Prof. Dr. Ajlan Tükün

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Prof. Dr. Ajlan Tükün

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SCI Kapsamındaki Dergilerde Yayınlanan Eserler

Hazan F, Gürsoy S, Unalp A, Yılmaz U, Demirağ B, Aydin Köker S, Ozyılmaz B, Erdogan KM, Kalenderer Ö, Erkuş S, Gürçınar M, Tükün A. Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants. Neurol Sci 2021 Jan 14. doi: 10.1007/s10072-020-04988-0. Online ahead of print
Gürsoy S, Hazan F, Kaderli B, Meşe T, Tükün A. Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric Study. J Clin Pediatr Dent. 2020 Aug 1;44(4):262-267.
Çevik B, Mance Calisir O, Atbaşoğlu C, Saka MC, Alptekin K, Ucok A, Sırmatel B, Guloksuz S, Tükün A, van Os J, Gümüş Akay G. Liability to psychosis and childhood adversities are associated with shorter telomere length: Study on schizophrenia patients, unaffected siblings and non-clinical controls. Journal of Psychiatric Research 2019 Apr;111:169-185.
Eren-Keleş E, Karabulut HG, Çakmaklı HF, Adaklı B, Köse SK, Uğur-Dinçaslan H, Yavuz G, Ertem M, Tükün A. Expression of survivin and its splice variants in pediatric acute lymphoblastic leukemia. Leukemia Research. Genet Test Mol Biomarkers. 2018 Nov 29. doi: 10.1089/gtmb.
Yararbaş K, Tükün A: Frequency of Anaplastic Lymphoma Kinase (ALK) Rearrangement in Turkish Patients with Non-small Cell Lung Carcinoma Int J Hum Genet 2018 Mar; 18(1): 1-6
Tunç S, Demir K, Tükün FA, Topal C, Hazan F, Sağlam B, Nalbantoğlu Ö, Yıldız M, Özkan B. Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents. J Clin Res Pediatr Endocrinol. 2017 Sep 1;9(3):216-221.
Kaymak-Cihan M, Karabulut HG, Yürür-Kutlay N, Ilgın-Ruhi H, Tükün A, Olcay L. Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment. Turk J Haematol 2017 Jun; 5;34(2):151-158..
Altıner Ş, Karabulut HG, Yararbaş K, Tükün A, Collet C, Kocaay P, Berberoğlu M, Ilgın-Ruhi H: A Novel TWIST1 Gene Mutation in a Patient with Saethre – Chotzen Syndrome. Clin Dysmorphol. 2017 Jul; 26(3):175-178.
Hazan F, Korkmaz HA, Yararbaş K, Wuyts W, Tükün A: Trichorhinophalangeal syndrome type II presenting with short stature in a child. Arch Argent Pediatr. 2016 Dec 1;114(6):e403-e407
Kutlay NY, Pekpak E, Altıner Ş, İleri T, Vicdan AN, Dinçaslan H, İnce EU, Tukun FA. Prognostic impact of RUNX1 and ETV6 gene copy number on pediatric B-cell precursor acute lymphoblastic leukemia with or without hyperdiploidy. Int J Hematol. 2016 Sep;104(3):368-77
Durmaz CD, Yararbaş K, Yürür-Kutlay N, Türedi Ö, Akın İ, Karataş G, Gürbüz C, Tükün A. Unusual chromosomal rearrangement resulted in interstitial monosomy 9p: case report. Cytogenet Genome Res. 2016;148(1):19-24.
Atik T, Aykut A, Hazan F, Onay H, Gökşen D, Darcan Ş, Tükün A, Özkınay F: Mutational Analysis of the PTPN11 Gene in Turkish Patient with Noonan Syndrome. Indian J Pediatr. 2016 Jun; 83(6):517-21.
Delil K, Karabulut HG, Hacıhamdioğlu B, Şıklar Z, Berberoğlu M, Öçal G, Tükün A, Ilgın Ruhi H. Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature. J Clin Res Pediatr Endocrinol. 2016 Jun 5; 8(2):144-9.
