Akademik Bilgiler



MUHSİN ÖZGÜR ÇOĞULU
PROFESÖR
Tıp Fakültesi
Dahili Tıp Bilimleri Bölümü
Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı
İletişim Bilgileri- E-posta: ozgur.cogulu@ege.edu.tr
- Telefon: (232) 3904917
Eğitim Bilgileri- Lisans: Ege Üniversitesi Tıp Fakültesi, Türkiye, 1989
- Doktora: Dicle Üniversitesi Tıp Fakültesi, Türkiye, 1993
- Yardımcı Doçentlik: Ege Üniversitesi, Türkiye , 2000
- Doçentlik: Ege Üniversitesi, Tıp Fakültesi, Türkiye, 2003
- Profesörlük: Ege Üniversitesi, Türkiye , 2011

İdari ve Akademik Görevleri (7 adet)- Milli Pediatri Derneği İzmir Yönetim Kurulu Üyeliği, 2009-
- Ege Pediatri Bülteni Yönetim Kurulu Üyeliği, 2009-
- Perinatoloji Derneği İzmir Yönetim Kurulu Üyeliği, 2008-
- Araştırma Eğitim Laboratuvarı Komisyon Üyeliği, 2005-
- Ulusal Sitogenetik Kalite Kontrol Komisyon Üyeliği, 2001-
- EGETAM Mesul Müdürlüğü, 1997-
- Journal of Biotechnology and Biomedicine Special Issue editörlüğü,
Mesleki Faaliyetleri (2 adet)- Birmingham Heartlands Hastanesi Regional Genetics, 1994-1996
- Basel Kinderspital Genetik Bölümü, 1991-1992
Uzmanlık Alanları- Genetik (1010103)
- Çocuk Sağlığı ve Hastalıkları (1011200)
İndekslerce Taranan Dergilerdeki Yayınları (110 adet)- Erturk B, Karaca E, Aykut A, Durmaz B, Guler A, Buke B, Yeniel AO, Ergenoglu AM, Ozkinay F, Ozeren M, Kazandi M, Akercan F, Sagol S, Gunduz C, Cogulu O. Prenatal Evaluation of MicroRNA Expressions in Pregnancies with Down Syndrome. Biomed Res Int. 2016;2016:5312674.
- Solmaz AE, Durmaz B, Braekeleer MD, Cogulu O, Ozkinay F. A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS. Genet Couns. 2016;27(1):1-8.
- Midyat L, Gulen F, Karaca E, Ozkinay F, Tanac R, Demir E, Cogulu O, Aslan A, Ozkinay C, Onay H, Atasever M.MicroRNA expression profiling in children with different asthma phenotypes.Pediatr Pulmonol. 2016 Jun;51(6):582-7.
- Ozkinay F, Onay H, Karaca E, Arslan E, Erturk B, Ece Solmaz A, Tekin IM, Cogulu O, Aydinok Y, Vergin C.Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation. Hemoglobin. 2015;39(4):230-4.
- Onay H, Aykut A, Karaca E, Durmaz A, Solmaz AE, Çoğulu Ö, Aydınok Y, Vergin C, Özkınay F.Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population.Int J Hematol. 2015 Jul;102(1):1-6.
- Cogulu O, Schoumans J, Toruner G, Demkow U, Karaca E, Durmaz AA.Laboratory genetic testing in clinical practice 2014.Biomed Res Int. 2015;2015:574798.
- Durmaz AA, Karaca E, Demkow U, Toruner G, Schoumans J, Cogulu O.Evolution of genetic techniques: past, present, and beyond.Biomed Res Int. 2015;2015:461524.
- Atik T, Torun HO, Cogulu O, Ozkinay F.A new patient with LACHT syndrome (Mardini-Nyhan association). Am J Med Genet A. 2015 Feb;167A(2):400-2
- Atik T, Atik SS, Çoğulu O, Özkinay F. MEGALOCORNEA SHOULD BE INVESTIGATED IN CASES WITH HYPOTONIA AND MENTAL RETARDATION: NEUHAUSER SYNDROME--AN EASILY MISSED DIAGNOSIS. Genet Couns. 2015;26(4):443-5.
- Atik T, Karaca E, Ozkinay E, Cogulu O.TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION. Genet Couns. 2015;26(4):431-5.
- Karaca E, Harel T, Pehlivan D, Jhangiani SN, Gambin T, Coban Akdemir Z, Gonzaga-Jauregui C, Erdin S, Bayram Y, Campbell IM, Hunter JV, Atik MM, Van Esch H, Yuan B, Wiszniewski W, Isikay S, Yesil G, Yuregir OO, Tug Bozdogan S, Aslan H, Aydin H, Tos T, Aksoy A, De Vivo DC, Jain P, Geckinli BB, Sezer O, Gul D, Durmaz B, Cogulu O, Ozkinay F, Topcu V, Candan S, Cebi AH, Ikbal M, Yilmaz Gulec E, Gezdirici A, Koparir E, Ekici F, Coskun S, Cicek S, Karaer K, Koparir A, Duz MB, Kirat E, Fenercioglu E, Ulucan H, Seven M, Guran T, Elcioglu N, Yildirim MS, Aktas D, Alikaşifoğlu M, Ture M, Yakut T, Overton JD, Yuksel A, Ozen M, Muzny DM, Adams DR, Boerwinkle E, Chung WK, Gibbs RA, Lupski JR.Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease. Neuron. 2015 Nov 4;88(3):499-513.
- Sahin ON, Atik T, Coğulu O, Ozkinay F. THE SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH KLIPPEL-TRENAUNAY-WEBER SYNDROME. Genet Couns. 2015;26(2):249-51.
- Atik T, Aykut A, Karaca E, Onay H, Ozkinay F, Cogulu O.A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization. Genet Couns. 2014;25(4):433-7.
- Atik T, Cogulu O, Ozkinay F.Results of fifteen-year follow-up from a single center: findings and risks for tumor development in isolated hemihyperplasia cases. Genet Couns. 2014;25(4):417-21.
- Atik T, Cogulu O, Ozkinay F.Results of fifteen-year follow-up from a single center: findings and risks for tumor development in isolated hemihyperplasia cases. Genet Couns. 2014;25(4):417-21.
- Atik T, Dervisoglu H, Onay H, Ozkinay F, Cogulu O.A new mutation in the TBX5 gene in Holt-Oram syndrome: two cases in the same family and prenatal diagnosis.J Trop Pediatr. 2014 Jun;60(3):257-9.
- 2014, Aykut A, Onay H, Sagol S, Gunduz C, Ozkinay F, Cogulu O. Determination of fetal rhesus d status by maternal plasma DNA analysis.Balkan J Med Genet. 2013 Dec;16(2):33-8.
- Durmaz A, Atik T, Onay H, Canda EE, Uçar SK, Bademkıran F, Coker M, Coğulu Ö, Özkınay F.Molecular analysis in X-linked adrenoleukodystrophy patients: identification of a novel mutation.Metab Brain Dis. 2014 Sep;29(3):809-12.
- Duyu M, Durmaz B, Gunduz C, Vergin C, Yilmaz Karapinar D, Aksoylar S, Kavakli K, Cetingul N, Irken G, Yaman Y, Ozkinay F, Cogulu O.Prospective evaluation of whole genome microRNA expression profiling in childhood acute lymphoblastic leukemia.Biomed Res Int. 2014;2014:967585.
- Pariltay E, Durmaz A, Durmaz B, Aykut A, Onay H, Ak H, Aydin HH, Ozkinay F, Cogulu O. Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies.Genet Couns. 2014;25(2):221-9.
- Özbaran B, Özen S, Gökşen D, Korkmaz Ö, Onay H, Özkınay F, Çoğulu Ö, Erermiş S, Köse S, Avanoğlu A, Ulman İ, Darcan Ş.Psychiatric approaches for disorders of sex development: experience of a multidisciplinary team. J Clin Res Pediatr Endocrinol. 2013;5(4):229-35.
- Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation. Atik T, Durmaz B, Yorganci OU, Cogulu O, Kioutsouk M, Ozkinay F. Genet Couns. 2013;24(2):179-84.
- Durmaz B, Karaca E, Durmaz A, Atik T, Akin H, Cogulu O, Ozkinay F.Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experience.Genet Couns. 2013;24(2):167-77.
- Aykut A, Ozen S, Sımsek DG, Onay H, Cogulu O, Darcan S, Ozkinay F.Multiple cutaneous hemangiomas in a patient with combined pituitary hormone deficiency.J Pediatr Endocrinol Metab. 2013 Sep 11:1-4.
- Schreml J, Durmaz B, Cogulu O, Keupp K, Beleggia F, Pohl E, Milz E, Coker M, Ucar SK, Nürnberg G, Nürnberg P, Kuhn J, Ozkinay F.The missing "link": an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation.Hum Genet. 2013 Aug 27. [
- Cogulu O, Alanay Y, Toruner GA.Laboratory genetic testing in clinical practice.Biomed Res Int. 2013;2013:532897.
- Zeytinoglu M, Aykut A, Hazan F, Torrente I, Akay MC, Karapinar DY, Vergin C, Cogulu O, Ozkinay F.A novel mutation, IVS13+5G>A, in Ellis-van Creveld syndrome associated with haemophagocytic lymphohistiocytosis.Clin Dysmorphol. 2013 Aug 6.
- Wieczorek D, Bögershausen N, Beleggia F, Steiner-Haldenstätt S, Pohl E, Li Y, Milz E, Martin M, Thiele H, Altmüller J, Alanay Y, Kayserili H, Klein-Hitpass L, Böhringer S, Wollstein A, Albrecht B, Boduroglu K, Caliebe A, Chrzanowska K, Cogulu O, Cristofoli F, Czeschik JC, Devriendt K, Dotti MT, Elcioglu N, Gener B, Goecke TO, Krajewska-Walasek M, Guillén-Navarro E, Hayek J, Houge G, Kilic E, Simsek-Kiper PO, López-González V, Kuechler A, Lyonnet S, Mari F, Marozza A, Mathieu Dramard M, Mikat B, Morin G, Morice-Picard F, Ozkynay F, Rauch A, Renieri A, Tinschert S, Utine GE, Vilain C, Vivarelli R, Zweier C, Nürnberg P, Rahmann S, Vermeesch J, Lüdecke HJ, Zeschnigk M, Wollnik B.A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling.Hum Mol Genet. 2013 Aug 14.
