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Author

Engin Atlı

Observed names: Atlı E, E Atli, E Atlı, E Ikbal Atli, E Ikbal Atlı, E İkbal Atli, E. Atli, E. Atlı, E., Atli, Engin ATLI, Engin Atli
Institution: Trakya University
ORCID: 0000-0002-3937-5243
Observed ORCID: 0000-0002-3937-5243
OpenAlex ID: A5016476925
The Analysis of the Relationship Between A1298C and C677T Polymorphisms of the MTHFR Gene with Prostate Cancer in Eskisehir Population
2009 · Muhammed H. Muslumanoglu, Emre Tepeli, et al. · Genetic Testing and Molecular Biomarkers · 25
Placental and serum levels of human Klotho in severe preeclampsia: A potential sensitive biomarker
2019 · Isil Uzun Cilingir, Fusun Varol, et al. · Placenta · 20
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
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
Genetic screening results of individuals with high risk BRCA-related breast/ovarian cancer in Trakya region of Turkey.
2020 · Selma Demir, Hilmi Tozkir, et al. · PubMed · 11
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 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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Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders
2017 · Isik Gorker, Hakan Gurkan, et al. · Nöro Psikiyatri Arşivi · 10
The possible role of epigenetics in the etiology of hypospadias
2024 · Yıldız S, Inanç I, et al. · Journal of Pediatric Urology · 9
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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Investigation of Relationship Between Small Noncoding RNA (sncRNA) Expression Levels and Serum Iron, Copper, and Zinc Levels in Clinical Diagnosed Multiple Sclerosis Patients
2022 · Arzu Ay, Nevra Alkanli, et al. · Molecular Neurobiology · 6
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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Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus Erythematosus
2021 · Mehmet Ali BALCI, Engin ATLI, et al. · Archives of Rheumatology · 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 case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother
2015 · E İkbal Atli, H Gürkan, et al. · Balkan Journal of Medical Genetics · 6
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A Study of FoxO1, mTOR, miR-21, miR-29b, and miR-98 Expression Levels Regarding Metabolic Syndrome in Acne Vulgaris Patients
2024 · Nazan Akdağ, Engin Atli, et al. · Cureus · 4
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The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method
2023 · Sinem Yalcintepe, Yasemin Karal, et al. · Global Medical Genetics · 4
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Works count: 72
Citation count: 325
H-index: 10
I10-index: 13
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