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1:

Birben E, Oner R, Oner C, Gumruk F, Altay C, Gurgey A.

Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion.
Br J Haematol. 2002 Jul;118(1):278-81.
PMID: 12100162 [PubMed - indexed for MEDLINE]

2: Birben E, Oner C, Oner R, Mergen H, Yesilipek A, Gumruk F, Gurgey A, Altay C.: Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype.
Hemoglobin. 2001 Nov;25(4):441-5. No abstract available.
PMID: 11791880 [PubMed - in process]

3: Birben E, Oner R, Oner C, Gumruk F, Gurgey A, Altay C.: Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patient.
Hemoglobin. 2001 Nov;25(4):409-15.
PMID: 11791874 [PubMed - in process]

4: Oner R, Acar C, Oner C, Yenicesu I, Gumruk F, Gurgey A, Altay C.: Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient.
Pediatr Hematol Oncol. 2002 Jan-Feb;19(1):39-44.
PMID: 11787865 [PubMed - indexed for MEDLINE]

5: Oner R, Oner C, Birben E, Sozen M, Gumruk F, Gurgey A, Altay C.: beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap site.
Br J Haematol. 2001 Oct;115(1):90-4. Review.
PMID: 11722417 [PubMed - indexed for MEDLINE]

6: Mergen M, Mergen H, Ozata M, Oner R, Oner C.: A novel melanocortin 4 receptor (MC4R) gene mutation associated with morbid obesity.
J Clin Endocrinol Metab. 2001 Jul;86(7):3448.
PMID: 11443223 [PubMed - indexed for MEDLINE]

7: Ozisik G, Mergen H, Ozata M, Uyanik C, Caglayan S, Turan M, Bolu E, Ilgin S, Oner R, Ozdemir IC, Oner C.: Vitamin d-receptor gene polymorphisms and vertebral bone density in men with idiopathic hypogonadotrophic hypogonadism.
Med Sci Monit. 2001 Mar-Apr;7(2):233-7.
PMID: 11257727 [PubMed - indexed for MEDLINE]

8: Oner R, Birben E, Acar C, Oner C, Kara A, Gumruk F, Gurgey A, Altay C.: Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels.
Hemoglobin. 2000 Aug;24(3):195-201.
PMID: 10975439 [PubMed - indexed for MEDLINE]

9: Mergen H, Acar C, Birben E, Oner R, Oner C.: A safer and relatively shorter method for Southern blot hybridization analysis.
J Biochem Biophys Methods. 2000 Jul 10;44(1-2):73-6.
PMID: 10889277 [PubMed - indexed for MEDLINE]

10: Berkel AI, Birben E, Oner C, Oner R, Loos M, Petry F.: Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey.
Immunobiology. 2000 Jan;201(3-4):347-55.
PMID: 10776791 [PubMed - indexed for MEDLINE]

11: Gumruk F, Mergen H, Oner R, Ozcebe O, Sayinalp N, Oner C, Gurgey A, Altay C.: Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
Hemoglobin. 2000 Feb;24(1):23-9.
PMID: 10722112 [PubMed - indexed for MEDLINE]

12: Oner R, Gumruk F, Acar C, Oner C, Gurgey A, Altay C.: Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.
Haematologica. 2000 Mar;85(3):320-1. No abstract available.
PMID: 10702825 [PubMed - indexed for MEDLINE]

13: Koc A, Oner R, Oner C, Aktas D, Sozen M, Tuncbilek E, Altay C.: Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient.
Hematol Cell Ther. 1999 Aug;41(4):187-9.
PMID: 10543376 [PubMed - indexed for MEDLINE]

14: Oner C, Oner R, Balkan H, Gumruk F, Gurgey A.: Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha].
Hemoglobin. 1998 May;22(3):273-6. No abstract available.
PMID: 9629502 [PubMed - indexed for MEDLINE]

15: Altay C, Oner C, Oner R, Gumruk F, Mergen H, Gurgey A.: Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)0-thalassemia traits.
Hum Hered. 1998 May-Jun;48(3):121-5.
PMID: 9618059 [PubMed - indexed for MEDLINE]

16: Oner C, Oner R, Birben E, Balkan H, Gumruk F, Gurgey A, Altay C.: HB H disease with homozygosity for red cell G6PD deficiency in a Turkish female.
Hemoglobin. 1998 Mar;22(2):157-60. No abstract available.
PMID: 9576333 [PubMed - indexed for MEDLINE]

17: Altay C, Oner C, Oner R, Mesci L, Balkan H, Tuzmen S, Basak AN, Gumruk F, Gurgey A.: Genotype-phenotype analysis in HbS-beta-thalassemia.
Hum Hered. 1997 May-Jun;47(3):161-4.
PMID: 9156327 [PubMed - indexed for MEDLINE]

18: Gurgey A, Balkan H, Irken G, Gumruk F, Altay S, Kalaycioglu A, Oner C, Oner R.: Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutation.
Turk J Pediatr. 1997 Apr-Jun;39(2):253-7.
PMID: 9223924 [PubMed - indexed for MEDLINE]

19: Oner C, Oner R, Balkan H, Gurgey A, Yalcin A, Avcu F, Altay C.: Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia.
Br J Haematol. 1997 Feb;96(2):229-34.
PMID: 9029004 [PubMed - indexed for MEDLINE]

