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19 results for ATLI,+Engin

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Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss
Author / Creator:Zhuri, Drenushe ; Guler, Hazal Sezginer ; Yalcintepe, Sinem ; Demir, Selma ; Atli, Engin ; Atli, Emine Ikbal ; Gurkan, Hakan
Publisher:Ankara: AVES
Journal title:The journal of international advanced otology, 2024-07, Vol.20 (4), p.312-324
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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
Author / Creator:Akdağ, Nazan ; Atli, Engin ; Zhuri, Drenushe ; Sezgi Ner Güler, Hazal ; Gürsel Ürün, Yıldız
Publisher:United States: Cureus Inc
Journal title:Curēus (Palo Alto, CA), 2024-03, Vol.16 (3), p.e56562-e56562
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Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma
Author / Creator:Yalcintepe, Sinem ; Gurkan, Hakan ; Korkmaz, Fatma Nur ; Demir, Selma ; Atli, Engin ; Eker, Damla ; Guler, Hazal Sezginer ; Zhuri, Drenusha ; Atli, Emine Ikbal ; Salt, Semra Ayturk ; Sahin, Mustafa ; Guldiken, Sibel
Publisher:Australia: Codon Publications
Journal title:Journal of kidney cancer and VHL, 2021-03, Vol.8 (1), p.19-24
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The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region
Author / Creator:Yalçıntepe, Sinem ; Özgüç Çömlek, Fatma ; Gürkan, Hakan ; Demir, Selma ; Atlı, Emine İkbal ; Atlı, Engin ; Eker, Damla ; Tütüncüler Kökenli, Filiz
Publisher:Turkey: Galenos Yayinevi Tic. Ltd
Journal title:Journal of clinical research in pediatric endocrinology, 2021-09, Vol.13 (3), p.320-331
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Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique
Author / Creator:Atlı, Engin ; Gürkan, Hakan ; Güldiken, Babürhan ; Eker, Damla ; Yalçıntepe, Sinem ; Demir, Selma ; Atlı, Emine İkbal
Publisher:Turkey: Galenos Yayinevi Tic. Ltd
Journal title:Balkan medical journal, 2023-01, Vol.40 (1), p.13-20
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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
Author / Creator:Ay, Arzu ; Alkanli, Nevra ; Atli, Engin ; Gurkan, Hakan ; Gulyasar, Tevfik ; Guler, Sibel ; Sipahi, Tammam ; Sut, Necdet
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2023-02, Vol.60 (2), p.875-883
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Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time
Author / Creator:Yalcintepe, Sinem ; Gurkan, Hakan ; Atli, Engin ; Sayin, Niyazi Cenk ; Basaran, Umit Nusret
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:Balkan medical journal, 2020-09, Vol.37 (5), p.297-298
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Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants
Author / Creator:Demir, Selma ; Yalçıntepe, Sinem ; Atlı, Engin ; Yalçın, Yelda ; İkbal Atlı, Emine ; Eker, Damla ; Karal, Yasemin ; Gürkan, Hakan
Publisher:Turkey: Galenos Yayinevi Tic. Ltd
Journal title:Balkan medical journal, 2021-11, Vol.38 (6), p.341-347
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Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus Erythematosus
Author / Creator:Balci, Mehmet Ali ; Atli, Engin ; Gürkan, Hakan
Publisher:Istanbul: Prof Sebnem Ataman, President Turkish League Against Rheumatism
Journal title:Turkish journal of rheumatology, 2021-06, Vol.36 (2), p.287-295
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The Correlation of Cystic Fibrosis Screening Test Results with Ultrasonographically Detected Fetal Anomalies in Prenatal Diagnosis
Author / Creator:Atlı, Emine İkbal ; Atlı, Engin ; Demir, Selma ; Yalçıntepe, Sinem ; Gürkan, Hakan
Journal title:Medical journal of Bakirköy, 2023-06, Vol.19 (2), p.191-199
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The Correlation of Cystic Fibrosis Screening Test Results with Ultrasonographically Detected Fetal Anomalies in Prenatal Diagnosis/Prenatal Tanida Kistik Fibroz Tarama Testi Sonuclarinin Ultrasonograf...
Author / Creator:Atli, Emine Ikbal ; Atli, Engin ; Demir, Selma ; Yalcintepe, Sinem ; Gurkan, Hakan
Publisher:Galenos Yayinevi Tic. Ltd
Journal title:Medical journal of Bakirköy, 2023-06, Vol.19 (2), p.191
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RETROSPECTIVE ANALYSIS OF ALPHA GLOBIN COPY NUMBER VARIATIONS DETERMINED BY MLPA IN THE TRAKYA REGION/TRAKYA BOLGESINDE MLPA ILE BELIRLENEN ALFA GLOBIN KOPYA SAYISI DEGISIKLIKLERININ RETROSPEKTIF ANAL...
Author / Creator:Demir, Selma ; Gurkan, Hakan ; Eker, Damla ; Yalcintepe, Sinem ; Atli, Emine Ikbal ; Atli, Engin
Publisher:AVES
Journal title:İstanbul Tıp Fakültesi dergisi = Journal of the Istanbul Faculty of Medicine, 2021-09, Vol.84 (3), p.348
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Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders
Author / Creator:Gürkan, Hakan ; Atli, Emine İkbal ; Atli, Engin ; Bozatli, Leyla ; Altay, Mengühan Araz ; Yalçintepe, Sinem ; Özen, Yasemin ; Eker, Damla ; Akurut, Çisem ; Demır, Selma ; Görker, Işık
Publisher:Turkey: AVES Yayincilik A.S
Journal title:Noro-Psikiyatri Arsivi, 2020-09, Vol.57 (3), p.177-191
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Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes
