1 - 25 of 35 results for author:"Ozen S." in Literature citations
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| Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism. Gurbuz F., Kotan L.D., Mengen E., Sıklar Z., Berberoglu M., Dokmetas S., Kılıclı M.F., Guven A., Kirel B., Saka N. et al. J Clin Res Pediatr Endocrinol 4:121-126(2012) · Mapped (4) |
| Homozygous M694V as a risk factor for amyloidosis in Turkish FMF patients. Akpolat T., Ozkaya O., Ozen S. Gene 492:285-289(2012) · Mapped (6) |
| Neuroendocrine immune system in familial Mediterranean fever. Topaloglu R., Bilginer Y., Alikasifoglu A., Ozaltin F., Besbas N., Ozen S., Bakkaloglu A. Turk. J. Pediatr. 52:588-593(2010) · Mapped (2) |
| Expression of laminin receptor 1 in human placentas from normal and preeclamptic pregnancies and its relationship with the severity of preeclampsia. Kurdoglu M., Kurdoglu Z., Ozen S., Kucukaydin Z., Bulut G., Erten R., Kamaci M. J Perinat Med 39:411-416(2011) · Mapped (1) |
| The association of inflammatory bowel disease and Mediterranean fever gene (MEFV) mutations in Turkish children. Uslu N., Yuce A., Demir H., Saltik-Temizel I.N., Usta Y., Yilmaz E., Besbas N., Gurakan F., Ozen H., Ozen S. Dig. Dis. Sci. 55:3488-3494(2010) · Mapped (6) |
| Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. Choi M., Scholl U.I., Ji W., Liu T., Tikhonova I.R., Zumbo P., Nayir A., Bakkaloglu A., Ozen S., Sanjad S. et al. Proc. Natl. Acad. Sci. U.S.A. 106:19096-19101(2009) · UniProtKB (1) |
| Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene. Gok F., Crettol L.M., Alanay Y., Hacihamdioglu B., Kocaoglu M., Bonafe L., Ozen S. Eur. J. Pediatr. 169:363-367(2010) · Mapped (2) |
| The analysis of interleukin-1 receptor antagonist and interleukin-1beta gene polymorphisms in Turkish FMF patients: do they predispose to secondary amyloidosis? Balci-Peynircioglu B., Taskiran Z.E., Turel B., Arici M., Bakkaloglu A., Ozen S., Yilmaz E. Clin. Exp. Rheumatol. 26:S99-102(2008) · Mapped (5) |
| MEFV mutations in systemic onset juvenile idiopathic arthritis. Ayaz N.A., Ozen S., Bilginer Y., Erguven M., Taskiran E., Yilmaz E., Besbas N., Topaloglu R., Bakkaloglu A. Rheumatology (Oxford) 48:23-25(2009) · Mapped (6) |
| Eye involvement in children with primary focal segmental glomerulosclerosis. Ozaltin F., Heeringa S., Poyraz C.E., Bilginer Y., Kadayifcilar S., Besbas N., Topaloglu R., Ozen S., Hildebrandt F., Bakkaloglu A. Pediatr. Nephrol. 23:421-427(2008) · Mapped (4) |
| Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa. Yalcinkaya F., Ozcakar Z.B., Kasapcopur O., Ozturk A., Akar N., Bakkaloglu A., Arisoy N., Ekim M., Ozen S. J. Pediatr. 151:675-678(2007) · Mapped (6) |
| Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever. Touitou I., Sarkisian T., Medlej-Hashim M., Tunca M., Livneh A., Cattan D., Yalcinkaya F., Ozen S., Majeed H., Ozdogan H. et al. Arthritis Rheum. 56:1706-1712(2007) · Mapped (6) |
| Is the CD14 C159T polymorphism effective in the development of secondary amyloidosis in Familial Mediterranean fever? Keskin O., Yilmaz E., Kutlay S., Bakkaloglu A., Topaloglu R., Arici M., Kalayci O., Ozen S. Rheumatol. Int. 27:691-694(2007) · Mapped (2) |