- Dodurga Y, Avcı CB, Yılmaz S, Nazlı O, Coğulu O, Cankaya T, Gündüz C.UroVysion fluorescence in situ hybridization (UroVysion FISH) assay for detection of bladder cancer in voided urine of Turkish patients: a preliminary study.Contemp Oncol (Pozn). 2013;17(2):156-60.
- Ozdemir TR, Atik T, Karaca E, Onay H, Ozkinay F, Cogulu O.A novel mutation in two families with pycnodysostosis.Clin Dysmorphol. 2013 Jul;22(3):102-5.
- Aykut A, Karaca E, Onay H, Ucar SK, Coker M, Cogulu O, Ozkinay F.Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann-Pick disease patients: mutation profile and description of a novel mutation.Gene. 2013 Sep 10;526(2):484-6.
- Cogulu O, Pariltay E, Koroglu OA, Aykut A, Ozyurek R, Levent E, Kultursay N, Ozkinay F.Genome wide analysis in a discordant monozygotic twin with caudal appendage and multiple congenital anomalies.Genet Couns. 2013;24(1):85-91.
- Cogulu O, Pariltay E, Durmaz AA, Aykut A, Gunduz C, Ozbaran B, Aydin HH, Erermis S, Aydin C, Ozkinay F. Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis. J Neuropsychiatry Clin Neurosci. 2012 Dec 1;24(1):E13-4.
- Cogulu O, Durmaz B, Wollnik B, Durmaz A, Darcan S, Ozkinay F.A new clinical presentation associated with pontine clefting, hyperpigmentation and short stature in addition to craniofacial, cardiac and developmental anomalies.Genet Couns. 2012;23(2):281-7.
- Kavakli K, Cogulu O, Karaca E, Durmaz B, Ozkinay F, Aydogdu S, Ozkilic H, Balkan C, Karapinar D, Ay Y. Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia. Ann Nucl Med. 2012 Jan;26(1):41-6. doi: 10.1007/s12149-011-0540-9.
- Ataman E, Cogulu O, Durmaz A, Karaca E, Durmaz B, Akin H, Ozkinay F.The Rate of Sex Chromosome Aneuploidies in Prenatal Diagnosis and Subsequent Decisions in Western Turkey. Genet Test Mol Biomarkers. 2012 Feb;16(2):150-3. Epub 2011 Oct 6.
- Aykut A, Cogulu O, Ozkinay F.Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney.Genet Couns. 2012;23(1):77-80.
- Chabchoub E, Cogulu O, Durmaz B, Vermeesch JR, Ozkinay F, Fryns JP.Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29.Dermatology. 2011;223(4):306-10. Epub 2012 Feb 7. Review.
- 2012, Tumgor G, Cogulu O, Onay H, Ekmekci AY, Aydogdu S, Durmaz B, Kilic M, Ozkinay F.Unusual presentation of biliary atresia splenic malformation syndrome with autosomal dominant hypospadias.Genet Couns. 2011;22(4):347-51.
- 2012, Durmaz B, Cogulu O, Dizdarer C, Stobbe H, Pfaeffle R, Ozkinay F.A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies.J Pediatr Endocrinol Metab. 2011;24(9-10):779-82.
- Okada I, Hamanoue H, Terada K, Tohma T, Megarbane A, Chouery E, Abou-Ghoch J, Jalkh N, Cogulu O, Ozkinay F, Horie K, SMOC1 is essential for ocular and limb development in humans and mice. Am J Hum Genet. 2011 Jan 7:88(1):30-41.
- Cogulu O, Ozkinay F, Akin H, Onay H, Karaca E, Durmaz AA, Durmaz B, Aykut A, Pariltay E, Kirbiyik O, Gunduz C, Ozkinay C. Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven-Year Period. Genet Couns. 2011 Jan 8.
- Durmaz A, Durmaz B, Kadioglu B, Aksoylar S, Karapinar D, Koturoglu G, Orman MN, Ozkinay F, Cogulu O. The Association of minor congenital anomalies and childhood cancer. Pediatr Blood Cancer. 2011 Feb 25.
- 2011, Karaca E, Durmaz B, Altug H, Yildiz T, Guducu C, Irgi M, Koksal MG, Ozkinay F, Gunduz C, Cogulu O.The genotoxic effect of radiofrequency waves on mouse brain.J Neurooncol. 2012 Jan;106(1):53-8.
- Durmaz A, Cankaya T, Durmaz B, Vahabi A, Gunduz C, Cogulu O, Ozkinay F.Interview with parents of children with Down syndrome: their perceptions and feelings.Indian J Pediatr. 2011 Jun;78(6):698-702.
- Durmaz B, Cogulu O, Dizdarer C, Stobbe H, Pfaeffle R, Ozkinay F.A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies. J Pediatr Endocrinol Metab. 2011;24(9-10):779-82.
- Avci CB, Susluer SY, Dodurga Y, Akalin T, Cogulu O, Dalbasti T, Oktar N, Gunduz C. The Emphasis of Tumor Suppressor Genes and Oncogenes in Diagnosis and Prognosis of Anaplastic Brain Tumors. Journal of Neurological Sciences [Turkish] 28:(4)# 29; 000-000, 2011
- Akin H, Onay H, Turker E, Cogulu O, Ozkinay F. MEFV mutations in patients with familial Mediterranean fever from the Aegean region of Turkey. Mol Biol Rep. 2010 Jan:37(1):93-8.
- Kavakli K, Cogulu O, Aydogdu S, Ozkiliç H, Durmaz B, Kirbiyik O, Ozkinay F, Balkan C, Karapinar D, Ay Y. Long-term evaluation of chromosomal breakages after radioisotope synovectomy for treatment of target joints in patients with haemophilia. Haemophilia. 2010 May:16(3):474-8.
- Durmaz B, Durmaz A, Karaca E, Saydam G, Cogulu O, Ozkinay F. A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow Turk J Hematol. Year: 2010 Volume: 27 Issue: 4 299-302
- Akgul M, Ozkinay F, Ercal D, Cogulu O, Dogan O, Altay B, Tavmergen E, Gunduz C, Ozkinay C. Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review.J Assist Reprod Genet. 2009 Jan 30.
- Durmaz B, Wollnik B, Cogulu O, Li Y, Tekgul H, Hazan F, Ozkinay F. Pontocerebellar hypoplasia type III (CLAM): Extended phenotype and novel molecular findings. J Neurol. 2009 Mar 14.
- Durmaz B, Alpman A, Pariltay E, Akgul M, Ataman E, Kirbiyik O, Cogulu O, Ozkinay F.The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey. Genet Test Mol Biomarkers. 2009 Apr:13(2):163-6.
- Cogulu O, Durmaz B, Pehlivan S, Alpman A, Ozkinay F.Evaluation of the SMN and NAIP Genes in a Family: Homozygous Deletion of the SMN2 Gene in the Fetus and Outcome of the Pregnancy. Genet Test Mol Biomarkers. 2009 Apr 27.
- Kirbiyik O, Durmaz B, Cogulu O, Akin H, Avci CB, Gunduz C, Ercal D, Ozkinay F. Intracardiac echogenic focus and cytogenetic abnormalities.Genet Couns. 2009:20(1):73-5.
- Alpman A, Cogulu O, Akgul M, Arikan EA, Durmaz B, Karaca E, Sağol S, Ozkinay C, Ozkinay F. Prenatally diagnosed Turner syndrome and cystic hygroma: incidence and reasons for referrals Fetal Diagn Ther. 2009:25(1):58-61.
- Durmaz AA, Akin H, Ekmekci AY, Onay H, Durmaz B, Cogulu O, Aydinok Y, Ozkinay F. A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletion. J Pediatr Hematol Oncol. 2009 Aug:31(8):592-4.
- Onay H, Balkan C, Cogulu O, Aydinok Y, Karapinar DY, Ozkinay F.A further Turkish case of Griscelli syndrome with new RAB27A mutation. J Am Acad Dermatol. 2008 May:58(5 Suppl 1):S115-6.
- Durmaz B, Karaca E, Vural F, Cogulu O, Alpman A, Tombuloglu M, Ozkinay F.Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome. Acta Oncol. 2008 Apr 30:1-3.
- Aykut A, Cogulu O, Ekmekci AY, Ozkinay F.An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia Genet Couns. 2008:19(2):237-40
- Tarhan F, Vural F, Kosova B, Aksu K, Cogulu O, Keser G, Gündüz C, Tombuloglu M, Oder G, Karaca E, Doganavsargil E.Telomerase activity in connective tissue diseases: elevated in rheumatoid arthritis, but markedly decreased in systemic sclerosis. Rheumatol Int. 2008 Apr:28(6):579-83.
- Cogulu O, Kosova B, Gunduz C, Karaca E, Aksoylar S, Erbay A, Karapinar D, Vergin C, Vural F, Tombuloglu M, Cetingul N, Ozkinay F.The evaluation of hTERT mRNA expression in acute leukemia children and 2 years follow-up of 40 cases. Int J Hematol. 2008 Apr:87(3):276-83.
- 2008, Cogulu O, Biray C, Gunduz C, Karaca E, Aksoylar S, Sorkun K, Salih B, Ozkinay F.Effects of Manisa propolis on telomerase activity in leukemia cells obtained from the bone marrow of leukemia patients.
- Cogulu O, Onay H, Uzunkaya D, Gunduz C, Pehlivan S, Vardar F, Atlihan F, Ozkinay C, Ozkinay FRole of angiotensin-converting enzyme gene polymorphisms in children with sepsis and septic shock. Pediatr Inter, 50: 477-480, 2008
- Cogulu O, Onay H, Aykut A, Wilson NJ, Smith FJ, Dereli T, Ozkinay F. Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view. Eur J Pediatr. 2008 Dec 24
- Alpman A, Cogulu O, Akgul M, Ataman Arıkan E, Durmaz B, Karaca E, Sağol S, Ozkinay C, Ozkinay F. Prenatally Diagnosed Turner Syndrome and Cystic Hygroma: Incidence and Reasons for Referrals. Fetal Diagn Ther. 2008 Mar 12:25(1):58-61.
