Pınar Ata

577 total citations
50 papers, 371 citations indexed

About

Pınar Ata is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Pınar Ata has authored 50 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Nephrology and 11 papers in Genetics. Recurrent topics in Pınar Ata's work include Renal Transplantation Outcomes and Treatments (8 papers), Parathyroid Disorders and Treatments (7 papers) and Organ Transplantation Techniques and Outcomes (4 papers). Pınar Ata is often cited by papers focused on Renal Transplantation Outcomes and Treatments (8 papers), Parathyroid Disorders and Treatments (7 papers) and Organ Transplantation Techniques and Outcomes (4 papers). Pınar Ata collaborates with scholars based in Türkiye, United States and Antigua and Barbuda. Pınar Ata's co-authors include Selvinaz Özkara, Leyla Özel, Kadir Turan, Melih Kara, M.İ. Titiz, Tayfun Hakan, Fügen Aker, Önder Peker, Yusuf Günerhan and Şafak Kızıltaş and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Pınar Ata

45 papers receiving 363 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Pınar Ata 73 71 64 63 63 50 371
Ben Ponvilawan 57 0.8× 78 1.1× 37 0.6× 71 1.1× 46 0.7× 75 445
Gérard Abadjian 75 1.0× 50 0.7× 38 0.6× 43 0.7× 90 1.4× 46 377
Bülend Yüksel 132 1.8× 53 0.7× 84 1.3× 28 0.4× 123 2.0× 7 433
Shigeo Yamanaka 159 2.2× 71 1.0× 64 1.0× 49 0.8× 109 1.7× 19 657
Bheemanathi Hanuman Srinivas 30 0.4× 43 0.6× 43 0.7× 42 0.7× 44 0.7× 75 264
A K Karak 37 0.5× 65 0.9× 54 0.8× 49 0.8× 18 0.3× 43 442
Corinne Fisher 108 1.5× 23 0.3× 65 1.0× 75 1.2× 49 0.8× 29 470
J. Smith 44 0.6× 81 1.1× 74 1.2× 70 1.1× 48 0.8× 11 462
Ryuichiro Konda 68 0.9× 63 0.9× 43 0.7× 51 0.8× 151 2.4× 44 474
Mustafa Yılmaz 86 1.2× 43 0.6× 33 0.5× 29 0.5× 118 1.9× 41 417

Countries citing papers authored by Pınar Ata

Since Specialization
Citations

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

Fields of papers citing papers by Pınar Ata

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pınar Ata

This figure shows the co-authorship network connecting the top 25 collaborators of Pınar Ata. A scholar is included among the top collaborators of Pınar Ata 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 Pınar Ata. Pınar Ata 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.
Doğru, Ömer, et al.. (2025). Multigene Panel Testing Revealed Novel Variants in Hereditary Spherocytosis Patients in Türkiye. Turkish Journal of Hematology. 42(1). 25–32. 1 indexed citations
2.
Eltan, Sevgi Bilgiç, Asena Pınar Sefer, Tülay Güran, et al.. (2024). Expanding the Clinical Features of Schimke Immuno-Osseous Dysplasia: A New Patient with a Novel Variant and Novel Clinical Findings. Journal of Clinical Research in Pediatric Endocrinology. 17(2). 126–135. 1 indexed citations
3.
Ergenekon, Pınar, Yasemi̇n Gökdemi̇r, Ela Erdem Eralp, et al.. (2024). Beyond the 10%: Unraveling the genetic diversity in Turkish cystic fibrosis patients not eligible for CFTR modulators. Pediatric Pulmonology. 59(12). 3250–3259. 1 indexed citations
4.
Ergenekon, Pınar, Yasemi̇n Gökdemi̇r, Ela Erdem Eralp, et al.. (2024). Exploring Turkey's mosaic of novel variants and complex alleles in cystic fibrosis genetics. Pediatric Pulmonology. 59(12). 3540–3549.
5.
Alpay, Harika, et al.. (2022). Clinical and genetic characterization of children with cubilin variants. Pediatric Nephrology. 38(4). 1381–1385. 4 indexed citations
6.
Geçkinli, Bilgen Bilge, et al.. (2022). Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency. Journal of Assisted Reproduction and Genetics. 39(3). 695–710. 12 indexed citations
7.
Gökçe, İbrahim, et al.. (2022). Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia. Turkish Archives of Pediatrics. 57(4). 432–440.
8.
Ata, Pınar, et al.. (2022). Phenotypic and genotypic characteristics of children with Bartter syndrome. The Turkish Journal of Pediatrics. 64(5). 825–838. 2 indexed citations
9.
Ilgın, Can, et al.. (2021). Effects of vitamin D receptor gene polymorphisms on the prognosis of COVID‐19. Clinical Endocrinology. 96(6). 819–830. 34 indexed citations
10.
Kurnaz, Erdal, et al.. (2021). The Spectrum of Low-Density Lipoprotein Receptor Mutations in a Large Turkish Cohort of Patients with Familial Hypercholesterolemia. Metabolic Syndrome and Related Disorders. 19(6). 340–346. 6 indexed citations
11.
Geçkinli, Bilgen Bilge, et al.. (2021). Biallelic Mutations in <b><i>DNAJB11</i></b>are Associated with Prenatal Polycystic Kidney Disease in a Turkish Family. Molecular Syndromology. 12(3). 179–185. 1 indexed citations
12.
Demirtaş, Coşkun Özer, et al.. (2020). A large Turkish pedigree with multiple endocrine neoplasia type 1 syndrome carrying a rare mutation: c.1680_1683 del TGAG. The Turkish Journal of Gastroenterology. 31(7). 508–514. 1 indexed citations
13.
Abalı, Zehra Yavaş, Pınar Ergenekon, Adnan Dağçınar, et al.. (2020). A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age. Calcified Tissue International. 107(1). 96–103. 10 indexed citations
14.
Yağcı, İlker, et al.. (2018). Challenges in the treatment of fibrodysplasia ossificans progressiva. Rheumatology International. 39(3). 569–576. 11 indexed citations
15.
Kızıltaş, Şafak, Pınar Ata, Yaşar Çolak, et al.. (2014). TLR4 Gene Polymorphism in Patients with Nonalcoholic Fatty Liver Disease in Comparison to Healthy Controls. Metabolic Syndrome and Related Disorders. 12(3). 165–170. 31 indexed citations
16.
Ata, Pınar, et al.. (2013). Monitoring of CD3+ T-Cell Count in Patients Receiving Antithymocyte Globulin Induction After Cadaveric Renal Transplantation. Transplantation Proceedings. 45(3). 929–931. 10 indexed citations
17.
Ata, Pınar, et al.. (2012). Flow Cytometric Detection of Anti-AB Antibody Titers in Blood Group O Recipients of Blood Group A2 Donor Kidneys. Transplantation Proceedings. 44(6). 1706–1709. 3 indexed citations
18.
Çağlayan, Kasım, et al.. (2012). The impact of preoperative immunonutrition and other nutrition models on tumor infiltrative lymphocytes in colorectal cancer patients. The American Journal of Surgery. 204(4). 416–421. 25 indexed citations
19.
Turan, Kadir & Pınar Ata. (2011). Effects of intra- and extracellular factors on anti-aging klotho gene expression. Genetics and Molecular Research. 10(3). 2009–2023. 15 indexed citations
20.
Aker, Fügen, et al.. (2005). Cerebellar liponeurocytoma/lipidized medulloblastoma. Journal of Neuro-Oncology. 71(1). 53–59. 31 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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