Publications:
Specialty in Medical Genetics Dissertation
SYP1 ve SYP2 genlerinin kromozomal lokalizasyonları, 8/1990, Uta Francke, Stanford University.
Chapters in books
Özçelik T., "Moleküler Genetikte Temel Kavramlar" in OBSTETRİK: Maternal·Fetal Tıp ve Perinatoloji (Edited by MS Beksaç, N. Demir, A. Koç). pp. 641-51, Ankara: Medical Network, (2001).
Hüner, M. Demirkol, N. Çine, T. Baykal, G. Çarbat, M. Çalışkan, N. Aydınlı, M. Özmen,Y. Seçkin, Özçelik T,. "The PAH Splicing Mutation IVS10nt546 in Late Diagnosed PKU Patients is Associated with Hypsarrytmia", "Diagnosis and Treatment of Inborn Errors of Metabolism: Contributions to an Equal Opportunity for Children in Asia and Europe" M. Demirkol and Y.S. Shin .eds., 79-84, Published by the Turkish Society for PKU. Istanbul Branch, (1996).
Özçelik T, N. Çine, G. Hüner, T. Baykal, G. Şarbat, M. Demirkol. "Molecular Genetic Approaches to the Diagnosis of Phenylketonuria in Istanbul", "Diagnosis and Treatment of Inborn Errors of Metabolism: Contributions to an Equal Opportunity for Children in Asia and Europe" M. Demirkol and Y.S. Shin .eds., 73-78, Published by the Turkish Society for PKU. Istanbul Branch, (1996).
Reviews
Özçelik T., "Farmakogenetik" Dokuz Eylül Tıp Fak Der, (2001).
Özçelik T. "Adli AmaçlI DNA analizleri" Hacettepe Tip Derg 27(2): 50-55 (1996).
Özçelik T. "DNA polimorfizminin Tıp'da kullanımı" Hacettepe Tip Derg 27(1): 72-76 (1996).
Özçelik T. "Nöromusk hast neden olan genler ve tanı testleri" Klinik Gelisim 8: 3728-3742 (1995).
Publications in refereed journals
Genetic disorders & population genetics
X-chromosome inactivation and genetic diseases
Ozbalkan Z, Bagislar S, Kiraz S, Akyerli CB, Ozer HT, Yavuz S, Birlik AM, Calguneri M, Özçelik T. Skewed X chromosome inactivation in blood cells of women with scleroderma. Arthritis Rheum 52:1564-70 (2005). [ I.F. 7.190 ]
Rett syndrome
Özçelik T . "Uncovering the complex mysteries of mosaicism"
[ correspondence letter ] Nature 417:588 (2002). [ I.F. 30.4 ]
Topçu M, Akyerli C, Sayı A, Törüner G, Koçoğlu RS, Cimbiş M, Özçelik T. "Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy" Eur J Hum Genet 10:77-81 (2002). [ I.F. 3.175 ]
Archidiacono N, Rocchi M, Anvret M, Özçelik T, Francke U, and Romeo G. "Rett Syndrome: Exclusion mapping on the X chromosome following the hypothesis of germinal mosaicism for new X- linked mutation in the mother of two affected half-sisters" Hum Genet 86: 604-606 (1991). [ I.F. 3.29]
Hematological malignancies
Zhang H, Vakil V, Braunstein M, Smith EL, Maroney J, Chen L, Dai K, Berenson JR, Hussain MM, Klueppelberg U, Norin AJ, Akman HO, Özçelik T, Batuman OA. Circulating endothelial progenitor cells in multiple myeloma: implications and significance. Blood 105:3286-94 (2005). [ I.F. 10.12 ]
Akyerli CB, Beksac M, Holko M, Frevel M, Dalva K, Özbek U, Soydan E, Özcan M, Özet G, İlhan O, Gürman G, Akan H, Williams BRG, Özçelik T. Expression of IFITM1 in chronic myeloid leukemia patients. Leuk Res. 2005 Mar;29(3):283-6. [ I.F. 2.333 ]
