F. Ferda Özkinay: search on Z-Library

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1

Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patients

Mehmet Okyay Kılınç, Vasiliki Ninidu Ninis, Elif Dağlı, Mübeccel Demirkol, Ferda Özkınay, Zeliha Arıkan, Özgür Çoğulu, Gülden Hüner, Fazilet Karakoç, Aslıhan Tolun

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 168 KB

english, 2002

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

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

4

The Association of minor congenital anomalies and childhood cancer

Asude Durmaz, Burak Durmaz, Bengu Kadioglu, Serap Aksoylar, Deniz Karapinar, Guldane Koturoglu, Mehmet N. Orman, Ferda Ozkinay, Ozgur Cogulu

Journal:

Pediatric Blood & Cancer

Year:

2011

Language:

english

File:

PDF, 117 KB

english, 2011

5

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

6

Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes

Parenti, Ilaria, Teresa-Rodrigo, María E., Pozojevic, Jelena, Ruiz Gil, Sara, Bader, Ingrid, Braunholz, Diana, Bramswig, Nuria C., Gervasini, Cristina, Larizza, Lidia, Pfeiffer, Lutz, Ozkinay, Ferda,

Journal:

Year:

2017

Language:

english

File:

PDF, 1.14 MB

english, 2017

7

The first report of fibular agenesis, tibial campomelia, and oligosyndactyly syndrome with hydrocephaly

Isik, Esra, Atik, Tahir, Ozkinay, Ferda

Journal:

Clinical Dysmorphology

Year:

2019

Language:

english

File:

PDF, 134 KB

english, 2019

8

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

9

Waardenburg anophthalmia syndrome: Report and review

Cogulu, �zg�r, Ozkinay, Ferda, G�und�z, Cumhur, Sapmaz, G�l, Ozkinay, Cihangir

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 156 KB

english, 2000

10

Mandibuloacral dysplasia with absent breast development

Özgür Cogulu, Cumhur Gunduz, Remide Arkun, Sukran Darcan, Bengü Kadioglu, Ferda Ozkinay, Cihangir Ozkinay

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 71 KB

english, 2003

11

Sliding type hernia and ectopic pancreatic tissue in the stomach with renal agenesis and ear abnormalities: Branchio-oto-renal syndrome or hemifacial microsomia with additional findings

Ferda Ozkinay, Ozgur Cogulu, Cihangir Ozkinay, Sema Aydogdu, Cumhur Gunduz, Sukran Tacoy

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 52 KB

english, 2003

12

A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II

Deniz Yilmaz, Özgür Çogǧulu, Ferda Ozkinay, Kaan Kavakli, Dirk Roos

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 41 KB

english, 2005

13

Unusual course of an acute lymphoblastic leukemia case with i(9q) as a sole cytogenetic abnormality

Ozgur Cogulu, Deniz Yilmaz Karapinar, Emin Karaca, Yesim Aydinok, Ferda Ozkinay

Journal:

Leukemia Research

Year:

2006

Language:

english

File:

PDF, 115 KB

english, 2006

14

Sister chromatid exchange (SCE) analysis in periodontitis

Gülnur Emingil, Gül Sapmaz, Nurgün Biçakçi, Ferda Özkinay

Journal:

Journal of Clinical Periodontology

Year:

2002

Language:

english

File:

PDF, 87 KB

english, 2002

15

Griscelli syndrome: Report of a case and review of the literature

Zafer Kurugöl, Ferda Ozkinay, Fadil Vardar, Sabire Karaçali, Necil Kutukçuler, Remziye Deveci

Journal:

Pediatrics International

Year:

2001

Language:

english

File:

PDF, 410 KB

english, 2001

16

Cerebro-costo-mandibular syndrome: A case report

FERDA ÖZKINAY, ÖZGÜR ÇOĞULU, CUMHUR GÜNDÜZ, TUFAN ÇANKAYA, CIHANGIR ÖZKINAY**

Journal:

Pediatrics International

Year:

2001

Language:

english

File:

PDF, 110 KB

english, 2001

17

Celiac disease in children with Down syndrome: Importance of follow-up and serologic screening

Ozgur Cogulu, Ferda Ozkinay, Cumhur Gunduz, Tufan Cankaya, Sema Aydogdu, Funda Ozgenc, Necil Kutukculer, Cihangir Ozkinay

Journal:

Pediatrics International

Year:

2003

Language:

english

File:

PDF, 84 KB

english, 2003

18

Evaluation of 80 children with prolonged fever

Ozgur Cogulu, Guldane Koturoglu, Zafer Kurugol, Ferda Ozkinay, Fadil Vardar, Cihangir Ozkinay

Journal:

Pediatrics International

Year:

2003

Language:

english

File:

PDF, 94 KB

english, 2003

19

Prenatal detection of a pure trisomy 10p case

Cumhur Gunduz, Ozgur Cogulu, Sermet Sagol, Osman Zekioglu, Cihangir Ozkinay, Ferda Ozkinay

Journal:

Prenatal Diagnosis

Year:

2003

Language:

english

File:

PDF, 114 KB

english, 2003

20

Multiple pterygium syndrome

F. Ferda Özkinay, Cihangir Özkinay, Haluk Akin, Sertaç Azarsiz, Cumhur Gündüz

Journal:

Indian Journal of Pediatrics

Year:

1997

Language:

english

File:

PDF, 484 KB

english, 1997

21

Progressive pseudorheumatoid arthropathy of childhood

Ozgur Cogulu, Ferda Ozkinay, Cihangir Ozkinay, Gül Sapmaz, Osman Yalman, Helda Binnur Deveci

Journal:

Indian Journal of Pediatrics

Year:

1999

Language:

english

File:

PDF, 1.17 MB

english, 1999

22

Poland anomaly and ulna shortage in two cousins

Ozgur Cogulu, Ferda Ozkinay, Osman Yalman

Journal:

Indian Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 681 KB

english, 2000

23

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

24

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

25

Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients

Haluk Akin, Huseyin Onay, Emre Turker, Ferda Ozkinay

Journal:

Journal of Assisted Reproduction and Genetics

Year:

2011

Language:

english

File:

PDF, 119 KB

english, 2011

26

Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven-Year Period

Ozgur Cogulu, Ferda Ozkinay, Haluk Akin, Huseyin Onay, Emin Karaca, Asude Alpman Durmaz, Burak Durmaz, Ayca Aykut, Erhan Pariltay, Ozgur Kirbiyik, Cumhur Gunduz, Cihangir Ozkinay

Journal:

Journal of Genetic Counseling

Year:

2011

Language:

english

File:

PDF, 128 KB

english, 2011

27

MEFVmutations in patients with familial Mediterranean fever from the Aegean region of Turkey

Haluk Akin, Huseyin Onay, Emre Turker, Ozgur Cogulu, Ferda Ozkinay

Journal:

Molecular Biology Reports

Year:

2010

Language:

english

File:

PDF, 179 KB

english, 2010

28

The genotoxic effect of radiofrequency waves on mouse brain

Emin Karaca, Burak Durmaz, Huseyin Altug, Teoman Yildiz, Candan Guducu, Melis Irgi, Mehtap Gulcihan Cinar Koksal, Ferda Ozkinay, Cumhur Gunduz, Ozgur Cogulu

Journal:

Journal of Neuro-Oncology

Year:

2012

Language:

english

File:

PDF, 358 KB

english, 2012

29

Interview with Parents of Children with Down Syndrome: Their Perceptions and Feelings

Asude Durmaz, Tufan Cankaya, Burak Durmaz, Ali Vahabi, Cumhur Gunduz, Ozgur Cogulu, Ferda Ozkinay

Journal:

Indian Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 90 KB

english, 2011

30

Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia

Kaan Kavakli, Ozgur Cogulu, Emin Karaca, Burak Durmaz, Ferda Ozkinay, Semih Aydogdu, Hayal Ozkilic, Can Balkan, Deniz Karapinar, Yılmaz Ay

Journal:

Annals of Nuclear Medicine

Year:

2012

Language:

english

File:

PDF, 219 KB

english, 2012

31

The evaluation of hTERT mRNA expression in acute leukemia children and 2

Ozgur Cogulu, Buket Kosova, Cumhur Gunduz, Emin Karaca, Serap Aksoylar, Ayse Erbay, Deniz Karapinar, Canan Vergin, Filiz Vural, Murat Tombuloglu, Nazan Cetingul, Ferda Ozkinay

Journal:

International Journal of Hematology

Year:

2008

Language:

english

File:

PDF, 217 KB

english, 2008

32

Progressive morphea of early childhood tracing Blaschko’s lines on the face: involvement of X chromosome monosomy in pathogenesis and clinical prognosis

Neslihan E. Karaca, Guzide Aksu, Emin Karaca, Funda Tuzun, Ali T. Gunes, Ferda Ozkinay, Necil Kutukculer

Journal:

International Journal of Dermatology

Year:

2011

Language:

english

File:

PDF, 200 KB

english, 2011

33

Complications of varicella in healthy children in Izmir, Turkey

Güldane Koturoglu, Zafer Kurugöl, Nuran Çetin, Murat Hizarcioglu, Fadil Vardar, Mehmet Helvaci, Zafer Çapar, Ferda Özkinay, Cihangir Özkinay

Journal:

Pediatrics International

Year:

2005

Language:

english

File:

PDF, 135 KB

english, 2005

34

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

35

Ring chromosome 20 syndrome with intractable epilepsy

Asude Alpman, Gul Serdaroglu, Ozgur Cogulu, Hasan Tekgul, Sarenur Gokben, Ferda Ozkinay

Journal:

Developmental Medicine & Child Neurology

Year:

2005

Language:

english

File:

PDF, 826 KB

english, 2005

36

Interleukin-1 receptor antagonist and tumour necrosis factor-alpha gene polymorphisms in Turkish patients with allergic contact dermatitis

Ilgen Ertam, Gulcin Itirli, Huseyin Onay, Sibel Alper, Ferda Ozkinay

Journal:

Contact Dermatitis

Year:

2009

Language:

english

File:

PDF, 455 KB

english, 2009

37

A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family

Filiz Hazan, Pia Ostergaard, Taylan Ozturk, Esin Kantekin, Fusun Atlihan, Steve Jeffery, Ferda Ozkinay

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 132 KB

english, 2012

38

Erratum to: The genotoxic effect of radiofrequency waves on mouse brain

Emin Karaca, Burak Durmaz, Huseyin Aktug, Teoman Yildiz, Candan Guducu, Melis Irgi, Mehtap Gulcihan Cinar Koksal, Ferda Ozkinay, Cumhur Gunduz, Ozgur Cogulu

Journal:

Journal of Neuro-Oncology

Year:

2012

Language:

english

File:

PDF, 94 KB

english, 2012

39

SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

Ippei Okada, Haruka Hamanoue, Koji Terada, Takaya Tohma, Andre Megarbane, Eliane Chouery, Joelle Abou-Ghoch, Nadine Jalkh, Ozgur Cogulu, Ferda Ozkinay, Kyoji Horie, Junji Takeda, Tatsuya Furuichi, Shi

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 1.94 MB

english, 2011

40

Evaluation of the relationship between caries indices and salivary secretory IgA, salivary pH, buffering capacity and flow rate in children with Down's syndrome

Dilsah Cogulu, Ertugrul Sabah, Necil Kutukculer, Ferda Ozkinay

Journal:

Archives of Oral Biology

Year:

2006

Language:

english

File:

PDF, 105 KB

english, 2006

41

Genotyping of Streptococcus mutans by using arbitrarily primed polymerase chain reaction in children with Down Syndrome

Dilsah Cogulu, Ertugrul Sabah, Atac Uzel, Ferda Ozkınay

Journal:

Archives of Oral Biology

Year:

2006

Language:

english

File:

PDF, 132 KB

english, 2006

42

AO-27. Mannose-binding lectin (MBL) codon 54 gene polymorphism in relation to risk of nosocomial invasive fungal infection in preterm neonates in the neonatal intensive care unit

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

Journal:

Early Human Development

Year:

2010

Language:

english

File:

PDF, 66 KB

english, 2010

43

New chromosome rearrangement in acute lymphoblastic leukemia

Cumhur Gündüz, Özgür Çoğulu, Nazan Çetingül, Mehmet Kantar, Tufan Çankaya, Cihangir Özkınay, Ferda Özkınay

Journal:

Cancer Genetics and Cytogenetics

Year:

2002

Language:

english

File:

PDF, 819 KB

english, 2002

44

A case of epicanthus, telecanthus, high palate, transitional vertebra associated with vesicoureteral reflux

Ozgur Cogulu, Burak Durmaz, Cihangir Ozkinay, Ferda Ozkinay

Journal:

Acta Paediatrica

Year:

2007

Language:

english

File:

PDF, 141 KB

english, 2007

45

Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47, XXY karyotype

F. Ferda Özkinay, Mete Akisü, Nilgün Kültürsay, Resmiye Oral, Nermin Tansug, Gül Sapmaz

Journal:

Clinical Genetics

Year:

1996

Language:

english

File:

PDF, 958 KB

english, 1996

46

Four siblings with achalasia, alacrimia and neurological abnormalities in a consanguineous family

Erhun Kasirga, Ferda Özkinay, Sarenur Tütüncuoğlu, Sema Aydoğdu, Zafer Çolakoğlu, Ahmet Musoğlu, Ayşe Yağci, Baha Taneli, Raşit V. Yağci

Journal:

Clinical Genetics

Year:

1996

Language:

english

File:

PDF, 302 KB

english, 1996

47

Two Genes Are Responsible for Griscelli Syndrome at the Same 15q21 Locus

Elodie Pastural, Fügen Ersoy, Nevin Yalman, Nico Wulffraat, Eugênio Grillo, Ferda Ozkinay, Ilhan Tezcan, G. Gediköglu, Noël Philippe, Alain Fischer, Geneviève de Saint Basile

Journal:

Year:

2000

Language:

english

File:

PDF, 116 KB

english, 2000

48

Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children

Guldane Koturoglu, Huseyin Onay, Rasit Midilli, Sacide Pehlivan, Erdem Eren, Gulcin Itirli, Zafer Kurugol, Fazıl Apaydın, Cihangir Ozkınay, Ferda Ozkınay

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2007

Language:

english

File:

PDF, 149 KB

english, 2007

49

A further Turkish case of Griscelli syndrome with new RAB27A mutation

Huseyin Onay, Can Balkan, Ozgur Cogulu, Yesim Aydinok, Deniz Yılmaz Karapinar, Ferda Ozkinay

Journal:

Journal of the American Academy of Dermatology

Year:

2008

Language:

english

File:

PDF, 143 KB

english, 2008

50

Might there be a link between mannose-binding lectin polymorphism and dental caries?

Sacide Pehlivan, Makbule Sipahi, Ferda Ozkinay, Mustafa Pehlivan, Guldane Koturoglu, Ali Riza Alpoz

Journal:

Molecular Immunology

Year:

2005

Language:

english

File:

PDF, 92 KB

english, 2005

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