Fatih Kardaş

538 total citations
47 papers, 367 citations indexed

About

Fatih Kardaş is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Fatih Kardaş has authored 47 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Clinical Biochemistry, 15 papers in Physiology and 12 papers in Molecular Biology. Recurrent topics in Fatih Kardaş's work include Metabolism and Genetic Disorders (15 papers), Lysosomal Storage Disorders Research (7 papers) and Amino Acid Enzymes and Metabolism (6 papers). Fatih Kardaş is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Lysosomal Storage Disorders Research (7 papers) and Amino Acid Enzymes and Metabolism (6 papers). Fatih Kardaş collaborates with scholars based in Türkiye, United States and Japan. Fatih Kardaş's co-authors include Mustafa Kendırcı, Selim Kurtoğlu, Hüseyin Per, Leyla Akın, Ayşe Kaçar Bayram, Sefer Kumandaş, Mehmet Canpolat, Hakan Gümüş, Esra Demi̇rci̇ and Figen Narin and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Clinica Chimica Acta.

In The Last Decade

Fatih Kardaş

38 papers receiving 358 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fatih Kardaş Türkiye 11 87 77 68 53 50 47 367
İsmail Benli Türkiye 12 76 0.9× 35 0.5× 24 0.4× 13 0.2× 34 0.7× 34 350
T. Lightfoot Germany 3 80 0.9× 39 0.5× 18 0.3× 13 0.2× 39 0.8× 3 399
C W Lam Hong Kong 12 150 1.7× 79 1.0× 93 1.4× 19 0.4× 24 0.5× 28 440
Atilla Çayır Türkiye 12 94 1.1× 35 0.5× 16 0.2× 19 0.4× 56 1.1× 64 408
Ersin Gümüş Türkiye 9 46 0.5× 57 0.7× 11 0.2× 46 0.9× 49 1.0× 25 354
Yong Ding China 10 91 1.0× 76 1.0× 45 0.7× 11 0.2× 19 0.4× 28 337
Nasser A. Elhawary Saudi Arabia 11 139 1.6× 56 0.7× 35 0.5× 13 0.2× 39 0.8× 36 310
Yavuz Sanısoğlu Türkiye 10 75 0.9× 40 0.5× 48 0.7× 6 0.1× 48 1.0× 26 392
H Willgerodt Germany 15 211 2.4× 39 0.5× 50 0.7× 110 2.1× 81 1.6× 49 690

Countries citing papers authored by Fatih Kardaş

Since Specialization
Citations

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

Fields of papers citing papers by Fatih Kardaş

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatih Kardaş

This figure shows the co-authorship network connecting the top 25 collaborators of Fatih Kardaş. A scholar is included among the top collaborators of Fatih Kardaş 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 Fatih Kardaş. Fatih Kardaş 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.
2.
Baykan, Ali, et al.. (2023). Evaluation of the effect of obesity, dietary glycemic index and metabolic profiles on the cardiovascular risk in children with classical phenylketonuria. Molecular Genetics and Metabolism. 140(3). 107677–107677. 6 indexed citations
3.
Kardaş, Fatih, et al.. (2023). PPM1K defects cause mild maple syrup urine disease: The second case in the literature. American Journal of Medical Genetics Part A. 191(5). 1360–1365. 6 indexed citations
4.
Bayram, Fahrı, et al.. (2023). Characterization of peripheral blood T follicular helper (TFH) cells in patients with type 1 Gaucher disease and carriers. Blood Cells Molecules and Diseases. 100. 102728–102728. 1 indexed citations
5.
Canpolat, Mehmet, Fatih Kardaş, Mustafa Kendırcı, et al.. (2022). Serum Vitamin D and B12 Levels in School-aged Children and Adolescents with Frequent Primary Headache Attacks. SHILAP Revista de lepidopterología. 3(4). 149–155.
6.
Hatipoğlu, Nihal, et al.. (2022). Identifying the effects of excess weight, metabolic syndrome and insulin resistance on liver stiffness using ultrasound elastography in children. The Turkish Journal of Pediatrics. 64(4). 671–682. 1 indexed citations
7.
Tada, Hayato, Alper Özcan, Ebru Yılmaz, et al.. (2022). A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia. Clinica Chimica Acta. 529. 61–66. 5 indexed citations
8.
Güven, Ahmet Sami, et al.. (2019). Screening Inherited Metabolic Disorder in Children with Intellectual Disability and Epilepsy. SHILAP Revista de lepidopterología. 25(3). 135–139. 3 indexed citations
9.
Kardaş, Fatih, et al.. (2018). Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family. The Turkish Journal of Pediatrics. 60(3). 344–347. 5 indexed citations
10.
Baştuğ, Osman, et al.. (2017). A rare cause of opistotonus; fumaric aciduria: The first case presentation in Turkey. Türk Pediatri Arşivi. 49(1). 74–76. 3 indexed citations
11.
Kendırcı, Mustafa, et al.. (2015). Long-term efficacy of lipoprotein apheresis in the management of familial hypercholesterolaemia: Application of two different apheresis techniques in childhood. Transfusion and Apheresis Science. 54(2). 282–288. 3 indexed citations
12.
Öztürk, Mehmet, et al.. (2015). Effects of L-carnitine supplementation on respiratory distress syndrome development and prognosis in premature infants: A single blind randomized controlled trial. Experimental and Therapeutic Medicine. 11(3). 1123–1127. 15 indexed citations
13.
Kardaş, Fatih, et al.. (2014). Plasma Pentraxin 3 as a Biomarker of Metabolic Syndrome. The Indian Journal of Pediatrics. 82(1). 35–38. 12 indexed citations
14.
Keklık, Muzaffer, Serdar Şıvgın, Süleyman Baldane, et al.. (2013). A Case with Niemann-Pick Disease and Concomitant Kartagener's Syndrome. 35(3). 174–176. 1 indexed citations
15.
Kardaş, Fatih, et al.. (2012). Çocuklarda D Vitamini İntoksikasyonu. 8(2). 148–151.
16.
Fasano, Tommaso, Paolo Zanoni, Claudio Rabacchi, et al.. (2012). Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency. Molecular Genetics and Metabolism. 107(3). 534–541. 29 indexed citations
17.
Kardaş, Fatih, et al.. (2012). A novel homozygous GALC mutation: Very early onset and rapidly progressive Krabbe disease. Gene. 517(1). 125–127. 11 indexed citations
18.
Kendırcı, Mustafa, et al.. (2012). Alkaptonuria: a Presentation of Two Turkish Cases. 34(2). 88–90. 2 indexed citations
19.
Akın, Melih, et al.. (2011). Closed fontanel due to wormian bone: case report.. 33(1). 65–68. 2 indexed citations
20.
Kardaş, Fatih, Türkan Patıroğlu, Ekrem Ünal, et al.. (2011). Hemophagocytic syndrome in a 4‐month‐old infant with biotinidase deficiency. Pediatric Blood & Cancer. 59(1). 191–193. 24 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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