Onay Huseyin: search on Z-Library

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1

DSM outcomes of psychotic experiences and associated risk factors: 6-year follow-up study in a community-based sample

Kırlı, Umut, Binbay, Tolga, Drukker, Marjan, Elbi, Hayriye, Kayahan, Bülent, Keskin Gökçelli, Duygu, Özkınay, Ferda, Onay, Hüseyin, Alptekin, Köksal, van Os, Jim

Journal:

Psychological Medicine

Year:

2018

Language:

english

File:

PDF, 308 KB

english, 2018

2

Is BDNF-Val66Met polymorphism associated with psychotic experiences and psychotic disorder outcome? Evidence from a 6 years prospective population-based cohort study

Kirli, Umut, Binbay, Tolga, Drukker, Marjan, Elbi, Hayriye, Kayahan, Bülent, Gökçelli, Duygu Keskin, Özkınay, Ferda, Onay, Hüseyin, Alptekin, Köksal, van Os, Jim

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2018

Language:

english

File:

PDF, 566 KB

english, 2018

3

Genetic factors associated with the predisposition to late onset Alzheimer's disease

Durmaz, Asude, Kumral, Emre, Durmaz, Burak, Onay, Huseyin, Aslan, Gulcin Itirli, Ozkinay, Ferda, Pehlivan, Sacide, Orman, Mehmet, Cogulu, Ozgur

Journal:

Year:

2019

Language:

english

File:

PDF, 592 KB

english, 2019

4

Mannose binding lectin, innate immunity, early neonatal outcome

Nilgun Kultursay⁎, Ozge Altun Koroglu, Ferda Ozkinay, Onay Huseyin, Mehmet Yalaz, Guzide Aksu, Mete Akisu

Journal:

Early Human Development

Year:

2008

Language:

english

File:

PDF, 60 KB

english, 2008

5

Can mycoplasma-mediated oncogenesis be responsible for formation of conventional renal cell carcinoma?

Mustafa Pehlivan, Sacide Pehlivan, Huseyin Onay, Meral Koyuncuoglu, Ziya Kirkali

Journal:

Year:

2005

Language:

english

File:

PDF, 107 KB

english, 2005

6

Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations

Aykut, Ayça, Karaca, Emin, Onay, Hüseyin, Gökşen, Damla, Çetinkalp, Şevki, Eren, Erdal, Ersoy, Betül, Çakır, Esra Papatya, Büyükinan, Muammer, Kara, Cengiz, Anık, Ahmet, Kırel, Birgül, Özen, Samim, At

Journal:

Year:

2017

Language:

english

File:

PDF, 681 KB

english, 2017

7

Modelling and optimization of the pyrolysis of low-rank lignite by central composite design (CCD) method

Onay, Özlem, Koca, Hüseyin

Journal:

International Journal of Coal Preparation and Utilization

Year:

2019

Language:

english

File:

PDF, 1.73 MB

english, 2019

8

Vitamin D receptor gene polymorphism in children with urinary tract infection

Sule Aslan, Ipek Akil, Gulcin Aslan, Huseyin Onay, Beyhan Cengiz Ozyurt, Ferda Ozkinay

Journal:

Pediatric Nephrology

Year:

2012

Language:

english

File:

PDF, 106 KB

english, 2012

9

Mannose-Binding Lectin Gene Polymorphism and Early Neonatal Outcome in Preterm Infants

Koroglu, Ozge Altun, Onay, Huseyin, Erdemir, Gulin, Yalaz, Mehmet, Cakmak, Bilin, Akisu, Mete, Ozkinay, Ferda, Kultursay, Nilgun

Journal:

Year:

2010

Language:

english

File:

PDF, 264 KB

english, 2010

10

Hereditary thrombophilia (factor V R2-mutation) as a contributing factor in premature myocardial infarction associated with pregnancy

Kayıkcioglu, Meral, Yavuzgil, Oguz, Eroglu, Zuhal, Onay, Huseyin, Ergenoglu, Mete, Can, Levent

Journal:

Anadolu Kardiyoloji Dergisi/The Anatolian Journal of Cardiology

Year:

2014

Language:

english

File:

PDF, 191 KB

english, 2014

11

The effect of interleukin-10 gene promoter polymorphisms on early-onset coronary artery disease

Karaca, Emin, Kayikcioglu, Meral, Onay, Huseyin, Gunduz, Cumhur, Ozkinay, Ferda

Journal:

Anadolu Kardiyoloji Dergisi/The Anatolian Journal of Cardiology

Year:

2011

File:

PDF, 85 KB

2011

12

MicroRNA expression profiling in children with different asthma phenotypes

Midyat, Levent, Gulen, Figen, Karaca, Emin, Ozkinay, Ferda, Tanac, Remziye, Demir, Esen, Cogulu, Ozgur, Aslan, Asli, Ozkinay, Cihangir, Onay, Huseyin, Atasever, Mesude

Journal:

Pediatric Pulmonology

Year:

2016

File:

PDF, 288 KB

2016

13

Clinical and Genetic Features of L1 Syndrome Patients: Definition of Two Novel Mutations

Isik, Esra, Onay, Huseyin, Atik, Tahir, Akgun, Bilcag, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

Clinical Neurology and Neurosurgery

Year:

2018

Language:

english

File:

PDF, 340 KB

english, 2018

14

Management of a Patient With Congenital Biallelic CSF3R Mutation With GM-CSF

Yilmaz Karapinar, Deniz, Özdemir, Hamiyet Hekimci, Akinci, Burcu, Yaşar, Akkiz Şahin, Siviş, Zuhal Önder, Onay, Hüseyin, Özkinay, Ferda

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2018

File:

PDF, 119 KB

2018

15

Bio-fuel production from olive oil by transesterification reactions

Onay, Melih, Yücel, Meral, Öktem, Hüseyin Avni

Journal:

New Biotechnology

Year:

2012

Language:

english

File:

PDF, 73 KB

english, 2012

16

Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndrome

Cosar, Hese, Kahramaner, Zelal, Erdemir, Aydin, Turkoglu, Ebru, Kanik, Ali, Sutcuoglu, Sumer, Onay, Hüseyin, Alpman, Asude, Ozkinay, Ferda, Ozer, Esra Arun

Journal:

Clinical Dysmorphology

Year:

2011

Language:

english

File:

PDF, 110 KB

english, 2011

17

Spectrum of clinical manifestations in two young Turkish patients with congenital generalized lipodystrophy type 4

Akinci, Gulcin, Topaloglu, Haluk, Akinci, Baris, Onay, Huseyin, Karadeniz, Cem, Ergul, Yakup, Demir, Tevfik, Ozcan, Emin Evren, Altay, Canan, Atik, Tahir, Garg, Abhimanyu

Journal:

European Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 2.25 MB

english, 2016

18

Early-onset severe obesity due to complete deletion of the leptin gene in a boy

Ozsu, Elif, Ceylaner, Serdar, Onay, Huseyin

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2017

Language:

english

File:

PDF, 1.02 MB

english, 2017

19

Single center experience of biotinidase deficiency: 259 patients and six novel mutations

Canda, Ebru, Yazici, Havva, Er, Esra, Kose, Melis, Basol, Gunes, Onay, Huseyin, Ucar, Sema Kalkan, Habif, Sara, Ozkinay, Ferda, Coker, Mahmut

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2018

Language:

english

File:

PDF, 191 KB

english, 2018

20

Does Mycoplasma sp. play role in small cell lung cancer?

