1.Modulator Effects of the Methylenetetrahydrofolate Reductase C677T Polymorphism on Response to Vitamin B12 Therapy and Homocysteine Metabolism.

Sensoy N, Soysal Y, Kahraman A, Doğan N, İmirzalıoğlu N.

DNA Cell Biol. 2011 Nov, 15. [Epub ahead of print]

 

2.Molecular characterization of microduplication 22q11.2 in a girl with hypernasal speech.

Soysal Y, Vermeesch J, Davani NA, Şensoy N, Hekimler K, İmirzalıoğlu N.

Genet Mol Res. 2011 Sep, 21; 10(3): 2148-54.

 

3.Age-Related Macular Degeneration and Association of CFH Y402H and LOC387715 A69S Polymorphisms in a Turkish Population.

Soysal Y, İnan UU, Küsbeci T, İmirzalıoğlu N.

DNA Cell Biol. 2011 Jul, 26. [Epub ahead of print]

 

4.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.

Soysal Y, Vermeesch J, Davani NA, Hekimler K, İmirzalıoğlu N.

Am J Med Genet A. 2011 Jul; 155A(7): 1745-52. doi: 10.1002/ajmg.a.34101. Epub 2011 May, 27.

 

5.[Analysis of genetic penetrance in the pedigree of cases with Van der Woude syndrome: report of five cases].

Bozkurt M, Kapı E, Külahçı Y, Zor F, Benlier E, Balkan M, Kılınç N, İmirzalıoğlu N, Kuvat SV.

Kulak Burun Boğaz Ihtis Derg. 2010 Jul-Aug; 20(4): 200-4. Turkish.

 

6.Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy.

Soysal Y, Balci S, Hekimler K, Liehr T, Ewers E, Schoumans J, Bui TH, Içduygu FM, Kosyakova N, İmirzalıoğlu N.

Am J Med Genet A. 2009 Dec; 149A(12): 2782-7.

 

7.Surgery for acute abdomen and MEFV mutations in patients with FMF.

Samli H, Içduygu FM, Ozgöz A, Akbulut G, Hekimler K, İmirzalıoğlu N.

Acta Reumatol Port. 2009 Jul-Sep; 34(3): 520-4.

 

8.Analysis of PTEN gene mutations in a Turkish patient with Cowden syndrome.

Soysal Y, Tate G, Polat C, Polat N, Aktepe F, Sıvacı Y, İmirzalıoğlu N.

Genet Test Mol Biomarkers. 2009 Aug; 13(4): 547-51.

 

9.A patient with ascending aortic dilatation, similar to phenotypes of connective tissue disorders.

Onrat ST, Emmiler M, Sıvacı Y, Söylemez Z, Ozgöz A, İmirzalıoğlu N.

Genet Mol Res. 2009 Apr, 14; 8(2): 426-34.

 

10.Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I.

Karacay S, Saygun I, Tunca Y, İmirzalıoğlu N, Güvenç G.

J Indian Soc Pedod Prev Dent. 2007 Mar; 25(1): 43-5.

 

11.Familial secundum type atrial septal defect with normal karyotypes.

Büyükateş M, Turan SA, Altunkaya SA, İmirzalıoğlu N.

J Cardiovasc Surg (Torino). 2007 Apr; 48(2): 258. No abstract available.

 

in-6 levels in patients with Familial Mediterranean Fever.

Ozel AM, Demirtürk L, Aydoğdu A, Gültepe M, Yazgan Y, İmirzalıoğlu N, Gürbüz AK, Narin Y.

Int J Clin Pract. 2008 May; 62(5): 754-61. Epub 2007 Mar, 1.

 

13.Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD).

Samli H, Samli MM, Yılmaz E, İmirzalıoğlu N.

Arch Androl. 2006 Nov-Dec; 52(6): 471-7.

 

14.Investigating the in vitro effect of taurine on the infant lymphocytes by sister chromatid exchange.

Ergun MA, Soysal Y, Kısmet E, Akay C, Dündaröz R, İlhan M, İmirzalıoğlu N.

Pediatr Int. 2006 Jun; 48(3): 284-6.

 

15.Genetic anomalies detected in patients with non-obstructive azoospermia and oligozoospermia.

Samli H, Samli MM, Solak M, İmirzalıoğlu N.

Arch Androl. 2006 Jul-Aug; 52(4): 263-7.

 

16.The vitamin D receptor fokI start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism.

Bolu SE, Orkunoğlu Suer FE, Deniz F, Uçkaya G, İmirzalıoğlu N, Kutlu M.

J Endocrinol Invest. 2005 Oct; 28(9): 810-4.

 

17.The cell based dressing with living allogenic keratinocytes in the treatment of foot ulcers: a case study.

Bayram Y, Deveci M, İmirzalıoğlu N, Soysal Y, Şengezer M.

Br J Plast Surg. 2005 Oct; 58(7): 988-96.