- Cogulu O, Durmaz B, Ozkinay C, Ozkinay F.A case of epicanthus, telecanthus, high palate, transitional vertebra associated with vesicoureteral reflux.Acta Paediatr. 2007 Jan:96(1):147-8.
- Cogulu O, Aykut A, Kutukculer N, Ozkinay C, Ozkinay F.Two cases of macrocephaly and immune deficiency.Clin Dysmorphol. 2007 Apr:16(2):81-4.
- Bora E, Cankaya T, Alpman A, Karaca E, Cogulu O, Tekgul H, Ozkinay F.A new case of Martsolf syndrome.Genet Couns. 2007:18(1):71-5.
- Cogulu O, Gunduz C, Karaca E, Onay H, Superti-Furga A, Ozkinay F.Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girl.Genet Couns. 2007:18(1):77-83.
- Onder A, Cogulu O, Ekmekci A, Pariltay E, Kirbiyik O, Ozkinay F.Seckel syndrome with Morgagni hernia.Clin Dysmorphol. 2007 Jul:16(3):209-10.
- Zatterale A, Kelly FJ, Degan P, d'Ischia M, Pallardo FV, Calzone R, Dunster C, Lloret A, Manini P, Cogulu O, Kavakli K, Pagano G. Oxidative stress biomarkers in four Bloom syndrome (BS) patients and in their parents suggest in vivo redox abnormalities in BS phenotype.Clin Biochem. 2007 Oct:40(15):1100-1103
- Cogulu O, Alpman A, Durmaz B, Özkınay F. The molecular mechanism of meisosis and mitosis: Review Turkiye Klinikleri J Med Sci 2007, 27:725-737
- Cogulu O, Karapinar DY, Karaca E, Aydinok Y, Ozkinay F.Unusual course of an acute lymphoblastic leukemia case with i(9q) as a sole cytogenetic abnormality.Leuk Res. 2006 Nov:30(11):1461-3.
- Ozkinay F, Kanit H, Onay H, Cogulu O, Gunduz C, Ercal D, Ozkinay C.Prenatal diagnosis of de novo unbalanced translocation 8p:21q using subtelomeric probes.Genet Couns. 2006:17(3):315-20.
- Cogulu O, Gunduz C, Karaca E, Onay H, Ozkinay C, Ozkinay F.Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.Genet Couns. 2006:17(3):321-31.
- Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK. A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia.J Clin Endocrinol Metab. 2005 Sep:90(9):5259-64. Epub 2005 Jul 5. Review
- Cogulu O, Onay H, Ozgenc F, Karaca E, Gunduz C, Tzetis M, Cankaya T, Kanavakis E, Ozkinay F. Trigonocephaly and Wilson's disease in two siblings. Clin Dysmorphol. 2005 Jul:14(3):161-4.
- Alpman A, Serdaroglu G, Cogulu O, Tekgul H, Gokben S, Ozkinay F. Ring chromosome 20 syndrome with intractable epilepsy. Dev Med Child Neurol. 2005 May:47(5):343-6.
- Egemen A, Ulger Z, Ozkinay F, Gulen F, Cogulu O. A de novo t (X:8)(p11.2:q24.3) demonstrating Cornelia de Lange syndrome phenotype. Genet Couns. 2005:16(1):27-30.
- Gunduz C, Biray C, Kosova B, Yilmaz B, Eroglu Z, Sahin F, Omay SB, Cogulu O. Evaluation of Manisa propolis effect on leukemia cell line by telomerase activity. Leuk Res. 2005 Nov:29(11):1343-6.
- 2005, Ozkinay F, Onay H, Giray O, Cogulu O, Ercal D, Sagol S. A rare chromosomal rearrangement [inv (2)(p11.q13)] was found in a 37-year-old normal male who had an offspring having 46,X,+mar/45,X0. Genet Couns. 200: 16: 317-318.
- 2005, Yilmaz D, Cogulu O, Ozkinay F, Kavakli K, Roos D., A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II. Am J Med Genet A. 2004 Dec 22:133A(1):101-102.
- Cogulu O, Kosova B, Karaca E, Gunduz C, Ozkinay F, Aksoylar S, Gulen H, Kantar M, Oniz H, Karapinar D, Cetingul N, Erbay A, Vergin C, Ozkinay C., Evaluation of telomerase mRNA (hTERT) in childhood acute leukemia. Leuk Lymphoma. 2004 Dec:45(12):2477-80
- Yenigun A, Ozkinay F, Cogulu O, Coker C, Cetiner N, Ozden G, Aksu O, Ozkinay C., Hair zinc level in Down syndrome., Downs Syndr Res Pract. 2004 Jul:9(2):53-7.
- Cogulu O, Munanoglu D, Karaca E, Onay H, Ozkinay F., Cleidocranial dysplasia with new additional findings., Genet Couns. 2004:15(2):229-31.
- Gündüz, C., Ö. Çoğulu, S. Sağol, O. Zekioğlu, C. Özkınay ve F. Özkınay, ‘Prenatal Detection of a Pure Trisomy 10p case’, Prenat Diagn, 23, 352-358, (2003).
- Çoğulu, Ö., C. Gündüz, R. Arkun, Ş. Darcan, B. Kadıoğlu, F. Özkınay ve C. Özkınay, ‘Mandibuloacral Dysplasia With Absent Breast Development’, Am J Med Genet, 119A: 391-392, (2003).
- Çoğulu, Ö., F. Özkınay, C. Gündüz, T. Çankaya ve C. Özkınay,’ Paracentric Inversion in the Short Arm of Chromosome 1. Report of a Family and Review of the Literature’, Genet Couns, 14: 419-423, (2003).
- Pehlivan, S., F. Özkınay, Ö. Okutman, Ö. Çoğulu, A. Özcan ve T. Çankaya,’ Achondroplasia in Turkey is Defined by Recurrent G380R Mutation of the PGFR3 Gene’, Turk J Pediatr, 45: 99-101, (2003).
- Çoğulu, Ö., F. Özkınay, C. Gündüz, T. Çankaya, S. Aydoğdu, F. Özgenç, N. Kütükçüler ve C. Özkınay, ‘Celiac Disease in Children with Down Syndrome: The Importance of Follow up and Serologic Screening’, Pediatr Int, 45, 395-399, (2003).
- Çoğulu, Ö., G. Koturoğlu, F. Özkınay, Z. Kurugöl, F. Vardar ve C. Özkınay,’ Evaluation of 80 Children With Prolonged Fever’, Pediatr Int, 45: 564-569, (2003).
- Gündüz, C., Ö. Çoğulu, T. Çankaya, E. Bora, E. Karaca, A. Akman, S. Sağol, H. Onay, F. Özkınay ve C. Özkınay,’Trends in Cytogenetic Prenatal Diagnosis in a Reference Hospital in İzmir/Turkey: A Comparative Study for 4 Years’, Genet Couns, 15: 53-59, (2003).
- Özkınay, F., Ö. Çoğulu, C. Özkınay, S. Aydoğdu, C. Gündüz ve Ş. Taçoy, ‘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’, Am J Med Genet, 120A: 562-563, (2003).
- Alpman, A., G. Sapmaz, E. Karaca, T. Çankaya, E. Bora, Ö. Çoğulu, C. Gündüz, W.J. Kleijer ve F. Özkınay, ‘Detection of Trisomy 21 in a Fetus During the Investigation for Tay Sach Disease’, Genet Couns, 15: 99-100, (2003).
- Çoğulu, Ö., C. Tırpan, F. Özkınay, C. Gündüz ve C. Özkınay, ‘The Second Case With 47,XY,+8 [38] / 45,X0 [12] Karyotype,’ Turk J Pediatr, 44, 86-89, (2002).
- Gündüz, G., Ö. Çoğulu, N. Çetingül, M. Kantar, T. Çankaya, C. Özkınay ve F. Özkınay, ‘ New Chromosome Rearrangement in Acute Lymphoblastic Leukemia’, Cancer Genet Cytogenet, 137, 150-152, (2002).
- 2002, Özkınay, F., Ö. Çoğulu, C. Gündüz, D. Yılmaz ve N. Kültürsay, ‘Valproic acid and Lamotrigine Treatment During Pregnancy The Risk of Chromosomal Abnormality’, Mutat Res, 534, 197-199, (2003).
- Savas, S., S. Eraslan, S. Kantarcı, B. Karaman, D. Acarsöz, T. Tükel, O. Çoğulu, F. Özkınay, S. Başaran, K. Aydınlı, M. Yüksel Apak ve B. Kırdar, ‘ Prenatal Prediction of Childhood-Onset Spinal Muscular Atrophy (SMA) in Turkish Families’, Prenat Diagn, 22, 703-709, (2002).
- Kılınç, M.O., V.N. Ninis, E. Dağlı, M. Demirkol, F. Özkınay, Z. Arıkan, Ö. Çoğulu, G. Hüner, F. Karakoç ve A. Tolun, ‘Highest heterogeneity for Cystic Fibrosis: 36 Mutations Account for 75% of All CF Chromosomes in Turkish Patients’, Am J Med Genet, 113, 250-257, (2002).
- Özkınay, F., Ö. Çoğulu, C. Gündüz, T. Çankaya ve C. Özkınay, ‘Cerebro-costo-mandibular Syndrome: A Case Report,’ Pediatr Int, 43, 522-524, (2001).
- Cogulu, O., F. Ozkinay, ve O. Yalman, ‘Poland Anomaly and Ulna Shortage in Two Cousins,’ Indian J Pediatr, 67, 23-24, (2000).
- Çoğulu, Ö., F. Ozkinay, C. Gündüz, G. Sapmaz ve C. Ozkinay, ‘Waardenburg Anophthalmia Syndrome: Report and Review,’ Am J Med Genet, 90, 173-174, (2000).
- Özkınay, F., Ö. Çoğulu, İ. Akil, C. Gündüz ve C. Özkınay, ‘Fronto-Facio-Nasal Dysplasia in Two Sisters With Additional Findings,’ Acta Pediatr, 89, 1-3, (2000).
