Emine İkbal Atlı - Concepedia

Author

Emine İkbal Atlı

Also Known As

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

Publications

385

Citations

H-Index

Concepts

All Affiliations

Trakya University Ankara University Eskişehir Osmangazi University Dr. John T. Macdonald Foundation University of Miami

Eİ

About

Emine İkbal Atlı is an author at Trakya University specializing in medicine, health sciences, and gene expression.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	88
2	Health Sciences	2	2	70
3	Molecular Genetics	2	2	59
4	Cell Biology	1	1	18
5	Pathology	1	1	29

Emine İkbal Atlı

Publications

241

Citations

H-Index

Page 1

	Year	Citations
Concepts of Double Hit and Triple Hit Disease in Multiple Myeloma, Entity and Prognostic Significance Mehmet Baysal, Ufuk Demirci, Emine İkbal Atlı, Scientific Reports	2020	52
<i>FOXF2</i>is required for cochlear development in humans and mice Güney Bademci, Clemer Abad, Armağan İncesulu, Human Molecular Genetics GeneticsGenomic MechanismHuman CochleaGene CharacterizationMolecular Genetics	2018	41
IDH1 mutations is prognostic marker for primary glioblastoma multiforme but MGMT hypermethylation is not prognostic for primary glioblastoma multiforme Rasime Kalkan, Emine İkbal Atlı, Muhsin Özdemir, Gene Neuro-oncologyOncologySomatic VariantGliomaTumor Heterogeneity	2014	29
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development Güney Bademci, Clemer Abad, Filiz Başak Cengiz, Journal of Clinical Investigation Long-range Cis-regulatory ElementsEar DevelopmentGeneticsMolecular GeneticsEpigenetics	2020	18
Wiedemann-Steiner Syndrome as a Differential Diagnosis of Cornelia de Lange Syndrome Using Targeted Next-Generation Sequencing: A Case Report Hakan Gürkan, Veysel Öz, Sinem Yalçıntepe, Molecular Syndromology	2020	15
Genetic analyses of the <i>NF1</i> gene in Turkish neurofibromatosis type I patients and definition of three novel variants SD Ulusal, Hakan Gürkan, Emine İkbal Atlı, Balkan Journal of Medical Genetics	2017	14
Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report Cihan İnan, N. Cenk Sayın, Hakan Gürkan, Fetal and Pediatric Pathology	2019	14
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, Journal of Clinical Research in Pediatric Endocrinology	2021	14
Clinical Implications of Chromosome 16 Copy Number Variation Emine İkbal Atlı, Sinem Yalçıntepe, Cisem Mail, Molecular Syndromology	2021	13
Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy Emine İkbal Atlı Internal Medicine Journal	2021	11

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