Pehlivan, Mustafa, Itirli, Gulcin, Onay, Huseyin, Bulut, Haydar, Koyuncuoglu, Meral, Pehlivan, Sacide

Journal:

Year:

2004

Language:

english

File:

PDF, 77 KB

english, 2004

21

Association of mannose binding lectin codon 54 polymorphism with predisposition to Henoch-Schönlein purpura in childhood

Durmaz, Burak, Aykut, Ayca, Hursitoglu, Gultac, Bak, Mustafa, Serdaroglu, Erkin, Onay, Huseyin, Ozkinay, Ferda

Journal:

International Journal of Rheumatic Diseases

Year:

2014

Language:

english

File:

PDF, 82 KB

english, 2014

22

Cross-reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasia

Tuhan, Hale Unver, Catli, Gonul, Anik, Ahmet, Onay, Huseyin, Dundar, Bumin, Bober, Ece, Abaci, Ayhan

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2015

Language:

english

File:

PDF, 395 KB

english, 2015

23

LOXL1 gene analysis in Turkish patients with exfoliation glaucoma

Yilmaz, Suzan Guven, Palamar, Melis, Onay, Huseyin, Ilim, Orhan, Aykut, Ayca, Ozkinay, Feristah Ferda, Yagci, Ayse

Journal:

International Ophthalmology

Year:

2016

Language:

english

File:

PDF, 376 KB

english, 2016

24

A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N)

Kutbay, Nilufer Ozdemir, Yurekli, Banu Sarer, Onay, Huseyin, Altay, Canan Tuncer, Atik, Tahir, Hekimsoy, Zeliha, Saygili, Fusun, Akinci, Baris

Journal:

European Journal of Internal Medicine

Year:

2016

Language:

english

File:

PDF, 878 KB

english, 2016

25

Associations of interleukin (IL)-1β, IL-1 receptor antagonist, and IL-10 with dental caries

Cogulu, Dilsah, Onay, Huseyin, Ozdemir, Yasemin, I. Aslan, Gulcin, Ozkinay, Ferda, Kutukculer, Necil, Eronat, Cemal

Journal:

Journal of Oral Science

Year:

2015

Language:

english

File:

PDF, 424 KB

english, 2015

26

Congenital Neutropenia Patient With Hypomorphic Biallelic CSF3R Mutation Responding to GCSF

Yilmaz Karapinar, Deniz, Akinci, Burcu, Şahin Yaşar, Akkiz, Hekimci Özdemir, Hamiyet, Önder Siviş, Zuhal, Onay, Hüseyin, Özkinay, Ferda

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2018

Language:

english

File:

PDF, 120 KB

english, 2018

27

Poster #T7 FAMILIAL LIABILITY THE BDNF-VAL66MET POLYMORPHISM AND PSYCHOTIC-LIKE EXPERIENCES

Alptekin, Koksal, Binbay, Tolga, Elbi, Hayriye, Zağli, Nesli, Onay, Huseyin, Ozkinay, Ferda, van Os, Jim

Journal:

Schizophrenia Research

Year:

2014

Language:

english

File:

PDF, 92 KB

english, 2014

28

Association of vitamin D receptor gene polymorphisms and bronchopulmonary dysplasia

Koroglu, Ozge Altun, Onay, Huseyin, Cakmak, Bilin, Bilgin, Betul, Yalaz, Mehmet, Tunc, Seckin, Ozkinay, Ferda, Kultursay, Nilgun

Journal:

Pediatric Research

Year:

2014

Language:

english

File:

PDF, 285 KB

english, 2014

29

Mannose-binding lectin gene polymorphism and chronic hepatitis B infection in children

Erdemir, Gulin, Kilic, SaraS, Onay, Huseyin, Ozgur, Taner, Ozkan, TanjuB, Budak, Ferah

Journal:

Saudi Journal of Gastroenterology

Year:

2015

Language:

english

File:

PDF, 624 KB

english, 2015

30

A Novel Mutation of AMHR2 In Two Siblings with Persistent Müllerian Duct Syndrome

Çakır, Aydilek D., Turan, Hande, Onay, Hüseyin, Emir, Haluk, Emre, Senol, Comunoglu, Nil, Ercan, Oya, Evliyaoglu, Olcay

Journal:

Sexual Development

Year:

2018

Language:

english

File:

PDF, 251 KB

english, 2018

31

A novel CYP11B1 mutation in a Turkish patient with 11β-hydroxylase deficiency: An association with the severe hypokalemia leading to rhabdomyolysis