- Koçyiğit, H., R. Arkun, F. Özkınay, Ö. Çoğulu, N. Hızlı ve A. Memiş, ‘Spondyloepiphyseal Dysplasia Tarda with Progressive Arthropathy,’ Clin Rheumatol, 19, 238-241, (2000).
- Kurugöl, Z., Ö. Çoğulu ve K. Kavaklı, ‘A Case Of Primary Chylous Ascites Cured By Breastfeeding Within 4 Months,’ Turk J Pediatrics, 42, 165-167, (2000).
- Cogulu, O., F. Ozkinay, C. Ozkinay, G. Sapmaz, O. Yalman ve H. Deveci, ‘Progressive Pseudorheumatoid Arthropathy Of Chilhood: A Case Report,’ Indian J Pediatr, 66, 455-460 (1999).
- KOÇYİĞİT, Hikmet: ARKUN, Remide: ÖZKINAY, Ferda: ÇOĞULU, Özgür: HIZLI, Nail: MEMİŞ, Asuman Progresif artropati ile seyreden spondiloepifiziyal displazi tarda: Olgu sunumu Romatoloji ve Tibbi Rehabilitasyon Dergisi, 1999,10(2):80-84
- Çetingül, N., H. Öniz, Ö. Çoğulu, F. Özkınay, K. Kavaklı, M. Kantar, Y. Aydınok, A. Polat, G. Nişli ve S. Öztop, ‘A New Chromosomal Rearrangement in Acute Myeloid Leukemia,’ Cancer Genet Cytogenet, 107, 153-154 (1998).
- Ozkinay, F., O. Çogulu, C. Gündüz, E. Levent ve C. Ozkinay, ‘A Case Of Brachman De Lange Syndrome With Cerebellar Vermis Hypoplasia,’ Clinical Dysmorphology: 7, 1-3 (1998).

İndekslerce Taranmayan Dergilerdeki Yayınları (52 adet)- Asude Durmaz, Burak Durmaz, Emin Karaca, Orkan Ergün, Özgür Çoğulu. Pediatrik Cerrahide Sık Karşılaşılan Konjenital Anomalilere Genetik Yaklaşım. Bakırköy Tıp Dergisi 2013;9:91-104.
- Atik T, Onay H, Aykut A, Cogulu O, Ozkinay F. Smith-Lemli-Opitz Sendromu: Olgu Sunumu. Erciyes Med J 2013;35(2):83-6.
- Çoğulu Ö, Durmaz A.A, Durmaz B, Atik T. Nörotransmitter ilişkili hastalıklar genetiği. Turkiye Klinikleri J Pediatr Sci 2013; 9(4), 47-59.
- Özgür Çoğulu, Genodermatozlar.Turkiye Klinikleri J Pediatr Sci 2011;7(2):62-72.
- Burak Durmaz, Asude Alpman Durmaz, Ferda Özkınay, Özgür Çoğulu. Genetik danışmanlık ve önemi. Cumhuriyet Tıp Derg 2011; 33: 259-265
- Hazan F, Aykut A, Serdaroğlu G, Gökben S, Akın H, Çoğullu Ö, Özkınay F. Angelman sendromu: bir olgu sunumu, Ege Tıp Dergisi/ Ege Journal of Medicine 48 (3) :195-198, 2009
- Çoğulu O, Onay H, Uzunkaya D, Gunduz C, Vardar F, Atlıhan F, Özkınay F. Role of thrombosis factors in the development of sepsis Ege Tıp Dergisi, 2008
- Kosova B, Eroğlu Z, Yılmaz B, Gunduz C, Özel R, Sayın E, Çoğulu Ö, Özkınay F, Özkınay C, Topçuoğlu N. F508, I507 ve F508C kistik fibroz mutasyonlarının gerçek-zamanlı multipleks PCR ile hızlı analizleri Ege Tıp Dergisi / Ege Journal of Medicine 47(2) : 103 -109, 2008
- 2008, 38. Onay H, Özkınay F, Çoğulu Ö, Kütükçüler N, Sağol S, Özkınay C. Otozomal Resesif SCID ve Prenatal Tanı: Olgu Sunumu. Gaziantep Tıp Dergisi: 14: 47-49,
- 2008, 37. Pehlivan S, Onay H, Tavmergen E, Tavmergen Göker N, Çoğulu Ö, Özkınay F. Erkek İnfertilitesinde Anjiotensin Konverting Enzim Polimorfizmleri. Gaziantep Tıp Dergisi: 14: 15-17
- Özgür Çoğulu, Burak Durmaz, Ferda Özkınay. Genetik hastalıklara temel yaklaşım Ege Pediatri Bülteni, 2006,13(1):57-66
- Özgür Çoğulu, Emin Karaca, Ferda Özkınay Mental retardasyon ve kromozomlarda subtelomerik bölge Bakırköy Tıp Dergisi, 2006,2(3):73-81
- 2006, ÇANKAYA, Tufan: BİRAY, Çığır: GÜNDÜZ, Cumhur: ÇOĞULU, Özgür: ERÇAL, Derya: ÖZKINAY, Cihangir: ÖZKINAY, Ferda Prenatal tanıda saptanan satellitli Y kromozomunun (Yqs) değerlendirilmesi Ege Tıp Dergisi, 2004,43(3):193-196
- Tufan Cankaya, Cumhur Gunduz, Özgür Çoğulu, Sermet Sağol, Ferda Özkınay. İnterfaz hücrelerinde flüoresan in-situ hibridizasyon yöntemi ile anoploidi aranması Ege Tıp Dergisi, 2006,45(3):149-154
- Çoğulu Ö, Özkınay F. The Effect Of Vitamins And Minerals On Fetus Turkiye Klinikleri J Pediatr Sci 2006, 2(11):108-115
- Beyhan Tüysüz, Özgür Çoğulu. İskelet Displazileri, Türkiye Klinikleri Pediatrik Bilimler Pediatrik Genetik Özel sayısı 2005 1(2): 93100.
- Çoğulu, Ö., F. Özkınay, C. Tırpan, C. Gündüz ve C. Özkınay, ‘Bir Olgu Nedeniyle X’e Bağlı Mental Retardasyonla Giden Marfanoid Habitus’, Ege Pediatri Bülteni, 9, 199-202 (2002).
- Çoğulu, Ö., Ş. Darcan, F. Özkınay, C. Gündüz ve C. Özkınay, ‘Melnick-Needles Sendromu: Ek Bulgularıyla Birlikte İki Ayrı Olgu’, Ege Pediatri Bülteni, 9, 89-94 (2002).
- Pehlivan, S., F. Özkınay, S. İzzetoğlu, Ö. Çoğulu, A. Kunt, T. Çankaya, E. Demirtaş ve S. Tütüncüoğlu,’Spinal Muskuler Atrofi’de Moleküler Tanı: Ege Bölgesinde Bir Referans Merkezindeki Uygulamalar’, Ege Tıp Dergisi, 41, 7-10 (2002).
- Çankaya, T., F. Özkınay, Ö. Çoğulu, C. Gündüz ve C. Özkınay, ‘Neu-laxova Sendromlu Bir Olgu Sunumu’, Ege Tıp Dergisi, 40, 67-70 (2001).
- Çoğulu, Ö., Z. Ülger, T. Çankaya, C. Gündüz ve F. Özkınay, ‘Wolf-Hirschorn Sendromu: Olgu Sunumu’, Ege Tıp Dergisi, 40, 63-65 (2001).
- Kavaklı, K., M. Kantar, F. Özkınay, Ö. Çoğulu, Y. Aydınok, N. Çetingül ve S. Kansoy, ‘Ehlers-Danlos Sendromu ve Kanama Bulgularının Sağıltımında Desmopressin Kullanımı’, Ege Pediatri Bülteni, 8, 93-94 (2001).
- Çoğulu, Ö., F. Özkınay, C. Gündüz, T. Çankaya, S. Aydoğdu, N. Kütükçüler ve C. Özkınay, ‘Down Sendromlu Olgularda Anti-gliadin ve Anti-endomisyum Antikorları: Bir Ön Çalışma’, Ege Pediatri Bülteni, 8, 147-149 (2001).
- Pehlivan, S., F. Özkınay, Ö. Okutman, Ö. Çoğulu, A. Özcan, T. Çankaya ve A. Ülgenalp,’Akondroplazide Moleküler Genetik Analizler: Bir Ön Çalışma’, Ege Pediatri Bülteni, 8, 205-208 (2001).
- Gündüz, C., F. Özkınay, Ö. Çoğulu, G. Sapmaz, T. Çankaya ve C. Özkınay, ‘A Father Born To Consanguineous Parents Had Double Translocation 21:22 (44,XY, t(21q:22q),t(21q:22q) Due To Familial Translocation In Four Generations’, Turkish Journal of Medical Sciences, 31, 275-277 (2001).
- Çoğulu, Ö., C. Gündüz, G. Sapmaz, N. Terzibaşıoğlu ve F. Özkınay, ‘Amniyotik Sıvı Hücre Kültüründe Açık ve Kapalı Sistemlerin Değerlendirilmesi’, Ege Tıp Dergisi, 39, 19-223 (2000).
- Özkınay, F., Z. Kurugöl, F. Vardar, Ö. Çoğulu ve C. Özkınay, ‘Down Sendromlu Olgularda Hepatit B Aşısı’, Turkish Journal of Infectious Disease, 14, 335-338 (2000).
- Serdaroğlu, G., M. Yiğit, F. Ünal, F. Özgenç, G. Aksu, Ö. Çoğulu, N. Kütükçüler, F. Özkınay ve S. Aydoğdu, ‘Down Sendromu ve Çölyak Hastalığı Birlikteliği’, Ege Pediatri Bülteni, 7, 89-91 (2000).
- Tırpan, T., Ş. Darcan, Ö. Çoğulu ve F. Özkınay, ‘Rieger Sendromu: Olgu sunumu’, Ege Pediatri Bülteni, 7, 37-40 (2000).
- Gündüz, C., Ö. Çoğulu, C. Özkınay, S. Tütüncüoğlu, G. Sapmaz, M. Kösem ve F. Özkınay, ‘İdiyopatik Mental Retardasyonlarda Frajil-X Sendromu Araştırılması’, Ege Tıp Dergisi, 39, 97-104 (2000).
