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

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

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)

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)

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)

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)

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)

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)

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

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

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)

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)

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

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)

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)

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)

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)

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)

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)

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

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)

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)

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)

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)

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)

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)

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)

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)

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

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

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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