Uluslararası Hakemli Dergilerde Yayımlanan Yazılar

1- Barut MU, Bozkurt M, Kahraman M, Yıldırım E, Imirzalioğlu N, Kubar A, Sak S, Ağaçayak E, Aksu T, Çoksüer H. Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues.Med Sci Monit. 2018 Jun 22;24:4288-4294.


2- Barut MU, Yildirim E, Kahraman M, Bozkurt M, Imirzalioğlu N, Kubar A, Çalişkan E, Sak S, Aksu T.Human Papilloma Viruses and Their Genotype Distribution in Women with High Socioeconomic Status in Central Anatolia, Turkey: A Pilot Study.Med Sci Monit. 2018 Jan 4;24:58-66.


3- Ozgöz A, Samli H, Oztürk KH, Orhan B, Icduygu FM, Aktepe F, Imirzalioglu N. An investigation of the effects of FGFR2 and B7-H4 polymorphisms in breast cancer. J Cancer Res Ther. 2013 Jul-Sep;9(3):370-5.


4- Sensoy N, Şoysal Y, Kahraman A, Doğan N, Imirzalioğlu N. Modulator effects of the methylenetetrahydrofolate reductase C677T polymorphism on response to vitamin B12 therapy and homocysteine metabolism. DNA Cell Biol. 2012 May;31(5):820-5.


5- Soysal Y, Vermeesch J, Davani NA, Şensoy N, Hekimler K, İmirzalıoğlu N. Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech. Genet Mol Res. 2011 Sep 21;10(3):2148-54


6- Soysal Y, Inan UÜ, Küsbeci T, Imirzalioğlu N. Age-related macular degeneration and association of CFH Y402H and LOC387715 A69S polymorphisms in a Turkish population. DNA Cell Biol. 2012 Mar;31(3):323-30.


7- Soysal Y, Vermeesch J, Davani NA, Hekimler K, Imirzalioğlu N. A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism.Am J Med Genet A. 2011 Jul;155A(7):1745-52.


8- Bozkurt M, Kapı E, Külahçı Y, Zor F, Benlier E, Balkan M, Kılınç N, Imirzalıoğlu N, Kuvat SV. [Analysis of genetic penetrance in the pedigree of cases with Van der Woude syndrome: report of five cases]. Kulak Burun Bogaz Ihtis Derg. 2010 Jul-Aug;20(4):200-4. Turkish.


9- Soysal Y, Balci S, Hekimler K, Liehr T, Ewers E, Schoumans J, Bui TH, Içduygu FM, Kosyakova N, Imirzalioğlu N. Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. Am J Med Genet A. 2009 Dec;149A(12):2782-7. 


10- Samli H, Içduygu FM, Ozgöz A, Akbulut G, Hekimler K, Imirzalioglu N. Surgery for acute abdomen and MEFV mutations in patients with FMF. Acta Reumatol Port. 2009 Jul-Sep;34(3):520-4.


11- Soysal Y, Tate G, Polat C, Polat N, Aktepe F, Sivaci Y, Imirzalioglu N. Analysis of PTEN gene mutations in a Turkish patient with Cowden syndrome. Genet Test Mol Biomarkers. 2009 Aug;13(4):547-51.


12- Onrat ST, Emmiler M, Sivaci Y, Söylemez Z, Ozgöz A, Imirzalioğlu N. A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders. Genet Mol Res. 2009 Apr 14;8(2):426-34.


13- Karacay S, Saygun I, Tunca Y, Imirzalioglu N, Guvenc G. Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I. J Indian Soc Pedod Prev Dent. 2007 Mar;25(1):43-5.


14- Buyukates M, Turan SA, Altunkaya SA, Imirzalioglu N. Familial secundum type atrial septal defect with normal karyotypes. J Cardiovasc Surg (Torino). 2007 Apr;48(2):258.


15- Ozel AM, Demirturk L, Aydogdu A, Gultepe M, Yazgan Y, Imirzalioglu N, Gurbuz AK, Narin Y. Effect of Helicobacter pylori infection and eradication therapy on interleukin-6 levels in patients with Familial Mediterranean Fever. Int J Clin Pract. 2008 May;62(5):754-61. Epub 2007 Mar 1.


16- Samli H, Samli MM, Yilmaz E, Imirzalioglu N. Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD). Arch Androl. 2006 Nov-Dec;52(6):471-7.


17- Ergun MA, Soysal Y, Kismet E, Akay C, Dundaroz R, Ilhan M, Imirzalioglu N. Investigating the in vitro effect of taurine on the infant lymphocytes by sister chromatid exchange. Pediatr Int. 2006 Jun;48(3):284-6.


