C. Öner

863 total citations
29 papers, 709 citations indexed

About

C. Öner is a scholar working on Genetics, Hematology and Physiology. According to data from OpenAlex, C. Öner has authored 29 papers receiving a total of 709 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Hematology and 10 papers in Physiology. Recurrent topics in C. Öner's work include Hemoglobinopathies and Related Disorders (18 papers), Iron Metabolism and Disorders (14 papers) and Erythrocyte Function and Pathophysiology (7 papers). C. Öner is often cited by papers focused on Hemoglobinopathies and Related Disorders (18 papers), Iron Metabolism and Disorders (14 papers) and Erythrocyte Function and Pathophysiology (7 papers). C. Öner collaborates with scholars based in Türkiye, United States and Tunisia. C. Öner's co-authors include KD Lanclos, Aleksandar Dimovski, YC Gu, Aytemiz Gürgey, R. Öner, TH Huisman, T. H. J. Huisman, Çiğdem Altay, F. Kutlar and T. H. J. Huisman and has published in prestigious journals such as Blood, British Journal of Haematology and Allergy.

In The Last Decade

C. Öner

28 papers receiving 687 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C. Öner Türkiye	14	512	439	179	160	127	29	709
YW Kan United States	17	615 1.2×	489 1.1×	155 0.9×	89 0.6×	220 1.7×	39	851
Fabienne Toutain France	10	162 0.3×	167 0.4×	52 0.3×	289 1.8×	159 1.3×	23	572
JULIAN R. DAVIS United States	5	385 0.8×	305 0.7×	89 0.5×	60 0.4×	57 0.4×	7	458
Bibi Shahin Shamsian Iran	11	111 0.2×	106 0.2×	47 0.3×	33 0.2×	36 0.3×	38	284
K. Punt Netherlands	11	149 0.3×	293 0.7×	39 0.2×	35 0.2×	106 0.8×	28	489
Hildegard Braun Germany	4	325 0.6×	371 0.8×	307 1.7×	122 0.8×	35 0.3×	7	644
Mary Link United States	4	309 0.6×	232 0.5×	178 1.0×	31 0.2×	101 0.8×	8	445
Samin Alavi Iran	12	155 0.3×	183 0.4×	47 0.3×	55 0.3×	22 0.2×	66	417
L L Chan Malaysia	11	419 0.8×	438 1.0×	91 0.5×	21 0.1×	39 0.3×	20	618
Maria Concetta Renda Italy	13	160 0.3×	115 0.3×	78 0.4×	19 0.1×	59 0.5×	25	458

Countries citing papers authored by C. Öner

Since Specialization

Citations

This map shows the geographic impact of C. Öner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by C. Öner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Öner more than expected).

Fields of papers citing papers by C. Öner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Öner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by C. Öner. The network helps show where C. Öner may publish in the future.

Co-authorship network of co-authors of C. Öner

This figure shows the co-authorship network connecting the top 25 collaborators of C. Öner. A scholar is included among the top collaborators of C. Öner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Öner. C. Öner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Saçkesen, Cansın, Çağatay Karaaslan, Özlem Keskin, et al.. (2005). The effect of polymorphisms at the CD14 promoter and the TLR4 gene on asthma phenotypes in Turkish children with asthma. Allergy. 60(12). 1485–1492. 81 indexed citations

Sozen, Mert, Çağatay Karaaslan, R. Öner, et al.. (2004). Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family. American Journal of Hematology. 76(4). 378–382. 8 indexed citations

Öner, R., Ceren Acar, C. Öner, et al.. (2002). CHRONIC HEMOLYTIC ANEMIA ASSOCIATED WITH GLUCOSE 6-PHOSPHATE DEHYDROGENASE (GUADALAJARA)1159 C → T (387 ARG → CYS) DEFICIENCY ASSOCIATED WITH GILBERT SYNDROME IN A TURKISH PATIENT. Pediatric Hematology and Oncology. 19(1). 39–44. 7 indexed citations

Öner, R., C. Öner, Esra Birben, et al.. (2001). β‐Thalassaemia intermedia in a Turkish girl: homozygosity for G→A substitution at +22 relative to the β‐globin cap site. British Journal of Haematology. 115(1). 90–94. 4 indexed citations

