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Özgür Balasar

Observed names: Balasar, Ozgur, O., Balasar, Ozgur Balasar, Ozgür Balasar, Ö., Balasar, Özgur Balasar, Özgür BALASAR
Institution: Konya City Hospital
ORCID: 0000-0002-2945-9355
Observed ORCID: 0000-0002-2945-9355
OpenAlex ID: A5017184594
The effect of rs9939609 FTO gene polymorphism on weight loss after laparoscopic sleeve gastrectomy
2015 · Özgür Balasar, Tuğrul Çakır, et al. · Surgical Endoscopy · 18
Male infertility associated with de novo pericentric inversion of chromosome 1
2017 · Özgür Balasar, Ayşe Gül Zamani, et al. · Urology Research and Practice · 17
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HLA-B*51 in Patients with Recurrent Aphthous Stomatitis
2008 · Mustafa Özdemir, Hasan Acar, et al. · Acta Dermato Venereologica · 13
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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 · 11
Importance of targeted next-generation sequencing in pediatric patients with developmental epileptic encephalopathy
2023 · Savaş Bariş, Serkan Kırık, et al. · Revista da Associação Médica Brasileira · 9
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Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey
2022 · Atil Bisgin, Sebnem Ozemri Sag, et al. · The Breast · 9
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Assessment of whole-exome sequencing results in neurogenetic diseases
2023 · Özgür Balasar, Müşerref Başdemirci · Journal of Human Genetics · 8
Batı Ege Bölgesinde α-Talasemi Genotipleri ve α-Talasemi Genotip Frekansı
2023 · Savaş BARIŞ, Cüneyd YAVAŞ, et al. · Sağlık Bilimlerinde Değer · 8
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Investigation of the interchromosomal effects in male carriers with structural chromosomal abnormalities using FISH
2020 · Özgür Balasar, Hasan Acar · Urology Research and Practice · 8
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Variable expressivity of renal involvement in a further family with Townes–Brocks syndrome
2014 · Hatice Koçak Eker, Özgür Balasar · Clinical Dysmorphology · 7
Status dystonicus associated with CLN8 disease
2020 · Miraç Yıldırım, Engin Köse, et al. · Brain and Development · 5
Lenz-Majewski syndrome and recurrent otitis media: Are they related or not?
2024 · Fayize Maden Bedel, Özgür Balasar, et al. · European Journal of Medical Genetics · 4
Assessment of Pathogenic Variants in the PAH Gene and Genotype–Phenotype Correlation in Phenylketonuria Patients from Turkey
2024 · Özgür Balasar, Banu Kadıoğlu Yılmaz, et al. · Biochemical Genetics · 3
Distinct Distribution of HBB Variants in Two Cohorts of Beta Thalassemia Patients, and a Novel Variant from Turkey
2024 · Hatice Kocak Eker, Ozgur Balasar · Molecular Syndromology · 3
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A rare CALR variant mutation and efficient peginterferon alfa-2a response in a patient with essential thrombocythemia
2023 · Rafiye Ciftciler, Ozgur Balasar · Cancer Genetics · 2
Mild congenital myopathy due to a novel variation in SPEG gene
2021 · Mirac Yildirim, Ozgur Balasar, et al. · Intractable & Rare Diseases Research · 2
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Case of twin achondroplasia and autism coexistence and literature review
2023 · Nagehan Bilgeç, Özgür Balasar, et al. · Psychiatric Genetics · 1
Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report
2023 · Rafiye Ciftciler, Özgur Balasar, et al. · Transfusion and Apheresis Science · 1
A rare variant Klinefelter syndrome seen 40 years later: 47,X,del(Xq24),Y
2021 · Mehmet Serkan Özkent, Özgür Balasar · Andrologia · 1
From Family History to Structural Insight: The TP53 c.1024C>T [p.(Arg342*)] Variant in Li–Fraumeni Syndrome
2026 · Emir Nekay, Savas Baris, et al. · Biomedicines
Radiomic Analysis of Mandibular Bone Changes in Patients with Chronic Myeloid Leukemia on Panoramic Radiographs
2026 · Taha Zirek, Sultan Uzun, et al. · Journal of Imaging Informatics in Medicine
Sotos and Malan Syndromes in Childhood: Molecular and Clinical Findings From a Nationwide Cohort of 48 Patients
2026 · Ceren Yılmaz Uzman, Semra Gürsoy, et al. · Clinical Genetics
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Characterization of FMR1 CGG Repeat Structure and AGG Interruption Patterns in Turkish and Syrian Individuals
2026 · Hatice Koçak Eker, Sümeyye Kara, et al. · Gazi Medical Journal
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The Association of FMR1 Gene Low-Normal and High-Normal Alleles with Ovarian Dysfunctions: A Retrospective Analysis from the Turkish Population
2026 · Hatice Kocak Eker, Levent Simsek, et al. · Molecular Syndromology
Supplementary Material for: The Association of FMR1 Gene Low-Normal and High-Normal Alleles with Ovarian Dysfunctions: A Retrospective Analysis from the Turkish Population
2026 · karger, figshare admin, H., KocakEker, et al. · Figshare
Works count: 36
Citation count: 130
H-index: 8
I10-index: 4
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