Serap Sivri

819 total citations
53 papers, 342 citations indexed

About

Serap Sivri is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Serap Sivri has authored 53 papers receiving a total of 342 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Clinical Biochemistry, 24 papers in Physiology and 21 papers in Molecular Biology. Recurrent topics in Serap Sivri's work include Metabolism and Genetic Disorders (32 papers), Mitochondrial Function and Pathology (13 papers) and Lysosomal Storage Disorders Research (12 papers). Serap Sivri is often cited by papers focused on Metabolism and Genetic Disorders (32 papers), Mitochondrial Function and Pathology (13 papers) and Lysosomal Storage Disorders Research (12 papers). Serap Sivri collaborates with scholars based in Türkiye, United States and Germany. Serap Sivri's co-authors include Turgay Coşkun, Ali Dursun, Ayşegül Tokatlı, Rıza Köksal Özgül, Şafak Güçer, Yılmaz Yıldız, Taner Yılmaz, Kamer Kılınç, Özlem Ünal and Didem Aliefendioğlu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Nutrients.

In The Last Decade

Serap Sivri

45 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Serap Sivri Türkiye 11 182 145 120 62 52 53 342
Ayesha Ahmad United States 13 120 0.7× 85 0.6× 151 1.3× 62 1.0× 66 1.3× 37 392
İlyas Okur Türkiye 12 78 0.4× 136 0.9× 124 1.0× 86 1.4× 42 0.8× 62 372
P. J. Lee United Kingdom 13 170 0.9× 186 1.3× 109 0.9× 156 2.5× 48 0.9× 20 366
Mary Anne D. Chiong Philippines 10 142 0.8× 54 0.4× 168 1.4× 55 0.9× 41 0.8× 31 295
Tanyel Zübarioğlu Türkiye 10 121 0.7× 56 0.4× 108 0.9× 41 0.7× 32 0.6× 52 281
Yılmaz Yıldız Türkiye 11 120 0.7× 75 0.5× 149 1.2× 47 0.8× 32 0.6× 57 317
A Baldellou Spain 10 163 0.9× 194 1.3× 160 1.3× 80 1.3× 38 0.7× 23 392
Sabrina Paci Italy 12 196 1.1× 169 1.2× 148 1.2× 132 2.1× 44 0.8× 31 404
Boris Gebhardt Germany 10 176 1.0× 64 0.4× 219 1.8× 31 0.5× 72 1.4× 12 422
Lénaïg Abily-Donval France 10 104 0.6× 112 0.8× 157 1.3× 32 0.5× 63 1.2× 22 311

Countries citing papers authored by Serap Sivri

Since Specialization
Citations

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

Fields of papers citing papers by Serap Sivri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Serap Sivri

