Vedat Uygun

1.1k total citations
57 papers, 486 citations indexed

About

Vedat Uygun is a scholar working on Hematology, Immunology and Genetics. According to data from OpenAlex, Vedat Uygun has authored 57 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Hematology, 16 papers in Immunology and 13 papers in Genetics. Recurrent topics in Vedat Uygun's work include Hematopoietic Stem Cell Transplantation (19 papers), Immunodeficiency and Autoimmune Disorders (13 papers) and Hemoglobinopathies and Related Disorders (10 papers). Vedat Uygun is often cited by papers focused on Hematopoietic Stem Cell Transplantation (19 papers), Immunodeficiency and Autoimmune Disorders (13 papers) and Hemoglobinopathies and Related Disorders (10 papers). Vedat Uygun collaborates with scholars based in Türkiye, United States and Italy. Vedat Uygun's co-authors include Gülsün Karasu, Akif Yeşilipek, Volkan Hazar, Alphan Küpesiz, Erdal Kurtoğlu, Oğuz Dursun, Özgür Tosun, Koray Yalçın, Dilara Öğünç and Dilara Fatma Kocacık Uygun and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and International Journal of Cancer.

In The Last Decade

Vedat Uygun

55 papers receiving 481 citations

Peers

Vedat Uygun

HEMAT

IMMUN

PPCH

GENET

EPIDE

Gülsün Karasu Türkiye

Reiji Fukano Japan

Alaa Elhaddad Egypt

Hagit Miskin Israel

Abdullah Al‐Jefri Saudi Arabia

Jesús Estella Spain

Karim Boudjedir France

Jolanta Goździk Poland

Éric Hermet France

Abraham S. Kanate United States

Gülsün Karasu Türkiye

Vedat Uygun

148 ×0.9

HEMAT

107 ×0.9

IMMUN

109 ×1.0

PPCH

71 ×0.7

GENET

58 ×0.7

EPIDE

Citations per year, relative to Vedat Uygun Vedat Uygun (= 1×) peers Gülsün Karasu

Countries citing papers authored by Vedat Uygun

Since Specialization

Citations

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

Fields of papers citing papers by Vedat Uygun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vedat Uygun

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

All Works

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20 of 20 papers shown

Uygun, Vedat, et al.. (2025). Hematopoietic stem cell transplantation in pediatric patients with type VI mucopolysaccharidosis. Clinical and Experimental Pediatrics. 68(8). 601–607. 1 indexed citations

Sayar, Esra Hazar, Hasan Kapaklı, Vedat Uygun, et al.. (2024). Variable clinical presentation of hypomorphic DCLRE1C deficiency from childhood to adulthood. Pediatric Allergy and Immunology. 35(10). e14260–e14260. 1 indexed citations

Uygun, Dilara Fatma Kocacık, et al.. (2024). High malignancy rate in IgE‐deficient children. International Journal of Cancer. 156(5). 964–968. 1 indexed citations

Shiraishi, Akira, Vedat Uygun, Nigel Sharfe, et al.. (2023). Novel immunodeficiency caused by homozygous mutation in SLC19A1 encoding the reduced folate carrier. Blood. 141(26). 3226–3230.

Uygun, Vedat, et al.. (2023). Combined Haploidentical Hematopoetic Stem Cell Transplantation and Liver Transplantation in a Pediatric Patient. International Journal of Hematology-Oncology and Stem Cell Research. 17(4). 291–295.

Uygun, Vedat, et al.. (2021). Pearson syndrome in a child transplanted for Diamond-Blackfan anemia. Archivos Argentinos de Pediatria. 119(5). e559–e561. 2 indexed citations

Uygun, Vedat, Dilek Çolak, Derya Mutlu, et al.. (2020). Incidence of BKV in the urine and blood samples of pediatric patients undergoing HSCT. Pediatric Transplantation. 25(2). e13894–e13894. 2 indexed citations

Sharapova, Svetlana, Emma Haapaniemi, Inga Sakovich, et al.. (2019). Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections. Clinical Immunology. 205. 1–5. 21 indexed citations

Artaç, Hasibe, et al.. (2019). Infliximab therapy for inflammatory colitis in an infant with NEMO deficiency. Immunologic Research. 67(4-5). 450–453. 6 indexed citations

10.

Karasu, Gülsün, Vedat Uygun, & Akif Yeşilipek. (2017). Factors associated with peripheral blood stem cell yield in healthy pediatric donors. Transfusion and Apheresis Science. 56(6). 819–824. 4 indexed citations

11.

Uygun, Vedat, et al.. (2016). Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children. Medicine. 95(44). e5242–e5242. 4 indexed citations

12.

Hazar, Volkan, et al.. (2012). Hematopoietic stem cell transplantation activity and trends in a single pediatric transplantation center in Turkey during 1998-2008. SHILAP Revista de lepidopterología. 29(2). 143–149. 5 indexed citations

13.

Filiz, Serkan, Dilara Fatma Kocacık Uygun, Jaap T. van Dissel, et al.. (2012). Cutaneous Leukocytoclastic Vasculitis due to Salmonella enteritidis in a Child with Interleukin‐12 Receptor Beta‐1 Deficiency. Pediatric Dermatology. 31(2). 236–240. 10 indexed citations

14.

Yeşilipek, M. Akif, et al.. (2010). POSTTRANSPLANT ORAL IRON-CHELATING THERAPY IN PATIENTS WITH β-THALASSEMIA MAJOR. Pediatric Hematology and Oncology. 27(5). 374–379. 10 indexed citations

15.

Hazar, Volkan, et al.. (2010). Childhood Acute Lymphoblastic Leukemia in Turkey: Factors Influencing Treatment and Outcome. Journal of Pediatric Hematology/Oncology. 32(8). e317–e322. 21 indexed citations

16.

Russo, Roberta, Maria Rosaria Esposito, Antonella Gambale, et al.. (2010). Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene. American Journal of Hematology. 85(12). 915–920. 31 indexed citations

17.

Yeşilipek, M. Akif, Gülsün Karasu, Alphan Küpesiz, Vedat Uygun, & Volkan Hazar. (2009). Better Posttransplant Outcome With Fludarabine Based Conditioning in Multitransfused Fanconi Anemia Patients Who Underwent Peripheral Blood Stem Cell Transplantation. Journal of Pediatric Hematology/Oncology. 31(7). 512–515. 4 indexed citations

18.

Yeşilipek, M. Akif, et al.. (2008). Unrelated cord blood transplantation in children with severe congenital neutropenia. Pediatric Transplantation. 13(6). 777–781. 3 indexed citations

19.

Akçam, Mustafa, Reha Artan, Tekinalp Gelen, et al.. (2007). Long‐term aspects of nodular gastritis in children. Pediatrics International. 49(2). 220–225. 9 indexed citations

20.

Akman, Sema, Vedat Uygun, & Ayfer Gür Güven. (2005). Value of the urine strip test in the early diagnosis of bacterial peritonitis. Pediatrics International. 47(5). 523–527. 13 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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