Diniz G, Tekgül H, Hazan F, Yararbas K, Tukun A: Sarcolemmal Deficiency Of Sarcoglycan Complex In An 18-Month-Old Turkish Boy With A Large Deletion In The Beta Sarcoglycan Gene. Balkan J Med Genet. 2016 Jul 9;18(2):71-76.
Seval M, Karabulut HG, Tükün A, Koç A: Cell free fetal DNA in the plasma of pregnant women with preeclampsia. Clinical and Experimental Obstetrics & Gynecology – CEOG 2015, 42 (6):787-91.
Topcu V, Ilgin-Ruhi H, Siklar Z, Karabulut HG, Berberoglu M, Hacihamdioglu B, Savas-Erdeve S, Aycan Z, Peltek-Kendirci HN, Ocal G, Tukun FA. Investigation of Androgen Receptor Gene mutations in a Series of 21 Patients with 46,XY Disorders of Sex Development. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1257-63.
Ekinci S, Ilgın-Ruhi H, Doğan M, Gürsoy S, Sak SD, Demirkazık A, Tükün A. Molecular Spectrum of PIK3CA Gene Mutations in Patients with Non-Small Cell Lung Cancer in Turkey. Genet Test Mol Biomarkers. 2015 Jul;19(7):353-8.
Borman P, Taşbaş O, Gürhan Karabulut H, Tükün A, Yorgancıoğlu R.Thymidylate synthase genetic polymorphism and plasma total homocysteine level in a group of Turkish patients with rheumatoid arthritis: relationship with disease activity and methotrexate toxicity. Rev Bras Reumatol. 2015 Nov-Dec;55(6):485-92.
Ocal G, Berberoğlu M, Sıklar Z, Aycan Z, Hacıhamdioglu B, Erdeve SS, Camtosun E, Kocaay P, Ruhi HI, Kılıç BG, Tukun A. Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification. J Pediatr Adolesc Gynecol. 2015 Feb;28(1):6-11
Kaymak-Cihan M, Tükün A, Kuşkonmaz B, Arıbaş B, Kuzu I, Dizbay-Sak S,Terzi N, Paç A, Arıyürek M, Olcay L: Chronic Eosinophilic Leukemia With Monosomy 8in A Five Years Old Girl: A Rare Case. The Turkish Journal of Pediatrics 2014; 55:444-451.
Diniz G, Tosun Yildirim H, Akıncı G, Hazan F, Öztürk A, Yararbas K, Tukun A:Sarcolemmal Alpha And Gamma Sarcoglycan Protein Deficiencies In Turkish Siblings With A Novel Missense Mutation In The Alpha Sarcoglycan Gene.Pediatric Neurology 2014; 50(6):640-7.
Doğan M, Demirkazık A, Tükün A, Sak SD, Ceyhan K, Yalçın B, Akbulut H, İçli F. The Relationship Between Common EGFR, BRAF, KRAS Mutations and Prognosis in Advanced Stage Non-Small Cell Lung Cancer with Response to the Treatment in Turkey. UHOD 2014;24(1):1-10.
Topçu V, Ruhi HI, Kutlay NY, Ekici C, Vicdan A, Tukun A: Pure partial trisomy 4q syndrome in a child with der(9)ins(9;4)(q34.3;q26q35.2)mat. Genet Couns.2014;25(1):1-6.
Hazan F, Güzel O, Celegen M, Tukun A: Genetic Approach To The Patient And The Family: A Rett Syndrome Case With R270X Mutation In MECP2 Gene. Turk J Biochem. 2013; 38 (1) ; 109–113.
Sancak S, Altun H, Aydın H, Tukun A, Mantoğlu B, Okuducu M, Onur E, Başkent A, Karip AB, Memişoğlu K. Bilateral Adrenal Myelolipoma in a Female Pseudohermaphroditism with Congenital Adrenal Hyperplasia (CAH) of 21-hydroxylase Deficiency (21-OHD) Acta Endocrinologica-Bucharest. 2013;9(1):109-119.