Akyerli BC, Özbek U, Aydın-Seyitoğlu M, Sırma S, Özçelik T. "Analysis of MYH Tyr382Asp variants in childhood leukemias" J Cancer Res Clin Oncol 129: 604-605 (2003). [ I.F. 2.66 ]
Üstün C, Arat M, Çelebi H, Akan H, Ilhan O, Özçelik T, Burgess RE, Koc H. "Extramedullary relapse following allogeneic stem cell transplantation in acute propmyelocytic leukemia: the role of ATRA" Haematologica 86: E31, 2001. [ I.F. 3.216 ] ,
Beksac M, Ma M, Akyerli C, DerDanielian M, Zhang L, Liu J, Arat M, Erekul S, Konuk S, Koc H, Özçelik T, Vescio R, Berenson JR. "Frequent demonstration of human herpesvirus 8 (HHV-8) in bone marrow samples from Turkish patients with multiple myeloma (MM)" Leukemia 15:1268-1273 (2001). [ I.F. 4.293 ]
Ustun C, Arslan O, Beksac M, Koc H, Gurman G, Özçelik T, Yılmaz B, Ilhan O, Akan H, Ozcan M, Demirer T, Uysan A, Konuk N, Arat M, Dilek I, Celebi H, Coskun HS. "A retrospective comparison of allogeneic peripheral blood stem cell and bone marrow transplantation results from a single center: a focus on the incidence of graft-vs- host disease and relapse" Biol Blood Marrow Transplant 5: 28-35 (1999).
Ricciardone MD, Özçelik T, Cevher B, Ozdag H, Tuncer M, Gurgey A, Uzunalimoglu O, Cetinkaya H, Tanyeli A, Erken E, Ozturk M. "Human MLH1 deficiency predisposes to hematological malignancy and Neurofibromatosis type 1" Cancer Res 59: 290-293 (1999). [ I.F. 8.614 ]
Breast cancer
Sevinç A, Yannoukakos D, Konstantopoulou I, Mangüoğlu E, Lüleci G, Çolak T, Akyerli C, Çolakoğlu G, Tez M, Sayek İ, Gerassimos V, Nasioulas G, Papadopoulou E, Florentin L, Kontogianni E, Yuluğ IG, Özçelik T. "Lack of association between RNASEL Arg462Gln variant and the risk of breast cancer."Anticancer Res 24:2547-9 (2004). [ I.F. 1.347 ]
Tez M, Göçmen E, Özçelik T. "HER2 overexpression and angiogenesis in breast cancer" [ correspondence letter ] The Lancet 362: 1503 (2003). [ I.F. 16.135 ]
Manguoglu EA, Lüleci G, Özçelik T, Çolak T, Schayek H, Akaydı M, Friedman E. "Germline mutations in BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients" Hum Mutat 21:444-50 (2003).
[ I.F. 6.134 ]
Sullivan A, Yuille M, Repellin C, Reddy A, Relfs O, Bell A, Dunne B, Gusterson BA, Osin P, Farrel PJ, Yulug I, Özçelik T, Evans A, Milena G and Crook T. "Concomitant inactivation of p53 and Chk2 in breast cancer" Oncogene 21:1316-24 (2002).
[ I.F. 6.737 ]
Mazoyer S, Özçelik T et al. The BRCA1 Exon 13 Duplication Screening Group. "The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations" Am JHum Genet 67: 207-212 (2000). [ I.F. 10.542 ]
Özdağ H, Tez M, Sayek İ, Müslümanoğlu M, Tarcan O, İçli F, Öztürk M, Özçelik T. "Germ-line BRCA1 and BRCA2 gene mutations in Turkish breast cancer patients" Eur J Cancer 36: 2076-2082 (2000). [ I.F. 3.46 ]
Population genetics
Vural B, Atlıoglu E, Kolusayın Ö, Togan İ, Büyükdevrim S, Özçelik T. "Turkish population data on the HLA-Da, LDLR, GYPA, HBGG, D7S8, and GC loci" Int J Legal Med 111: 43-45 (1998).