| Are carriers for MEFV mutations "healthy"? Kalyoncu M., Acar B.C., Cakar N., Bakkaloglu A., Ozturk S., Dereli E., Tunca M., Kasapcopur O., Yalcinkaya F., Ozen S. Clin. Exp. Rheumatol. 24:S120-2(2006) · Mapped (6) |
| Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease. Ozen S., Berdeli A., Turel B., Kutlay S., Yalcinkaya F., Arici M., Besbas N., Bakkaloglu A., Yilmaz E. J. Rheumatol. 33:2498-2500(2006) · Mapped (2) |
| NOD2/CARD15, NOD1/CARD4, and ICAM-1 gene polymorphisms in Turkish patients with inflammatory bowel disease. Ozen S.C., Dagli U., Kilic M.Y., Toruner M., Celik Y., Ozkan M., Soykan I., Cetinkaya H., Ulker A., Ozden A. et al. J. Gastroenterol. 41:304-310(2006) · Mapped (22) |
| Cytokine gene polymorphisms in Turkish patients with inflammatory bowel disease. Celik Y., Dagli U., Kilic M.Y., Toruner M., Ozen S.C., Ozkan M., Soykan I., Cetinkaya H., Ulker A., Ozden A. et al. Scand. J. Gastroenterol. 41:559-565(2006) · Mapped (11) |
| Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Tunca M., Akar S., Onen F., Ozdogan H., Kasapcopur O., Yalcinkaya F., Tutar E., Ozen S., Topaloglu R., Yilmaz E. et al. Medicine (Baltimore) 84:1-11(2005) · Mapped (6) |
| Influence of Serum Amyloid A (SAA1) and SAA2 gene polymorphisms on renal amyloidosis, and on SAA/C-reactive protein values in patients with familial mediterranean fever in the Turkish population. Bakkaloglu A., Duzova A., Ozen S., Balci B., Besbas N., Topaloglu R., Ozaltin F., Yilmaz E. J. Rheumatol. 31:1139-1142(2004) · Mapped (5) |
| Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis. Aganna E., Hawkins P.N., Ozen S., Pettersson T., Bybee A., McKee S.A., Lachmann H.J., Karenko L., Ranki A., Bakkaloglu A. et al. Genes Immun. 5:289-293(2004) · Mapped (14) |
| Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patients. Yilmaz E., Balci B., Kutlay S., Ozen S., Erturk S., Oner A., Besbas N., Bakkaloglu A. Turk. J. Pediatr. 45:198-202(2003) · Mapped (9) |
| Mutations in the gene for familial Mediterranean fever: do they predispose to inflammation? Ozen S., Bakkaloglu A., Yilmaz E., Duzova A., Balci B., Topaloglu R., Besbas N. J. Rheumatol. 30:2014-2018(2003) · Mapped (6) |
| No evidence for an association between the T102C and 1438 G/A polymorphisms of the serotonin 2A receptor gene in attention deficit/hyperactivity disorder in a Turkish population. Zoroglu S.S., Erdal M.E., Erdal N., Ozen S., Alasehirli B., Sivasli E. Neuropsychobiology 47:17-20(2003) · Mapped (2) |
| Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss. Stover E.H., Borthwick K.J., Bavalia C., Eady N., Fritz D.M., Rungroj N., Giersch A.B.S., Morton C.C., Axon P.R., Akil I. et al. J. Med. Genet. 39:796-803(2002) · UniProtKB (2) |
| MEFV gene mutations in familial Mediterranean fever phenotype II patients with renal amyloidosis in childhood: a retrospective clinicopathological and molecular study. Balci B., Tinaztepe K., Yilmaz E., Gucer S., Ozen S., Topaloglu R., Besbas N., Ozguc M., Bakkaloglu A. Nephrol. Dial. Transplant. 17:1921-1923(2002) · Mapped (6) |