20: Oner C, Gurgey A, Oner R, Balkan H, Gumruk F, Baysal E, Altay C.: The molecular basis of Hb H disease in Turkey.
Hemoglobin. 1997 Jan;21(1):41-51.
PMID: 9028822 [PubMed - indexed for MEDLINE]

21: Smetanina NS, Oner C, Baysal E, Oner R, Bozkurt G, Altay C, Gurgey A, Adekile AD, Gu LH, Huisman TH.: The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.
Biochim Biophys Acta. 1996 Aug 23;1316(3):176-82.
PMID: 8781536 [PubMed - indexed for MEDLINE]

22: Zareie MH, Erdem G, Oner C, Oner R, Ogus A, Piskin E.: Investigation of ascorbate-Cu (II) induced cleavage of DNA by scanning tunneling microscopy.
Int J Biol Macromol. 1996 Jul;19(1):69-73.
PMID: 8782722 [PubMed - indexed for MEDLINE]

23: Oner R, Oner C, Erdem G, Balkan H, Ozdag H, Erkan M, Gumruk F, Gurgey A, Altay C.: A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family.
Acta Haematol. 1996;96(4):232-6.
PMID: 8922490 [PubMed - indexed for MEDLINE]

24: Oner C, Oner R, Gurgey A, Altay C.: A new Turkish type of beta-thalassaemia major with homozygosity for two non-consecutive 7.6 kb deletions of the psi beta and beta genes and an intact delta gene.
Br J Haematol. 1995 Feb;89(2):306-12.
PMID: 7873380 [PubMed - indexed for MEDLINE]

25: Divoky V, Baysal E, Oner R, Curuk MA, Walker EL 3rd, Indrak K, Huisman TH.: The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed.
Hum Genet. 1994 Jan;93(1):77-8.
PMID: 8270260 [PubMed - indexed for MEDLINE]

26: Oner C, Dimovski AJ, Olivieri NF, Schiliro G, Codrington JF, Fattoum S, Adekile AD, Oner R, Yuregir GT, Altay C, et al.: Beta S haplotypes in various world populations.
Hum Genet. 1992 Apr;89(1):99-104.
PMID: 1577473 [PubMed - indexed for MEDLINE]

27: Rosatelli MC, Altay C, Oner R, Leoni GB, Moi B, Atzori G, Cao A.: Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemia.
Haematologica. 1992 Mar-Apr;77(2):106-9.
PMID: 1383103 [PubMed - indexed for MEDLINE]

28: Fei YJ, Oner R, Bozkurt G, Gu LH, Altay C, Gurgey A, Fattoum S, Baysal E, Huisman TH.: Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
Acta Haematol. 1992;88(2-3):82-5.
PMID: 1281602 [PubMed - indexed for MEDLINE]

29: Oner R, Oner C, Wilson JB, Tamagnini GP, Ribeiro LM, Huisman TH.: Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene.
Br J Haematol. 1991 Oct;79(2):306-10.
PMID: 1659862 [PubMed - indexed for MEDLINE]

30: Oner R, Kutlar F, Gu LH, Huisman TH.: The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C---T mutation at nucleotide-114 of the A gamma-globin gene.
Blood. 1991 Mar 1;77(5):1124-5. No abstract available.
PMID: 1704803 [PubMed - indexed for MEDLINE]

31: Fattoum S, Guemira F, Oner C, Oner R, Li HW, Kutlar F, Huisman TH.: Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
Hemoglobin. 1991;15(1-2):11-21.
PMID: 1917531 [PubMed - indexed for MEDLINE]

32: Gupta RB, Tiwary RS, Pande PL, Kutlar F, Oner C, Oner R, Huisman TH.: Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
Hemoglobin. 1991;15(5):441-58. Review.
PMID: 1802886 [PubMed - indexed for MEDLINE]

33: Altay C, Gurgey A, Oner R, Kutlar A, Kutlar F, Huisman TH.: A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site.
Hemoglobin. 1991;15(4):327-30. No abstract available.
PMID: 1787101 [PubMed - indexed for MEDLINE]

34: Beris PH, Darbellay R, Beck D, Oner R.: Concomitant inheritance of homozygous alpha-thalassemia-2 with homozygous IVS-I-5 G-C beta gene mutation does not influence the severity of the thalassemic phenotype.
Nouv Rev Fr Hematol. 1991;33(3):227-30.
PMID: 1720237 [PubMed - indexed for MEDLINE]

35: Oner R, Agarwal S, Dimovski AJ, Efremov GD, Petkov GH, Altay C, Gurgey A, Huisman TH.: The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.
Hemoglobin. 1991;15(1-2):67-76.
PMID: 1717406 [PubMed - indexed for MEDLINE]

36: Oner R, Altay C, Gurgey A, Aksoy M, Kilinc Y, Stoming TA, Reese AL, Kutlar A, Kutlar F, Huisman TH.: Beta-thalassemia in Turkey.
Hemoglobin. 1990;14(1):1-13. Review.
PMID: 2200760 [PubMed - indexed for MEDLINE]

37: Agarwal S, Oner R, Kutlar F, Huisman TH.: Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes.
Hemoglobin. 1990;14(4):471-5. No abstract available.
PMID: 1704359 [PubMed - indexed for MEDLINE]