Akyay A, Celkan T, Öztürkmen S, Bıçakçı Z, Tavil B, İskender G, Tükün A, Ogan C, Olcay L: Two Acute Myeloblastic Leukemia Cases Concomitant with Hemophagocytic Lymphohistiocytosis and Review of the Literature. Ann Clin Lab Sci. 2013;43(1):85-90.
Okten G, Gunes S, Onat OE, Tukun A, Ozcelik T, Kocak I.Disruption of HDX gene in premature ovarian failure. Syst Biol Reprod Med. 2013 Feb 26. [Epub ahead of print]
Hazan F, Ozturk T, Adibelli H, Unal N, Tukun A: Anovel mutation in PAX3 in eight members of a Turkish family with Waardenburg syndrome type 1.Mol Vis. 2013;19:196-202.
Atbasoglu EC, Sakarya D, Gümüş-Akay G, Sakarya A,Tukun A: Fragile X Premutation In Adult Psychiatry: Four Cases And Overview Of Clinical Presentation.Turk Psikiyatri Derg. 2013 Spring;24(1):63-7.
Korkmaz HA, Hazan F, Dizdarer C, Tükün A: Hypochondroplasia in A Child with 1620C>G (Asn540Lys) Mutation in FGFR3. J Clin Res Pediatr Endocrinol. 2012; 4(4):220-2.
Németh S, Riedl S, Kriegshäuser G, Baumgartner-Parzer S, Concolino P, Neocleous V, Phylactou LA, Borucka-Mankiewicz M, Onay H, TukunA, Oberkanins C.Reverse-hybridization assay for the rapid detection of common CYP21A2 mutations in dried blood spots from newborns with elevated 17-OH progesterone. Clinica Chimica Acta 2012;414:211-214.
Yürür-Kutlay N, Tukun A: Which is more effected on the leukomogenesis in Ph positive leukemias: Fusion or cell type? Turk J Biochem. 2012;37(2);181–187
Tos T, Karaman A, Aksoy A, Tukun A. Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patients. Genet Couns. 2012;23(2):289-96.
Doğan M, Karabulut HG, Tükün A, Demirkazık A, Özal G, Utkan G, Yalçın B, Dinçol D, Akbulut H, İçli F. The Relationship between antimetabolite toxicity and pharmacogenetics in Turkish cancer patients. Asian Pac J Cancer Prev. 2012;13(4):1553-6
Ekiz F, Ormeci N, Coban S, Karabulut HG, Aktas B, Tukun A, Tuncali T, Yüksel O, Alkış N. Association of methylenetetrahydrofolate reductase C677T-A1298C polymorphisms with risk for esophageal adenocarcinoma, Barrett's esophagus, and reflux esophagitis. Dis Esophagus.2012 Jul;25(5):437-41.
Ocal G, Berberoglu M, Siklar Z, Ertosun E, Erdeve Ş, Hacıhamdioğlu B, Ilgın-Ruhi H, Tukun A: The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD? .Eur J Pediatr. 2012:171(10):1497-1502
Taşbaş O, Borman P, Gürhan Karabulut H, Tükün A, Yorgancıoğlu R. The Frequency of A1298C and C677T Polymorphisms of the Methylentetrahydrofolate Gene in Turkish Patients with Rheumatoid Arthritis: Relationship with Methotrexate Toxicity. Open Rheumatol J. 2011;5:30-5
Savas-Erdeve S, Berberoglu M, Yurur-Kutlay N, Siklar Z, Hacıhamdioğlu B, Tukun A, Ocal G: Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche. J Pediatr Endocrinol Metab.2011;24(11-12):965-70.
Tos T, Karaman A, Aycan Z, Tükün A.: A rare case of monosomy 18p: translocation between chromosomes 18 and 21. Genet Couns. 2011; 22(2):227-31.
Akalın İ, Koca E, Karabulut HG, Haznedaroğlu İC, Çetiner D, Hayran M, Onal IK, Özcebe Oİ, Tükün A:Angiotensin Converting Enzyme Insertion/Deletion Gene Polymorphisms in Leukemic Hematopoiesis. International Journal of Hematology and Oncology 2011; 21(1): 1-9.
