Tepeli, Emre

	Issue Date	Title	Author(s)
1	2019	Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder	Aydin, S.U.; Kabukçu Başay, Bürge ; Çetin, Gökhan Ozan ; Güngör Aydın, Ayşegül ; Tepeli, E.
2	2018	Association of synaptosomal-associated protein 25 (SNAP-25) gene polymorphism with temperament and character traits in women with fibromyalgia syndrome	Dogru, A.; Balkarli, A.; Tepeli, Emre ; Aydin, E.; Cobankara, V.
3	2009	A case of schizophrenia accompanying velocardiofacial syndrome	Şengül, Cem ; Efe, Muharrem ; Tepeli, Emre ; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Herken, Hasan
4	2016	Comparison of IL-23 receptor gene polymorphisms in patients with primary sjögren syndrome, ankylosing spondylitis. and ankylosing spondylitis with sjögren’s syndrome [Article]	Temel, Şahin ; Balkarlı, Ayşe; Elmas, Levent ; Tepeli, Emre ; Çobankara, Veli
5	2014	Contribution of MLPA to routine testing to detect the prognostic chromosomal abnormalities in chronic lymphocytic leukemia	Ayaz, A.; Tepeli, Emre ; Sari, Hakan İsmail ; Cetin, O.; Eser, M.; Dogu, H.; Bağcı, Gülseren
6	2015	Could serum pentraxin 3 levels and IgM deposition in skin biopsies predict subsequent renal involvement in children with Henoch–Schönlein purpura?	Yüksel, Selçuk ; Çağlar, Murat ; Evrengül, Havva; Becerir, Tülay ; Tepeli, Emre ; Ergin, Ahmet ; Avcı Çiçek, Esin
7	2011	Determination of O-6-Methylguanine DNA Methyltransferase Promoter Methylation in Non-Small Cell Lung Cancer [Article]	Ekim, M.; Caner, Vildan ; Büyükpinarbaşili, N.; Tepeli, E. ; Elmas, L.; Bagcı, Gülseren
8	2012	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	Koç, Esin; Caner, Vildan ; Büyükpınarbaşılı, N.; Tepeli, Emre ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Bağcı, Gülseren
9	2015	Esansiyel hipertansiyonlu olgularda CHGA geni promotor bölge polimorfizmlerinin araştırılması	Eser, Metin ; Şanlıalp, Musa ; Tepeli, Emre ; Tufan, Lale Şatıroğlu ; Kaftan, Havane Asuman ; Semerci, Cavidan Nur
10	2012	Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer	Tepeli, Emre ; Caner, Vildan ; Büyükpınarbaşılı, N.; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Elmas, Levent ; Bağcı, Gülseren
11	2017	Familial mutation in caffey disease with reduced penetrance: A case report	Özdemir, Özmert Muhammet Ali ; Tancer-Elçi, Hazal ; Polat, Aziz ; Güçtürk, İnci ; Tepeli, Emre ; Zeybek, Selcan; Ayaz, Akif
12	2010	Familial translocation (2;18) ascertained through recurrent spontaneous abortions [Article]	Bağcı, Gülseren ; Tepeli, Emre ; Düzcan, Füsun ; Çetin, G. Ozan ; Alataş, Erkan
13	2003	Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss	Düzcan, F.; Wollnik, B.; Tepeli, E. ; Ardıç, Fazıl Necdet ; Uyguner, O.; Bağcı, Hüseyin.
14	2004	Femoral-facial syndrome with hemifacial microsomia and hypoglossia	Düzcan, F.; Ergin, H. ; Perçin, E.F.; Tepeli, E. ; Erkula, G.
15	2014	GADD45? methylation is more common in benign prostatic hyperplasia than in prostate cancer	Can, O.; Caner, Vildan ; Türk, Nilay Şen ; Tuncay, Ömer Levent ; Eskicorapci, S.Y. ; Tepeli, Emre ; Çetin, Ozan
16	2015	HIF1A as a major vascular endothelial growth factor regulator: Do its polymorphisms have an association with age-related macular degeneration?	Okur, Volkan ; Çetin, Ozan ; Çetin, Ebru ; Tepeli, E. ; Bulgu, Y.; Yildirim, C.
17	2022	IL-23R gene polymorphisms in rheumatoid arthritis	Soysal, Ergun ; Ulutas, Firdevs ; Tepeli, Emre ; Kaymaz, Serdar ; Cobankara, Veli
18	2019	Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss	Zeybek, S.; Tepeli, E. ; Çetin, Gökhan Ozan ; Caner, Vildan ; Şenol, Hande ; Yildirim, B.; Bağcı, Gülseren
19	2022	Interleukin-1 gene (IL-1) polymorphism in patients with Behcet's Disease, and its relationship with disease manifestations	Ozkan, Umit ; Ulutas, Firdevs ; Tepeli, Emre ; Cobankara, Veli
20	2014	Investigation of LRRK2 G2019S mutation in the patients with sporadic Parkinson's disease in Turkey	Aslan, H.; Ozkan, S. ; Tepeli, Emre ; Emre, R.; Kutlay, O.; Gurler, A.I.; Uludag, A.

