Prof. Dr. Tahsin Yakut hakkında bilgi ve randevu alabilir, hasta yorumlarını okuyabilir, doktorun uygun saatlerini görebilir ve online randevu alabilirsiniz.
Tıbbi İlgi Alanları
Klinik genetik
Düşük
Riskli gebelik
Tüp bebek
Kısırlık
Okullar / eğitimler
1989 - Uludağ Üniversitesi, Tıp Fakültesi - Tıp Eğitimi
2002 – Uludağ Üniversitesi Tıp Fakültesi - Tıbbi Genetik Bilim Dalı Uzmanlık Eğitimi
2006 - Uludağ Üniversitesi Tıp Fakültesi Tıbbi Genetik A.D.- Yrd. Doç. Dr.
2006 - Uludağ Üniversitesi Tıp Fakültesi Tıbbi Genetik A.D.- Doç. Dr.
2012 - Uludağ Üniversitesi Tıp Fakültesi Tıbbi Genetik A.D. - Prof. Dr.
Deneyimler
Uludağ Üniversitesi, Tıp Fakültesi, Tıbbi Genetik A.D
George-Agust Üniversity, Molecular Genetics Department
Innova Medicine - Sherr İnstitute, Amerika Birleşik Devletleri
Queen Elizabeth Hospital - MolecularCytogenetics Department, İngiltere
Özel Jimer Hastanesi
İstinye Üniversitesi Genetik Tanı Merkezi
BAU Medical Park Göztepe
1-Evaluation of relationship between chromosome 22 and p53 gene alterations and the subtype of meningiomas by the interphase-FISH technique.
Yakut T, Bekar A, Doygun M, Acar H, Egeli U, Ogul E.Teratog Carcinog Mutagen. 2002;22(3):217-25. doi: 10.1002/tcm.10013.PMID: 11948632
2-Comparison of genetic changes between interphase and metaphase nuclei in monitoring CML and APL treatment using DC-FISH technique.
Yakut T, Ali R, Egeli U, Ozkalemkas F, Ercan I, Ozçelik T, Ozkocaman V, Yigit B, Tunali A.Cancer Biol Ther. 2004 Sep;3(9):858-63. doi: 10.4161/cbt.3.9.1039. Epub 2004 Sep 18.PMID: 15254420
3-Investigation of c-myc and p53 gene alterations in the tumor and surgical borderline tissues of NSCLC and effects on clinicopathologic behavior: by the FISH technique.
Yakut T, Egeli U, Gebitekin C.Lung. 2003;181(5):245-58. doi: 10.1007/s00408-003-1026-x.PMID: 14705768
Cite
4-Toll-like receptor-9 gene polymorphism in common variable immunodeficiency.
Tanir S, Karkucak M, Yakut T, Kilic SS.J Investig Allergol Clin Immunol. 2010;20(3):267-8.PMID: 20635795 Free article. No abstract available.
5-Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mende-lian Neurologic Disease.
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, Isi-kay 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, Alika-şifoğlu M, Ture M, Yakut T, Overton JD, Yuksel A, Ozen M, Muzny DM, Adams DR, Boerwinkle E, Chung WK, Gibbs RA, Lupski JR.Neuron. 2015 Nov 4;88(3):499-513. doi: 10.1016/j.neuron.2015.09.048.PMID: 26539891 Free PMC article.
6-A fertile patient with 45X/47XXX mosaicism.
Sahinturk S, Ozemri Sag S, Ture M, Gorukmez O, Topak A, Yakut T, Gulten T.Genet Couns. 2015;26(1):29-34.PMID: 26043504
Cite
7-De novo partial trisomy distal 4q: a case report.
Gorukmez O, Sag SO, Gorukmez O, Ture M, Gulten T, Yakut T.Genet Couns. 2014;25(4):423-8.PMID: 25804022
8-MMP2 gene-735 C/T and MMP9 gene -1562 C/T polymorphisms in JAK2V617F positive mye-loproliferative disorders.
Sag SO, Gorukmez O, Ture M, Gorukmez O, Topak A, Sahinturk S, Ocakoglu G, Gulten T, Ali R, Yakut T.Asian Pac J Cancer Prev. 2015;16(2):443-9. doi: 10.7314/apjcp.2015.16.2.443.PMID: 25684469 Free article.
9-Dyskeratosis Congenita: A Case Report.