Tecder Ünal M, Karabulut H, Gümüş-Akay G, Dölen Y, Elhan A, Tükün A, Ünal AE:Endothelial nitric oxide synthase gene polymorphism in gastric cancer. Turk J Gastroenterol 2010; 21 (4): 338-344
Tükün A, Koca E, Akalın İ, Çetiner D, Tuncali T, Kutlay N, Karabulut H, Özcebe O, Haznedaroğlu İ: Sudden Blastic Transformation During Cytogenetic Remission Of Imatinib Treated Chronic Myeloid Leukemia. Clinical Genetics 2010, 78(suppl1):3-6.
Demirkazık A, Tukun A: Individualized Therapy in Cancer: Why Pharmacogenetics? J Med Sci 2010;30(Suppl 1):S1-S4
Akyay A, Olcay L, Kuzu I, Bozdoğan N, Unal-İnce E, Ileri T, Tükün A, Yürür-Kutlay N. A Child With Myelodysplastic Syndrome With Hypocellular Fibrosis. J Pediatr Hematol Oncol. 2010,32(8):617-20
Ocal G, Berberoglu M, Siklar Z, Bilir P, Uslu R, Yagmurlu A, Tükün A, Akar N, Soygur T, Gultan S, Tonyukuk Gedik V: Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University. J Pediatr Endocrinol Metab. 2010, 23:1123-32.
Sagnak L, Ersoy H, Ozok U, Eraslan A, Yararbas K, Goktug G, Tukun A: Clinical research The significance of Y chromosome microdeletion analysis in subfertile men with clinical variocele. Arch Med Sci 2010; 6, 3: 382-387.
Unal S, Cetin M, Kutlay NY, Elmas SA, Gumruk F, Tukun A, Tuncer M, Gurgey A.Hemophagocytosis Associated with Leukemia: a striking association with Juvenile Myelomonocytic Leukemia. Annals of Hematology Ann Hematol. 2010; 89(4):359-64,
Polat O, Polat G, Karahüseyinoğlu S, Kutlay NY, Taşcı AG, Erdemli E, Tükün A, Avunduk MC, Kuplulu S, Demirtaş M: Bone Fracture Healing with Umbilicoplacental Mononuclear Cells: A controlled animal study. European Journal of Trauma and Emergency Surgery, 2010;36(1):60-66
Yakut S, Cetin Z, Simsek M, Karauzum Sb, Tukun A, Luleci G: Prenatal Diagnosis Of A De Novo Supernumerary Marker Chromosome Originated From Chromosome 16. Genetic Counseling 2009, 20(4):327-32
Gümüş-Akay G, Ünal AE, Elhan AH, Bayar S, Karadayı K, Sunguroğlu A, Kadıkıran A, Tükün A: DNA Copy Number Changes in Gastric Adenocarcinomas: High Resolutione Comparative Genomic Hybridization Study in Turkey. Archives of Medical Research 2009;Oct;40(7):551-560
Gümüş-Akay G, Elhan AH, Ünal AE, Demirkazık A, Sunguroğlu A, Tükün A: Effects of Genomic Imbalances on Telomerase Activity in Gastric Cancer: Clues to Telomerase Regulation. Oncol Res. 2009;17(10):455-62.
Sayıtoglu M, Haznedaroğu IC, Hatırnaz O, Erbılgın Y, Aksu S, Koca E, Adıguzel C, Bayık M, Akalın I, Gülbas Z, Akay M, Unal A, Kaynar L, Ovalı E, Yılmaz M, Yenerel M, Dagdas S, Ozet G, Ar C, Aydın Y, Soysal T, Durgun B, Ozcebe O, Tukun A, Ilhan O, Ozbek U: Effects of Imatinib Mesylate on Renin–Angiotensin System (RAS) Activity During the Clinical Course of Chronic Myeloid Leukaemia. The Journal of International Medical Research 2009, 37:1018-28.
