Gülden Gökçay

1.2k total citations
30 papers, 492 citations indexed

About

Gülden Gökçay is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Gülden Gökçay has authored 30 papers receiving a total of 492 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in Gülden Gökçay's work include Metabolism and Genetic Disorders (9 papers), Neonatal Health and Biochemistry (4 papers) and Biotin and Related Studies (4 papers). Gülden Gökçay is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Neonatal Health and Biochemistry (4 papers) and Biotin and Related Studies (4 papers). Gülden Gökçay collaborates with scholars based in Türkiye, United States and Germany. Gülden Gökçay's co-authors include Mübeccel Demirkol, T. Baykal, Barry Wolf, Ferhat Demir, Kevin P. Jensen, Steven F. Dobrowolski, Wouter F. Visser, Trent Miller, Mine Güllüoğlu and Özlem Durmaz and has published in prestigious journals such as Human Molecular Genetics, Nutrients and Clinica Chimica Acta.

In The Last Decade

Gülden Gökçay

27 papers receiving 481 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gülden Gökçay Türkiye 13 277 213 100 86 78 30 492
Xia Zhan China 13 181 0.7× 69 0.3× 127 1.3× 62 0.7× 28 0.4× 39 376
Hidde H. Huidekoper Netherlands 15 208 0.8× 187 0.9× 127 1.3× 31 0.4× 102 1.3× 44 651
Coleman Turgeon United States 13 380 1.4× 404 1.9× 307 3.1× 29 0.3× 132 1.7× 26 821
Khaja Basheeruddin United States 15 239 0.9× 43 0.2× 234 2.3× 79 0.9× 68 0.9× 25 605
B. M. Tracey United Kingdom 13 384 1.4× 363 1.7× 133 1.3× 43 0.5× 71 0.9× 29 615
Maciej Adamowicz Poland 11 357 1.3× 44 0.2× 94 0.9× 35 0.4× 52 0.7× 14 471
Marinus Duran Netherlands 9 584 2.1× 232 1.1× 86 0.9× 25 0.3× 43 0.6× 9 732
Christina Lam United States 10 312 1.1× 65 0.3× 72 0.7× 56 0.7× 11 0.1× 31 455
Tom Wagemans Netherlands 12 147 0.5× 42 0.2× 383 3.8× 142 1.7× 73 0.9× 14 510
A Grenier Canada 13 231 0.8× 402 1.9× 121 1.2× 33 0.4× 92 1.2× 24 616

Countries citing papers authored by Gülden Gökçay

Since Specialization
Citations

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

Fields of papers citing papers by Gülden Gökçay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gülden Gökçay

This figure shows the co-authorship network connecting the top 25 collaborators of Gülden Gökçay. A scholar is included among the top collaborators of Gülden Gökçay 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 Gülden Gökçay. Gülden Gökçay 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.
Toksoy, Güven, et al.. (2023). Novel GALT variations and genetic spectrum in Turkish population with the correlation of genotype and phenotype. Annals of Human Genetics. 87(6). 285–294.
2.
Kesim, Yeşim, Barış Salman, Emrah Yücesan, et al.. (2023). Reanalysis of exome sequencing data reveals a treatable neurometabolic origin in two previously undiagnosed siblings with neurodevelopmental disorder. Neurological Sciences. 44(7). 2527–2540. 1 indexed citations
3.
Bılgıç, Başar, Ali Bayram, Haşmet Hanağası, et al.. (2021). Functional Connectivity Analysis in Heterozygous Glucocerebrosidase Mutation Carriers. Journal of Parkinson s Disease. 11(2). 559–568. 5 indexed citations
4.
Yıldırım, Zeynep Yürük, Güven Toksoy, Zehra Oya Uyguner, et al.. (2019). Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype. European Journal of Medical Genetics. 63(1). 103621–103621. 11 indexed citations
5.
Demi̇r, Sevliya Öcal, Manolya Kara, Selda Hançerlı Törün, et al.. (2018). Dirençli Gram Pozitif İnfeksiyon Tedavisinde Vankomisin ve Linezolid Kombinasyonu: Vaka Sunumu. Çocuk Dergisi / Journal of Child. 18(2). 93–96. 1 indexed citations
6.
Ghosh, Arunabha, Kirk Aleck, Miika Arvonen, et al.. (2018). Experience of the nutritional management of infantile onset lysosomal acid lipase deficiency (LALD). Molecular Genetics and Metabolism. 123(2). S51–S51. 2 indexed citations
7.
Demmelmair, Hans, Anita MacDonald, Urania Kotzaeridou, et al.. (2018). Determinants of Plasma Docosahexaenoic Acid Levels and Their Relationship to Neurological and Cognitive Functions in PKU Patients: A Double Blind Randomized Supplementation Study. Nutrients. 10(12). 1944–1944. 12 indexed citations
8.
Gökçay, Gülden, et al.. (2017). The quality of sleep in nurses. P1–P1. 5 indexed citations
9.
Tamay, Zeynep, et al.. (2016). Rapid Desensitization for Immediate Hypersensitivity to Galsulfase Therapy in Patients with MPS VI. JIMD Reports. 30. 53–57. 6 indexed citations
10.
Kara, Bülent, et al.. (2014). Adult phenotype and further phenotypic variability in SRD5A3-CDG. BMC Medical Genetics. 15(1). 10–10. 22 indexed citations
11.
Garbade, Sven F., Cheryl R. Greenberg, Mübeccel Demirkol, et al.. (2014). Unravelling the complex MRI pattern in glutaric aciduria type I using statistical models—a cohort study in 180 patients. Journal of Inherited Metabolic Disease. 37(5). 763–773. 29 indexed citations
12.
Janzen, Nils, Michael Terhardt, Stefanie Sander, et al.. (2013). Towards newborn screening for ornithine transcarbamylase deficiency: Fast non-chromatographic orotic acid quantification from dried blood spots by tandem mass spectrometry. Clinica Chimica Acta. 430. 28–32. 14 indexed citations
13.
Sütçü, Murat, Ayşe Kılıç, Emin Ünüvar, et al.. (2011). Hipofosfatemik Raşitizm ile Gelen Herediter Tirozinemili On beş Yaşında Erkek Hasta: Ender Bir Vaka Sunumu. Çocuk Dergisi / Journal of Child. 11(1). 32–35.
14.
Aoyama, Yoshiko, Tetsu Ebara, Toshio Murase, et al.. (2010). Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa. Pediatrics International. 52(1). 145–147. 2 indexed citations
15.
Sander, Johannes, Nils Janzen, Michael Terhardt, et al.. (2010). Monitoring tyrosinaemia type I: Blood spot test for nitisinone (NTBC). Clinica Chimica Acta. 412(1-2). 134–138. 23 indexed citations
16.
Aoyama, Yoshiko, Mübeccel Demirkol, Tetsu Ebara, et al.. (2009). Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations. Journal of Human Genetics. 54(11). 681–686. 21 indexed citations
17.
Yekeler, Ensar, et al.. (2007). Prediction of premature atherosclerosis by endothelial dysfunction and increased intima-media thickness in glycogen storage disease types Ia and III.. PubMed. 49(2). 115–9. 4 indexed citations
18.
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
19.
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
20.
Gökçay, Gülden. (2003). Growth of Infants during the First Year of Life According to Feeding Regimen in the First 4 Months. Journal of Tropical Pediatrics. 49(1). 6–12. 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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