Author / Creator:Yalçintepe, Sinem ; Görker, Işık ; Demir, Selma ; Atli, Emine İkbal ; Atli, Engin ; Tozkir, Hilmi ; Süt, Necdet ; Özen, Yasemin ; Eker, Damla ; Mail, Çisem ; Güler, Hazal Sezginer ; Zhuri, Drenushe ; Gurkan, Hakan
Publisher:Turkey: AVES Yayincilik A.S
Journal title:Noro-Psikiyatri Arsivi, 2021-09, Vol.58 (3), p.171-175
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Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders
Author / Creator:Görker, Işık ; Gürkan, Hakan ; Ulusal, Selma ; Atli, Engin ; Ayaz, Güçlü ; Ceylan, Cansın ; Tozkir, Hilmi ; Altay, Mengühan Araz ; Erol, Ali ; Yildiz, Nazike ; Direk, Ceren ; Akköprü, Hilal ; Kilit, Neriman ; Aykutlu, Hasan Cem ; Bozatli, Leyla ; Çelik, Zeki ; Berberoğlu, Kıvanç Kudret
Publisher:Turkey: BAYT Ltd. Co
Journal title:Noro-Psikiyatri Arsivi, 2018-09, Vol.55 (3), p.215-219
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Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders
Author / Creator:Gorker, Isik ; Gurkan, Hakan ; Ulusal, Selma ; Atli, Engin ; Ayaz, Guclu ; Ceylan, Cansin ; Tozkir, Hilmi ; Altay, Menguhan Araz ; Erol, Ali ; Yildiz, Nazike ; Direk, Ceren ; Akkopru, Hilal ; Kjut, Neriman ; Aykutlu, Hasan Cem ; Bozatli, Leyla ; Celik, Zeki ; Berberoglu, Kivanc Kudret
Publisher:AVES Yayincilik A.S
Journal title:Noro-Psikiyatri Arsivi, 2018-09, Vol.55 (3), p.215
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The analysis of the relationship between A1298C and C677T polymorphisms of the MTHFR gene with prostate cancer in Eskisehir population
Author / Creator:Muslumanoglu, Muhammed H ; Tepeli, Emre ; Demir, Selma ; Uludag, Ahmet ; Uzun, Derya ; Atli, Engin ; Canturk, Kemal M ; Ozdemir, Muhsin ; Turgut, Mehmet
Publisher:United States: Mary Ann Liebert, Inc
Journal title:Genetic testing and molecular biomarkers, 2009-10, Vol.13 (5), p.641-645
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Y chromosome polymorphism in Turkish patients with reproductive problems: a genetic centre experience
Author / Creator:ATLI, Emine İkbal ; MAİL, Çisem ; GURKAN, Hakan ; YALÇINTEPE, Sinem ; DEMİR, Selma ; ATLI, Engin
Publisher:Bursa: The Association of Health Research & Strategy
Journal title:The European research journal, 2023-07, Vol.9 (4), p.725-729
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Two Cystic Fybrosis Cases with Firstly Reported Compund Heterozygous Variants
Author / Creator:Yalçıntepe, Sinem ; Gürkan, Hakan ; Atlı, Engin ; Sayın, Niyazi Cenk ; Başaran, Ümit Nusret
Publisher:Turkey
Journal title:Balkan medical journal, 2020-02
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Investigation of Targeted Genes and Identification of Novel Variants with Next Generation Sequencing Method in Hearing Loss

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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

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Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma

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The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region

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Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

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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

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Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time

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Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants

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Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus Erythematosus

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The Correlation of Cystic Fibrosis Screening Test Results with Ultrasonographically Detected Fetal Anomalies in Prenatal Diagnosis

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The Correlation of Cystic Fibrosis Screening Test Results with Ultrasonographically Detected Fetal Anomalies in Prenatal Diagnosis/Prenatal Tanida Kistik Fibroz Tarama Testi Sonuclarinin Ultrasonograf...

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RETROSPECTIVE ANALYSIS OF ALPHA GLOBIN COPY NUMBER VARIATIONS DETERMINED BY MLPA IN THE TRAKYA REGION/TRAKYA BOLGESINDE MLPA ILE BELIRLENEN ALFA GLOBIN KOPYA SAYISI DEGISIKLIKLERININ RETROSPEKTIF ANAL...

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Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders

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Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes

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Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders

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Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders

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The analysis of the relationship between A1298C and C677T polymorphisms of the MTHFR gene with prostate cancer in Eskisehir population

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Y chromosome polymorphism in Turkish patients with reproductive problems: a genetic centre experience

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Two Cystic Fybrosis Cases with Firstly Reported Compund Heterozygous Variants

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