T. Baykal

598 total citations
18 papers, 449 citations indexed

About

T. Baykal is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, T. Baykal has authored 18 papers receiving a total of 449 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Clinical Biochemistry, 9 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in T. Baykal's work include Metabolism and Genetic Disorders (11 papers), Neonatal Health and Biochemistry (6 papers) and Biotin and Related Studies (6 papers). T. Baykal is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Neonatal Health and Biochemistry (6 papers) and Biotin and Related Studies (6 papers). T. Baykal collaborates with scholars based in Türkiye, United States and Switzerland. T. Baykal's co-authors include Mübeccel Demirkol, Gülden Gökçay, Barry Wolf, Yasemi̇n Gökdemi̇r, Beat Thöny, Nenad Blau, Kevin P. Jensen, Ferhat Demir, Fatih Demir and Ertan Mayatepek and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Mutation and Human Genetics.

In The Last Decade

T. Baykal

18 papers receiving 438 citations

Peers

T. Baykal

RHEUM

R. Baumgartner Switzerland

S Scheibenreiter Austria

Maria Luı́s Cardoso Portugal

D. Leupold Germany

H. Niederhoff Germany

Mercedes Martínez‐Pardo Spain

H. D. Bakker Netherlands

F. Šmíd Czechia

I. Hargreaves United Kingdom

Jinqing Song China

R. Baumgartner Switzerland

T. Baykal

310 ×1.3

293 ×1.3

201 ×1.5

102 ×0.9

168 ×1.9

RHEUM

Citations per year, relative to T. Baykal T. Baykal (= 1×) peers R. Baumgartner

Countries citing papers authored by T. Baykal

Since Specialization

Citations

This map shows the geographic impact of T. Baykal'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 T. Baykal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Baykal more than expected).

Fields of papers citing papers by T. Baykal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Baykal

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

All Works

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18 of 18 papers shown

Dobrowolski, Steven F., Caroline Heintz, Trent Miller, et al.. (2010). Molecular genetics and impact of residual in vitro phenylalanine hydroxylase activity on tetrahydrobiopterin responsiveness in Turkish PKU population. Molecular Genetics and Metabolism. 102(2). 116–121. 71 indexed citations

Özdemir, Nihal, et al.. (2006). Corticospinal Tract Involvement in a Patient With 3-HMG Coenzyme A Lyase Deficiency. Pediatric Neurology. 35(2). 139–141. 20 indexed citations

Aydınli̇, Nur, Burak Tatlı, Mine Çalışkan, et al.. (2006). Stroke in Childhood: Experience in Istanbul, Turkey. Journal of Tropical Pediatrics. 52(3). 158–162. 14 indexed citations

Giovannini, Marcello, Laura M. Fiori, Yasemi̇n Gökdemi̇r, et al.. (2005). Screening for tetrahydrobiopterin deficiencies using dried blood spots on filter paper. Molecular Genetics and Metabolism. 86. 96–103. 32 indexed citations

Wolf, Barry, Kevin P. Jensen, Bruce A. Barshop, et al.. (2005). Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates. Human Mutation. 25(4). 413–413. 30 indexed citations

Baykal, T., Gülden Gökçay, Yasemi̇n Gökdemi̇r, et al.. (2005). Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases. Journal of Inherited Metabolic Disease. 28(6). 903–912. 37 indexed citations

Gökçay, Gülbin, et al.. (2005). Breast feeding in organic acidaemias. Journal of Inherited Metabolic Disease. 29(2-3). 304–310. 7 indexed citations

Baykal, T., Gülden Gökçay, Zeynep İnce, et al.. (2005). Consanguineous 3‐methylcrotonyl‐CoA carboxylase deficiency: Early‐onset necrotizing encephalopathy with lethal outcome. Journal of Inherited Metabolic Disease. 28(2). 229–233. 19 indexed citations

Mungan, Neslihan Önenli, et al.. (2004). Type II hyperprolinemia: a case report.. SHILAP Revista de lepidopterología. 46(2). 167–9. 13 indexed citations

10.

Baykal, T., et al.. (2004). Breastfeeding experience in inborn errors of metabolism other than phenylketonuria. Journal of Inherited Metabolic Disease. 28(4). 457–465. 20 indexed citations

11.

Baykal, T., et al.. (2004). Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry. Journal of Inherited Metabolic Disease. 27(6). 781–782. 10 indexed citations

12.

Spiekerkoetter, Ute, T. Baykal, Mübeccel Demirkol, et al.. (2003). Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2. Journal of Inherited Metabolic Disease. 26(6). 613–615. 46 indexed citations

13.

Uyguner, Zehra Oya, Elena Goicoechea de Jorge, Ayşe Çefle, et al.. (2003). Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from Central Asia and was spread throughout Europe and Anatolia by human migrations. Journal of Inherited Metabolic Disease. 26(1). 17–23. 15 indexed citations

14.

Wolf, Barry, Kevin P. Jensen, Mübeccel Demirkol, et al.. (2002). Seventeen novel mutations that cause profound biotinidase deficiency. Molecular Genetics and Metabolism. 77(1-2). 108–111. 31 indexed citations

15.

Romstad, Anne, H. Serap Kalkanoğlu, Turgay Coşkun, et al.. (2000). Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE). Human Genetics. 107(6). 546–553. 16 indexed citations

16.

Pomponio, Robert J., Turgay Coşkun, Mübeccel Demirkol, et al.. (2000). Novel mutations cause biotinidase deficiency in Turkish children. Journal of Inherited Metabolic Disease. 23(2). 120–128. 39 indexed citations

17.

Podskarbi, Teodor, et al.. (1998). Molecular aspects of glycogen storage disease type Ia in Turkish patients: A novel mutation in the glucose‐6‐phosphatase gene. Journal of Inherited Metabolic Disease. 21(4). 445–446. 19 indexed citations

18.

Baykal, T., et al.. (1998). Incidence of biotinidase deficiency in Turkish newborns. Acta Paediatrica. 87(10). 1102–1103. 10 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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