Ozemri Sag S, Topak A, Gorukmez O, Gorukmez O, Ture M, Carrillo J, Sahinturk S, Gulten T, Perona R, Yakut T.Genet Couns. 2016;27(2):263-7.PMID: 29485835 No abstract available.
10-Meiotic segregation analysis of reciprocal translocations both in sperms and blastomeres.
Yakut T, Ercelen N, Acar H, Kimya Y, Egeli U.Am J Med Genet A. 2006 May 15;140(10):1074-82. doi: 10.1002/ajmg.a.31215.PMID: 16596678
11-Association and Prognostic Significance of the Functional -1562C/T Polymorphism in the Promoter Region of MMP-9 in Turkish Patients with Gastric Cancer.
Avcı N, Ture M, Deligonul A, Cubukcu E, Olmez OF, Sahinturk S, Topak A, Kurt E, Evrensel T, Şahin AB, Yakut T.Pathol Oncol Res. 2015 Sep;21(4):1243-7. doi: 10.1007/s12253-015-9950-7. Epub 2015 Jul 9.PMID: 26156886
12-GSTT1 and GSTM1 gene polymorphisims in sarcoidosis.
Coskun F, Karkucak M, Yilmaz D, Yakut T, Uzaslan E.Sarcoidosis Vasc Diffuse Lung Dis. 2016 Oct 7;33(3):253-257.PMID: 27758991
13-Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation.
14-Investigation of MEFV gene polymorphisms (G138G and A165A) in adult patients with fami-lial Mediterranean fever.
Öksuz MF, Karkucak M, Görukmez O, Ocakoğlu G, Yıldız A, Ture M, Yakut T, Dilek K.Rev Bras Reumatol Engl Ed. 2017 Nov-Dec;57(6):501-506. doi: 10.1016/j.rbre.2016.02.004. Epub 2016 Mar 10.PMID: 29173686 Free article. English, Portuguese.
15-TURNER SYNDROME WITH 45,X/46,X,I(Xq)/47,X,I(Xq),I(Xq) KARYOTYPE.
Gorukmez O, Sag SO, Gulten T, Gorukmez, Ture M, Yakut T.Genet Couns. 2015;26(2):267-9.PMID: 26349201 No abstract available.
16-Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel synd-rome.
Eroğlu P, Erkol İnal E, Sağ ŞÖ, Görükmez Ö, Topak A, Yakut T.Clin Rheumatol. 2016 May;35(5):1245-51. doi: 10.1007/s10067-014-2855-0. Epub 2015 Jan 9.PMID: 25566970
17-Association of GSTM1, GSTT1, GSTP1-ILE105VAL and ACE I/D polymorphisms with ankylosing spondylitis.
18-Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis.
Ceylan E, Karkucak M, Coban H, Karadag M, Yakut T.J Infect Public Health. 2017 Nov-Dec;10(6):774-777. doi: 10.1016/j.jiph.2016.11.003. Epub 2017 Feb 8.PMID: 28189510 Free ar-ticle.
19-Association between the catechol-o-methyltransferase val158met polymorphism with sus-ceptibility and severity of carpal tunnel syndrome.
Erkol İnal E, Eroğlu P, Görükmez O, Özemri Sağ Ş, Yakut T.Balkan J Med Genet. 2016 Jul 9;18(2):43-48. doi: 10.1515/bjmg-2015-0085. eCollection 2015 Dec 1.PMID: 27785396 Free PMC article.
20-Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Pati-ents.
Gorukmez O, Yakut T, Gorukmez O, Sag SO, Karkucak M, Kanat O.Asian Pac J Cancer Prev. 2016;17(3):1175-9. doi: 10.7314/apjcp.2016.17.3.1175.PMID: 27039744 Free article.
21-CLINICAL EFFECT OF A MUTATION (p.Glu322Asp, c.966 G>T) IN PANK2 GENE IN A FAMILY WITH ATYPICAL PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION.
22-Glutathione S-transferase T1, M1 and P1 Genetic Polymorphisms and Susceptibility to Colo-rectal Cancer in Turkey.
Gorukmez O, Yakut T, Gorukmez O, Sag SO, Topak A, Sahinturk S, Kanat O.Asian Pac J Cancer Prev. 2016;17(8):3855-9.PMID: 27644629 Free article.
23-Glutathione S-Transferase M1 and T1 Gene Polymorphisms in Patients with Chronic Plaque-Type Psoriasis: A Case-Control Study.