Sadeghi F, Yurur-Kutlay N, Berberoglu M, Cetinkaya E, Aycan Z, Kara C, Ilgin Ruhi H, Ocal G, Siklar Z, Elhan A, Tukun A.Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in Turkey.J Pediatr Endocrinol Metab. 2008 Aug;21(8):781-7
Siklar Z, Berberoglu M, Adiyaman P, Salih M, Tukun A, Cetinkaya E, Aycan Z, Evliyaoglu O, Ergur AT, Ocal G. Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum. Pediatr Endocrinol Rev. 2007 Mar;4(3):210-7
Aydos S, Tukun A: Does telomere length affect blood pressure? Adv Therapy 2007 Mar-Apr;24(2):269-72
Gümüş-Akay G, Ünal AE, Bayar S, Karadayı K, Elhan AH, Sunguroğlu A, Tükün A: Telomerase activity could be used as a marker for neoplastic transformation in gastric adenocarcinoma: but it has not a prognostic significance Genetics and Molecular Research Genet Mol Res. 2007 Feb 15;6(1):41-9.
Sivaslı E, Yurdakök M, Babaoğlu E, Karabulut HG, Yiğt Ş, Babaoğlu M, Tekinalp G, Tukun A: ACE gene deletion/deletion polymorphism may be a protective factor for respiratory distress in preterm infants. The Turkish Journal of Pediatrics 2007; 49:69-74.
Çabuk F, Karabulut HG, Tuncali T, Karademir S, Bozdayi M, Tukun A: TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy. The Turkish Journal of Pediatrics 2007; 49:61-8.
Akalin İ, Yurur Kutlay N, İlhan O, Tukun A:Novel chromosomal translocations in multiple myeloma: t(13;16)(q14;q24) and t(1;15)(q10;q26) Int Jnl Lab Hem. 2007 29:1-6
Karahuseyinoglu S, Cinar O, Kilic E, Kara F, Gumus Akay G, Ozel Demiralp D, Tukun A, Uckan D, Can A. Biology of the Stem Cells in Human Umbilical Cord Stroma: In situ and in vitro Surveys. Stem Cells. 2007 Feb;25(2):319-31
Aydos SE, Tukun A. Infertility in a man with oligoasthenoteratozoospermia associated with nonrobertsonian translocation t(9;15)(p10;q10). Fertil Steril. 2006 Oct;86(4):1001.e7-9.
Akalin İ, Yararbas K, Akgul N, Babaoglu E, Gumus Akay G, Dyer S, Yurur Kutlay N, Ilgin Ruhi H, Kog G, Tukun A: del5p/dup5q in a 'Cri du Chat' patient without parental chromosomal rearrangement. Am J Med Genet A. 2006 Apr 17;140A(9):1016-1020
Turhan N, Yürür-Kutlay N, Topcuoglu P, Saykı M, Yüksel M, Gürman G,Tükün A: Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4. Leukemia Research 2006 30(7):903-905
Aydos SE, Tükün A: Analysis of the factors that are thought to have an effect on reproductive life span. Proceedings of the 13th World Congress on In Vitro Fertilization, Assisted Reproduction & Genetics; 91-94, 2005
Akalin I, Senses DA, Ilgin-Ruhi H, Misirlioglu E, Yalçiner M, Çetinkaya E, Fryns JP, Tükün A.: A novel Fryns ‘anophthalmia-plus’ syndrome associated with (concomitant) primary hypothyrodism. Genet Counsel 16(2): 145-8 ,2005.
Aydos SE, Elhan A, Tükün A: Is telomere length one of the determinants of reproductive lifespan? Archives of Gynecology and Obstetrics 272(2):113-6, 2005.
Ilgin-Ruhi H, Yürür-Kutlay N, Tükün A, Bökesoy I: The role of genetic counceling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey. Eur J Med Genet. 48(1): 13-19, 2005
Idilman R, Erden E, Kuzu I, Ersöz S, Karasu Z, Karayalçin K, Yüce G, Tokat Y, Sahin Y, Tükün A, Akarca US, Karayalçin S: Recipient-derived hepatocytes in sex-mismatched liver allografts after liver transplantation: early versus late transplant biopsies. Transplantation. 78(11):1647-52, 2004
Deda G, Çaksen H, Kansu A, Girgin N, Suskan E, Uysal S, Tukun A. Toxic hepatitis in a case of Angelman syndrome associated with Lennox-Gastaut syndrome. Genet Counsel,15(3):357-61, 2004.
