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Emine İkbal Atlı

Observed names: Atli, Emine Ikbal, E Atlı, E Ikbal Atli, E. Atli, E.İ. Atli, Emine Atli, Emine Atlı, Emine I. Atli, Emine Ikbal Atli, Emine İ. Atlı, Emine İkbal ATLI, Emine İkbal Atli, EmineIkbal Atli, emine ikbal atli
Institution: Trakya University
Observed institutions: Trakya University, Bursa Uludağ Üni̇versi̇tesi̇, Acıbadem University, Sağlık Bilimleri Üniversitesi, Eskişehir Osmangazi University, Near East University
ORCID: 0000-0001-9003-1449
Observed ORCID: 0000-0001-9003-1449
OpenAlex ID: A5030957598
Concepts of Double Hit and Triple Hit Disease in Multiple Myeloma, Entity and Prognostic Significance
2020 · Mehmet Baysal, Ufuk Demirci, et al. · Scientific Reports · 64
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FOXF2 is required for cochlear development in humans and mice
2018 · Guney Bademci, Clemer Abad, et al. · Human Molecular Genetics · 33
IDH1 mutations is prognostic marker for primary glioblastoma multiforme but MGMT hypermethylation is not prognostic for primary glioblastoma multiforme
2014 · Rasime Kalkan, Emine İkbal Atli, et al. · Gene · 30
The Impacts of miRNAs in Glioblastoma Progression
2016 · Rasime Kalkan, Emine İkbal Atli · Critical Reviews in Eukaryotic Gene Expression · 27
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development
2020 · Guney Bademci, Clemer Abad, et al. · Journal of Clinical Investigation · 20
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The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region
2021 · Sinem Yalçıntepe, Fatma Özgüç Çömlek, et al. · Journal of Clinical Research in Pediatric Endocrinology · 18
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Clinical Implications of Chromosome 16 Copy Number Variation
2021 · Emine Ikbal Atli, Sinem Yalcintepe, et al. · Molecular Syndromology · 17
Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants
2017 · SD Ulusal, H Gürkan, et al. · Balkan Journal of Medical Genetics · 17
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Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report
2020 · Selma Demir, Hakan Gürkan, et al. · Molecular Syndromology · 15
Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype
2022 · Drenushe Zhuri, Hakan Gurkan, et al. · Global Medical Genetics · 12
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Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report
2019 · Cihan Inan, N. Cenk Sayin, et al. · Fetal and Pediatric Pathology · 12
Routine Chromosomal Microarray Analysis Is Necessary in Turkish Patients with Unexplained Developmental Delay/Intellectual Disability Disorder
2020 · Hakan Gurkan, Emine Ikbal Atli, et al. · Nöro Psikiyatri Arşivi · 11
The evaluation of risk factors leading to early deaths in patients with acute promyelocytic leukemia: a retrospective study
2022 · Mehmet Baysal, Vildan Gürsoy, et al. · Annals of Hematology · 10
Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy
2021 · Emine Ikbal Atli, Engin Atli, et al. · Internal Medicine Journal · 10
The importance of multiple gene analysis for diagnosis and differential diagnosis in charcot marie tooth disease
2021 · Sinem Yalcintepe, Hakan Gurkan, et al. · Turkish Neurosurgery · 10
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Pros and cons for fluorescent in situ hybridization, karyotyping and next generation sequencing for diagnosis and follow-up of multiple myeloma
2020 · E Ikbal Atli, H Gurkan, et al. · Balkan Journal of Medical Genetics · 10
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The Importance of Targeted Next-generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies
2020 · Emine Atli, Hakan Gurkan, et al. · Mediterranean Journal of Hematology and Infectious Diseases · 9
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De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype–Phenotype Correlation
2019 · Emine Ikbal Atli, Hakan Gurkan, et al. · Journal of Pediatric Genetics · 9
Identification of a novel homozygous TBC1D24 mutation in a Turkish family with DOORS syndrome
2017 · Engin Atli, Hakan Gurkan, et al. · Clinical Dysmorphology · 9
Y chromosome polymorphism in Turkish patients with reproductive problems: a genetic centre experience
2023 · Emine İkbal Atlı, Çisem Mail, et al. · The European Research Journal · 6
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Comprehensive Genetic Analysis of RASopathy in the Era of Next-Generation Sequencing and Definition of a Novel Likely Pathogenic KRAS Variation
2022 · Selma Demir, Hümeyra Yaşar Köstek, et al. · Molecular Syndromology · 6
Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants
2021 · Selma Demir, Sinem Yalçıntepe, et al. · Balkan Medical Journal · 6
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Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey
2021 · Selma Demir, Sinem Yalçıntepe, et al. · Genetic Testing and Molecular Biomarkers · 6
Investigation of the Relationship between Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2 and GABRA4 Genes
2021 · Sinem Yalcintepe, Isik Gorker, et al. · Nöro Psikiyatri Arşivi · 6
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A large posterior encephalocele associated with severe ventriculomegaly, cerebellar atrophy and transposition of the great arteries
2018 · Cihan Inan, Niyazi Cenk Sayin, et al. · Journal of Clinical Ultrasound · 5
Works count: 82
Citation count: 453
H-index: 11
I10-index: 16
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