[ I.F. 1.626 ]
Hatemi AC, Cine N, Özçelik T. "Allele and genotype frequencies of the insertion/deletion polymorphism in the human angiotensin converting enzyme in the Turkish population" Turkish J Med 27:205-208 (1997).
Özbek U, Vural B, Kalayoglu S, Soysal T, Bilgen H, Yavuz S, Anak S, Sargin D, Gedikoglu G, Ferhanoglu B, Akoglu T, Tangun Y, Özçelik T. "Evaluation of chimerism with DNA polymorphisms in the Turkish population" Turkish J Ped 39:303-312 (1997). [ I.F. 0.122 ]
Atlıoğlu E, Canlı MA, Öztürk M, Kolusayın Ö, Olgun A, Özçelik T. "Türk popülasyonunda alyuvar antijen sistemlerinin gen frekansları" Adli Tıp Derg 10: 23-28 (1994).
Other publications (cancer, genetic disorders, general)
Buyukderim-Ozcelik I, Özçelik T. Science flourishes in a secular democracy. Nature 433:355 (2005). [ correspondence letter ] [ I.F. 30.4 ]
Akgül H, Tez M, Ünal AE, Keşkek M, Sayek İ, Özçelik T. "Echinococcus against cancer: Why not?" Cancer 98: 1998-99 (2003). [ I.F. 3.99 ]
Törüner GA, Uçar A, Tez M, Çetinkaya M, Özen H, Özçelik T. "p53 codon 72 polymorphism in bladder cancer - no devidence of association with increased risk or invasiveness" Urol Res 29: 393-395(2001). [ I.F. 0.993 ]
Törüner GA, Akyerli C, Uçar A, Akı T, Atsu N, Özen H, Tez M, Çetinkaya M, Özçelik T. "Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and bladder cancer susceptibility" Arch Toxicol 75: 459-464, (2001). [ I.F. 1.683 ]
Topaloğlu R, Akyerli C, Bakkaloğlu A, Aydıntuğ O, Özen S, Beşbaş N, Özçelik T. "Survey of factor V Leiden and prothrombin gene mutations in systemic lupus erythematosus" Clin Rheumatology 20: 259-261 (2001). [ I.F. 0.838 ]
Gul A, Aslantas AB, Tekinay T, Konice M, Özçelik T. Procoagulant mutations and venous thrombosis in Behçet's disease" Rheumatology 38: 1298-1299 (1999). [ I.F. 3.62 ]
Deymeer F, Serdaroglu P, Poda M, Gulsen-Parman Y, Özçelik T, Ozdemir C. "Segmental distribution of muscle weakness in SMAIII: implications for deterioration in muscle strength with time" Neuromuscul Disord7: 521-528 (1997). [ I.F. 2.749 ]
Kyriallis K, Christodoulou K, Al-Shehab A, Barba V, Mylonas Y, Mavromatis J, Serdaroglu P, Özçelik T, Deymeer F,Ozdemir C, Middleton LT. "Familial Infantile Myasthenia in Eastern Mediterranean Countries" Neurology 46: P04.089 (1996). [ I.F. 5.232 ]
Gül A, Özbek U, Öztürk C, İnanç M, Koniçe M, Özçelik T. "Coagulation factor V mutation and the development of venous thrombosis in Behcet's disease" Revue du Rheumatisme No 7-8: F10 545 (1996). [ I.F. 0.774 ]
Gül A, Özbek U, Öztürk C, İnanç M, Koniçe M, Özçelik T. "Coagulation factor V gene mutation increases the risk of venous thrombosis in Behcet's disease" Brit J Rheum 5:1178-1180 (1996). [ I.F. 3.949 ]
Gene mapping
Anders DA, Milatovich A, Özçelik T, Wenzlau JM, Brown MS, Goldstein JL, Francke U. "cDNA cloning of the two subunits of human CAAX Farnesyltransferase gene and mapping of FTNA and FTNB loci and related sequences" Genomics 18:105-112 (1993). [ I.F. 6.726 ]
Ibraghimov-Beskrovnaya O, Milatovich A, Özçelik T, Yang B, Koepnick K, Francke U, and Campbell K. "Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization" Hum Molec Genet 2:1651-1657 (1993). [ I.F. 9.318 ]
