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Author

Haldun Doğan

Observed names: DOĞAN, HALDUN, Haldun Dogan
Institution: Intergen (Turkey)
ORCID: 0000-0003-1667-1987
Observed ORCID: 0000-0003-1667-1987
OpenAlex ID: A5027996497
Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing
2015 · Sebahat Yılmaz Ağladıoğlu, Zehra Aycan, et al. · Journal of Pediatric Endocrinology and Metabolism · 42
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey
2021 · Rabia Miray Kisla Ekinci, Sibel Balci, et al. · Molecular Syndromology · 25
MaFOS-GDM trial: Maternal fish oil supplementation in women with gestational diabetes and cord blood DNA methylation at insulin like growth factor-1 (IGF-1) gene
2017 · Dilek Dilli, Nazan Neslihan Doğan, et al. · Clinical Nutrition ESPEN · 16
The potential utility of real-time PCR of the 16S-rRNA gene in the diagnosis of neonatal sepsis
2019 · Kenan İstanbullu, Nilgün Köksal, et al. · The Turkish Journal of Pediatrics · 14
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Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity
2016 · Mehmet Boyraz, Ediz Yeşilkaya, et al. · Journal of Clinical Research in Pediatric Endocrinology · 10
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Rapid screening of 10 common mutations in Turkish Gaucher patients using electronic DNA microarray
2007 · Fatih Ezgu, Alev Hasanoglu, et al. · Blood Cells Molecules and Diseases · 8
Significance of O6-methyl guanine methyltransferase promoter methylation in high grade glioma patients: optimal cutoff point, CpG locus, and genetic assay
2023 · Murat Buyuktepe, Ibrahim Kaplan, et al. · Journal of Neuro-Oncology · 7
Iron Refractory Iron Deficiency Anemia Due to 374 Base Pairs Deletion in the TMPRSS6 Gene
2018 · Seda Çakmakli, Can Acipayam, et al. · Journal of Pediatric Hematology/Oncology · 4
Evaluation of MSX1 gene as the common candidate gene of nonsyndromic congenital hypodontia and cleft lip and palate
2017 · AyseTuba Altug, Asli Senol, et al. · Journal of Cleft Lip Palate and Craniofacial Anomalies · 3
A Novel Beta Globin Gene Polymorphism in Turkish Population: IVS-II 706 G>A
2015 · Nejat Akar, Serdar Ceylaner, et al. · The Journal of Pediatric Research · 1
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MYH2 as a Potential Modifier of Clinical Severity in Facioscapulohumeral Muscular Dystrophy
2026 · Ceren Hangül, Ayse Esra Manguoglu, et al. · Journal of Molecular Neuroscience
Allojeneik Hematopoetik Kök Hücre Nakli Sonrası Aseptik Nekroz Gelişen Olgularda Vitamin D Reseptör Gen Polimorfizmi
2023 · Ender Soydan, Uğur Şahin, et al. · LLM Dergi
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Use of immunohistochemical versus microsatellite analyses as markers for colorectal cancer
2017 · Utku Tantoğlu, Seher Yüksel, et al. · Turkish Journal of Biochemistry
Ai̇lesel Hi̇perkolesterolemi̇ Olgularinin Geneti̇k, Demografi̇k Ve Kli̇ni̇k Özelli̇kleri̇
2017 · DOĞAN, HALDUN, BİLGİN, MÜGE, et al. · Van Yüzüncü Yıl University Academic Data Management System
Sendromik Olmayan Konjenital Maksiller Lateral Kesici Diş Eksikliği ve Dudak Damak Yarıklarının Ortak Genetik Alt Yapısı
2016 · A. Ataç, Aslı Şenol, et al. · Turkiye Klinikleri Orthodontics - Special Topics
A Novel Mutation of SCL26A4 gene in Turkish Family with Pendred Syndrome
2015 · Özgür Aldemir, Kadri Karaer, et al. · Mustafa Kemal Üniversitesi Tıp Dergisi
Sequence Analysis of 11 Known Causative Genes in Clinically Diagnosed Children as Maturity Onset Diabetes of Youth by Next Generation Sequencing
2014 · Sebahat Yılmaz Ağladıoğlu, Zehra Aycan, et al. · ESPE 2014
Tip 2 herediter anjioödem tanısı alan bir aile
2013 · AYDIN, ÖMÜR, SİN, BETÜL AYŞE, et al. · AYBU AVESIS
Hereditary angioedema A turkish family
2013 · DOĞAN, HALDUN, SOYYİĞİT, ŞADAN, et al. · AYBU AVESIS
Works count: 19
Citation count: 130
H-index: 7
I10-index: 5
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