Author(s)

1

2019

Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder

Aydin, S.U.; Kabukçu Başay, Bürge ; Çetin, Gökhan Ozan ; Güngör Aydın, Ayşegül ; Tepeli, E.

2

2018

Association of synaptosomal-associated protein 25 (SNAP-25) gene polymorphism with temperament and character traits in women with fibromyalgia syndrome

Dogru, A.; Balkarli, A.; Tepeli, Emre ; Aydin, E.; Cobankara, V.

3

2009

A case of schizophrenia accompanying velocardiofacial syndrome

Şengül, Cem ; Efe, Muharrem ; Tepeli, Emre ; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Herken, Hasan

4

2016

Comparison of IL-23 receptor gene polymorphisms in patients with primary sjögren syndrome, ankylosing spondylitis. and ankylosing spondylitis with sjögren’s syndrome [Article]

Temel, Şahin ; Balkarlı, Ayşe; Elmas, Levent ; Tepeli, Emre ; Çobankara, Veli

5

2014

Contribution of MLPA to routine testing to detect the prognostic chromosomal abnormalities in chronic lymphocytic leukemia

Ayaz, A.; Tepeli, Emre ; Sari, Hakan İsmail ; Cetin, O.; Eser, M.; Dogu, H.; Bağcı, Gülseren

6

2015

Could serum pentraxin 3 levels and IgM deposition in skin biopsies predict subsequent renal involvement in children with Henoch–Schönlein purpura?

Yüksel, Selçuk ; Çağlar, Murat ; Evrengül, Havva; Becerir, Tülay ; Tepeli, Emre ; Ergin, Ahmet ; Avcı Çiçek, Esin

7

2011

Determination of O-6-Methylguanine DNA Methyltransferase Promoter Methylation in Non-Small Cell Lung Cancer [Article]

Ekim, M.; Caner, Vildan ; Büyükpinarbaşili, N.; Tepeli, E. ; Elmas, L.; Bagcı, Gülseren

8

2012

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

Koç, Esin; Caner, Vildan ; Büyükpınarbaşılı, N.; Tepeli, Emre ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Bağcı, Gülseren

9

2015

Esansiyel hipertansiyonlu olgularda CHGA geni promotor bölge polimorfizmlerinin araştırılması

Eser, Metin ; Şanlıalp, Musa ; Tepeli, Emre ; Tufan, Lale Şatıroğlu ; Kaftan, Havane Asuman ; Semerci, Cavidan Nur

10

2012

Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer

Tepeli, Emre ; Caner, Vildan ; Büyükpınarbaşılı, N.; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Elmas, Levent ; Bağcı, Gülseren

11

2017

Familial mutation in caffey disease with reduced penetrance: A case report

Özdemir, Özmert Muhammet Ali ; Tancer-Elçi, Hazal ; Polat, Aziz ; Güçtürk, İnci ; Tepeli, Emre ; Zeybek, Selcan; Ayaz, Akif

12

2010

Familial translocation (2;18) ascertained through recurrent spontaneous abortions [Article]

Bağcı, Gülseren ; Tepeli, Emre ; Düzcan, Füsun ; Çetin, G. Ozan ; Alataş, Erkan

13

2003

Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss

Düzcan, F.; Wollnik, B.; Tepeli, E. ; Ardıç, Fazıl Necdet ; Uyguner, O.; Bağcı, Hüseyin.

14

2004

Femoral-facial syndrome with hemifacial microsomia and hypoglossia

Düzcan, F.; Ergin, H. ; Perçin, E.F.; Tepeli, E. ; Erkula, G.

15

2014

GADD45? methylation is more common in benign prostatic hyperplasia than in prostate cancer

Can, O.; Caner, Vildan ; Türk, Nilay Şen ; Tuncay, Ömer Levent ; Eskicorapci, S.Y. ; Tepeli, Emre ; Çetin, Ozan

16

2015

HIF1A as a major vascular endothelial growth factor regulator: Do its polymorphisms have an association with age-related macular degeneration?

Okur, Volkan ; Çetin, Ozan ; Çetin, Ebru ; Tepeli, E. ; Bulgu, Y.; Yildirim, C.

17

2022

IL-23R gene polymorphisms in rheumatoid arthritis

Soysal, Ergun ; Ulutas, Firdevs ; Tepeli, Emre ; Kaymaz, Serdar ; Cobankara, Veli

18

2019

Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss

Zeybek, S.; Tepeli, E. ; Çetin, Gökhan Ozan ; Caner, Vildan ; Şenol, Hande ; Yildirim, B.; Bağcı, Gülseren

19

2022

Interleukin-1 gene (IL-1) polymorphism in patients with Behcet's Disease, and its relationship with disease manifestations

Ozkan, Umit ; Ulutas, Firdevs ; Tepeli, Emre ; Cobankara, Veli

20

2014

Investigation of LRRK2 G2019S mutation in the patients with sporadic Parkinson's disease in Turkey

Aslan, H.; Ozkan, S. ; Tepeli, Emre ; Emre, R.; Kutlay, O.; Gurler, A.I.; Uludag, A.

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