Lindgren V, Bryke CR, Özçelik T, Yang-Feng TL, Francke U. "Reply to Rivera" Am J Hum Genet 53:533-534 (1993). [ I.F. 10.542 ]
Davidson JJ, Özçelik T, Hamacher C, Willems PJ, Francke U, Kilimann MW. "cDNA cloning of a liver soform of the phosphorylase kinase a subunit and mapping of the gene to Xp22.2-p22.1, the region of the human X-linked liver glycogenosis" Proc Natl Acad Sci, USA 89: 2096-2100 (1992). [ I.F. 9.04 ]
Murphy PM, Özçelik T, Kenney RT, Tiffany HL, McDermott D, and Francke U. "A structural homologue of the N-formyl peptide receptor: Characterization and chromosome mapping of a peptide chemoattractant receptor family" J Biol Chem 267:7637-7643 (1992). [ I.F. 7.716 ]
Suter U, Welcher AA, Özçelik T, Snipes GJ, Kosaras B, Francke U, Billings-Gagliardi S, Sidman RL, and Shooter EM. "Trembler mouse carries a point mutation in a myelin gene" Nature356: 241-244 (1992). [ I.F. 30.4 ]
Lindgren V, Bryke CR, Özçelik T, Yang-Feng TL, and Francke U. "Phenotypic cytogenetic and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis" Am J Hum Genet 50: 988-997 (1992). [ I.F. 10.542 ]
Özçelik T , Porteus MH, Rubenstein JLR, and Francke U. "DLX2 (TES1), a homeobox gene for the Distal-less family, assigned to conserved regions on human and mouse chromosome 2" Genomics 13:1157-1161 (1992). [ I.F. 6.726 ]
Berkemeier LR, Özçelik T, Francke U, and Rosenthal A. "Human chromosome 19 contains the Neurothrophin-5 gene locus and three related genes that may encode novel acidic neurotrophins" SomatCell and Molec Genet 18: 3, 233-245 (1992). [ I.F. 2.374 ]
Rupp F, Özçelik T, Linial M, Peterson U, Francke U, and Scheller R. "Structure and chromosomal localization of the mammalian agrin gene" J of Neurosci 12: 9, 3535-3544 (1992). [ I.F. 8.955 ]
Ahuja SK, Özçelik T, Milatovich A, Francke U and Murphy P. "Molecular evolution of the human interleukin-8 receptor gene cluster" Nature Genet 2: 31-36 (1992). [ I.F. 29.6 ]
Özçelik T , Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, and Francke U. "Small nuclear ribonucleoprotein N (SNRPN), an expressed gene in thePrader-Willi syndrome critical region" Nature Genet 2: 265-269 (1992). [ I.F. 29.6 ]
Leff SE, Brannan CI, Reed ML, Özçelik T, Francke U, Copeland NG, Jenkins NA. "Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region" Nature Genet 2: 259-264 (1992). [ I.F. 29.6 ]
Perin MS, Johnston PA, Özçelik T, Jahn R, Francke U, and Sudhof TC. "Structural and functional conservation of synaptotagmin (p65) in drosophila and humans" J Biol Chem 266:615-622 (1991).[ I.F. 7.716 ]
Özçelik T , Rosenthal A, Francke U. "Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse" Genomics 10:569-575 (1991). [ I.F. 6.726 ]
Özçelik T , Suedhof TC, Francke, U. " Chromosomal assignments of genes for vacuolar (endomembrane) proton pump subunits VPP1/Vpp-1(116 kDa) and VPP3/Vpp-3 (58 kDa) in human and mouse" Cytogenet Cell Genet 58 : 2008-2009 (1991). [ I.F. 4.185 ]
Özçelik T, Suedhof TC, Francke U. " The genes for nositol1,4,5-triphosphate receptors 1 (ITPR1) and 3 (ITPR3) are localized on human chromosomes 3p and 6pter-p21, respectively" Cytogenet Cell Genet 58 :1880 (1991). [ I.F. 4.185 ]
