Publications by authors named "Senol Citli"

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Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases.
Zeynep Esener, Mehmet Akif Yücesoy, Alper Gezdirici, Mustafa Dogan, Ayberk Turkyilmaz, Senol Citli

Clin Genet· January 2026

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Novel RORA Variants Reveal Genotype-Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders.
Gul Unsel-Bolat, Hilmi Bolat, Senol Citli, Ozlem Ozdemir, Ibrahim Baris

Clin Genet· December 2025

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Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757].
Nalan Yakici, Alexandra Y Kreins, Mehmet Cihangir Catak, Royala Babayeva, Baran Erman, Senol Citli

Clin Immunol· November 2023

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Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells.
Feyzanur Caldiran, Caglar Berkel, Esra Yilmaz, Burak Kucuk, Aslihan Hatun Cacan, Senol Citli

Biochem Biophys Res Commun· October 2023

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Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.
Nalan Yakici, Alexandra Y Kreins, Mehmet Cihangir Catak, Royala Babayeva, Baran Erman, Senol Citli

Clin Immunol· October 2023

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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay.
Pınar Özkan Kart, Senol Citli, Nihal Yildiz, Ali Cansu

Brain Dev· May 2023

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Investigation of sub-chromosomal changes in males with idiopathic azoospermia by chromosomal microarray analysis.
Şenol Çitli, Ahmet Cevdet Ceylan, Fikret Erdemir

Andrologia· October 2022

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Maternal Germline Mosaicism of a TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings.
Şenol Çitli, Esra Serdaroglu

Fetal Pediatr Pathol· February 2022

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ASD with the Bor Syndrome: A Case Report.
Ferhat Yaylaci, Begum Sahbudak, Senol Citli, Neriman Kilit

Psychopharmacol Bull· May 2020

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IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease.
Ulas Emre Akbulut, Hamdi Cihan Emeksiz, Senol Citli, Alper Han Cebi, Hatice Ayca Ata Korkmaz

J Pediatr (Rio J)· October 2019

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Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders.
Ahmet Cevdet Ceylan, Senol Citli, Haktan Bagis Erdem, Ibrahim Sahin, Elif Acar Arslan

Mol Cytogenet· September 2018

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Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers.
Oztürk Ozdemir, Ilhan Sezgin, Hande Kucuk Kurtulgan, Ferhan Candan, Binnur Koksal, Senol Citli

Mol Biol Rep· June 2011

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