F. Kutlar

4.2k total citations
157 papers, 3.3k citations indexed

About

F. Kutlar is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, F. Kutlar has authored 157 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 136 papers in Genetics, 94 papers in Hematology and 34 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in F. Kutlar's work include Hemoglobinopathies and Related Disorders (135 papers), Iron Metabolism and Disorders (69 papers) and Blood groups and transfusion (34 papers). F. Kutlar is often cited by papers focused on Hemoglobinopathies and Related Disorders (135 papers), Iron Metabolism and Disorders (69 papers) and Blood groups and transfusion (34 papers). F. Kutlar collaborates with scholars based in United States, Türkiye and Spain. F. Kutlar's co-authors include Abdullah Kutlar, T. H. J. Huisman, T. A. Stoming, T. H. J. Huisman, J. M. Gonzalez‐Redondo, KD Lanclos, Aytemiz Gürgey, M Aksoy, T. Nakatsuji and J. B. Wilson and has published in prestigious journals such as New England Journal of Medicine, Blood and FEBS Letters.

In The Last Decade

F. Kutlar

154 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F. Kutlar United States 34 2.8k 2.1k 705 614 504 157 3.3k
T. H. J. Huisman United States 35 2.5k 0.9× 1.9k 0.9× 692 1.0× 774 1.3× 530 1.1× 135 3.2k
G Stamatoyannopoulos United States 29 1.5k 0.5× 1.1k 0.5× 557 0.8× 999 1.6× 618 1.2× 104 2.6k
J. B. Wilson United States 24 1.8k 0.7× 1.1k 0.5× 543 0.8× 464 0.8× 602 1.2× 144 2.6k
T. H. J. Huisman United States 23 1.3k 0.5× 911 0.4× 357 0.5× 269 0.4× 272 0.5× 81 1.5k
Junius G. Adams United States 20 981 0.4× 727 0.3× 250 0.4× 229 0.4× 252 0.5× 64 1.2k
Theodosia A. Kalfa United States 27 661 0.2× 676 0.3× 282 0.4× 818 1.3× 1.2k 2.3× 111 2.5k
ME Fabry United States 21 1.3k 0.5× 806 0.4× 199 0.3× 257 0.4× 707 1.4× 39 1.5k
D. Mark Layton United Kingdom 19 368 0.1× 653 0.3× 227 0.3× 378 0.6× 387 0.8× 62 1.5k
P Vuopio Finland 27 495 0.2× 879 0.4× 154 0.2× 402 0.7× 171 0.3× 92 1.9k
Lesley J. Bruce United Kingdom 29 415 0.2× 572 0.3× 677 1.0× 1.1k 1.9× 1.7k 3.5× 80 2.7k

Countries citing papers authored by F. Kutlar

Since Specialization
Citations

This map shows the geographic impact of F. Kutlar'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 F. Kutlar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Kutlar more than expected).

Fields of papers citing papers by F. Kutlar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. Kutlar. 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 F. Kutlar. The network helps show where F. Kutlar may publish in the future.

Co-authorship network of co-authors of F. Kutlar

This figure shows the co-authorship network connecting the top 25 collaborators of F. Kutlar. A scholar is included among the top collaborators of F. Kutlar 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 F. Kutlar. F. Kutlar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Meiler, Steffen E., Marlene Wade, F. Kutlar, et al.. (2011). Pomalidomide augments fetal hemoglobin production without the myelosuppressive effects of hydroxyurea in transgenic sickle cell mice. Blood. 118(4). 1109–1112. 61 indexed citations
2.
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Dınçol, Günçağ, et al.. (2006). Hb J- Meerut [α 120 (H3) Ala ->Glu (α1)] In A Turkish Male. International Journal of Medical Sciences. 3(1). 26–27. 7 indexed citations
5.
6.
Tadmouri, Ghazi Omar, et al.. (1999). Identification of the Chinese IVS-II-654 (C-->T) beta-thalassemia mutation in an immigrant Turkish family: recurrence or migration?. PubMed. 71(2). 295–302. 3 indexed citations
7.
Çürük, Mehmet Akif, Aleksandar Dimovski, E. Baysal, et al.. (1993). Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients. American Journal of Hematology. 44(4). 270–275. 64 indexed citations
8.
Adekile, Adekunle, Kathleen McKie, O O Adeodu, et al.. (1993). Spleen in sickle cell anemia: Comparative studies of Nigerian and U.S. patients. American Journal of Hematology. 42(3). 316–321. 36 indexed citations
9.
Wilson, J. B., M. Ramachandran, B. B. Webber, et al.. (1991). HB Cleveland or α2β293(F9)CYS→ARG;121(GH4)GLU→GLN. Hemoglobin. 15(4). 269–278. 7 indexed citations
10.
Plaseska‐Karanfilska, Dijana, et al.. (1990). Hb F-Jiangsu, The First γ Chain Variant with a Valine -Methionine Substitution: αγ2134(H12) Val→Met. Hemoglobin. 14(2). 177–183. 3 indexed citations
11.
Codrington, John, et al.. (1990). Compound Heterozygosity for a Mild β<sup>+</sup> and a Rare β°-Thalassemia Allele. Acta Haematologica. 84(3). 135–138. 2 indexed citations
12.
Gürgey, Aytemiz, et al.. (1989). Hydrops fetalis due to Homozygosity for α-Thalassemia-1, -(α)-20.5 kb: The First Observation in a Turkish Family. Acta Haematologica. 81(3). 169–171. 14 indexed citations
13.
Kutlar, F., et al.. (1989). The Types of Hemoglobins and Globin Chains in Hydrops Fetalis. Hemoglobin. 13(7-8). 671–683. 16 indexed citations
14.
Codrington, John, et al.. (1989). Hb A2-Wrens or α2δ298(FG5)Val → MEt, an unstable δ chain variant identified by sequence analysis of amplified DNA. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1009(1). 87–89. 18 indexed citations
15.
Yang, K. G., F. Kutlar, Elizabeth George, et al.. (1989). Molecular characterization of β‐globin gene mutations in Malay patients with Hb E‐β‐thalassaemia and thalassaemia major. British Journal of Haematology. 72(1). 73–80. 81 indexed citations
16.
Kutlar, F., P Sciacca, G. Schiliró, et al.. (1989). A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns. Hemoglobin. 13(1). 45–65. 46 indexed citations
17.
Kutlar, Abdullah, F. Kutlar, J. B. Wilson, et al.. (1988). HB F-Austell or α2Gγ240(c6)ARG→LYS. Hemoglobin. 12(4). 409–411. 4 indexed citations
18.
Ma, Minghong, et al.. (1987). HB F-Xin-Su orAγT73(E17)Asp→His: A New Slow-Moving Fetal Hemoglobin Variant. Hemoglobin. 11(5). 473–479. 4 indexed citations
19.
Daenen, Simon, et al.. (1987). An Indonesian Family with the Southeast Asian Type of α-Thalassemia-1 and a γ-Globin Gene Triplication. Acta Haematologica. 78(1). 23–27. 2 indexed citations
20.
Wilson, J. B., et al.. (1986). The Identification of Five Rare β-Chain Abnormal Hemoglobins by High Performance Liquid Chromatographic Procedures. Hemoglobin. 10(1). 49–63. 14 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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