Aydos S, Tükün A, Bökesoy I: Gonadal Dysgenesis and Mayer-Rokitansky-Kuster-Hauser Syndrome in a girl with 46,X,del(X) (pterq22:). Archives of Gynecology and Obstetrics, 267(3): 173-174, 2003.
Gümüs G, Sunguroglu A, Tukun A, Sayin B, Bökesoy I: Fragile sites associated with the breakpoints of chromosomal aberrations in hematologic neoplasms. Cancer Cenetics Cytogenetics, 133(2):61-4, 2002.
Toydemir PB, Elhan A.H, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I: Assessment of prothrombotic risk in patients with Behcet's disease should include homocysteine plasma levels - Reply.Journal of Rheumatology, 28(12);2765, 2001.
Ilgin Ruhi H, Tükün A, Karabulut HG, Bayazit P, Bökesoy I:A Down syndrome Case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21. Clinical Genetics, 59(5):368-70, 2001.
Tükün A, Renda Y, Topçu M, Tuncali T, Bökesoy I: Mental retardation with rare fragile site expressed at 2q11. Brain & Development, 22(8):498-500, 2000.
Toydemir PB, Elhan A.H, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I: The effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothrombin gene G20210A mutations on deep venous thrombogenesis in Behçet’s disease. Journal of Rheumatology, 27(12);2849-54, 2000.
Peller S, Yona R, Kopilova Y, Prokocimer M, Goldfinger N, Uysal A, Karabulut HG, Tükün A, Bökesoy I, Tunçman G, Rotter V: Molecular Alterations in the TP53 Gene of Peripheral Blood Cells of Patients With Chronic myeloid Leukemia. Genes, Chromosomes & Cancer, 21:2-7, 1998.
Tunçman G, Tükün A, Yalaz K, Bökesoy I: A case of Prader Willi syndrome with del 15(q11-->q13). The Turkish Journal of Pediatrics, 35:333-6,1993.
Diğer uluslararası/ulusal dizinlerde yer alan dergilerdeki yayınlar:
Yararbas K, Ilgin Ruhi H, Aydos K, Elhan A, Tukun A. Is idiopathic male infertility really idiopathic? Detection of DNA copy number variations and candidate chromosomal loci among azoospermic males by high resolution comparative genomic hybridization. Pamukkale Tıp Dergisi, 2019;12(1): 199 – 208
Çelik VD, Orhan-Kılıç B, Ardiçoğlu-Akişin Y, Tükün FA, Akar N. Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3,.7 kb deletion. The Egyptian Journal of Medical Human Genetics. 2018; 19:433–435
Tunçer C, Tükün A: Epigenetik kalıtım ve kanser. Turkiye Klinikleri Kanser Mutagenezis Ve Moleküler/Genetik Etiyolojik Sebepleri Özel Sayısı J Med Genet-Special Topics 2017;2(2):99-106
Khosroshahi HE, Özdamar MY, Tükün FA, Akyüz-Özkan E, Yararbas K, Adnan M. A novel mosaic 22q11.2 micro-duplication syndrome: A novel mosaic 22q11.2 micro-duplication syndrome: clinical report and literature review. Cerebro-oculo-facio-urethrogenito-skeletal syndrome: de novo condition Int J Clin Exp Med 2016;9(6):9734-9743
Tükün A, Bilecen K: Evrimsel Tip Perspektifi İle Genetik Hastaliklar, TOPLUM ve HEKİM 2016;31(5):334-9.