Solak B, Karkucak M, Turan H, Ocakoğlu G, Özemri Sağ Ş, Uslu E, Yakut T, Erdem T.Med Princ Pract. 2016;25(2):155-8. doi: 10.1159/000442165. Epub 2015 Nov 4.PMID: 26535568 Free PMC article.
24Spectrum of EGFR gene mutations and ALK rearrangements in lung cancer patients in Turkey.
Sag SO, Gorukmez O, Ture M, Gorukmez O, Deligonul A, Sahinturk S, Topak A, Gulten T, Kurt E, Yakut T.Springerplus. 2016 Apr 19;5:482. doi: 10.1186/s40064-016-2150-4. eCollection 2016.PMID: 27217997 Free PMC article.
25-Oxytocin system social function impacts in children with attention-deficit/hyperactivity di-sorder.
Ayaz AB, Karkucak M, Ayaz M, Gokce S, Kayan E, Güler EE, Güngen BD, Kuşcu TD, Ocakoğlu G, Yakut T.Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):609-16. doi: 10.1002/ajmg.b.32343. Epub 2015 Jul 14.PMID: 26174935
26-The Effects of Bundles on Catheter-Associated Urinary Tract Infections in the Pediatric Inten-sive Care Unit.
33-Association of the ACE I/D gene polymorphisms with JAK2V617F-positive polycythemia vera and essential thrombocythemia.
Gorukmez O, Sag ŞO, Gorukmez Ö, Ture M, Topak A, Sahinturk S, Ozkaya G, Gulten T, Ali R, Yakut T.Genet Test Mol Biomarkers. 2015 Jun;19(6):303-8. doi: 10.1089/gtmb.2014.0334. Epub 2015 May 8.PMID: 25955555
34-Does MBL2 codon 54 polymorphism play a role in the pathogenesis of psoriasis?
Turan H, Karkucak M, Yakut T, Ozsahin M, Gurlevik Z, Yanik ME, Ucgun T, Aliagaoglu C, Yaykasli KO.Int J Dermatol. 2014 Jan;53(1):34-8. doi: 10.1111/j.1365-4632.2012.5657.x. Epub 2012 Nov 1.PMID: 23113841
35-Association between p16(CDKN2A) C540G polymorphism and tumor behavior in prolactino-ma: A single-center study.
Cander S, Karkucak M, Gul OO, Sag SO, Yakut T, Ersoy C, Tuncel E, Erturk E.Biomed Rep. 2014 Jul;2(4):589-595. doi: 10.3892/br.2014.281. Epub 2014 May 19.PMID: 24944814 Free PMC ar-ticle.
36-Esophageal muscle cell interaction with biopolymers.
Korkmaz M, Yakut T, Narci A, Güvenç BH, Güilten T, Yağmurca M, Yiğit B, Bilir A.Med Sci Mo-nit. 2007 Feb;13(2):BR46-9.PMID: 17261980
37-A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
38-Effect of cyclin [corrected] D1 (CCND1) gene polymorphism on tumor formation and beha-vior in patients with prolactinoma.
Cander S, Ertürk E, Karkucak M, Oz Gül O, Görükmez O, Yakut T, Unal OK, Ersoy C, Tuncel E, Imamoğlu S.Gene. 2012 Nov 1;509(1):158-63. doi: 10.1016/j.gene.2012.07.056. Epub 2012 Aug 8.PMID: 22967707
39-Cathecol-O-methyl transferase Val158Met genotype is not a risk factor for conversion disor-der.
Armagan E, Almacıoglu ML, Yakut T, Köse A, Karkucak M, Köksal O, Görükmez O.Genet Mol Res. 2013 Mar 19;12(1):852-8. doi: 10.4238/2013.March.19.1.PMID: 23613193 Free article.
40-Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malforma-tions.
Rainger J, Pehlivan D, Johansson S, Bengani H, Sanchez-Pulido L, Williamson KA, Ture M, Barker H, Rosendahl K, Spranger J, Horn D, Meynert A, Floyd JA, Prescott T, Anderson CA, Rainger JK, Karaca E, Gonzaga-Jauregui C, Jhangiani S, Muzny DM, Seawright A, Soares DC, Kharbanda M, Murday V, Finch A; UK10K; Baylor-Hopkins Center for Mendelian Genomics, Gibbs RA, van Hey-ningen V, Taylor MS, Yakut T, Knappskog PM, Hurles ME, Ponting CP, Lupski JR, Houge G, Fitz-Patrick DR.Am J Hum Genet. 2014 Jun 5;94(6):915-23. doi: 10.1016/j.ajhg.2014.05.005.PMID: 24906020 Free PMC article.