This figure shows the co-authorship network connecting the top 25 collaborators of Serap Sivri. A scholar is included among the top collaborators of Serap Sivri 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 Serap Sivri. Serap Sivri 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.
Rocha, Júlio César, Á. Hermida Ameijeiras, Sarah Rose, et al.. (2024). Meta-analysis of bone mineral density in adults with phenylketonuria. Orphanet Journal of Rare Diseases. 19(1). 338–338. 1 indexed citations
2.
Rose, Sarah, Kirsten Ahring, Deborah A. Bilder, et al.. (2024). Systematic literature review of the somatic comorbidities experienced by adults with phenylketonuria. Orphanet Journal of Rare Diseases. 19(1). 293–293. 4 indexed citations
3.
Rocha, Júlio César, Kirsten Ahring, Deborah A. Bilder, et al.. (2023). Expert Consensus on the Long-Term Effectiveness of Medical Nutrition Therapy and Its Impact on the Outcomes of Adults with Phenylketonuria. Nutrients. 15(18). 3940–3940. 3 indexed citations
4.
Yıldız, Yılmaz, et al.. (2023). COVID-19 in inherited metabolic disorders: Clinical features and risk factors for disease severity. Molecular Genetics and Metabolism. 139(2). 107607–107607. 4 indexed citations
5.
Yıldız, Yılmaz, et al.. (2023). Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency. Neuromuscular Disorders. 33(4). 315–318. 1 indexed citations
6.
Tokgöz-Yılmaz, Suna, et al.. (2022). Does glutaric aciduria type 1 affect hearing function?. Metabolic Brain Disease. 37(6). 2121–2132.
7.
8.
Yıldız, Yılmaz, et al.. (2021). DNACJ12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant. Metabolic Brain Disease. 36(6). 1405–1410. 8 indexed citations
9.
Yıldız, Yılmaz & Serap Sivri. (2021). Difficulties Associated with Enzyme Replacement Therapy for Mucopolysaccharidoses. Turkish Archives of Pediatrics. 56(6). 602–609. 4 indexed citations
10.
Burton, Barbara K., Anne Skalicky, Christoph Baerwald, et al.. (2021). A non-interventional observational study to identify and validate clinical outcome assessments for adults with phenylketonuria for use in clinical trials. Molecular Genetics and Metabolism Reports. 29. 100810–100810. 3 indexed citations
11.
Yıldız, Yılmaz, et al.. (2021). Correction to: DNAJC12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant. Metabolic Brain Disease. 36(6). 1411–1411. 1 indexed citations
12.
Özdemir, Dilşad Foto, Yılmaz Yıldız, Ali Dursun, et al.. (2018). Cognitive and behavioral impairment in mild hyperphenylalaninemia. The Turkish Journal of Pediatrics. 60(6). 617–624. 10 indexed citations
13.
Tekşam, Özlem, et al.. (2017). A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis. The Turkish Journal of Pediatrics. 59(6). 693–695. 2 indexed citations
14.
Alikaşifoğlu, Ayfer, Nurgün Kandemir, Munis Dündar, et al.. (2016). A Nonvirilized form of Classic 3[beta]-Hydroxysteroid Dehydrogenase Deficiency Due to a Homozygous S218P Mutation in the HSD3B2 Gene in a Girl with Classic Phenylketonuria. 86. 1 indexed citations
15.
16.
Özgül, Rıza Köksal, Halil Dündar, Turgay Coşkun, et al.. (2013). Galactosemia in the Turkish population with a high frequency of Q188R mutation and distribution of Duarte-1 and Duarte-2 variations. Journal of Human Genetics. 58(10). 675–678. 9 indexed citations
17.
Aydın, Halil İbrahim, et al.. (2012). Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosis. Clinical Biochemistry. 45(7-8). 571–574. 6 indexed citations
18.
Taşkesen, Mustafa, Turgay Coşkun, Figen Gürakan, et al.. (2011). A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene. JIMD Reports. 2. 25–28. 9 indexed citations
19.
Sivri, Serap, et al.. (2011). Gyrate atrophy of the choroid and retina: a case report. SHILAP Revista de lepidopterología. 4 indexed citations
20.
Dursun, Ali, Rıza Köksal Özgül, Serap Sivri, et al.. (2011). Mutation Spectrum of Fumarylacetoacetase Gene and Clinical Aspects of Tyrosinemia Type I Disease. JIMD Reports. 1. 17–21. 17 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ayesha Ahmad Breakdown of academic impact, for papers by İlyas Okur Breakdown of academic impact, for papers by P. J. Lee Breakdown of academic impact, for papers by Mary Anne D. Chiong Breakdown of academic impact, for papers by Tanyel Zübarioğlu Breakdown of academic impact, for papers by Yılmaz Yıldız Breakdown of academic impact, for papers by A Baldellou Breakdown of academic impact, for papers by Sabrina Paci Breakdown of academic impact, for papers by Boris Gebhardt Breakdown of academic impact, for papers by Lénaïg Abily-Donval
Rankless by CCL
2026