Sağlam-Ada B, Tükün A: Kalıtsal Kanserler ve Genetiği. Turkiye Klinikleri J Med Genet-Special Topics 2016;1(1):119-24
Tükün A: Genetik Tanı Uygulamalarında Etik Sorunlar. Turkiye Klinikleri J Med Ethics Law Hist-Special Topics 2015;1(3): 51-55
Dinççelik M, Gümüş-Akay G, Elhan AH, Ünal AE, Tükün A: Diagnostic And Prognostic Significance Of Glypican 5 And Glypican 6 Expression Levels In Gastric Cancer. Molecular and Clinical Oncology 2015, 3: 584-590
Diniz G, Tosun Yildirim H, Gokben S, Serdaroğlu G, Hazan F, Yararbas K, Tukun A: Concomittant Alpha And Gamma Sarcoglycan Deficiencies In A Turkish Family With A Novel Deletion In The Alpha Sarcoglycan Gene. Case Rep Genet. 2014;2014:248561
Yürür-Kutlay N, Tuncalı T, Ilgın-Ruhi H, Karabulut HG,Tukun A: An evaluation of the phenotypic features of Fanconi Anemia together with DEB/MMC positivity in 199 Turkish patients. J Med Sci 2013;33(1):1-8
Tos T, Özkaya E, Korkmaz V, Özkaya Y,Tükün A, Gökmen O, Küçüközkan T. Nuchal Translucency Measurement Did Not Significantly Predict Trisomy Cases in Tertiary Referral Center. Gynecology Obstetrics & Reproductive Medicine 2012;18(3):127-30.
Korkmaz HA, Hazan F, Dizdarer C, Tükün A: Hypochondroplasia in A Child With 1620C>G (Asn540Lys) Mutation in FGFR3. J Clin Res Pediatr Endocrinol. 2012;4(4):220-2.
Tos T, Özkaya E, Korkmaz V, Özkaya Y,Tükün A, Gökmen O, Küçüközkan T. Nuchal Translucency Measurement Did Not Significantly Predict Trisomy Cases in Tertiary Referral Center. Gynecology Obstetrics & Reproductive Medicine 2012;18(3):127-30.
Tukun A: Clinical Utility of Medical Genetics in Oncology. J Med Oncol-Special Topics 2011;4(2):7-15
S. Koçak, L. Çelik, S. Özbaş, S. Dizbay Sak, A. Tükün, B. Yalçın: Meme Kanserinde Risk Faktörleri, Riskin Değerlendirilmesi Ve Prevansiyon: İstanbul 2010 Konsensus Raporu. The Journal of Breast Health 7(2):47-67, 2011.
Demirkazık A, Tükün A: Indıvıdualızed Therapy In Cancer: Why Pharmacogenetıcs? Turkiye Klinikleri J Med Sci 2010;30(2EK):1-4
Tükün A: Akut Lösemilerde Sitogenetik ve Moleküler Genetiğin Önemi. Türk Çocuk Hematoloji Dergisi 3(1):120-3, 2009.
Ilgın-Ruhi H, Tükün A:Fanconi anemia: Moleküler Bozukluklar ve Önemi. Turkiye Klinikleri 2(2): 27-31, 2009.
Gümüş-Akay G, Elhan AH, Ünal AE, Demirkazık A, Sunguroğlu A, Tükün A: Mide kanserinde genomik değişikliklerin telomeraz aktivitesi üzerine etkisi. Moleküler Tanı Dergisi: 3(2):6-12, 2007.
Tukun A, Gümüs G, Yurur Kutlay N: Telomere and telomerase in hematological malignancies. Turk J Hematol 2006; 23.77-83, 2006.
Yürür-Kutlay N, Tükün A : Akciğer hastalıklarına moleküler yaklaşım. Türkiye Klinikleri 2(9): 81-8, 2006
Ilgin-Ruhi H, Tuncali T, Tükün A: Kromozomal kirik sendromlari. Türkiye Klinikleri 1(2): 101-6, 2005
Yirmibeş-Karaoguz M, Tükün A: Mitokondriyal hastaliklar ve genetik danisma. Türkiye Klinikleri 1(2): 56-60, 2005
Babaoglu E, Ilgin-Ruhi H, Tükün A; From gene to disorder: Fanconi Anemia. Journal of Ankara Medical School, 26(1):27-33, 2004.