 

18.MEFV gene is a probable susceptibility gene for Behçet’s disease.

İmirzalıoğlu N, Dursun A, Tastan B, Soysal Y, Yakicier MC.

Scand J Rheumatol. 2005; 34(1): 56-8.

 

19.HLA-DR B1 and DQ B1 polymorphisms in patients with coronary artery ectasia.

Akdemir R, Özhan H, Gündüz H, Erbilen E, Yazıcı M, Duran S, Orkunoğlu F, Albayrak S, İmirzalıoğlu N, Uyan C.

Acta Cardiol. 2004 Oct; 59(5): 499-502.

 

20.Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G.

Köseoğlu V, Kısmet E, Soysal Y, Ulucan H, Dündaröz R, İmirzalıoğlu N, Gökçay E.

Pediatr Int. 2004 Aug; 46(4): 415-8. Erratum in: Pediatr Int. 2004 Dec; 46(6): 756. İmirzalıoğlu, Necat [corrected to İmirzalıoğlu, Necat].

 

21.Complete atrioventricular block in Becker muscular dystrophy.

Akdemir R, Özhan H, Gündüz H, Yazıcı M, Erbilen E, Uyan C, İmirzalıoğlu N.

N Z Med J. 2004 May, 21; 117(1194): U895. No abstract available.

 

22.Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture.

Samli H, Solak M, İmirzalıoğlu N, Beyatlı Y, Şimşek S, Kahraman S.

Prenat Diagn. 2003 Oct; 23(10): 847-50.

 

23.Essential palatal myoclonus in monozygotic male twins.

Kütükçü Y, İmirzalıoğlu N, Odabaşı Z, Gökçil Z, Vural O.

J Neurol. 2003 Jul; 250(7): 885-6. No abstract available.

 

24.New heritable fragile site at 15q13 in both members of a non-consanguineous couple.

Karadeniz NN, Tunca Y, İmirzalıoğlu N.

Am J Med Genet A. 2003 Apr, 30; 118A(3): 290-2.

 

25.Ebstein’s anomaly in siblings: an original observation.

Uyan C, Yazıcı M, Uyan AP, Akdemir R, İmirzalıoğlu N, Dokumacı B.

Int J Cardiovasc Imaging. 2002 Dec; 18(6): 435-8.

 

26.Prolongation of skin xenograft survival with modified cultured fibroblasts.

Işık S, Er E, Soysal Y, İmirzalıoğlu N.

Plast Reconstr Surg. 2003 Jan; 111(1): 275-82; discussion 283-5.

 

27.The effects of folic acid application on IL-1beta levels of human gingival fibroblasts stimulated by phenytoin and TNFalpha in vitro: a preliminary study.

Doğan A, Tunca Y, Özdemir A, Şengül A, İmirzalıoğlu N.

J Oral Sci. 2001 Dec; 43(4): 255-60.

 

28.Relationship between granular cytoplasm of oocytes and pregnancy outcome following intracytoplasmic sperm injection.

Kahraman S, Yakın K, Dönmez E, Samli H, Bahçe M, Cengiz G, Sertyel S, Samli M, İmirzalıoğlu N.

Hum Reprod. 2000 Nov; 15(11): 2390-3.

 

29.Healthy births and ongoing pregnancies obtained by preimplantation genetic diagnosis in patients with advanced maternal age and recurrent implantation failure.

Kahraman S, Bahçe M, Samli H, İmirzalıoğlu N, Yakisn K, Cengiz G, Dönmez E.

Hum Reprod. 2000 Sep; 15(9): 2003-7.

 

30.Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.

Güran S, Tunca Y, İmirzalıoğlu N.

Cancer Genet Cytogenet. 1999 Sep; 113(2): 145-51.

 

31.Variable clinical expression of Holt-Oram syndrome in three generations.

Oğur G, Gül D, Lenk MK, İmirzalıoğlu N, Alpay F, Oğur E.

Turk J Pediatr. 1998 Oct-Dec; 40(4): 613-8.

 

32.Application of the ‘Apt test’ in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: results of 30 pregnancies.

Oğur G, Gül D, Özen S, İmirzalıoğlu N, Cankuş G, Tunca Y, Bahçe M, Güran S, Başer I.

Prenat Diagn. 1997 Sep; 17(9): 879-82.

 

33.Prenatal diagnosis of autosomal recessive osteopetrosis, infantile type, by X-ray evaluation.

Oğur G, Oğur E, Celasun B, Başer I, İmirzalıoğlu N, Öztürk T, Alemdaroğlu A.

Prenat Diagn. 1995 May; 15(5): 477-81.

 

34.Prenatal diagnosis of autosomal recessive osteopetrosis, infantile type, by X-ray evaluation.

Oğur G, Oğur E, Celasun B, Başer I, İmirzalıoğlu N, Öztürk T, Alemdaroğlu A. Prenat Diagn. 1995 May; 15(5): 477-81.

 

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