- Çoğulu, Ö., C. Gündüz, F. Özkınay, N. Çetingül, G. Sapmaz ve C. Özkınay, ‘Ege Üniversitesi Tıp Fakültesi Genetik Laboratuvarlarında 1993-97 Yılları Arasında Kemik iİliğinde Yapılan Sitogenetik Çalışma Sonuçları’, Ege Pediatri Bülteni, 7, 129-135 (2000)
- Çoğulu, Ö., ‘Dismorfoloji’, Ege Pediatri Bülteni, 7, 217-222 (2000).
- Özkınay, F., Ö. Çoğulu, N. Bayram, C. Gündüz ve C. Özkınay, ‘ Proteus Sendromu: Olgu Sunumu’, Ege Tıp Dergisi, 39, 213-215 (2000).
- Çoğulu, Ö., F. Vardar ve C. Özkınay, ‘Sepsis’, Turkish Journal of Infectious Diseases, 13, 611-616 (1999).
- Çoğulu, Ö., ‘Kanser ve Genetik Danışma’, Klinik Bilimler ve Doktor, 5, 523-531 (1999).
- Özkınay, F., Ö. Çoğulu, C. Gündüz, H. Akın ve C. Özkınay, ‘Trizomi 9p: Olgu Sunumu’, Ege Tıp Dergisi, 1, 41-43 (1999).
- Gündüz, C., F. Özkınay, H. Kanıt, G. Sapmaz, Ö. Çoğulu, T. Çankaya ve C. Özkınay, ‘Ultrasonda Choroid Plexus Kisti Saptanan Gebelerin sitogenetik Analiz Değerlendirilmesi’, Ege Tıp Dergisi, 38, 65-68 (1999).
- Söker, M., Ö. Çoğulu, K. Topal, C. Devecioğlu ve F. Gürkan, ‘Nörofibromatozus Tanılı Bir Olguda Kronik Myelositer Lösemi’, Türkiye Tıp Dergisi, 6, 313-317 (1999).
- KOÇYİĞİT, Hikmet: ARKUN, Remide: ÖZKINAY, Ferda: ÇOĞULU, Özgür: HIZLI, Nail: MEMİŞ, Asuman Progresif artropati ile seyreden spondiloepifiziyal displazi tarda: Olgu sunumu Romatoloji ve Tibbi Rehabilitasyon Dergisi, 1999,10(2):80-84
- Çoğulu, Ö., M.A. Taş, R. Bozoklar ve F. Özkınay, ‘Evaluation of 437 Amniotic Fluid Samples in Prenatal Diagnosis’, Journal of Neonatalogy, 5, 25-31 (1998).
- Özkınay, F., Ö. Çoğulu, C. Gündüz ve C. Özkınay, ‘Popliteal Pterygium Sendromu: Olgu Sunumu’, Klinik Bilimler & Doktor, 4, 601-603 (1998).
- Çoğulu, Ö., M.A. Taş, R. Bozoklar ve F. Özkınay, ‘Evaluation of 394 Chorionic Villus Samples in Prenatal Diagnosis’, Journal of Neonatalogy, 5, 63-69 (1998).
- Çoğulu, Ö., F. Özkınay, C. Gündüz ve H. Demir, ‘Bir Olgu Nedeniyle Frontonasal Displazi ve Frontofasionasal Displazi’, Klinik Bilimler & Doktor, 2, 248-250 (1998).
- Ülger, Z., K. Kavaklı ve Ö. Çoğulu, ‘Konjenital Pernisiöz Anemili Bir Olgu’, Ege Pediatri Bülteni, 4, 139-143 (1998).
- Özkınay, F., A. Yenigün, Ö. Çoğulu, M. Çoker, G. Sarı ve C. Özkınay, ‘Ehlers Danlos Sendromu Tip VI: Olgu Sunumu’, Ege Tıp Dergisi, 37, 1-4 (1998).
- Çoğulu, Ö., F. Vardar ve C. Özkınay, ‘Sepsiste Tedavi’, Ege Pediatri Bülteni, 1, 31-37 (1998).
- Çoğulu, Ö., ‘Turner Sendromu’, Ege Pediatri Bülteni, 2, 73-85 (1998).
- Çoğulu, Ö., ‘DNA ve Gen’, Ege Pediatri Bülteni, 3, 125-128 (1998).
- Çoğulu, Ö., M.A. Taş, S. Günbey ve F. Özkınay, ‘İmmubaskılanmış Hastalarda Israrlı Ateş ve Ampirik Flukonazol Kullanımı’, Ege Tıp Dergisi, 36, 143-146 (1997).
- Çoğulu, Ö., ‘Prenatal Tanıda Koryonik Villüs Biyopsisi ve Amniyotik Sıvı İncelemesi’, Jinekoloji ve Obstetrik Bülteni, 6, 165-74 (1997).
- Günbey, S., Ö. Çoğulu, M.Ali Taş ve M. Kılınç, ‘Lupus Hücresi Pozitif Bir Dermatomyozit Olgusu’, Ege Tıp Dergisi, 33, 295-299 (1994).
- Elevli, M., Ö. Çoğulu, N. Narlı ve S. Günbey, ‘Bir Olgu Nedeniyle Bartter Sendromu’, Dicle Tıp Dergisi, 20, 185-188 (1993).

Uluslararası Toplantılarda Sunulan Bildirileri (32 adet)- H. Onay, F. Ozkinay, O. Cogulu, N. Kutukculer, S. Sagol, C. Ozkinay; Autosomal Recessive Type SCID and Prenatal Diagnosis: Case Report. European Human Genetics Conference, Book of Abstracts, 162, Münih, 2004
- F. Ozkinay, H. Kanıt, H. Onay, O. Cogulu, C. Gündüz, D. Erkal, C. Ozkinay; Prenatal diagnosis of de nova unbalanced translocation 8p;21q using subtelomeric probes European Human Genetics Conference, Book of Abstracts, 162, Münih, 2004
- C. Ozkinay, A. Ekmekci, H. Onay, T. Cankaya, O. Cogulu, F. Ozkinay; A case of fetal hydantoin syndome having hemangioma associated with hemiatrophy at the left side of the body European Human Genetics Conference, Book of Abstracts, 116, Münih, 2004
- Cogulu O, Kosova B, Karaca E, Gunduz C, Ozkinay F, Aksoylar S, Gulen H, Kantar M, Oniz H, Karapinar D, Cetingul N, Erbay A, Vergin C, Ozkinay C., Evaluation of telomerase mRNA (hTERT) in childhood acute leukemia. European Human Genetics Conference, Book of Abstracts, 189, Münih, 2004
- A. Alpman, T. Cankaya, O. Cogulu, S. Sagol, F. Ozkinay Prenatal diagnosis of 47,XX,t(2;18)(p21-q23),+18 due to maternal balanced translocation of t(2;18)(p21-q23) European Human Genetics Conference, Book of Abstracts, 160, Münih, 2004
- Çoğulu, Ö., G. Koturoğlu, F. Özkınay, Z. Kurugöl, F. Vardar ve C. Özkınay,’Hepatitis A and B Seropositivity in the Patients Hospitalized in the Department of Pediatrics, Medical School Hospital, Ege University, izmir, Turkey’, 21st Annual Meeting of the European Society for Paediatrics Infectious Diseases, Book of Abstracts, 154, Sicily, 2003.
- Karaca, E., O. Cogulu, A. Alpman, C. Ozkinay ve F. Ozkinay,’ Further case of Frontonasaldysplasia and Dilated Virchow Robin Spaces’ European Human Genetics Conference, Book of Abstracts, 99, Birmingham, 2003.
- Pehlivan, S., F. Ozkinay, O. Okutman, O. Cogulu, A. Ozcan ve T. Cankaya,’ Achondroplasia In Turkey Is Defined By Recurrent G380R Mutation Of The FGFR3 Gene’, European Human Genetics Conference, Book of Abstracts,197, Birmingham, 2003.
- Alpman, A., G. Serdaroğlu, O. Cogulu, H. Tekgül, S. Tütüncüoğlu, ve F. Özkınay. ‘ Ring Chromosome 20 Syndrome: An Additional Case With Intractable Epilepsy’ Fourth European Cytogenetics Conference, Ann Genet, 226, Bologna, 2003.
- Ozkinay, C., F. Özkınay, O. Cogulu, E. Bora, H. Kirayoğlu ve O. Sudekan’ A Woman Having a Sibling With Trisomy 21, Had Two Babıes With Different Trisomy (13 and 21) in Two Seperate Pregnancıes’ Fourth European Cytogenetics Conference, Ann Genet, 254, Bologna, 2003.
- Ozkinay, F., H. Onay, O. Giray, O. Cogulu, D. Ercal ve S. Sagol’ A rare chromosomal rearrangement [inv(2)(p11q13)] in a 37-year-old Normal Male With an Offspring With 46,X,+mar/45,X Karyotype’ Fourth European Cytogenetics Conference, Ann Genet, 254, Bologna, 2003.
- Pehlivan, S., F. Ozkinay, O. Okutman, O. Cogulu, A. Ozcan ve T. Cankaya,’ Achondroplasia In Turkey Is Defined By Recurrent G380R Mutation Of The FGFR3 Gene’, European Human Genetics Conference, Book of Abstracts,197, Birmingham, 2003.
- Alpman, A., G. Serdaroğlu, O. Cogulu, H. Tekgül, S. Tütüncüoğlu, ve F. Özkınay. ‘ Ring Chromosome 20 Syndrome: An Additional Case With Intractable Epilepsy’ Fourth European Cytogenetics Conference, Ann Genet, 226, Bologna, 2003.
- Ozkinay, C., F. Özkınay, O. Cogulu, E. Bora, H. Kirayoğlu ve O. Sudekan. A Woman Having a Sibling With Trisomy 21, Had Two Babıes With Different Trisomy (13 and 21) in Two Seperate Pregnancıes’ Fourth European Cytogenetics Conference, Ann Genet, 254, Bologna, 2003.