Yurekli, Banu Sarer, Kutbay, Nilufer Ozdemir, Onay, Huseyin, Simsir, Ilgin Yildirim, Kocabas, Gokcen Unal, Erdogan, Mehmet, Cetinkalp, Sevki, Ozgen, Gokhan, Saygili, Fusun

Journal:

Year:

2016

File:

PDF, 759 KB

2016

32

A hereditary angioedema screening in two villages, based on an index case, and identification of a novel mutation, “1033G>T”, at the SERPING1 gene

Ozkars, Mehmet, Keskın, Ozlem, Bayram, Nazan, Onay, Huseyin, Keskın, Mehmet, Bayram, Hasan, Sahın, Yavuz, Küçükosmanoğlu, Ercan, Kırık, Serkan

Journal:

Advances in Dermatology and Allergology

Year:

2019

File:

PDF, 328 KB

2019

33

Exon-3 polymorphism of CTLA-4 gene in Turkish patients with vitiligo

Itırlı, Gülçin, Pehlivan, Mustafa, Alper, Sibel, Yüksel, S. Eda, Onay, Hüseyin, Özkınay, Ferda, Pehlivan, Sacide

Journal:

Journal of Dermatological Science

Year:

2005

Language:

english

File:

PDF, 82 KB

english, 2005

34

HIGH PREVALENCE OF PSYCHOSIS CONTINUUM IN A HIGHLY URBANIZED AREA OF TURKEY: TüRKSCH STUDY

Tolga Binbay, Hayriye Elbi, Feride Aksu, Ferda Özkınay, Hüseyin Önay, Marjan Drukker, Jim van Os, Köksal Alptekin

Journal:

Schizophrenia Research

Year:

2010

Language:

english

File:

PDF, 70 KB

english, 2010

35

Multiple cutaneous hemangiomas in a patient with combined pituitary hormone deficiency

Aykut, Ayca, Ozen, Samim, Sımsek, Damla Gokşen, Onay, Huseyin, Cogulu, Ozgur, Darcan, Sukran, Ozkinay, Ferda

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2014

Language:

english

File:

PDF, 1.61 MB

english, 2014

36

A novel mutation in two families with pycnodysostosis

Ozdemir, Taha R., Atik, Tahir, Karaca, Emin, Onay, Huseyin, Ozkinay, Ferda, Cogulu, Ozgur

Journal:

Clinical Dysmorphology

Year:

2013

Language:

english

File:

PDF, 283 KB

english, 2013

37

Whole-genome gene expression analysis in urine samples of patients with prostate cancer and benign prostate hyperplasia

Özdemir, Taha Reşid, Şimşir, Adnan, Onay, Hüseyin, Cüreklibatır, İbrahim, Özkınay, Ferda, Akın, Haluk

Journal:

Urologic Oncology: Seminars and Original Investigations

Year:

2017

Language:

english

File:

PDF, 1.28 MB

english, 2017

38

Moniliform blepharosis in lipoid proteinosis with a homozygous ECM1 gene mutation

Barut Selver, Ozlem, Palamar, Melis, Onay, Huseyin, Furundaoturan, Onur, Akalın, Taner, Noyan, Mukaddes Aysin

Journal:

Ophthalmic Genetics

Year:

2018

Language:

english

File:

PDF, 959 KB

english, 2018

39

Coexistence of Gaucher Disease and severe congenital neutropenia

Köse, Melis Demir, Canda, Ebru, Kağnıcı, Mehtap, Uçar, Sema Kalkan, Onay, Hüseyin, Yıldırım, Eser Sözmen, Karapınar, Deniz, Özkınay, Ferda, Çoker, Mahmut

Journal:

Blood Cells, Molecules, and Diseases

Year:

2018

Language:

english

File:

PDF, 1.19 MB

english, 2018

40

Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view

Ozgur Cogulu, Huseyin Onay, Ayca Aykut, Neil J. Wilson, Frances J. D. Smith, Tugrul Dereli, Ferda Ozkinay

Journal:

European Journal of Pediatrics

Year:

2009

Language:

english

File:

PDF, 207 KB

english, 2009

41

Targeted multi-gene panel testing for the diagnosis of Bardet Biedl Syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes

Ece Solmaz, Asli, Onay, Huseyin, Atik, Tahir, Aykut, Ayca, Cerrah Gunes, Meltem, Ozalp Yuregir, Ozge, Bas, Veysel Nijat, Hazan, Filiz, Kirbiyik, Ozgur, Ozkinay, Ferda

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 296 KB

english, 2015

42

A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion

Durmaz, Asude Alpman, Akin, Haluk, Ekmekci, Aslihan Yilmaz, Onay, Huseyin, Durmaz, Burak, Cogulu, Ozgur, Aydinok, Yesim, Ozkinay, Ferda

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2009

Language:

english

File:

PDF, 83 KB

english, 2009

43

Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice

Rashnonejad, Afrooz, Amini Chermahini, Gholamhossein, Gündüz, Cumhur, Onay, Hüseyin, Aykut, Ayça, Durmaz, Burak, Baka, Meral, Su, Qin, Gao, Guangping, Özkınay, Ferda

Journal:

Molecular Therapy

Year:

2019

Language:

english

File:

PDF, 2.46 MB

english, 2019

44

Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele

Karaca, Emin, Kalkan, Sema, Onay, Huseyin, Aykut, Ayca, Coker, Mahmut, Ozkinay, Ferda

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2012

Language:

english

File:

PDF, 405 KB

english, 2012

45

Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice

Rashnonejad, Afrooz, Amini Chermahini, Gholamhossein, Gündüz, Cumhur, Onay, Hüseyin, Aykut, Ayça, Durmaz, Burak, Baka, Meral, Su, Qin, Gao, Guangping, Özkınay, Ferda

Journal:

Molecular Therapy

Year:

2019

File:

PDF, 2.46 MB

2019

46

Homozygous LMNA p.R582H pathogenic variant reveals increasing effect on the severity of fat loss in lipodystrophy

Soyaltin, Utku Erdem, Simsir, Ilgin Yildirim, Akinci, Baris, Altay, Canan, Adiyaman, Suleyman Cem, Lee, Kristen, Onay, Huseyin, Oral, Elif Arioglu

Journal:

Clinical Diabetes and Endocrinology

Year:

2020

File:

PDF, 2.24 MB

2020

47

Role of angiotensin-converting enzyme gene polymorphisms in children with sepsis and septic shock

Ozgur Cogulu, Huseyin Onay, Demet Uzunkaya, Cumhur Gunduz, Sacide Pehlivan, Fadil Vardar, Fusun Atlihan, Cihangir Ozkinay, Ferda Ozkinay

Journal:

Pediatrics International

Year:

2008

Language:

english

File:

PDF, 63 KB

english, 2008

48

Mannose-binding lectin codon 54 gene polymorphism in relation to risk of nosocomial invasive fungal infection in preterm neonates in the neonatal intensive care unit

Aydemir, Cumhur, Onay, Huseyin, Oguz, Serife Suna, Ozdemir, Taha Resid, Erdeve, Omer, Ozkinay, Ferda, Dilmen, Ugur

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Year:

2011

Language:

english

File:

PDF, 178 KB

english, 2011

49

Association of vitamin D receptor polymorphisms and type 1 diabetes susceptibility in children: a meta-analysis

Sahin, Ozlem Atan, Goksen, Damla, Ozpinar, Aysel, Serdar, Muhittin, Onay, Huseyin

Journal:

Endocrine Connections

Year:

2017

Language:

english

File:

PDF, 14.18 MB

english, 2017

50

Rapid Prenatal Diagnosis of Common Aneuploidies in Amniotic Fluid Using Quantitative Fluorescent Polymerase Chain Reaction

Onay, Huseyin, Ugurlu, Timur, Aykut, Ayca, Pehlivan, Sacide, Inal, Murat, Tinar, Sivekar, Ozkinay, Cihangir, Ozkinay, Ferda

Journal:

Gynecologic and Obstetric Investigation

Year:

2008

Language:

english

File:

PDF, 194 KB

english, 2008

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