41-Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods.
Ozemri Sag S, Yakut T, Gorukmez O, Gorukmez O, Ture M, Karkucak M, Gulten T, Ali R.Genet Test Mol Biomarkers. 2015 Oct;19(10):584-8. doi: 10.1089/gtmb.2015.0056. Epub 2015 Aug 26.PMID: 26308792
42-ACE gene I/D polymorphism and risk of sarcoidosis development in Turkish patients.
43-Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential throm-bocythemia and polycythemia vera.
Karkucak M, Yakut T, Ozkocaman V, Ozkalemkas F, Ali R, Bayram M, Gorukmez O, Ocakoglu G.Mol Biol Rep. 2012 Sep;39(9):8663-7. doi: 10.1007/s11033-012-1721-x. Epub 2012 Jun 22.PMID: 22722988
44-A novel mutation in the FRAS1 gene in a patient with Fraser syndrome.
Ozemri Sag S, Gorukmez O, Gorukmez O, Ture M, Sahinturk S, Topak A, Gulten T, Schanze D, Yakut T, Zenker M.Genet Couns. 2015;26(1):21-7.PMID: 26043503
45-A RARE COMBINATION OF 45,X/46,XY MOSAICISM AND Y CHROMOSOME MICRODELETION IN AN INFERTILE MAN WITH AZOOSPERMIA.
Aydemir H, Karkucak M, Cimen HI, Halis F, Kumsar S, Sonbahar AE, Yakut T.Genet Couns. 2016;27(1):95-8.PMID: 27192898 No abstract available.
46-An Unusual Case of LCHAD Deficiency Presenting With a Clinical Picture of Hemophagocytic Lymphohistiocytosis: Secondary HLH or Coincidence?
47-Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroi-dism.
Cangul H, Morgan NV, Forman JR, Saglam H, Aycan Z, Yakut T, Gulten T, Tarim O, Bober E, Ce-sur Y, Kirby GA, Pasha S, Karkucak M, Eren E, Cetinkaya S, Bas V, Demir K, Yuca SA, Meyer E, Kendall M, Hogler W, Barrett TG, Maher ER.Clin Endocrinol (Oxf). 2010 Nov;73(5):671-7. doi: 10.1111/j.1365-2265.2010.03849.x.PMID: 20718767
48-A NOVEL MUTATION IN NPR2 GENE IN A PATIENT WITH ACROMESOMELIC DYSPLASIA, MA-ROTEAUX TYPE.
Sag SO, Gorukmez O, Topak A, Gorukmez O, Ture M, Sahinturk S, Gulten T, Yakut T.Genet Co-uns. 2015;26(2):219-25.PMID: 26349192
49-Glutathione s-transferase m1 and t1 gene polymorphisms are not associated with increased risk of gestational diabetes mellitus development.
Orhan O, Atalay MA, Orhan F, Karkucak M, Centinkaya Demir B, Yakut T, Cengiz C.West Indian Med J. 2014 Aug;63(4):300-6. doi: 10.7727/wimj.2013.128. Epub 2014 May 15.PMID: 25429472 Free PMC article.
50-Investigation of TNF-alpha gene (G308A) and GSTP1 gene (Ilel05Val) polymorphisms in Tur-kish patients with retinopathy of prematurity.
Türe M, Yildiz M, Karkucak M, Gülten ET, Siğirli D, Özmen AT, Yakut T.Turk J Med Sci. 2015;45(1):164-9. doi: 10.3906/sag-1307-94.PMID: 25790547 Free article.
51-Vitamin a deficiency in patients with common variable immunodeficiency.
52-Comparison of aneuploidy frequencies between in vitro matured and unstimulated cycles oocytes by metaphase comparative genomic hybridization (mCGH).
Yakut T, Karkucak M, Sher G, Keskintepe L.Mol Biol Rep. 2012 May;39(5):6187-91. doi: 10.1007/s11033-011-1436-4. Epub 2011 Dec 30.PMID: 22207182
53-MULTIPLE CONGENITAL ANOMALIES IN A CHILD WITH 47,XY,+der(8;9)(p10;p10): A CASE REPORT.