Özçelik T , Murphy M, Francke U. "Chromosomal assignment of genes for formyl peptide receptor (FPR1),a structural homolog of the formyl peptede receptor (FPRL1) and a low affinity interleukin-8 receptor (IL8RA) in human" Cytogenet Cell Genet 58: 2023-2024 (1991). [ I.F. 4.185 ]
Özçelik T, Lafreniere RG, Archer III BT, Johnston PA,Willard HF, Francke U, Sudhof TC. "Synaptophysin: Structure of the human gene and assignment to the X chromosome in man and mouse" Am J Hum Genet 47:551-561 (1990). [ I.F. 10.542 ]
Archer III BT, Özçelik T, Jahn R, Francke U, Sudhof TC. "Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2" J Biol Chem 265:7267-7273 (1990). [ I.F. 7.716 ]
Heart physiology
Becker BF, Reinholz N, Özçelik T, Leipert B, Gerlach E. "Uric acid as radical scavenger and antioxidant in the heart" Pflugers Arch 415:127-135 (1989). [ I.F. 3.115 ]
Karakullukcu YE, Özçelik T, Gokhan N. "Changes of cyclic AMP and cyclic GMP levels during the calcium paradox in the isolated rat heart" Pflugers Arch 410: 657-663 (1987). [ I.F. 3.115 ]
Özçelik T , Erbengi T, Gokhan N, Karakullukcu YE. "The influence of acetylcholine on the occurrence of the ultrastructural changes of the calcium paradox in isolated rat heart" IRCS Med Sci 14:996-997 (1986).
Özçelik T , Karakullukcu YE, Unal, T, Gokhan N. "Positive inotropy seen following calcium-free, acetylcholine added perfusion in cardiac muscle of the rat" IRCS Med Sci 13:128 (1985).
Ünal T, Özçelik T, Karakullukcu YE, Gokhan N. "Catecholamine independent positive inotropy in cardiac muscle of the rat" Tip Fak Mecm 46:513-518 (1983).
Published congress abstracts
Akyerli CB, Beksac M, Holko M, Frevel M, Dalva K, Gurman G, Ilhan O, Ozcan M, Akan H, Williams BRG, Özçelik T. "Analysis of high and low risk chronic myeloid leukemia by gene expression profiling" Blood 100 (11): 1412 (2002).
Aydemir AEM, Luleci G, Özçelik T, Colak T, Schayek H, Akaydin M, Friedman E. "Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients" Int J Cancer Suppl 13, 387 (2002).
Akyerli C, Sayi A, Kocoglu RS, Cimbis M, Topcu M, Özçelik T. "Analysis of MECP2 gene mutations in Turkish Rett syndrome patients" Eur J Hum Genet 9: Suppl.1, P1450 (2001).
Toruner GA, Akyerli C, Ucar A, Aki T, Atsu N, Ozen H, Tez M, Özçelik T. "Combination of GSTM1 null genotype and GSTP1 105 Val allele leads to increased risk of bladder cancer in the Turkish population" Eur J Hum Genet 9: Suppl.1, P0054 (2001).
Topcu M, Cimbis M., Haliloglu G, Akyerli C, Sayi A, Kocoglu RS, Özçelik T. "Genotype-phenotype correlation in Turkish patients with Rett syndrome" Eur J Paediatr Neurol, 5 (5): O47, (2001).
Törüner G, Bozkurt B, Atalay A, Kocabaş NA, Özçelik T. Yuluğ IG, "Glutatyon S-transferaz gen polimorfizmleri (GSTM1, GSTP1, ve GSTT1) ile meme kanseri riski arasındaki ilişkinin araştırılması", in the proceedings of the 6th Natl. Breast Cancer Congress and 1st Congress of the World Society for Breast Health, İstanbul, Turkey, 22-26 September 2001.
Özçelik T. "Yüzyılımızın moleküler teknolojileri ve uygulamaları" in the proceedings of the "Uluslararası Katılımlı" 23. Pediatri ve 3. Pediatri Hemşireliği Günleri, s. 46, İstanbul, Turkey, 2001.