Koç, Ahmet, R. Öner, C. Öner, et al.. (1999). Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient. PubMed. 41(4). 187–189. 2 indexed citations

Tezcan, İlhan, Özden Sanal, F Ersoy, et al.. (1999). Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvement. Bone Marrow Transplantation. 24(8). 931–933. 18 indexed citations

Altay, Çiğdem, C. Öner, R. Öner, et al.. (1998). Effect of α-Gene Numbers on the Expression of β-Thalassemia intermedia, β-Thalassemia and (δβ)°-Thalassemia Traits. Human Heredity. 48(3). 121–125. 13 indexed citations

Öner, C., Aytemiz Gürgey, R. Öner, et al.. (1997). The Molecular Basis of HB H Disease in Turkey. Hemoglobin. 21(1). 41–51. 40 indexed citations

Gürgey, Aytemiz, et al.. (1995). HB Hakkari or α₂β₂31(B13)LEU→ARG, A Severely Unstable Hemoglobin Variant Associated with Numerous Intra-Erythroblastic Inclusions and Erythroid Hyperplasia of the Bone Marrow. Hemoglobin. 19(3-4). 165–172. 7 indexed citations

10.

Öner, C., et al.. (1995). A new Turkish type of β‐thalassaemia major with homozygosity for two non‐consecutive 7.6 kb deletions of the Ψβ and β genes and an intact δ gene. British Journal of Haematology. 89(2). 306–312. 14 indexed citations

11.

Gu, L-H., C. Öner, & T. H. J. Huisman. (1995). The^Gγ^TChain (^Gγ75 Thr; 136 Gly) In Hb F-Charlotte Is The Product Of An^Aγ Gene With A Limited Gene Conversion And That In Hb F-Waynesboro Of A Mutated^Gγ Gene. Hemoglobin. 19(6). 413–418. 6 indexed citations

12.

Dimovski, Aleksandar, et al.. (1993). Haplotype-Specific Sequence Variations in the Locus Control Region (5′ Hypersensitive Sites 2, 3, 4) OF β^SChrwosomes. Hemoglobin. 17(5). 475–478. 11 indexed citations

13.

Baysal, E., C. Öner, KD Lanclos, et al.. (1992). Black β‐thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site‐2 of the locus control region have high levels of fetal hemoglobin. American Journal of Hematology. 41(2). 97–101. 18 indexed citations

14.

Öner, C., Aleksandar Dimovski, Çiğdem Altay, et al.. (1992). Sequence variations in the 5' hypersensitive site-2 of the locus control region of beta S chromosomes are associated with different levels of fetal globin in hemoglobin S homozygotes. Blood. 79(3). 813–819. 87 indexed citations

15.

Kutlar, F., et al.. (1991). Hemoglobinopathies Among the Gond Tribal Groups of Central India; Interaction of α- and β-Thalassemia with β Chain Variants. Hemoglobin. 15(5). 441–458. 25 indexed citations

16.

Fattoum, S., Fethi Guémira, C. Öner, et al.. (1991). β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians. Hemoglobin. 15(1-2). 11–21. 48 indexed citations

17.

Dimovski, Aleksandar, et al.. (1991). Certain Mutations Observed in the 5´ Sequences of the Gγ- and Aγ-Globin Genes of βs Chromosomes Are Specific for Chromosomes with Major Haplotypes. Acta Haematologica. 85(2). 79–87. 25 indexed citations

18.

Lanclos, KD, C. Öner, Aleksandar Dimovski, YC Gu, & T. H. J. Huisman. (1991). Sequence variations in the 5' flanking and IVS-II regions of the G gamma- and A gamma-globin genes of beta S chromosomes with five different haplotypes. Blood. 77(11). 2488–2496. 86 indexed citations

19.

Öner, R., C. Öner, J. B. Wilson, et al.. (1991). Dominant β‐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 β‐globin gene. British Journal of Haematology. 79(2). 306–310. 27 indexed citations

20.

Öner, C., Aytemiz Gürgey, Çiğdem Altay, F. Kutlar, & T. H. J. Huisman. (1990). Variation in the level of fetal hemoglobin in (δβ)°‐thalassemia heterozygotes with different numbers of α‐globin genes. American Journal of Hematology. 34(3). 230–231. 7 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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