Gorukmez O, Gorukmez O, Sag OS, Yakut T, Gulten T.Genet Couns. 2015;26(2):163-9.PMID: 26349185
54-Polymorphisms of glutathione-s-transferase M1, T1, and P1 genes in endometrial carcino-ma.
Ozerkan K, Atalay MA, Yakut T, Doster Y, Yilmaz E, Karkucak M.Eur J Gynaecol Oncol. 2013;34(1):42-7.PMID: 23589999
55-FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.
Yakut T, Kilic SS, Cil E, Yapici E, Egeli U.Pediatr Surg Int. 2006 Apr;22(4):380-3. doi: 10.1007/s00383-006-1641-8. Epub 2006 Feb 4.PMID: 16463032
56-GST (GSTM1, GSTT1, and GSTP1) polymorphisms in the genetic susceptibility of Turkish pati-ents to cervical cancer.
57-Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Mul-tiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome.
Karkucak M, Bülbül EB, Turan H, Yakut T, Toka S, Sarıcaoğlu H.Balkan Med J. 2012 Sep;29(3):310-3. doi: 10.5152/balkanmedj.2012.018. Epub 2012 Sep 1.PMID: 25207021 Free PMC article.
58-Investigation of ABCB1 gene polymorphism with colchicine response in Behçet's disease.
Saricaoglu H, Yilmaz M, Karkucak M, Ozturk HZ, Yakut T, Gulten T, Baskan EB, Aydogan K, Dilek K.Genet Mol Res. 2011 Jan 4;10(1):1-6. doi: 10.4238/vol10-1gmr824.PMID: 21218380 Free ar-ticle.
59-The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels.
Sogutlu Sari E, Yazici A, Eser B, Erol MK, Kilic A, Ermis SS, Koytak A, Akşit H, Yakut T.Cutan Ocul Toxicol. 2014 Dec;33(4):270-4. doi: 10.3109/15569527.2013.854372. Epub 2014 Jan 22.PMID: 24446892
60-Assessment of molecular events in squamous and non-squamous cell lung carcinoma.
Yakut T, Schulten HJ, Demir A, Frank D, Danner B, Egeli U, Gebitekin C, Kahler E, Gunawan B, Urer N, Oztürk H, Füzesi L.Lung Cancer. 2006 Dec;54(3):293-301. doi: 10.1016/j.lungcan.2006.08.011. Epub 2006 Sep 29.PMID: 17011066
61-Frequency of recombinant and nonrecombinant products of pericentric inversion of chromo-some 1 in sperm nuclei of carrier: by FISH technique.
Yakut T, Acar H, Egeli U, Kimya Y.Mol Reprod Dev. 2003 Sep;66(1):67-71. doi: 10.1002/mrd.10325.PMID: 12874801
62-Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures.
Yildiz M, Karkucak M, Yakut T, Gorukmez O, Ozmen A.Genet Mol Res. 2010 Oct 26;9(4):2131-9. doi: 10.4238/vol9-4gmr887.PMID: 21038299 Free article.
63-Effect of Pressure Injury Prevention Guides Used In a Pediatric Intensive Care.
64-NOVEL MUTATION OF THE ELECTRON TRANSFERRING FLAVOPROTEIN DEHYDROGENASE (ETFDH) GENE IN THE ISOLATED MYOPATHIC FORM OF COENZYME q10 DEFICIENCY.
Gorukmez O, Gorukmez O, Sag SO, Erdol S, Saglam H, Yakut T.Genet Couns. 2015;26(2):259-62.PMID: 26349199 No abstract available.
Polymorphisms in angiotensin-converting enzyme and glutathione s-transferase genes in Tur-kish population and risk for preeclampsia.
Atalay MA, Ozerkan K, Karkucak M, Yakut T, Atik Y, Develioglu OH.Clin Exp Obstet Gynecol. 2012;39(4):466-9.
65-Recurrence of Oligodendroglioma Remote From the Original Site: A Case ReportKocaeli H, Yakut T, Bekar A, Taşkapilioğlu O, Tolunay S.Surg Neurol. 2006 Dec;66(6):627-30; discussion 630-1. doi: 10.1016/j.surneu.2006.02.049. Epub 2006 Oct . 6.PMID: 17145331
66-Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome.