- Ozkinay, F., H. Onay, O. Giray, O. Cogulu, D. Ercal ve S. Sagol. A rare chromosomal rearrangement [inv(2)(p11q13)] in a 37-year-old Normal Male With an Offspring With 46,X,+mar/45,X Karyotype’ Fourth European Cytogenetics Conference, Ann Genet, 254, Bologna, 2003.
- Özkınay, F., T. Çankaya, Ö. Çoğulu ve C. Özkınay,’ Kabuki Make-Up Syndrome in Three Turkish Patients’, European Human Genetics Conference, Final Programme and Abstracts, 125, Strasbourg, 2002.
- Çoğulu, Ö., F.F. Özkınay, C. Gündüz, T. Çankaya, S. Aydoğdu, F. Özgenç, N. Kütükçüler ve C. Özkınay,’Antigliadin Antibodıes and Antiendomysıal Antıbodıes in Down Syndrome Children’, European Human Genetics Conference, Final Programme and Abstracts, 125, Strasbourg, 2002.
- Özkınay, C., C. Gündüz, T. Çankaya, E. Bora, E. Karaca, A. Alpman, S. Sağol, H. Onay, Ö. Çoğulu ve F. Özkınay,’ ’Trends in Cytogenetic Prenatal Diagnosis in a Reference Hospital in İzmir/Turkey: A Comparative Study for 4 Years’ European Human Genetics Conference, Final Programme and Abstracts, 282, Strasbourg, 2002.
- Gündüz, C., A. Alpman, Ö. Çoğulu, C. Özkınay ve F. Özkınay,’ Seven Cases of Chromosomal Mosaicism Detected in Amniocentesis and Karyotype Phenotype Correlations’, European Human Genetics Conference, Final Programme and Abstracts, 283, Strasbourg, 2002.
- Alpman, A., G. Sapmaz, E. Karaca, T. Çankaya, E. Bora, Ö. Çoğulu, C. Gündüz, W.J. Kleijer ve F. Özkınay, ‘Detection of Trisomy 21 in a Fetus During the Investigation for Tay Sachs Disease: Prenatal Cytogenetic Study Should be performed Associated With Molecular or Enzymatic Studies’ European Human Genetics Conference, Final Programme and Abstracts, 285, Strasbourg, 2002.
- Cogulu, O., C. Tirpan, F. Ozkinay, C. Gunduz ve C. Ozkinay, ‘A Second Case With 47,XY,+8[38]/45,X0[12] Karyotype’, Third European Cytogenetics Conference, Book of Abstract, 79, Paris, 2001.
- Gunduz, C., O. Cogulu, N. Çetingül, T. Cankaya Ozkinay ve F. Ozkinay, ‘A New Chromosome Rearrangement In Acute Lymphoblastic Leukemia’, Third European Cytogenetics Conference, Book of Abstract, 95, Paris, 2001.
- Ozkinay, C., O. Cogulu, C. Gündüz, G. Sapmaz, T. Cankaya ve F. Ozkinay, ‘Anophthalmia Waardenburg Syndrome,’ 31st Annual Meeting of the European Society of Human Genetics, Book of Abstract, Geneva, 64, 1999.
- Ozkinay, F., C. Gündüz, O. Cogulu, G. Sapmaz ve C. Özkınay, ‘Double Translocation 21:21 in a Normal Male Born to a Consanguineous Parents,’ 31st Annual Meeting of the European Society of Human Genetics, Book of Abstract, Geneva, 76, Stockton, 1999.
- Yenigun, A., F. Ozkinay, O. Cogulu, C. Coker, N. Cetiner, G. Özden, C. Ozkinay ve O. Aksu, ‘Hair Zinc Levels in Down Syndrome Children,’ 29th Annual Meeting of the European Society of Human Genetics, Book of Abstract, Genoa, 24, 1997.
- Cogulu, O., F. Ozkinay, C. Ozkinay, G. Sapmaz ve O. Yalman, ‘A Case of Progressive Pseudorheumatoid Arthropathy of Chilhood,’ 29th Annual Meeting of the European Society of Human Genetics, Book of Abstract, Genoa, 26, 1997.
- Gündüz, C., F. Ozkinay, O. Cogulu, N. Terzibasioglu, E. Levent ve C. Ozkinay, ‘A Case of KBG Syndrome,’ 29th Annual Meeting of the European Society of Human Genetics, Book of Abstract, Genoa, 28, 1997.
- Ozkinay, F., O. Cogulu, C. Ozkinay, I. Akil ve N. Terzibaşıoğlu, ‘A Case of Frontofacionasal Dysplasia,’ 29th Annual Meeting of the European Society of Human Genetics, Book of Abstract, Genoa, 29, 1997.
- Vatansever, S., C. Tuncer, F. Ozkinay, O. Cogulu, C. Gündüz ve C. Ozkinay, ‘Medical Knowledge and Social Opinions of the Medical School Students About Down Syndrome, 29th Annual Meeting of the European Society of Human Genetics, Book of Abstract, Genoa, 188, 1997.
- Yenigün, A., F. Ozkinay, O. Cogulu, C. Coker, N. Cetiner, G. Ozden, C. Ozkinay ve O. Aksu, ‘Hair Zinc Levels in Down Syndrome Children,’ International Conference On Chromosome 21 and Medical Research On Down Syndrome, Program and Abstracts, Barcelona, N C-15, 1997.
- Ozkinay, F., S. Vatansever, C. Tuncer, O. Cogulu, C. Gündüz ve C. Ozkinay, ‘Medical Knowledge and Social Opinions of the Medical School Students About Down Syndrome,’ International Conference On Chromosome 21 and Medical Research On Down Syndrome, Program and Abstracts, Barcelona, N C-16, 1997.
- Çoğulu, Ö., M.A. Taş ve E. Bühler, ‘Amniocentesis in Prenatal Diagnosis And Results of 447 Cases,’ XXI. Ortadoğu ve Akdeniz Pediatri Dernekleri Birliği Kongresi, İzmir, 97, Ege Basım, 1993. (SÖZLÜ BİLDİRİ)

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İndeksli Yayınlarını Kaynak Gösteren Yayınlar (119 adet)- 2008, Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands
- 2008, Multiplex ligation-dependent probe amplification identification of whole exon and single nucleotide deletions in the CFTR gene of Hispanic individuals with cystic fibrosis
- 2008, CFTR mutations in Turkish and north African cystic fibrosis patients in Europe: Implications for screening
- 2008, Identification of a novel mutation and polymorphic change in the NIPBL gene of subjects with Cornelia de Lange syndrome
- 2008, Cohesin and human disease
- 2008, Spondyloepiphyseal dysplasia tarda with progressive arthropathy with delayed diagnosis
- 2008, Refractory and lethal status epilepticus in a patient with ring chromosome 20 syndrome
- 2008, X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
- 2008, Cohesin and human disease
- 2008, Genetics of intellectual disability
- 2008, Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes
- 2008, Severe Mandibuloacral Dysplasia-Associated Lipodystrophy and Progeria in a Young Girl with a Novel Homozygous Arg527Cys LMNA Mutation
- 2008, Microcephalia with mandibular and dental dysplasia in adult Zmpste24-deficient mice
- 2008, Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome
- 2008, HGPS and related premature aging disorders: From genomic identification to the first therapeutic approaches
- 2008, The R527H mutation in LMNA gene causes an increased sensitivity to ionizing radiation
- 2008, Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings
- 2008, Association of homozygous LMNA mutation R471C with new phenotype: Mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy
- 2008, Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure
- 2008, Dental eruption in afrotherian mammals
- 2008, The evaluation of hTERT mRNA expression in acute leukemia children and 2 years follow-up of 40 cases
- 2008, Celiac disease: What's new about it?
- 2008, Clinical spectrum of fever of unknown origin among Indian children
- 2008, Evaluation of an in-house protocol for prenatal molecular diagnosis of SMA in Chinese
- 2008, Quantification of SMN1 and SMN2 genes by capillary electrophoresis for diagnosis of spinal muscular atrophy
- 2008, The population-based prevalence of achondroplasia and thanatophoric dysplasia in selected regions of the US
- 2007, Application of medical genetics in Turkey
- 2007, The Haemophilus influenzae hFbpABC Fe3+ transporter: Analysis of the membrane permease and development of a gallium-based screen for mutants
- 2007, Association between inflammatory markers in induced sputum and clinical characteristics in children with non-cystic fibrosis bronchiectasis
- 2007, Spectrum of mutations in the CFTR gene in cystic fibrosis patients of spanish ancestry
- 2007, The PDAC syndrome (Pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): Report of eight cases including a living child and further evidence for autosomal recessive inheritance
- 2007, Ophthalmo-acromelic syndrome: Report of a case with vertebral anomalies
- 2007, Anophthalmia-Waardenburg syndrome with expanding phenotype: Does neural crest play a role?
- 2007, The nuclear envelope, a key structure in cellular integrity and gene expression
- 2007, Mandibuloacral dysplasia and a novel LMNA mutationin in a woman with severe progressive skeletal changes
- 2007, A der(1:15)(q10:q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia
- 2007, Cornelia de Lange syndrome: Clinical review, diagnostic and scoring systems, and anticipatory guidance
- 2007, Natural history of aging in Cornelia de Lange syndrome
- 2007, Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X:19)(q11.1-11.2:p13-3)
- 2007, Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type a phenotype
- 2007, Mandibuloacral dysplasia and a novel LMNA mutationin in a woman with severe progressive skeletal changes
- 2007, Werner and Hutchinson-Gilford progeria syndromes: mechanistic basis of human progeroid diseases
- 2007, The nuclear envelope, a key structure in cellular integrity and gene expression
- 2007, Concise review: Telomere biology in normal and leukemic hematopoietic stem cells
- 2007, Telomere biology of pediatric cancer
- 2007, Protein phosphatase 2A (PP2A) has a potential role in CAPE-induced apoptosis of CCRF-CEM cells via effecting human telomerase reverse transcriptase activity
- 2007, Apoptosis of human melanoma cells induced by the novel compounds propolin A and propolin B from Taiwenese propolis
- 2007, Tissue transglutaminase antibodies are a useful serological marker for the diagnosis of Celiac disease in patients with Down syndrome
- 2007, Crohn's disease: Is still the reason of fever of unknown origin?
