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Havva Çobanoğulları

Observed names: Cobanogullari, H., H Cobanogullari, H. Cobanogullari, Havva Cobanogullari, Havva Cobanogulları, Havva Çobanogullari, Havva Çobanoğullari, Çobanoğulları, Havva
ORCID: 0000-0003-4153-7739
Observed ORCID: 0000-0003-4153-7739
OpenAlex ID: A5040013822
Gold Nanoparticle-Modified Molecularly Imprinted Polymer-Coated Pencil Graphite Electrodes for Electrochemical Detection of Bisphenol A
2024 · Fatma Yılmaz, Nemah Abu Shama, et al. · ACS Omega · 19
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Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia
2023 · Aslıhan Kiraz, Ozlem Sezer, et al. · Journal of Medical Virology · 8
Strong association between angiotensin-converting enzyme gene InDel polymorphism and COVID-19 diseases
2023 · Havva Çobanogullari, Emine Unal Evren, et al. · Medicina Clínica · 5
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Periconceptional Mediterranean Diet during Pregnancy on Children’s Health
2022 · Çobanoğulları, Havva, Ergoren, Mahmut Cerkez, et al. · Journal of preventive medicine and hygiene · 4
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Integrated Biotechnological Strategies for Planetary Health and Ecosystem Restoration
2026 · Duygu T. Yildirim, A. Baki Yildirim, et al. · The EuroBiotech Journal · 1
Molecular insights into Wnt3a and Wnt5a gene expression in venous insufficiency
2024 · Fatima Eltayb M. Ageed, Fadumo Ali Tifow, et al. · Molecular Biology Reports · 1
Strong association between angiotensin-converting enzyme gene InDel polymorphism and COVID-19 diseases
2023 · Havva Çobanogullari, Emine Unal Evren, et al. · Medicina Clínica (English Edition) · 1
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Association of the 5HTR2C gene Ser23 variation with childhood allergic asthma
2022 · Sehime Gulsun Temel, Mahmut Cerkez Ergoren, et al. · The EuroBiotech Journal · 1
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The Biennial report: The collaboration between MAGI Research, Diagnosis and Treatment Center of Genetic and Rare Diseases and Near East University DESAM Institute
2020 · Mahmut Cerkez Ergoren, Elena Manara, et al. · The EuroBiotech Journal · 1
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Functional coding/non-coding variants in EGFR, ROS1 and ALK genes and their role in liquid biopsy as a personalized therapy
2020 · Mahmut Cerkez Ergoren, Havva Cobanogulları, et al. · Critical Reviews in Oncology/Hematology · 1
A Pilot Evaluation of Spinal Muscular Atrophy Carrier Frequency Among Newborns in Northern Cyprus
2026 · Haniyeh Rahbar Kafshboran, John Demey, et al. · Current Genetic Medicine Reports
Low Prevalence of the HBB c.20A > T (HbS) Allele in a Turkish Cypriot Cohort: A Molecular Screening Study
2026 · Emine Kandemis, Saadatu Sani Sulamain, et al. · Hemoglobin
AI-Powered Synthetic Biology: Current Situation, Challenges, and Future Perspectives
2026 · Izem Olcay Sahin, Nuriye Gokce, et al. · The EuroBiotech Journal
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Gastroprotective Potential of Wild-Grown Rheum rhabarbarum from Northern Iraq: A Preliminary Pharmacological Study on Ethanol-Induced Gastric Ulcers in Rats
2026 · Halo Hameed, Esref Celik, et al. · kerbala journal of pharmaceutical sciences
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Long-read sequencing bridges germline and somatic variant detection: a multi-modal approach for hereditary cancer diagnostics
2026 · Behich Koyutourk, Havva Çobanoğulları, et al. · Clinical & Translational Oncology
Investigating the Relationship between COVID-19 Vaccination and ACE2 Gene Expression in Cardiovascular Disease
2026 · Nabaa Shihab Shihab, Havva Cobanogullari, et al. · Journal of Clinical Medicine of Kazakhstan
Allele frequencies of ACE I/D and CCR5- Δ32 variants in the Jordanian cohort residing in Northern Cyprus
2026 · Havva Cobanogullari, Behich Koyutourk, et al. · Human Gene
Determination of the Frequency of HBB (c.20 A > T) Gene Mutation in the Nigerian and Zimbabwean Populations in Northern Cyprus
2025 · Havva Çobanoğulları, Dabbah Maima Gbassay, et al. · Biochemical Genetics
Investigation of balanced chromosomal aberrations prevalence in healthy Turkish Cypriot couples
2025 · Dize Deryali, Havva Cobanogullari, et al. · Global Medical Genetics
Correlation of ITGB3 Gene rs5918T>C and APOA1 Gene rs1799837C>T Variants with Serum Lipid Profiles in Turkish Cypriot Patients with Coronary Artery Disease
2025 · Cenk Conkbayir, Mahmut Cerkez Ergoren, et al. · Cor et Vasa
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A frameshift mutation in the PRG4 gene causing camptodactyly-arthropathy-coxa vara-pericarditis syndrome: a case report
2025 · Behich Koyutourk, Havva Cobanogullari, et al. · Modern Rheumatology Case Reports
Non-Invasive Screening Test Paradox in a Case Born with Mixed Gonadal Dysgenesis (45,X/46,Xy)
2023 · H. Cobanogullari, N. Akcan, et al. · Balkan Journal of Medical Genetics
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Associations of the ITGB3 gene rs5918T>C and the APOA1 gene rs1799837C>T markers with serum lipid metabolism in coronary artery disease patients
2021 · C Conkbayir, M Ergoren, et al. · European Heart Journal
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Associations of the ITGB3 gene rs5918T > C and the APOA1 gene rs1799837C > T markers with serum lipid metabolism in coronary artery disease patients
2021 · TEMEL, ŞEHİME GÜLSÜN, Ugurlucan, M., et al. · Bursa Uludag University - AVESIS
Meeting Reports: Notes and commentaries on Turkish Medical Genetics Association and Cyprus Turkish Genetic Union Meeting
2020 · Mahmut Çerkez Ergören, Havva Çobanoğullari, et al.
Works count: 25
Citation count: 42
H-index: 4
I10-index: 1
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