Voravarn S. Tanphaichitr

1.0k total citations
39 papers, 807 citations indexed

About

Voravarn S. Tanphaichitr is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Voravarn S. Tanphaichitr has authored 39 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 25 papers in Hematology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Voravarn S. Tanphaichitr's work include Hemoglobinopathies and Related Disorders (29 papers), Iron Metabolism and Disorders (18 papers) and Erythrocyte Function and Pathophysiology (10 papers). Voravarn S. Tanphaichitr is often cited by papers focused on Hemoglobinopathies and Related Disorders (29 papers), Iron Metabolism and Disorders (18 papers) and Erythrocyte Function and Pathophysiology (10 papers). Voravarn S. Tanphaichitr collaborates with scholars based in Thailand, United Kingdom and Australia. Voravarn S. Tanphaichitr's co-authors include Vip Viprakasit, Parichat Pung‐Amritt, Douglas R. Higgs, Gavivann Veerakul, Kleebsabai Sanpakit, C Mahasandana, V Suvatte, Mitchell J. Weiss, Achra Sumboonnanonda and S Ong-Ajyooth and has published in prestigious journals such as New England Journal of Medicine, Blood and Cancer.

In The Last Decade

Voravarn S. Tanphaichitr

39 papers receiving 776 citations

Peers

Voravarn S. Tanphaichitr
F Argiolu Italy
Sandra Gualandro Brazil
Vivien Sheehan United States
Jacqueline S. Davis United States
María de Fátima Sonati Brazil
Catherine Driscoll United States
Satheesh Chonat United States
Aderson S. Araújo Brazil
Frank Shafer United States
Idowu Akinsheye United States
F Argiolu Italy
Voravarn S. Tanphaichitr
Citations per year, relative to Voravarn S. Tanphaichitr Voravarn S. Tanphaichitr (= 1×) peers F Argiolu

Countries citing papers authored by Voravarn S. Tanphaichitr

Since Specialization
Citations

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

Fields of papers citing papers by Voravarn S. Tanphaichitr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Voravarn S. Tanphaichitr. 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 Voravarn S. Tanphaichitr. The network helps show where Voravarn S. Tanphaichitr may publish in the future.

Co-authorship network of co-authors of Voravarn S. Tanphaichitr

This figure shows the co-authorship network connecting the top 25 collaborators of Voravarn S. Tanphaichitr. A scholar is included among the top collaborators of Voravarn S. Tanphaichitr 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 Voravarn S. Tanphaichitr. Voravarn S. Tanphaichitr 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.
2.
Viprakasit, Vip, et al.. (2013). Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand. Clinical Chemistry and Laboratory Medicine (CCLM). 51(8). 1605–1614. 26 indexed citations
3.
4.
Viprakasit, Vip, et al.. (2004). Identification of Hb Q-India (64 Asp→His) in Thailand. Hematology. 9(2). 151–155. 4 indexed citations
5.
Viprakasit, Vip, et al.. (2004). Co‐inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α0 thalassemia associated with transfusion‐dependent Hb H disease. American Journal of Hematology. 75(3). 157–163. 26 indexed citations
6.
Viprakasit, Vip, et al.. (2004). Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report. Annals of Tropical Paediatrics. 24(4). 323–328. 8 indexed citations
7.
Viprakasit, Vip & Voravarn S. Tanphaichitr. (2004). Unusual phenotype of Hemoglobin EE with Hemoglobin H disease: a pitfall in clinical diagnosis and genetic counseling. The Journal of Pediatrics. 144(3). 391–393. 5 indexed citations
8.
Viprakasit, Vip, et al.. (2004). Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder*. European Journal Of Haematology. 73(1). 43–49. 9 indexed citations
9.
Tanphaichitr, Voravarn S., et al.. (2003). Homozygous Hemoglobin Tak Causes Symptomatic Secondary Polycythemia in a Thai Boy. Journal of Pediatric Hematology/Oncology. 25(3). 261–265. 22 indexed citations
10.
Sumboonnanonda, Achra, et al.. (2003). Renal tubular dysfunction in α-thalassemia. Pediatric Nephrology. 18(3). 257–260. 32 indexed citations
11.
Durongpisitkul, Kritvikrom, et al.. (2002). Early detection of cardiac involvement in beta-thalassemia children.. PubMed. 85 Suppl 2. S667–73. 2 indexed citations
12.
Viprakasit, Vip, et al.. (2002). Complex interactions of δβ hybrid haemoglobin (Hb Lepore‐Hollandia) Hb E (β26 G→A) and α+ thalassaemia in a Thai family. European Journal Of Haematology. 68(2). 107–111. 21 indexed citations
13.
Viprakasit, Vip, et al.. (2002). Baseline levels of plasma endothelin‐1 (ET‐1) and changes during transfusion in thalassemic patients. American Journal of Hematology. 70(3). 260–262. 12 indexed citations
14.
Viprakasit, Vip & Voravarn S. Tanphaichitr. (2002). COMPOUND HETEROZYGOSITY FORα0-THALASSEMIA (−−THAI) AND Hb CONSTANT SPRING CAUSES SEVERE Hb H DISEASE. Hemoglobin. 26(2). 155–162. 16 indexed citations
15.
Viprakasit, Vip, et al.. (2002). Clinical phenotypes and molecular characterization of Hb H-Paksé disease.. PubMed. 87(2). 117–25. 69 indexed citations
16.
Sumboonnanonda, Achra, et al.. (1998). Renal tubular function in β-thalassemia. Pediatric Nephrology. 12(4). 280–283. 65 indexed citations
17.
Issaragrisil, Surapol, et al.. (1995). Collection of cord blood stem cells for transplantation in thalassemic patients. Stem Cells. 13(S3). 71–75. 3 indexed citations
18.
Issaragrisil, Surapol, V Suvatte, Voravarn S. Tanphaichitr, et al.. (1995). Transplantation of Cord-Blood Stem Cells into a Patient with Severe Thalassemia. New England Journal of Medicine. 332(6). 367–369. 58 indexed citations
19.
Kanokpongsakdi, Sujin, et al.. (1987). Prenatal diagnosis of the fetus at risk for beta-thalassemia/hemoglobin E disease: a report of the first case in Thailand.. PubMed. 70(1). 38–43. 1 indexed citations
20.
Tanphaichitr, Voravarn S. & Jan van Eys. (1972). The assay of pyruvate kinase activity in blood cells. Clinica Chimica Acta. 41. 41–45. 9 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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