2013, pp.461, (Full Text)
63. TEKHARF çalışmasında dislipidemi ve apolipoprotein genleri
27. Ulusal Kardiyoloji Kongresi, İstanbul, Turkey, 27 - 30 October 2011, pp.60, (Summary Text)
64. Association found between the promoter region polymorphism in the APOC3 gene and the serum triglyceride level in Tukish adults
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 05 December 2010, pp.26, (Summary Text)
65. . The effect of APOA4-T347S polymorphism on obesity and serum triglycerides in Turkish adults
9. Ulusal Tıbbi Genetik Kongresi , İstanbul, Turkey, 1 - 05 December 2010, pp.25, (Summary Text)
66. Tekharf Çalışmasında Metabolik Sendrom Gelişimini Etkileyen Genetik Risk Faktörlerinin Belirlenmesi
26. Ulusal Kardiyoloji Kongresi, İstanbul, Turkey, 21 - 24 October 2010, pp.22, (Summary Text)
67. TEKHARF çalışması ile IL-6 promotor gen varyantlarının ilişkileri
XXIV. Ulusal Kardiyoloji Kongresi, İstanbul, Turkey, 24 - 27 October 2009, pp.121, (Summary Text)
68. Türk erişkinlerinde Apolipoprotein AIV gen polimorfizminin plazma lipid seviyeleri ve obezite ile ilişkisi
XXV. Ulusal Kardiyoloji Kongresi, İstanbul, Turkey, 22 - 25 October 2009, pp.49, (Summary Text)
69. Türk erişkinlerinde apolipoprotein C3 geninin abdominal obezite ile ilişkisi
XXV. Ulusal Kardiyoloji Kongresi, İstanbul, Turkey, 22 - 25 October 2009, pp.45, (Summary Text)
70. ATP-binding Kaset Transporter A1 (ABCA1) Geninin Düşük HDL-kolesterol Seviyesi Üzerine Etkisi
XXIII. Ulusal Kardiyoloji Kongresi, Antalya, Turkey, 19 - 23 October 2007, pp.32, (Summary Text)
71. Metabolik Sendromda Lipoprotein Lipaz Geni S447X Varyantının Önemi
XXII. Ulusal Kardiyoloji Kongresi, Turkey, 24 - 28 November 2006, (Summary Text)
Books
7
2. TEKHARF Genetik Kanadı Koroner Kalp Hastalığı ve Metabolik Sendrom genetik Risk Faktörleri
in: TEKHARF 2017, Tıp Dünyasının Kronik Hastalıklara Yaklaşımına Öncülük, Altan Onat, Editor, Logos Yayıncılık Tic. AŞ., İstanbul, pp.263-275, 2017
3. TEKHARF Genetik Kanadı Koroner Kalp Hastalığı ve Metabolik Sendrom Genetik Risk Faktörleri
in: TEKHARF 2015 Yetişkinlerimizin Sağlığı ve Kronik Hastalıklara Tıbbın Yaklaşımına Öncülük, Altan Onat, Editor, Logos Yayınevi, İstanbul, pp.329-252, 2015
4. TEKHARF Genetik Kanadı: Koroner Kalp Hastalığı ve Metabolik Sendrom Genetik Risk Faktörleri
in: TEKHARF ÇALIŞMASI 2015 Yetişkinlerimizin Sağlığı ve Kronik Hastalıklara Tıbbın Yaklaşımına Öncülük, Onat A., Editor, Logos Yayıncılık, İstanbul, pp.239-252, 2015
5. Genetik Kanadı: Koroner Kalp Hastalığı ve Metabolik Sendrom Genetik Risk Faktörleri
in: TEKHARF ÇALIŞMASI 2013 Halkımızın Sağlığına Işık Tıbba Çığır Açabilecek Katkı, Altan Onat, Editor, Logos Yayıncılık, İstanbul, pp.221-234, 2013
6. TEKHARF 2011, Halkımızın Kusurlu Kalp Sağlığına Işık Yoluyla, Tıbba Büyük Katkı
in: TEKHARF Genetik Kanadı Koroner Kalp Hastalığı ve Metabolik Sendrom Genetik Risk Faktörleri, Onat A., Editor, Logos Yayıncılık Tic. A.Ş., İstanbul, pp.209-219, 2011
7. TEKHARF Genetik Kanadı: Koroner Kalp Hastalıkları ve Metabolik Sendrom Genetik Risk Faktörleri
in: TEKHARF ÇALIŞMASI 2011 HALKIMIZIN KUSURLU KALP SAĞLIĞINA IŞIK YOLUYLA TIBBA BÜYÜK KATKI, Altan Onat, Editor, Logos yayıncılık, İstanbul, pp.209-219, 2011