- 2007, Evidence of a segregation ratio distortion of SMN1 alleles in spinal muscular atrophy
- 2007, Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis
- 2007, Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia
- 2006, Lee, Susie K: Green, Peter HRCeliac sprue (the great modern-day imposter). Current Opinion in Rheumatology. 18(1):101-107, January 2006.
- 2006, Comprehensive genetic analysis of the cystic fibrosis transmembrane conductance regulator from dried blood specimens - Implications for newborn screening
- 2006, Phenotypic consequences of branch point substitutions
- 2006, A haplotype framework for cystic fibrosis mutations in Iran
- 2006, Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): Report of a new Italian case with renal anomaly and review
- 2006, Osteoarthritis
- 2006, 'Epilepsy responds to vagus nerve stimulation in ring chromosome 20 syndrome'
- 2006, Electroclinical evolution in ring chromosome 20 epilepsy syndrome: A case with severe phenotypic features followed for 25 years
- 2006, X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
- 2006, Genetic disorders of adipose tissue development, differentiation, and death
- 2006, Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency
- 2006, The laminopathies: a clinical review
- 2006, Stabilization of the retinoblastoma protein by A-type nuclear lamins is required for INK4A-mediated cell cycle arrest
- 2006, Nuclear lamins: Laminopathies and their role in premature ageing
- 2006, Genetic basis of lipodystrophies and management of metabolic complications
- 2006, Cytogenetic results of amniocentesis materials: Incidence of abnormal karyotypes in the Turkish collaborative study
- 2006, In situ detection of hTERT variants in anaplastic large cell lymphoma
- 2006, Chemical composition effects onto antimicrobial and antioxidant activities of propolis collected from different regions of Turkey
- 2006, Natural products and the treatment of leukemia
- 2006, Embryopathy due to valproic acid with severe malformations in the central nervous system
- 2006, American Gastroenterological Association (AGA) Institute Technical Review on the Diagnosis and Management of Celiac Disease
- 2006, Celiac sprue (the great modern-day imposter)
- 2006, A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review
- 2005, Garg A, Cogulu O, Ozkinay F, et al. A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 90 (9): 5259-5264 SEP 2005
- 2005, Polityko A, Starke H, Rumyantseva N, et al. Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding CYTOGENETIC AND GENOME RESEARCH 111 (2): 171-174 2005
- 2005, Young SG, Fong LG, Michaelis S Prelamin A, Zmpste24, misshapen cell nuclei, and progeria - new evidence suggesting that protein farnesylation could be important for disease pathogenesis JOURNAL OF LIPID RESEARCH 46 (12): 2531-2558 DEC 2005
- 2005, Ram R, Uziel O, Lahav M The importance of the telomere and telomerase system in hematological malignancies LEUKEMIA & LYMPHOMA 46 (8): 1121-1135 AUG 2005
- 2005, Alanay Y, Boduroglu K, Tuncbilek E Celiac disease screening in 100 Turkish children with Down syndrome TURKISH JOURNAL OF PEDIATRICS 47 (2): 138-140 APR-JUN 2005
- 2005, Botta A, Tacconelli A, Bagni I, et al. Transmission ratio distortion in the spinal muscular atrophy locus - Data from 314 prenatal tests NEUROLOGY 65 (10): 1631-1635 NOV 22 2005
- 2005, Niessen RC, Jonkman MF, Muis N, et al. Pigmentary mosaicism following the lines of Blaschko in a girl with a double aneuploidy mosaicism: (47,XX,+7/45,X) AMERICAN JOURNAL OF MEDICAL GENETICS PART A 137A (3): 313-322 SEP 1 2005
- 2005, Barisic I. Down Syndrome, Medicina, 42:69-75, 2005
- 2005, Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number: {248370}: {2/21/2005}: . World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/
- 2005, Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number: {119600}: {8/31/2005}: . World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/
- 2005, Hyperechogenic fetal bowel: counseling difficulties
- 2005, A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia
- 2005, Prelamin A, Zmpste24, misshapen cell nuclei, and progeria - new evidence suggesting that protein farnesylation could be important for disease pathogenesis
- 2005, Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding
- 2005, Mandibuloacral dysplasia: A report of two Egyptian cases
- 2005, The importance of the telomere and telomerase system in hematological malignancies
- 2005, Celiac disease screening in 100 Turkish children with Down syndrome
- 2005, Transmission ratio distortion in the spinal muscular atrophy locus - Data from 314 prenatal tests
- 2005, Pigmentary mosaicism following the lines of Blaschko in a girl with a double aneuploidy mosaicism: (47,XX,+7/45,X)
- 2004, Dayangac D, Erdem H, Yilmaz E, et al. Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens HUMAN REPRODUCTION 19 (5): 1094-1100 MAY 2004
- 2004, Caridi G, Berdeli A, Dagnino M, et al. Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin AMERICAN JOURNAL OF KIDNEY DISEASES 43 (4): 727-732 APR 2004
- 2004, Audrezet M, Chen JM, Raguenes O, et al. Genomic rearrangements in the CFTR gene: Extensive allelic heterogeneity and diverse mutational mechanisms HUMAN MUTATION 23 (4): 343-357 2004
- 2004, Rahmah R, Yong JF, Sharifa NA, et al. Bilateral adrenal cysts and ectopic pancreatic tissue in Beckwith-Wiedemanin syndrome: Is a conservative approach acceptable? JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM 17 (6): 909-912 JUN 2004
- 2004, Tsao L, Draoua HY, Osunkwo I, et al. Mature B-cell acute lymphoblastic leukemia with t(9:11) translocation: a distinct subset of B-cell acute lymphoblastic leukemia MODERN PATHOLOGY 17 (7): 832-839 JUL 2004
- 2004, Kaptanoglu E, Percin F, Percin S, et al. Spondyloepiphyseal dysplasia tarda with progressive arthropathy TURKISH JOURNAL OF PEDIATRICS 46 (4): 380-383 OCT-DEC 2004
- 2004, Buckwalter JA, Saltzman C, Brown T The impact of osteoarthritis - Implications for research CLINICAL ORTHOPAEDICS AND RELATED RESEARCH (427): S6-S15 Suppl. S OCT 2004
- 2004, Chen CP, Lin SP Detection of chromosome aberrations during prenatal genetic testing for single gene disorders PRENATAL DIAGNOSIS 24 (11): 924-925 NOV 2004
- 2004, Ostrea EM, Mantaring JB, Silvestre MA Drugs that affect the fetus and newborn infant via the placenta or breast milk PEDIATRIC CLINICS OF NORTH AMERICA 51 (3): 539+ JUN 2004
- 2004, Chen CP, Chang TY, Town DD, et al. Partial trisomy 10 (10q11.2 -> pter) and partial trisomy 18 (18p11.2 -> pter) associated with abnormal sonographic findings and a maternal serum screen-positive result ULTRASOUND IN OBSTETRICS & GYNECOLOGY 23 (2): 202-204 FEB 2004
- 2004, John Wiley & Sons, Ltd.Current awareness in prenatal diagnosis, Prenatal Diagnosis,Volume 24, Issue 9, 2004. Pages 755-760
- 2004, Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens
- 2004, Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin
- 2004, Genomic rearrangements in the CFTR gene: Extensive allelic heterogeneity and diverse mutational mechanisms
- 2004, Drugs that affect the fetus and newborn infant via the placenta or breast milk
- 2004, Partial trisomy 10 (10q11.2 -> pter) and partial trisomy 18 (18p11.2 -> pter) associated with abnormal sonographic findings and a maternal serum screen-positive result
- 2003, Semerci CN, Zorlu P, Topal Y, et al. Is it a new syndrome or a clinical variability in cerebro-oculo-nasal syndrome? AMERICAN JOURNAL OF MEDICAL GENETICS PART A 120A (2): 253-255 JUL 15 2003
- 2003, Lao O, Andres AM, Mateu E, et al. Spatial patterns of cystic fibrosis mutation spectra in European populations EUROPEAN JOURNAL OF HUMAN GENETICS 11 (5): 385-394 MAY 2003
- 2003, Emmanouil-Nikoloussi EN, Goret-Nicaise M, Manthos A, et al. Histological study of anophthalmia observed in exencephalic rat embryos after all-trans-retinoic acid administration JOURNAL OF TOXICOLOGY-CUTANEOUS AND OCULAR TOXICOLOGY 22 (1-2): 33-46 2003
- 2003, Padmanabhan R, Abdulrazzaq YM, Bastaki SMA, et al. Experimental studies on reproductive toxicologic effects of lamotrigine in mice BIRTH DEFECTS RESEARCH PART B-DEVELOPMENTAL AND REPRODUCTIVE TOXICOLOGY 68 (5): 428-438 OCT 2003
- 2003, Is it a new syndrome or a clinical variability in cerebro-oculo-nasal syndrome?
- 2003, Spatial patterns of cystic fibrosis mutation spectra in European populations
- 2003, Experimental studies on reproductive toxicologic effects of lamotrigine in mice
- 2002, Male A, Davies A, Bergbaum A, et al. Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region EUROPEAN JOURNAL OF HUMAN GENETICS 10 (12): 807-812 DEC 2002
- 2002, Gunduz C, Cogulu O, Cetingul N, et al. New chromosome rearrangement in acute lymphoblastic leukemia CANCER GENETICS AND CYTOGENETICS 137 (2): 150-152 SEP 2002
Kitapları (10 adet)- 2007, Laboratuvar kılavuzu Sitogenetik-Moleküler sitogenetik Ege Üniversitesi Tıp Fakültesi Tıbbi Genetik Anabilim Dalı İzmir
- 2007, Laboratuvar kılavuzu Moleküler Genetik Ege Üniversitesi Tıp Fakültesi Tıbbi Genetik Anabilim Dalı İzmir
- 2007, Özgür Çoğulu, Ferda Özkınay. Dismorfoloji, Klinik Pediatri Kitabı Bölüm Yazarlığı
- 2007, 6. Özgür Çoğulu, Ferda Özkınay., Dismorfoloji, In: Pediatrik Tanı ve Tedavide Pratik Yaklaşımlar, Nobel Tıp Kitabevi, Robert M Kliegman, Ed. Nejat Narlı, Çeviri,
- Çoğulu, Ö.,’Genetik hastalıklara Temel yaklaşım’, Moleküler Tanı ve Uygulamaları Yaz Okulu, Proceedings, 23-39, İzmir, 2002.
