Ozcelik, T. - A Web Based Annotated Bibliography - Aigaion 2.0

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First name(s):	T.
Last name(s):	Ozcelik

Gul, A., Aslantas, A.B., Tekinay, T., Konice, M. and Ozcelik, T., Procoagulant mutations and venous thrombosis in Behcet's disease (2000), in: Rheumatology, 38(1298-1299)

Gul, A., Ozbek, U., Ozturk, C., Inanc, M., Konice, M. and Ozcelik, T., Coagulation factor V gene mutation increases the risk of venous thrombosis in Behcet's disease (1997), in: British J of Rheumatology, 35(1178-1180)

Sullivan, A., Yuille, M., Repellin, C., Reddy, A., Reelfs, O., Bell, A., Dunne, B., Gusterson, B.A., Osin, P., Farrell, P.J., Yulug, I., Evans, A., Ozcelik, T., Gasco, M. and Crook, T., Concomitant inactivation of p53 and Chk2 in breast cancer (2002), in: Oncogene, 21(1316-1324)

Sullivan, A., Yuille, M., Repellin, C., Reddy, A., Reelfs, O., Bell, A., Dunne, B., Gusterson, B.A., Osin, P., Farrell, P.J., Yulug, I., Evans, A., Ozcelik, T., Gasco, M. and Crook, T., Concomitant inactivation of p53 and Chk2 in breast cancer (2002), in: Oncogene, 21(1316-1324)

Sevinc, A, Yannoukakos, D, Konstantopoulou, I, Manguoglu, E, Luleci, G, Colak, T, Akyerli, C, Colakoglu, G, Tez, M, Sayek, I, Gerassimos, V, Nasioulas, G, Papadopoulou, E, Florentin, L, Kontogianni, E, Bozkurt, B, Kocabas, N, Karakaya, A, Yulug, I. and Ozcelik, T., Lack of Association Between RNASEL Arg462Gln Variant and the Riskof Breast Cancer (2005), in: Anticancer Research, 24(2547-2550)

Sevinc, A, Yannoukakos, D, Konstantopoulou, I, Manguoglu, E, Luleci, G, Colak, T, Akyerli, C, Colakoglu, G, Tez, M, Sayek, I, Gerassimos, V, Nasioulas, G, Papadopoulou, E, Florentin, L, Kontogianni, E, Bozkurt, B, Kocabas, N, Karakaya, A, Yulug, I. and Ozcelik, T., Lack of Association Between RNASEL Arg462G1n Variant and the Risk of Breast Cancer (2005), in: Anticancer Research, 24(2547-2550)

Karahalil, B., Kocabas, N.A. and Ozcelik, T., DNA repair gene polymorphisms and bladder cancer susceptibility in a Turkish population (2007), in: Anticancer Research, 26(4955-4958)

Vural, B., Atlioglu, E., Kolusayin, O., Togan, I., Buyukdevrim, S. and Ozcelik, T., Turkish population data on the HLA-DQ, LDLR, GYPA, HBGG, D7S8 and GC loci (1998), in: Int J of Legal Medicine, 111(43-45)

Akyerli, B.C., Ozbek, U., Seyitoglu-Aydin, M., Sýrma, S. and Ozcelik, T., Analysis of MYH Tyr382Asp variants in childhood leukemias (2004), in: J of Cancer Research and Clinical Oncology, 129(604-605)

Ustun, C., Arat, M., Celebi, H., Akan, H., Ilhan, O., Ozcelik, T., Burgess, R.E. and Koc, H., Extramedullary relapse following allogeneic stem cell transplantation in acute propmyelocytic leukemia: the role of ATRA (2002), in: Haematologica (E-journal), 86(E31)

Akyerli, C.B., Beksac, M., Holko, M., Frevel, M., Dalva, K., Ozbek, U., Soydan, E., Ozcan, M., Ozet, G., Ilhan, O., Gurman, G., Akan, H., Williams, B.R.G. and Ozcelik, T., Expression of IFITM1 in chronic myeloid leukemia patients (2005), in: Leukemia Research, 29(283-6)

Uz, E., Mustafa, C., Topaloglu, R., Bilginer, Y., Dursun, A., Kasapcopur, O., Ozen, S., Bakkaloglu, A. and Ozcelik, T., Increased frequency of extremely skewed X chromosome inactivation in juvenile idiopathic arthritis (2010), in: Arthritis & Rheumatism, 60(3410-3412)