Turan H, Bulbul Baskan E, Yakut T, Karkucak M, Tunali S, Saricaoglu H.Bratisl Lek Listy. 2011;112(5):260-3.PMID: 21682079
67-Correlation of chromosomal imbalances by comparative genomic hybridization and expres-sion of EGFR, PTEN, p53, and MIB-1 in diffuse gliomas.
Yakut T, Gutenberg A, Bekar A, Egeli U, Gunawan B, Ercan I, Tolunay S, Doygun M, Schulten HJ.Oncol Rep. 2007 May;17(5):1037-43.PMID: 17390041
68-Oocyte karyotyping by comparative genomic hybridization [correction of hybrydization] pro-vides a highly reliable method for selecting "competent" embryos, markedly improving in vitro fertilization outcome: a multiphase study.
69-Sher G, Keskintepe L, Keskintepe M, Ginsburg M, Maassarani G, Yakut T, Baltaci V, Kotze D, Unsal E.Fertil Steril. 2007 May;87(5):1033-40. doi: 10.1016/j.fertnstert.2006.08.108. Epub 2007 Jan 29.PMID: 17258713
70-Pregnancy under treatment of imatinib and successful labor in a patient with chronic mye-logenous leukemia (CML). Outcome of discontinuation of imatinib therapy after achieving a molecular remission.
Ali R, Ozkalemkaş F, Ozçelik T, Ozkocaman V, Ozan U, Kimya Y, Köksal N, Gülten T, Yakut T, Tu-nali A.Leuk Res. 2005 Aug;29(8):971-3. doi: 10.1016/j.leukres.2005.01.009. Epub 2005 Feb 16.PMID: 15978950
71-Cytogenetic results of amniocentesis materials: incidence of abnormal karyotypes in the Turkish collaborative study.
Karaoguz MY, Bal F, Yakut T, Ercelen NO, Ergun MA, Gokcen AB, Biri AA, Kimya Y, Urman B, Gultomruk M, Egeli U, Menevse S.Genet Couns. 2006;17(2):219-30.PMID: 16970041 Clinical Trial.
72-Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mu-tation at the SOX9 locus.
Temel SG, Gulten T, Yakut T, Saglam H, Kilic N, Bausch E, Jin WJ, Leipoldt M, Scherer G.Sex Dev. 2007;1(1):24-34. doi: 10.1159/000096236.PMID: 18391513 Free article.
73-Sudden blastic crisis and additional chromosomal abnormalities during chronic myeloid leu-kemia in the imatinib era.
Ali R, Ozkalemkas F, Ozkocaman V, Yakut T, Nazlioglu HO, Budak F, Pekgoz M, Korkmaz S, Kar-kucak M, Ozcelik T, Tunali A.Int J Clin Oncol. 2009 Dec;14(6):545-50. doi: 10.1007/s10147-009-0884-5. Epub 2009 Dec 5.PMID: 19967494
74-Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y, Yakut T, Egelí U, Ozerkan K.Prenat Diagn. 2002 Nov;22(11):957-61. doi: 10.1002/pd.403.PMID: 12424755
75-Another small supernumerary marker chromosome derived from chromosome 9 in a Kline-felter patient.
Gulten T, Gorukmez O, Gorukmez O, Karkucak M, Ture M, Yakut T.West Indian Med J. 2012 Dec;61(9):924-7. doi: 10.7727/wimj.2012.027.PMID: 24020236
76-Low frequency of p53 and k-ras codon 12 mutations in non-small cell lung carcinoma (NSCLC) tumors and surgical margins.
Vatan O, Bilaloglu R, Tunca B, Cecener G, Gebitekin C, Egeli U, Yakut T, Urer N.Tumori. 2007 Sep-Oct;93(5):473-7.PMID: 18038880
77-Impact of concomitant obstructive sleep apnea on pulmonary involvement and main pulmo-nary artery diameter in adults with scleroderma.
78-Determination of allelic deletion of multiple endocrine neoplasm type 1 (MEN1) gene in acute myeloid leukemia (AML) by application of FISH-TSA technique.
Acar H, Kaynak M, Yakut T, Uçar F, Egeli U.Teratog Carcinog Mutagen. 2002;22(5):369-75. doi: 10.1002/tcm.10033.PMID: 12210500
79-Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene.
Cangül H, Ozdemir O, Yakut T, Okan M, Morgan NV, Baytan B, Kurian MA, Spiegel R, Maher ER.Turk J Pediatr. 2009 Mar-Apr;51(2):161-5.PMID: 19480328
80-Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients.
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