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Şenol Çitli

Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers
2010 · Oztürk Ozdemir, Ilhan Sezgin, et al. · Molecular Biology Reports · 41
Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders
2018 · Ahmet Cevdet Ceylan, Senol Citli, et al. · Molecular Cytogenetics · 19
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Steatohepatitis and liver cirrhosis in Chanarin-Dorfman syndrome with a new ABDH5 mutation
2012 · E. Cakmak, H. Alagozlu, et al. · Clinics and Research in Hepatology and Gastroenterology · 18
Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients
2023 · Nalan Yakici, Alexandra Y. Kreins, et al. · Clinical Immunology · 13
Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells
2023 · Feyzanur Caldiran, Caglar Berkel, et al. · Biochemical and Biophysical Research Communications · 13
IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease
2018 · Ulas Emre Akbulut, Hamdi Cihan Emeksiz, et al. · Jornal de Pediatria · 9
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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay
2023 · Pınar Özkan Kart, Senol Citli, et al. · Brain and Development · 6
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Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings
2020 · Şenol Çitli, Esra Serdaroglu · Fetal and Pediatric Pathology · 6
Novel RORA Variants Reveal Genotype–Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders
2025 · Gul Unsel‐Bolat, Hilmi Bolat, et al. · Clinical Genetics · 3
IL‐17A, MCP‐1, CCR‐2, and ABCA1 polymorphisms in children with non‐alcoholic fatty liver disease
2019 · Ulas Emre Akbulut, Hamdi Cihan Emeksiz, et al. · Jornal de Pediatria (Versão em Português) · 3
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IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period
2021 · Feyzanur Yildirimtepe Çaldiran, Şenol Çitli, et al. · Journal of Contemporary Medicine · 2
Mitochondrial DNA copy number alterations in familial mediterranean fever patients
2018 · H. B. Erdem, A. C. Ceylan, et al. · Bratislavské lekárske listy/Bratislava medical journal · 2
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ASD with the Bor Syndrome: A Case Report
2025 · Ferhat Yaylaci, Begum Sahbudak, et al. · Psychopharmacology Bulletin · 1
Beyond Coronary Obstruction: Genome-Wide Copy Number Variation Profiling in MINOCA and Atherosclerotic Acute Coronary Syndrome
2026 · Ahmet Seyda Yılmaz, Haldun Koç, et al. · Medicina
Compensated iron depletion in repeated blood donations: Stability of circulating microRNAs despite reduced ferritin stores
2026 · Aziz Karaca, Şenol Çitli, et al. · Vox Sanguinis
Differential regulation of erythropoiesis‐related microRNAs in blood donors: Erythrocyte glutathione predicts miR ‐142 expression
2026 · Aziz Karaca, Şenol Çitli, et al. · Transfusion Medicine
Novel ABCA12 frameshift variant in a preterm infant with harlequin ichthyosis
2026 · Ilkay Er, Senol Citli, et al. · Clinical Dysmorphology
Evaluation of plasma microRNA expressions in children with metabolic dysfunction-associated steatotic liver disease
2026 · Arzu Aras, Alperhan Cebi, et al. · The Annals of Clinical and Analytical Medicine
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HbJ Bangkok, a hemoglobin variant causing diagnostic confusion in HbA1c measurement in beta-thalassemia trait: A Case Report
2026 · Hülya Kılıç, Bayram Şen, et al. · The Annals of Clinical and Analytical Medicine
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Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases
2025 · Zeynep Esener, Mehmet Akif Yücesoy, et al. · Clinical Genetics
Author response for "Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases"
2025 · Esener, Zeynep, Yuecesoy, Mehmet Akif, et al. · Publons reviews and discussion
Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]
2023 · Nalan Yakici, Alexandra Y. Kreins, et al. · Clinical Immunology
Spectrum of Germline Cancer Susceptibility Gene Mutations in Breast and Ovarian Cancer Patients in the Black Sea Region of Turkey: Single Center Experience
2023 · Şenol Çitli, Yelda Dağcıoğlu, et al. · Eskisehir Medical Journal Eskisehir City Hospital
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Unbalanced distributions of paternal t(5;7)(p15-,q36+;q36-,p15+) balanced translocation and review of the literature: Unbalanced distributions of balanced translocation
2022 · Çitli, Şenol · International Journal of Current Medical and Biological Sciences
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Newly defined Unbalanced distributions of paternal balanced chromosomal translocation and review of the literature
2022 · Citli, Senol · Zenodo (CERN European Organization for Nuclear Research)
Works count: 38
Citation count: 136
H-index: 6
I10-index: 5
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