Nejat Akar

714 total citations
31 papers, 300 citations indexed

About

Nejat Akar is a scholar working on Hematology, Genetics and Physiology. According to data from OpenAlex, Nejat Akar has authored 31 papers receiving a total of 300 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Hematology, 12 papers in Genetics and 9 papers in Physiology. Recurrent topics in Nejat Akar's work include Hemoglobinopathies and Related Disorders (12 papers), Erythrocyte Function and Pathophysiology (8 papers) and Iron Metabolism and Disorders (5 papers). Nejat Akar is often cited by papers focused on Hemoglobinopathies and Related Disorders (12 papers), Erythrocyte Function and Pathophysiology (8 papers) and Iron Metabolism and Disorders (5 papers). Nejat Akar collaborates with scholars based in Türkiye, United States and Spain. Nejat Akar's co-authors include Duygu Özel Demiralp, Zümrüt Uysal, Ece Akar, Hakkı Taştan, Nilgün Çakar, Fatoş Yalçınkaya, Mustafa Tekin, A.O. Çavdar, Antonio Cao and Angela Loi and has published in prestigious journals such as Blood, Thrombosis and Haemostasis and Journal of Medical Genetics.

In The Last Decade

Nejat Akar

31 papers receiving 281 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nejat Akar Türkiye 11 145 125 85 58 52 31 300
Sonja Wagner Austria 8 116 0.8× 82 0.7× 41 0.5× 27 0.5× 38 0.7× 14 284
A. McCraw United Kingdom 8 251 1.7× 133 1.1× 19 0.2× 30 0.5× 31 0.6× 13 362
Karin P. Potoka United States 6 77 0.5× 106 0.8× 46 0.5× 166 2.9× 129 2.5× 6 302
Brigitte Onraed France 8 51 0.4× 60 0.5× 33 0.4× 30 0.5× 72 1.4× 17 268
M. Pilar Sardà Spain 12 190 1.3× 121 1.0× 56 0.7× 30 0.5× 19 0.4× 15 321
Hagit Hauschner Israel 11 167 1.2× 56 0.4× 16 0.2× 44 0.8× 25 0.5× 27 278
Muriel Giansily‐Blaizot France 18 605 4.2× 188 1.5× 44 0.5× 132 2.3× 18 0.3× 50 740
McDonald Tp United States 11 302 2.1× 77 0.6× 47 0.6× 133 2.3× 40 0.8× 22 379
Nadia Mirra Italy 9 93 0.6× 125 1.0× 85 1.0× 51 0.9× 10 0.2× 14 232
Matteo Francese Italy 11 109 0.8× 122 1.0× 127 1.5× 86 1.5× 45 0.9× 15 337

Countries citing papers authored by Nejat Akar

Since Specialization
Citations

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

Fields of papers citing papers by Nejat Akar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nejat Akar

This figure shows the co-authorship network connecting the top 25 collaborators of Nejat Akar. A scholar is included among the top collaborators of Nejat Akar 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 Nejat Akar. Nejat Akar 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.
Bakanay, Şule Mine, et al.. (2013). Blood group genotyping in multi-transfused patients. Transfusion and Apheresis Science. 48(2). 257–261. 31 indexed citations
2.
Demiralp, Duygu Özel, et al.. (2012). Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis. PROTEOMICS - CLINICAL APPLICATIONS. 6(7-8). 403–411. 10 indexed citations
3.
Akar, Nejat, et al.. (2011). Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis. Molecular Biology Reports. 39(3). 3161–3167. 13 indexed citations
4.
Tekeli, Oya, et al.. (2006). No Relation between Angiotensin-Converting Enzyme Gene Polymorphism and Pseudoexfoliation. Ophthalmic Research. 40(1). 32–34. 1 indexed citations
5.
Elhan, Atilla Halil, et al.. (2005). SERUM SOLUBLE TRANSFERRIN RECEPTOR IS A VALUABLE DIAGNOSTIC TOOL IN IRON DEFICIENCY OF BREATH-HOLDING SPELLS. Pediatric Hematology and Oncology. 22(8). 711–716. 7 indexed citations
6.
Akar, Nejat, et al.. (2002). Factor V 1691 G-A mutation in children with intracardiac thrombosis: a prospective study. Acta Paediatrica. 91(2). 168–171. 2 indexed citations
7.
Akar, Nejat, et al.. (2002). RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION. Pediatric Hematology and Oncology. 19(8). 569–573. 9 indexed citations
8.
Akar, Nejat, et al.. (2001). Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same Patient.. PubMed. 18(2). 137–41. 2 indexed citations
9.
Tekin, Mustafa, Fatoş Yalçınkaya, Nilgün Çakar, et al.. (2000). MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis?. Clinical Genetics. 57(6). 430–434. 32 indexed citations
10.
Avcu, Ferit, Ece Akar, Ufuk Demirkılıç, et al.. (2000). The Role of Prothrombotic Mutations in Patients with Buerger's Disease. Thrombosis Research. 100(3). 143–147. 28 indexed citations
11.
Küçük, Ömer, et al.. (1999). Evaluation of cardiac functions in patients with thalassemia major. Annals of Nuclear Medicine. 13(3). 175–179. 13 indexed citations
12.
Atalay, Semra, et al.. (1999). Plasma endothelin-1 levels in patients with left-to-right shunt with or without pulmonary hypertension. International Journal of Cardiology. 70(1). 57–62. 21 indexed citations
13.
Alhenc‐Gelas, Martine, et al.. (1998). Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr. Blood Coagulation & Fibrinolysis. 9(4). 351–354. 2 indexed citations
14.
Uysal, Zümrüt, Yıldız Yildirmak, Nejat Akar, Nazlı Başak, & Şükrü Cin. (1998). α-Thalassemia and Hereditary Spherocytosis in the Same Patient: The Interaction of two Diseases. Pediatric Hematology and Oncology. 15(3). 271–276. 7 indexed citations
15.
Çakar, Nilgün, Mesiha Ekim, Necmiye Tümer, et al.. (1997). Pharmacokinetics of recombinant human erythropoietin in children with chronic renal failure. International Urology and Nephrology. 29(3). 377–383. 3 indexed citations
16.
Akar, Nejat, Tansu Sipahi, & Feride Söylemez. (1997). Coffee beans pica causing iron and zinc deficiency. The Journal of Trace Elements in Experimental Medicine. 10(3). 205–208. 1 indexed citations
17.
Akar, Nejat, Ece Akar, Hakkı Taştan, & Ş. Cin. (1996). Direct detection of Hb C (B6 Glu-Lys) byBseRI analysis. American Journal of Hematology. 52(4). 325–326. 6 indexed citations
18.
Akar, Nejat, et al.. (1995). Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysis. Pediatric Nephrology. 9(4). 485–486. 3 indexed citations
19.
Erekul, Selim, et al.. (1995). p53 Codon 213 (A-G) Polymorphism in a Turkish Population. Pediatric Hematology and Oncology. 12(5). 499–501. 3 indexed citations
20.
Cin, Ş., Nejat Akar, Ayten Arcasoy, & A.O. Çavdar. (1988). Abnormal Hemoglobins in Turkish Cypriots. Hemoglobin. 12(4). 423–425. 2 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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