Aydos S, Tükün A: Ileri anne yasi ve kromozom ayrilamama, Türk Fertilite Dergisi 12(4): 329-38, 2004
Sayin B, Tükün A: Lösemi gelişiminde rol oynayan risk faktörleri, Optimal 16(4): 122-6, 2003
Aydos S, Tükün A: Reprodüktif yasam süresini etkileyen genetik faktörler, Klinik Laboratuvar Arastirma Dergisi 7(4): 118-26, 2003
Pekkurnaz G, Gümüs G, Yürür-Kutlay N, Akçay R, Kaya AI, Aydos S, Burhan B, Özer L, Özkal P, Rustamov A, Tükün A, Sunguroglu A: Kronik Myeloproliferatif hastaliklarda saptanan kromozomal anomaliler. Klinik Laboratuvar Arastirma Dergisi, Kanser Sitogenetigi Özel Sayisi: 124-8, 2002.
Çabuk F, Tükün A: Antiepileptik ve antipsikotik ilaçlarin teratojenik etkileri, Optimal 15(3): 83-9, 2002
Akçay R, Tükün A: Analjezik ilaçlarin teratojenik etkileri, Optimal 15(4): 116-9, 2002
Yürür-Kutlay N, Tükün A: Genomik Imprinting ve Kanser, Optimal, 14(3):87-91, 2001.
Tükün A, Aysun S, Bökesoy I: Two siblings with Fragile X syndrome, Journal of Ankara Medical School, 23(3):237-41, 2001.
Sunguroglu A, Akarsu N, Tükün A, Ilgin H, Tunçman G, Karabulut HG, Bökesoy I, Deniz E: Ataxia telengiectazia'li (AT) hasta periferik kan lenfositleri üzerine Bleomisin’in in vitro etkisi, Optimal, 8(1):27-9, 1995.
Tükün A, Karabulut HG, Tunçman G, Ilgin H, Toydemir R, Bayrak P, Bökesoy I: Martin-Bell fenotipi gösteren hastalarda frajil X bulgulari. Ankara Üniversitesi Tip Fakültesi Mecmuasi, 48:529-35, 1995.
Tükün A, Tunçman G, Sunguroglu A, Yapar G, Bökesoy I: Effects of sex steroids on metaphase chromosomes analyzed by Sister Chromatid Exchange, Turkish Journal of Medical Sciences, 24: 185-9, 1995.
Tükün A, Bayrak P, Sunguroglu A, Bökesoy I, Çavdar AO, Gözdasoglu S, Babacan E, Yavuz G, Ünal E: Chromosomal abnormalities in children with acute nonlymphocytic leukaemia, Turkish Journal of Medical Sciences, 22:111-2, 1994.
Sunguroglu A, Tükün A, Bökesoy I: Nor activity in chronic myeloid leukaemia, Turkish Journal of Medical Sciences, 20:95-7, 1994.
Tükün A, Bökesoy I, Gürsel T, Tümer L, Tunaoglu S, Uluoglu Ö:Two siblings with ICF syndrome; Case reports and review, Dysmorphology and Clinical Genetics, 6(3):135-40, 1992.
Tükün A, Sunguroglu A, Bayrak P, Topal M, Bökesoy I: Biyoritm ve cinsiyet farkinin kromozomlar üzerindeki etkilerinin SCE yöntemi ile analizi, Optimal 4(2):88-90, 1991.
Tükün A, Kuyucu N, Sunguroglu A, Öcal G, Bökesoy I: Fototerapinin hücre kinetigi üzerine etkisi, Ankara Üniversitesi Tip Fakültesi Mecmuasi, 43(3'e ek): 825-30, 1990.
Sunguroglu A, Koç E, Tükün A, Bökesoy I, Kerimoglu E: 48,XXXX sendromlu bir vaka, Optimal 3(4):216-9, 1990.
Balci S, Gögüs T, Hayran A: Femoral hipoplazi ve degisik yüz görünümü sendromlu iki vakanin takdimi, Çocuk Sagligi ve Hastaliklari Dergisi, 28:311-8, 1985.

Prof. Dr. Ajlan Tükün

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