18- Samli H, Samli MM, Solak M, Imirzalioglu N. Genetic anomalies detected in patients with non-obstructive azoospermia and oligozoospermia. Arch Androl. 2006 Jul-Aug;52(4):263-7.


19- Bolu SE, Orkunoglu Suer FE, Deniz F, Uckaya G, Imirzalioglu N, Kutlu M. The vitamin D receptor fokI start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism. J Endocrinol Invest. 2005 Oct;28(9):810-4.


20- Bayram Y, Deveci M, Imirzalioglu N, Soysal Y, Sengezer M. The cell based dressing with living allogenic keratinocytes in the treatment of foot ulcers: a case study. Br J Plast Surg. 2005 Oct;58(7):988-96.


21- Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC. MEFV gene is a probable susceptibility gene for Behçet's disease. Scand J Rheumatol. 2005;34(1):56-8.


22- Akdemir R, Ozhan H, Gunduz H, Erbilen E, Yazici M, Duran S, Orkunoglu F, Albayrak S, Imirzalioglu N, Uyan C. HLA-DR B1 and DQ B1 polymorphisms in patients with coronary artery ectasia. Acta Cardiol. 2004 Oct;59(5):499-502.


23- Köseoglu V, Kismet E, Soysal Y, Ulucan H, Dündaröz R, Imirzalioglu N, Gökçay E. Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G. Pediatr Int. 2004 Aug;46(4):415-8. Erratum in: Pediatr Int. 2004 Dec;46(6):756. 


24- Akdemir R, Ozhan H, Gunduz H, Yazici M, Erbilen E, Uyan C, Imirzalioglu N. Complete atrioventricular block in Becker muscular dystrophy. N Z Med J. 2004 May 21;117(1194):U895.


25- Samli H, Solak M, Imirzalioglu N, Beyatli Y, Simşek S, Kahraman S. Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture. Prenat Diagn. 2003 Oct;23(10):847-50.


26- Kutukcu Y, Imirzalioglu N, Odabasi Z, Gokcil Z, Vural O. Essential palatal myoclonus in monozygotic male twins. J Neurol. 2003 Jul;250(7):885-6.


27- Karadeniz NN, Tunca Y, Imirzalioğlu N. New heritable fragile site at 15q13 in both members of a nonconsanguineous couple. Am J Med Genet A. 2003 Apr 30;118A(3):290-2.


28- Uyan C, Yazici M, Uyan AP, Akdemir R, Imirzalioglu N, Dokumaci B. Ebstein's anomaly in siblings: an original observation. Int J Cardiovasc Imaging. 2002 Dec;18(6):435-8.


29- Işik S, Er E, Soysal Y, Imirzalioğlu N. Prolongation of skin xenograft survival with modified cultured fibroblasts. Plast Reconstr Surg. 2003 Jan;111(1):275-82; discussion 283-5.


30- Doğan A, Tunca Y, Ozdemir A, Sengül A, Imirzalioğlu N. The effects of folic acid application on IL-1beta levels of human gingival fibroblasts stimulated by phenytoin and TNFalpha in vitro: a preliminary study. J Oral Sci. 2001 Dec;43(4):255-60.


31- Kahraman S, Yakin K, Dönmez E, Samli H, Bahçe M, Cengiz G, Sertyel S, Samli M, Imirzalioğlu N. Relationship between granular cytoplasm of oocytes and pregnancy outcome following intracytoplasmic sperm injection. Hum Reprod. 2000 Nov;15(11):2390-3.


32- Kahraman S, Bahçe M, Samli H, Imirzalioğlu N, Yakisn K, Cengiz G, Dönmez E. Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure. Hum Reprod. 2000 Sep;15(9):2003-7.


33- Güran S, Tunca Y, Imirzalioğlu N. Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family. Cancer Genet Cytogenet. 1999 Sep;113(2):145-51.


34- Oğur G, Gül D, Lenk MK, Imirzalioğlu N, Alpay F, Oğur E. Variable clinical expression of Holt-Oram syndrome in three generations. Turk J Pediatr. 1998 Oct-Dec;40(4):613-8.


35- Ogur G, Gül D, Ozen S, Imirzalioglu N, Cankus G, Tunca Y, Bahçe M, Güran S, Baser I. Application of the 'Apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: results of 30 pregnancies. Prenat Diagn. 1997 Sep;17(9):879-82.


36- Oğur G, Oğur E, Celasun B, Baser I, Imïrzalioğlu N, Oztürk T, Alemdaroğlu A. Prenatal diagnosis of autosomal recessive osteopetrosis, infantile type, by X-ray evaluation. Prenat Diagn. 1995 May;15(5):477-81.