Özçelik T. "Meme kanserinin moleküler genetiği" in the proceedings of the "Natl. Medical Biology Congress", Eskişehir, Turkey, October 2001.
Sayan AE, Ozdag H, Findikli N, Unsal K, Özçelik T, Ozturk M. "Structure and expression of p73 gene in liver and hepatocellular carcinoma" EARC (European Association for Cancer Research) XVI-2000. Halkidi-Greece (2000).
Özdag H, Tez M, Sayek I, Muslumanoglu M, Tarcan O, Icli F, Ozturk M, Özçelik T. "Germ-line BRCA1 and BRCA2 mutations in Turkish breast cancer patients" EARC (European Association for Cancer Research) XVI-2000. Halkidi-Greece (2000).
Al-Otaibi, Ozturk M, Özçelik T, Ricciardone M. "NF1 mutation analysis in a child homozygous for HMLH1 mutation" II Pan Arab Congress of Diabetes and Endocrinology & The 10th Intl. Clinical Genetics Seminar, 120, Amman, Jordan, 20-24 October 2000.
Özdag H, Tez M, Muslumanoglu M, Tarcan O, Sayek I, Ozturk M, Özçelik T. "BRCA1 and BRCA2 mutations in Turkish breast cancer families" Eur J Hum Genet 7: 293 (1999).
Toruner G, Ucar A, Akın T, Atsu N, Ozen H, Özçelik T. "Analysis of GSTM1 and microsatellite instability in bladder cancer" Eur J Hum Genet 7: 293 (1999).Özçelik T. "Türkiye'deki bazi ailesel kanserlerin moleküler temelleri" KÜKEM Dergisi 23: 5-6 (1999).
Özçelik TH, Erken E, Cevher B, Tunçman G, Mesci L, Ozer H, Gunesacar R, Ozturk M. "MEFV mutation analysis in Turkish familial Mediterranean fever families" Am J Hum Genet 65: A484, 2751 (1999).
Özdag H, Tez M, Muslumanoglu M, Tarcan O, Ozturk M, Özçelik T. "Novel mutations in BRCA1 and BRCA2 genes in Turkish breast cancer families" Am J Hum Genet 63: 438 (1998).
Yalcinoz MC, Cine N, Özçelik T. "Clinical utility of PCR based .Tuberculosis detection in sputum samples of HIV seronegative patients" Annual Congress of the European Respiratory Society. Barcelona, Spain (1995).
Yilmaz G, Utku B, Kucukusta AR, Cine N, Özçelik T. "Polymerase chain reaction in diagnosing pleural effusions" Ann. Meet. of the Intl. Union Against Tuberculosis and Lung Disease. Paris, France (1995).
Yalcinoz MC, Cine N, Özçelik T. "Akciger tuberkulozu tanisinda PCR metodun klinik uygulamadaki yeri" Türkiye Solunum Arastirmalari Dernegi XIII. Ulusal Kongresi. Istanbul, Türkiye (1995).
Vural B, Özçelik T. "Individual identification from postmortem tissue samples by DNA analysis" XIIIth Meeting of the Intl. Society of Hematology. Istanbul, Turkey (1995).
Özçelik T, Ozbek U, Vural B, Bilgen H, Anak S, Gedikoglu G, Besisik S, Sargin D, Soysal T, Ferhanoglu B, Tangun Y. "Evaluation of chimerism with DNA polymorphisms in bone marrow transplantation" XIIIth Meeting of the Intl. Society of Hematology. Istanbul, Turkey (1995).
Hatemi AC, Özçelik T. "Allele and genotype frequencies of the insertion/deletion polymorphism in the human angiotensin converting enzyme in the Turkish population" XIIIth Meeting of the Intl. Society of
Hematology. Istanbul, Turkey (1995).
Çine N, Utku B, Yalcinoz C, Yilmaz G, Özçelik T. "PCR based M. Tuberculosis detection in sputum, bronchoalveolar lavage and pleural fluid samples of HIV seronegative patients" XIIIth Meeting of the
International Society of Hematology. Istanbul, Turkey (1995).