- 37. Türk Pediatri Kongresi Kurs Kitabı, Editör: R.V. Yağcı, Ö. Çoğulu, F. Özgenç, E. Levent, M. Yalaz, İzmir, 2001.
- Özkınay, F., Ö. Çoğulu, ‘Kulak, Burun, Boğaz Muayenesi’, ‘Çocuk Sağlığı ve Hastalıklar Propedötik’ Editör Alphan Cura, EÇV Yayınları No: 10, 21-54, İzmir, 2001.
- Çoğulu, Ö., ‘Talasemi ve Genetik’ ‘Talasemi’, Kurs Kitabı, 5-16, izmir, 2000.
- Özkınay, F., Ö. Çoğulu, ‘Hastalıkların Moleküler Genetik Temeli’, ‘Çocuk Sağlığı ve Hastalıkları’, Editör Alphan Cura, EÇV Yayınları No: 6, 21-54, İzmir, 1999.
- Özkınay, C., S. Aydoğdu, Ö. Çoğulu, F. Vardar, ‘Hasta Çocuk Beslenmesi, Ateşli Hastalıklarda ve Protein-Enerji Gereksinimi Artmış Çocuklarda Beslenme’, Kurs Kitabı, Editör Alphan Cura, EÇV Yayınları No: 3, 21-30, izmir, 1997.

Tamamlanmış Araştırma Projeleri (29 adet)- 2009, Araştırma Projesi, Çocukluk Çağı Lösemilerinde micro RNA Ekspresyonunun lösemi tipi, tedaviye yanıt ve prognoz ile ilişkisinin değerlendirilmesi, TÜBİTAK, Proje Yürütücüsü, 109S076
- 2008, Araştırma Projesi, Diffüz ve Yüksek Dereceli Glial Tümörlerde Tümör Süpressör Genlerin Epigenetik Değişimlerinin Realtime Online PCR Tabanlı Metillenmiş Alellerin Kantitatif Analizi Yöntemi ile Belirlenmesi, TÜBİTAK, Yardımcı araştırıcı
- 2008, Araştırma Projesi, Deneysel Nekrotizan Enterokolit Modelinde İnsulin Benzeri Büyüme Faktörü-1 ve Rekombine Eritropoetinin Apoptoz ve Telomeraz Aktivitesi Üzerine Etkileri, TÜBİTAK, Yardımcı araştırıcı
- Araştırma Projesi, Klinik olarak ilerleyici ailevi intrahepatik kolestaz ile uyumlu hastalarda FIC-1 mutasyonunun araştırılması, Proje Yürütücüsü, AREL, 2007-TIP-03
- 2006, Araştırma Projesi, Akut Post Streptokoksik Glomerulonefrit Geçirmiş Olgularda Mannoz Binding Lektin (MBL) Gen Polimorfizlerinin Araştırılması,Yardımcı araştırmacı, EBILTEM
- 2006, Araştırma Projesi, Emziren anne ve bebeklerindeki Vitamin D reseptör polimorfizimlerinin anne saç kökü hücrelerinde ekspresyonları, anne sütünde ve bebek serumundaki vitamin D düzeyleri ilişkisi, Yardımcı araştırmacı, TÜBİTAK
- 2006, Araştırma Projesi, Febril Nötropenik Kanserli Çocuklarda Toll-like Reseptör 2 ve 4’ün rolü, Yardımcı araştırmacı EBILTEM
- 2006, Araştırma Projesi, Türk Toplumunda Tüberküloza Yatkınlıkta Rol Oynayan Genlere Ait Polimorfizmlerin Araştırılması (DHPLC Yöntemi ile), EÜ Araştırma Fon Saymanlığı, Yardımcı araştırmacı,
- Araştırma Projesi, Lösemik Hücrelerde Propolis Aktivitesinin hTERT ile İncelenmesi, Proje Yöneticisi, EBİLTEM, 2005.
- Araştırma Projesi, Sepsisde Hemostazda etkili Genlerin Değerlendirilmesi, Proje Yöneticisi, EBİLTEM, 2005.
- 2005, Araştırma Projesi, 17. Prematür doğumlarda MBL gen polimorfizmlerinin araştırılması EBİLTEM
- 2005, Araştırma Projesi, 18. NTD hastalarda MTHFR polimorfizmlerin araştırılması, EBILTEM,
- 2005, Araştırma Projesi, Kronik Lenfositer Lösemililerde (KLL) Telomeraz Aktivitesinin Değerlendirilmesi ve Prognostik Belirleyici Olan Cd38 Ve Zap70 İle Karşılaştırılması, Proje Yürütücüsü, Proje No: 2004/GHUM/001, EBİLTEM
- 2005, Araştırma Projesi, Türk toplumunda tüberküloza yatkınlıkta NRAMP1 gen polimorfizmi, EBİLTEM
- 2005, Araştırma Projesi, Nadir görülen genetik sendromda(Pachoyonychia congenita) sorumlu genin araştırılması, Proje Yürütücüsü, AREL
- 2005, Araştırma Projesi, AREL WEB sitesinin hazırlanması ve projelerin elektronik ortamda hazırlanması, Proje Yürütücüsü, AREL
- Araştırma Projesi, Akut Lösemi Hücre Kültürlerinde Propolis Etkinliğinin Telomeraz Aktivitesi İle İlişkisi, Proje Yürütücüsü, Proje No: 2005/GHUM/001, EBİLTEM
- Araştırma Projesi, Akut Lösemilerde Telomeraz Aktivite Tayini, Proje Yöneticisi, EBİLTEM, 2004.
- Araştırma Projesi, Transizyonel Hücreli Kanserlerde Kromozomal Anomalilerin Fluoresan in situ Hibridizasyon (FISH) Yöntemi ile Tanısı, Ege Üniversitesi Araştırma Fon Saymanlığı, Yardımcı Araştırmacı, 2002/TIP/010, 2002.
- Araştırma Projesi, Fetal anomalili olan gebeler ile nikotin bağımlısı gebelerin amniyon hücreleri ve trofoblastlarında telomeraz aktivitesi ve rtelomer boyugebeliklerde telomeraz aktivitesi ve telomer boyunun tayini, Ege Üniversitesi Bilimsel Araştırma Uygulama Merkezi, Yardımcı Araştırmacı, 2002/BİL/01, 2002.
- Araştırma Projesi, İdiyopatik Mental Retardasyonda Kromozomlarda Subtelomerik bölgenin araştırılması, Proje Yöneticisi, TUBİTAK, SBAG-2546, 2002.
- Araştırma Projesi, Kistik Fibroz Hastalarındaki Mutasyonların Moleküler Yöntemlerle Saptanması, Ege Üniversitesi Araştırma Fon Saymanlığı, Yardımcı Araştırmacı, 2000/TIP/001, 2001.
- Araştırma Projesi, Hematolojik malignitelerde real time on line floresan PCR ile translokasyon (9:22) nin kantitatif tayini, Ege Üniversitesi Bilimsel Araştırma Uygulama Merkezi, Yardımcı Araştırmacı, 2001/GHUM/002, 2001.
- 2000, Araştırma Projesi, 6. Embriyonik Bölünme Gösteren Hücrelerde Telomeraz Aktivitesi, Ege Üniversitesi Bilimsel Araştırma Uygulama Merkezi, Proje Yöneticisi, 2001/GHUM/001, 2001.
- Araştırma Projesi, Akondroplazide Moleküler Genetik Analizler, Ege Üniversitesi Bilimsel Araştırma Uygulama Merkezi, Yardımcı Araştırmacı, 2000/FEN/007, 2000.
- Araştırma Projesi, Konjenital Kardiopati ve Di George Sendromu bulgularını gösteren olgularda 22q11 delesyonunun Fluoresans In Situ Hidridizasyon (FISH) yöntemiyle gösterilmesi, Ege Çocuk Vakfı Araştırma Projesi, Yardımcı Araştırmacı, Yardımcı Araştırmacı, Ege Çocuk Vakfı Araştırma Projesi, Yardımcı Araştırmacı, Yardımcı Araştırmacı, Ege Çocuk Vakfı, 2000.
- Araştırma Projesi, Prenatal Tanıdaİnterfaz Hücrelerinde Floresan İn Situ Hibridizasyon Yöntemi ile Anöploidi Aranması, Ege Üniversitesi Bilimsel Araştırma Uygulama Merkezi, Yardımcı Araştırmacı, 2000/GHUM /001, 2000.
- Araştırma Projesi, Parafin Bloktan ve Periferal Kan Lenfositlerinden İzole Edilen Spinal Muskuler Atrofi Hasta DNA’larında Delesyon Analizleri ve Prenatal Tanı, Ege Çocuk Vakfı Araştırma Projesi, Yardımcı Araştırmacı, Ege Çocuk Vakfı, 1999.
- Araştırma Projesi, 1. Antikanser Kemoterapide Mikotik Enfeksiyon Sıklığı, Dicle Üniversitesi Tıp Fakültesi, Proje Yöneticisi, 1990.
Bilimsel Kuruluş Üyeliklerim (5 adet)- European Cytogenetics association
- Milli Pediatri derneği
- Perinatoloji Derneği
- Tıbbi Genetik Derneği
- Türk Pediatri Kurumu
Kazanılan Burslar (1 adet)- 1983, TÜBİTAK
Kazandığı Ödüller (9 adet)- 2008, 8. Febril Nötropeni Simpozyumu Poster Birincilik Ödülü
- 2006, 7. Febril Nötropeni Sempozyumu Poster Ödülü
- 2006, TÜBİTAK Özendirme Ödülü
- 2006, Astrazeneca Poster Ödülü
- 2006, Türk Pediatri Kongresi Sözlü Sunum Birincilik
- 2004, EBİLTEM, Proje Yarışması-Temel Tıp Bilimleri Sözlü sunu Birincilik
- 2003, Güncel İnfertilite ve Yardımcı Üreme Teknikleri Sempozyumu Poster Birincilik
- 2003, 39. Türk Pediatri Kongesi-Sözlü sunu birincilik
- 2000, IV. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi-Poster Birincilik