Uz, E., Dolen, I., Al, A.R. and Ozcelik, T., Extremely skewed X-chromosome inactivation in pre-eclampsia (2007), in: Human Genetics, 121(101-105)

Uz, E., Loubiere, L.S., Gadi, V.K., Ozbalkan, Z., Stewart, J., Nelson, J.L. and Ozcelik, T., Skewed X-chromosome inactivation in scleroderma (2009), in: Clinical Reviews in Allergy & Immunology

Manguoglu, E.A., Luleci, G., Ozcelik, T., Colak, T., Schayek, H., Akaydi, M. and Friedman, E., Germline mutations in BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patterns (2004), in: Human Mutation, 21(444-450)

Chabchoub, G., Uz, E., Maalej, A., Mustafa, C.A., Rebai, A., Mnif, M., Bahloul, Z., Farid, N.R., Ozcelik, T. and Ayadi, H., Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases (2010), in: Arthritis & Rheumatism, 11(106-1--8)

Toruner, G.A., Ucar, A., Tez, M., Cetinkaya, M., Ozen, H. and Ozcelik, T., p53 codon 72 polymorphism in bladder cancer - no devidence of association with increased risk or invasiveness (2002), in: Urological Research, 29(393-395)

Toruner, G.A., Akyerli, C., Ucar, A., Aki, T., Atsu, N., Ozen, H., Tez, M., Cetinkaya, M. and Ozcelik, T., Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and bladder cancer susceptibility (2002), in: Archives of Toxicology, 75(459-464)

Akgul, H., Tez, M., Unal, A.E., Keskek, M., Sayek, I. and Ozcelik, T., Echinococcus against cancer: Why not? (2004), in: Cancer, 98(1998-1999)

Ozdag, H., Tez, M., Sayek, I., Muslumanoglu, M., Tarcan, O., Icli, F., Ozturk, M. and Ozcelik, T., Germ line BRCA1 and BRCA2 gene mutations in Turkish breast cancer patients (2001), in: European J of Cancer, 36(2076-2082)

Zhang, H., Vakil, V., Braunstein, M., Smith, E.L.P., Maroney, J., Chen, L., Dai, K., Berenson, J., Hussain, M., Klueppelberg, U., Norin, A.J., Akman, H.O., Ozcelik, T. and Batuman, O.A., Circulation Endothelial Progenitor Cells in Multiple Myeloma: Implications and Significance (2005), in: Blood, 105(3286-3294)

Buyukderim-Ozcelik, I. and Ozcelik, T., Science flourishes in a secular democracy (2006), in: Nature, 433(355)

Kolb, L.E., Arlier, Z., Yalcinkaya, C., Ozturk, A.K., Moliterno, J.A., Erturk, O., Bayrakli, F., Korkmaz, B., Bilguvar, K., DiLuna, M.L., Yasuno, K., Ozcelik, T., Tuysuz, B., State, M.W. and Gunel, M., Novel VLDLR microdeletion identified in two turkish siblings with pachygyria and pontocerebellar atrophy (2010), in: Neurogenetics, 11(319-325)

Bekaac, M., Ma, M., Akyerli, C., DerDanielian, M., Zhang, L., Liu, J., Arat, M., Erekul, S., Konuk, S., Koc, H., Ozcelik, T., Vescio, R. and Berenson, J.R., Frequent demonstration of human herpesvirus 8 (HHV-8) in bone marrow samples from Turkish patients with multiple myeloma (MM) (2002), in: Leukemia, 15(1268-1273)

Braunstein, M., Ozcelik, T., Bagislar, S., Vakil, V., Smith, E.L., Dai, K., Akyerli, C.B. and Batuman, O.A., Endothelial progenitor cells display clonal restriction in multiple myeloma (2007), in: BMC Cancer, 6(161)

Tez, M., Gocmen, E. and Ozcelik, T., HER2 overexpression and angiogenesis in breast cancer (2004), in: Lancet, 362(1503)

Topcu, M., Akyerli, C., Sayi, A., Toruner, G., Kocoglu, R.S., Cimbis, M. and Ozcelik, T., Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome ina boy (2002), in: European J of Human Genetics, 10(77-81)

Ricciardone, M.D., Ozcelik, T., Cevher, B, Ozdag, H., Tuncer, M., Gurgey, A., Uzunalimoglu, O., Cetinkaya, H., Tanyeli, A., Erken, E. and Ozturk, M., Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type I (1999), in: Cancer Research, 59(290-293)

