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Emre Tepeli
Observed names:
E Tepeli,
E. Tepeli,
Emre TEPELİ,
TEPELİ, EMRE,
Tepeli, Emre
Institution:
Atlas Üniversitesi
Observed institutions:
Istinye University,
Medeniyet Üniversitesi Göztepe Eğitim ve Araştırma Hastanesi,
Pamukkale Üniversitesi Hastaneleri,
Atlas Üniversitesi,
Pamukkale University,
Eskişehir Osmangazi University,
Istanbul Medeniyet University
show all 7
ORCID:
0000-0003-3771-2741
Observed ORCID:
0000-0003-3771-2741
OpenAlex ID:
A5047254619
Works
76
Awards
2
Vitamin D receptor gene polymorphisms and haplotypes (Apa I, Bsm I, Fok I, Taq I) in Turkish psoriasis patients
2012
·
Ibrahim Acikbas
, Berna Sanlı
, et al.
·
Medical Science Monitor
·
25
PDF
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
Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder
2019
·
Sezai Ustun Aydin
, Burge Kabukcu Basay
, et al.
·
Journal of Psychiatric Research
·
20
Synaptosomal-associated protein 25 (Snap-25) gene Polymorphism frequency in fibromyalgia syndrome and relationship with clinical symptoms
2014
·
Ayse Balkarli
, Cem Sengül
, et al.
·
BMC Musculoskeletal Disorders
·
19
PDF
IL-23R gene polymorphisms in rheumatoid arthritis
2021
·
Ergün Soysal
, Firdevs Ulutaş
, et al.
·
Rheumatology International
·
18
The miRNA content of circulating exosomes in DLBCL patients and in vitro influence of DLBCL-derived exosomes on miRNA expression of healthy B-cells from peripheral blood
2021
·
Vildan Caner
, Gokhan Ozan Cetin
, et al.
·
Cancer Biomarkers
·
14
Could serum pentraxin 3 levels and IgM deposition in skin biopsies predict subsequent renal involvement in children with Henoch–Schönlein purpura?
2014
·
Selçuk Yüksel
, Murat Çağlar
, et al.
·
Pediatric Nephrology
·
14
MYD88 Expression and L265P Mutation in Mature B-Cell Non-Hodgkin Lymphomas
2015
·
Vildan Caner
, Nilay Sen Turk
, et al.
·
Genetic Testing and Molecular Biomarkers
·
12
Determination of O 6 -Methylguanine DNA Methyltransferase Promoter Methylation in Non-Small Cell Lung Cancer
2011
·
Mehmet Ekim
, Vildan Caner
, et al.
·
Genetic Testing and Molecular Biomarkers
·
12
Angiotensin‐converting enzyme gene insertion/deletion polymorphism frequency in normotensive children with a positive family history of essential hypertension
2009
·
Lale Camci
, Zubeyir Kilic
, et al.
·
Journal of Paediatrics and Child Health
·
11
HIF1A as a major vascular endothelial growth factor regulator: do its polymorphisms have an association with age‐related macular degeneration?
2014
·
Volkan Okur
, Ozan Cetin
, et al.
·
Clinical and Experimental Ophthalmology
·
10
The determination of relationship between “excision repair cross-complementing group 1” (ERCC1) gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non-small cell lung cancer
2011
·
Esin Koç
, Vildan Caner
, et al.
·
Molecular Biology Reports
·
10
Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer
2011
·
Emre Tepeli
, Vildan Caner
, et al.
·
Molecular Biology Reports
·
10
Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss
2019
·
S Zeybek
, E Tepeli
, et al.
·
Balkan Journal of Medical Genetics
·
8
PDF
Relationship between the SNAP-25 gene and the effects of methylphenidate on the anterior cingulate cortex of patients with adult attention deficit hyperactivity disorder: a magnetic resonance spectroscopy study.
2016
·
G A Ünal
, A N İnci Kenar
, et al.
·
PubMed
·
7
Quantitative comparison of immunohistochemical and PCR analysis of midkine expression in breast cancer types and serum midkine level
2016
·
Hülya ÇETİN SORKUN
, Metin AKBULUT
, et al.
·
TURKISH JOURNAL OF MEDICAL SCIENCES
·
7
Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome
2010
·
C. Nur Semerci
, Mine Cinbis
, et al.
·
American Journal of Medical Genetics Part A
·
6
Femoral-facial syndrome with hemifacial microsomia and hypoglossia
2003
·
F??sun D??zcan
, Hacer Ergin
, et al.
·
Clinical Dysmorphology
·
6
Neonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare association
2016
·
Özmert MA Özdemir
, Ceren Çıralı
, et al.
·
Pediatrics International
·
5
Mutational status of EZH2 and CD79B hot spots in mature B-cell non-Hodgkin's lymphomas: novel CD79B variations have been revealed.
2016
·
G O Cetin
, I C Baris
, et al.
·
PubMed
·
5
Expression and Amplification of Topoisomerase-2α in Type 1 and Type 2 Papillary Renal Cell Carcinomas and Its Correlation with HER2/neu Amplification
2011
·
Fusun Duzcan
, Suleyman Ender Duzcan
, et al.
·
Pathology & Oncology Research
·
5
The mRNA expression of cytochrome P450 isoforms in human gastric tissue.
2010
·
Pakize Canturk
, Vildan Caner
, et al.
·
PubMed
·
5
Detection of deletions and/or amplifications of genes related with lung cancer by multiplex ligation-dependent probe amplification (MLPA) technique
2009
·
Emre Tepeli
, Muhammed Hamza Muslumanoglu
, et al.
·
Cancer Biology & Therapy
·
5
PDF
Sex chromosome aneuploidy rates in the somatic cells of infertile men.
2006
·
Fusun Duzcan
, Zafer Aybek
, et al.
·
PubMed
·
5
A Case of the Perinatal Form Hypophosphatasia Caused by a Novel Large Duplication of the ALPL Gene and Report of One Year Follow-up with Enzyme Replacement Therapy
2018
·
Bülent Hacıhamdioğlu
, Gamze Özgürhan
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
4
PDF
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Works count:
76
Citation count:
292
H-index:
10
I10-index:
13
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