Publications by authors named "Emine Atli"

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Comparison of Procedural Oxygen Mask Versus Conventional Nasal Cannula for Hypoxemia Prevention During Endoscopic Retrograde Cholangiopancreatography: A Randomized Controlled Trial.
Bedirhan Gunel, Ayse Sencan, Zeynep Yasemin Tavsanoglu, Tunahan Cevik, Emine Atli

Dig Dis Sci· December 2025

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Evaluation of Cardiomyopathy-Related Target Genes by Next-Generation Sequencing Method and Investigation of the Phenotype-Genotype Relationship.
Hazal Sezginer Guler, Drenushe Zhuri, Sinem Yalcintepe, Servet Altay, Murat Deveci, Engin Atli, Emine İkbal Atli

Mol Syndromol· May 2025

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Incidence of Thromboembolism in COVID-19 Patients in Intensive Care Units: A Retrospective Cohort Analysis.
Ayse Z Turan Civraz, Ipek Duzyol, Emine Atli, Cigdem Caglayan, Emine Ozer Yurt

Cureus· October 2023

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The Frequency of Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method.
Sinem Yalcintepe, Yasemin Karal, Selma Demir, Emine Ikbal Atli, Engin Atli

Glob Med Genet· June 2023

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Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique.
Engin Atlı, Hakan Gürkan, Babürhan Güldiken, Damla Eker, Sinem Yalçıntepe

Balkan Med J· January 2023

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Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype.
Drenushe Zhuri, Hakan Gurkan, Damla Eker, Yasemin Karal, Sinem Yalcintepe, Engin Atli, Emine Ikbal Atli

Glob Med Genet· September 2022

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Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy.
Emine Ikbal Atli, Engin Atli, Sinem Yalcintepe, Selma Demir, Rasime Kalkan

Intern Med J· July 2022

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The evaluation of risk factors leading to early deaths in patients with acute promyelocytic leukemia: a retrospective study.
Mehmet Baysal, Vildan Gürsoy, Fazil Cagri Hunutlu, Buket Erkan, Ufuk Demirci, Emine Ikbal Atli

Ann Hematol· May 2022

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Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies.
Emine Ikbal Atli, Engin Atli, Cihan Inan, Gülizar Fusun Varol, Cisem Mail

Taiwan J Obstet Gynecol· May 2022

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Clinical Implications of Chromosome 16 Copy Number Variation.
Emine Ikbal Atli, Sinem Yalcintepe, Engin Atli, Selma Demir, Cisem Mail

Mol Syndromol· May 2022

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First Report of Jacobsen Syndrome with Dextrocardia Diagnosed with del(11)(q24q25).
Sinem Yalcintepe, Drenushe Zhuri, Hazal Sezginer Guler, Engin Atli, Selma Demir, Emine Ikbal Atli

Mol Syndromol· May 2022

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Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period.
Emine Ikbal Atli, Engin Atli, Sinem Yalcintepe, Selma Demir, Rasime Kalkan

Glob Med Genet· March 2022

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Clinical Features of Aberrations Chromosome 22q: A Pilot Study.
Emine Ikbal Atli, Engin Atli, Sinem Yalcintepe, Selma Demir, Cisem Mail

Glob Med Genet· March 2022

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Comprehensive Genetic Analysis of RASopathy in the Era of Next-Generation Sequencing and Definition of a Novel Likely Pathogenic > Variation.
Selma Demir, Hümeyra Yaşar Köstek, Aslıhan Sanrı, Ruken Yıldırım, Fatma Özgüç Çömlek

Mol Syndromol· February 2022

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The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease.
Sinem Yalcintepe, Hakan Gurkan, Ipek Gungor Dogan, Selma Demir, Sebnem Ozemri Sag, Emine Ikbal Atli, Engin Atli

Turk Neurosurg· January 2022

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An unknown chromosomal aberration in a patient with chronic lymphocytic leukemia: Extra isochromosome 4q.
Emine Ikbal Atli, Hakan Gurkan, Ahmet Muzaffer Demir

J Cancer Res Ther· November 2021

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Chronic myeloid leukaemia after chemoradiotherapy for solid malignancies.
Mehmet Baysal, Gülcin Ulutas, Ali Gokyer, Elif Umit, Emine Ikbal Atli

Natl Med J India· October 2021

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The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region.
Sinem Yalçıntepe, Fatma Özgüç Çömlek, Hakan Gürkan, Selma Demir, Emine İkbal Atlı

J Clin Res Pediatr Endocrinol· August 2021

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Investigation the Relationship of Autism Spectrum Disorder and Genes.
Sinem Yalçintepe, Işık Görker, Selma Demir, Emine İkbal Atli, Engin Atli

Noro Psikiyatr Ars· August 2021

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A Pilot Study of Identification Genetic Background of Craniosynostosis Cases.
Emine Ikbal Atli, Sinem Yalcintepe, Engin Atli, Selma Demir, Cisem Mail

J Craniofac Surg· May 2021

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Prenatal diagnosis of 20p13 microdeletion syndrome.
Cem Yener, Cenk Sayın, Cihan İnan, Hakan Gürkan, Emine İkbal Atlı

Taiwan J Obstet Gynecol· March 2021

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Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report.
Selma Demir, Hakan Gürkan, Veysel Öz, Sinem Yalçıntepe, Emine I Atlı

Mol Syndromol· March 2021

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Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma.
Sinem Yalcintepe, Hakan Gurkan, Fatma Nur Korkmaz, Selma Demir, Engin Atli, Emine Ikbal Atli

J Kidney Cancer VHL· March 2021

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Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey.
Selma Demir, Sinem Yalçıntepe, Emine İkbal Atlı, Aslıhan Sanrı, Ruken Yıldırım

Genet Test Mol Biomarkers· January 2021

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The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies.
Emine Ikbal Atli, Hakan Gurkan, Engin Atli, Hakki Onur Kirkizlar, Sinem Yalcintepe

Mediterr J Hematol Infect Dis· January 2021

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