Ricciardone, M.D., Ozcelik, T., Cevher, B, Ozdag, H., Tuncer, M., Gurgey, A., Uzunalimoglu, O., Cetinkaya, H., Tanyeli, A., Erken, E. and Ozturk, M., Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type I (1999), in: Cancer Research, 59(290-293)

Hatirnaz, O., Ure, U., Ar, C., Akyerli, C., Sosyal, T., Ferhanoglu, B., Ozcelik, T. and Ozbek, U., The SOCS-1 gene methylation in chronic myleoid leukemia patients (2008), in: American J of Hematology, 82(729-730)

Onat, O.E., Tez, M., Ozcelik, T. and Toruner, G.A., MDM2 T309G polymorphism is associated with bladder cancer (2007), in: Anticancer Research, 26(3473-3475)

Topaloglu, R., Akyerli, C., Bakkaloglu, A., Aydintug, O., Ozen, S., Besbas, N. and Ozcelik, T., Survey of factor V leiden and prothrombin gene mutations in systemic lupus erythematosus (2002), in: Clinical Rheumatology, 20(259-261)

Bagislar, S., Ustuner, I., Cengiz, B., Soylemez, F., Akyerli, C.B., Ceylaner, S., Ceylaner, G., Acar, A. and Ozcelik, T., Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion (2007), in: Australian New Zealand J of Obstetrics Gynaecology, 46(384-387)

Mazoyer, S., …, ?, Ozcelik, T., Ozturk, M. and al, et, The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations (2001), in: American Journal of Human Genetics, 67(207-212)

Mazoyer, S., …, ?, Ozcelik, T., Ozturk, M. and al, et, The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations (2001), in: American Journal of Human Genetics, 67(207-212)

Ozcelik, T., X chromosome inactivation and female pred,sposition to autoimmunity (2009), in: Clinical Reviews in Allergy & Immunology

Ozcelik, T., To the editor: X-linked clonality testing and autoimmune diseases (2008), in: Blood, 110(2769)

Ozcelik, T., Uncovering the complex mysteries of mosaicism (2003), in: Nature, 417((6889):588)

Ozcelik, T., Uz, E., Bagislar, S., Mustafa, C.A., Gursoy, A., Akarsu, N., Toruner, G., Kamel, N. and Gullu, S., Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity (2007), in: European J of Human Genetics, 14(791-797)

Ozcelik, T., Kanaan, M., Avraham, K.B., Yannoukakos, D., Megarbane, A., Tadmouri, G.O., Middleton, L., Romeo, G., King, M.C. and Lahad, E.L., Collaborative genomics for human health and cooperation in the Mediterranean region (2011), in: Nature Genetics, 42(641-645)

Ozcelik, T., Akarsu, N., Uz, E., Caglayan, S., Gulsuner, S., Onat, O.E., Tan, M. and Tan, U., Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans (2009), in: Proceedings of National Academy of Sciences USA, 105(4232-4236)

Ozcelik, T., Akarsu, N., Uz, E., Caglayan, S., Gulsuner, S., Onat, O.E., Tan, M. and Tan, U., Reply to Herz et al. And Humprey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadruprdal locomotion (2009), in: Proceedings of National Academy of Sciences USA, 105(32-33)

Ozbek, U., Vural, B., Kalayoglu, S., Soysal, T., Bilgen, H., Yavuz, S., Anak, S., Sargin, D., Gedikoglu, G., Ferhanoglu, B., Akoglu, T., Tangun, Y. and Ozcelik, T., Evaluation of chimerism with DNA polymorphisms in bone marrow transplantation (1997), in: Turkish J of Pediatrics, 39(303-311)

Plagnol, V., Uz, E., Wallace, C., Stevens, H., Clayton, D., Ozcelik, T. and Todd, J.A., Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses (2009), in: Plos One, 3(2966)

Kaplan, Y., Vargel, I., Kansu, T., Akin, B., Rohmann, E., Kamaci, S., Uz, E., Ozcelik, T., Wollnik, B. and Akarsu, N.A., Skewed X-inactivation in an X-linked Nystagmus Family Resulted From a Novel, p.R229G, Missence Mutation in the FRMD7 Gene (2008), in: British J of Ophthalmology, 92(135-141)

Ozbalkan, Z., Bagislar, S., Kiraz, S., Akyerli, C.B., Ozer, H.T.E., Yavuz, S., Birlik, A.M., Calguneri, M. and Ozcelik, T., Skewed X-chromosome inactivation in blood cells of women with scleroderma (2006), in: Arthritis & Rheumatism, 52(1564-1570)

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