Özçelik T, Vural B, Atlioglu E, Kolusayin O, Buyukdevrim S. "Alti farkli lokusun allel ve genotip frekanslarinin Turk toplumunda dagiliminin DNA analizi ile saptanmasi ve nesep (babalik) tayininde kullanimi" I. Adli Bilimler Kongresi, Adana, Türkiye (1994).
Panayides K, Özçelik T, Serdaroglu P, Deymeer F, Ozdemir C, Topaloglu H, Georgiou DM, Christova A, Peterlin B, Kalaydjieva L, Zidar J, Ioannou P, Middleton L. "Molecular genetic analysis of Friedrich's ataxia in Eastern Mediterranean countries"
Christodoulou K, Özçelik T, Georgiou DM, Serdaroglu P, Deymeer F, Topaloglu H, Ozdemir C, Ioannou P, Middleton L. "Two recombination events detected in a large inbred Turkish Friedrich's ataxia family provide useful information regarding the position of the disease locus" Muscle and Nerve Suppl. 1, S239, No: 21-5-46 (1994).
Özçelik T, Cine N, Huner G, Kurdoglu G, Buyukdevrim S, Demirkol M. "Molecular genetic approaches to the diagnosis of PKU in Istanbul" 2nd Asian-European Workshop on Inborn Errors of Metabolism. Istanbul, Turkey (1994).
Özçelik T, Vural B, Atlioglu E, Kolusayin O, Buyukdevrim S. "HLA-DQA1 allel ve genotip frekanslarinin Turk toplumunda dagilimi ve DNA'ya bagli kimlik tespitinde kullanımı" Istanbul Tip Fak. 12. Kurultayi, Istanbul, Türkiye (1993).
Özçelik T, Vural B, Atlioglu E, Kolusayin O, Buyukdevrim S. "Turk toplumunda DNA analizi ile gerceklestirilen ilk nesep (babalik) tayinleri" 3. Klinik Molekuler Patoloji Kongresi, Ankara, Türkiye (1993).
Özçelik T, Archer BT, Sudhof TC, Francke U. "Mouse and human genes for two forms of synaptobrevin (or vesicle-associated membrane protein) are in conserved syntenic groups" 35; 4th Intl. Workshop on Mouse Genome Mapping, Annapolis MD (1991).
Özçelik T, Levitt D, Cole D, Budden S, Anvret M, Francke U. "Rett syndrome: Search for The molecular defect on the X chromosome" 8th Int. Cong. of Hum. Genet., Washington DC, USA (1991).
Özçelik T, Yuksel M, Tolun A, Kuseyri F, Partalci A, Apak S, Francke U. "Linkage analysis of a family with X-linked spinocerebellar ataxia and spastic diplegia" 8th Intl. Cong. of Hum. Genet., Washington
DC, USA (1991) and 23rd Ann. March of Dimes Meeting in Clin. Genet., Vancouver, Canada (1991).
Özçelik T, Sudhof TC, Francke U. "Chromosomal assignment of genes for vacuolar (endomembrane) proton pump subunits VPP1/Vpp-1 (116kD) and VPP3/Vpp-3 (58 kD) in human and mouse" HGM 11, London, England (1991)
Özçelik T, Sudhof TC, Francke U. "The genes for inositol 1,4,5-triphosphate receptors 1 (ITPR1) and 3 (ITPR3) are localized on human chromosomes 3p and 6pter-p21 respectively" HGM 11, London,
England (1991).
Özçelik T, Murphy PM, Francke U. "Chromosomal assignment of genes for a formyl peptide receptor (FPR2) and for two other members of this receptor family (FPRL1 and FPRL2) in human" HGM 11, London, England (1991).
Lindgren V, Bryke C, Özçelik T, Yang-Feng TL, Francke U. Cytogenetic and molecular characterization of two chromosome 5q deletions near the familial adenomatous polyposis coli gene" Am J Hum Genet 45: 4 (Suppl.): A81 (1989).
Becker BF, Özçelik T, Reinholz N, Leipert B, Gerlach E. "Oxygen radical scavenging, a possible physiological function of uric acid in the coronary system". Pflugers Arch 411: (Suppl. 1) R26 (1988).
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