Thongperm Munkongdee

995 total citations
27 papers, 675 citations indexed

About

Thongperm Munkongdee is a scholar working on Genetics, Hematology and Genetics. According to data from OpenAlex, Thongperm Munkongdee has authored 27 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 19 papers in Hematology and 6 papers in Genetics. Recurrent topics in Thongperm Munkongdee's work include Hemoglobinopathies and Related Disorders (24 papers), Iron Metabolism and Disorders (19 papers) and Blood groups and transfusion (6 papers). Thongperm Munkongdee is often cited by papers focused on Hemoglobinopathies and Related Disorders (24 papers), Iron Metabolism and Disorders (19 papers) and Blood groups and transfusion (6 papers). Thongperm Munkongdee collaborates with scholars based in Thailand, United States and Australia. Thongperm Munkongdee's co-authors include Suthat Fucharoen, Pranee Winichagoon, Saovaros Svasti, Orapan Sripichai, Wattanan Makarasara, Kittiphong Paiboonsukwong, Chutima Kumkhaek, Ping Chen, Chayanon Peerapittayamongkol and Suporn Chuncharunee and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

Thongperm Munkongdee

27 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thongperm Munkongdee Thailand 16 582 481 164 126 81 27 675
Nermeen Varawalla United Kingdom 5 448 0.8× 343 0.7× 116 0.7× 57 0.5× 47 0.6× 10 523
A Metaxotou-Mavromati Greece 14 501 0.9× 388 0.8× 140 0.9× 90 0.7× 68 0.8× 28 549
Rosalba Di Marzo Italy 10 251 0.4× 167 0.3× 66 0.4× 146 1.2× 34 0.4× 23 365
Núria Nogués Spain 13 72 0.1× 240 0.5× 58 0.4× 58 0.5× 142 1.8× 32 390
Geetha Puthenveetil United States 8 134 0.2× 105 0.2× 34 0.2× 165 1.3× 46 0.6× 16 352
Siris Patel India 11 253 0.4× 230 0.5× 84 0.5× 26 0.2× 18 0.2× 31 320
Hatsue Tsuneyama Japan 12 104 0.2× 284 0.6× 30 0.2× 45 0.4× 210 2.6× 40 331
Katarzyna Guz Poland 12 61 0.1× 301 0.6× 96 0.6× 50 0.4× 96 1.2× 49 417
Jonathan S. Smythe United Kingdom 9 100 0.2× 231 0.5× 72 0.4× 59 0.5× 288 3.6× 10 371
J.H. Maas Germany 8 103 0.2× 352 0.7× 83 0.5× 18 0.1× 243 3.0× 12 398

Countries citing papers authored by Thongperm Munkongdee

Since Specialization
Citations

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

Fields of papers citing papers by Thongperm Munkongdee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thongperm Munkongdee

This figure shows the co-authorship network connecting the top 25 collaborators of Thongperm Munkongdee. A scholar is included among the top collaborators of Thongperm Munkongdee 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 Thongperm Munkongdee. Thongperm Munkongdee 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
2.
Munkongdee, Thongperm, et al.. (2023). Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification. Scientific Reports. 13(1). 9612–9612. 1 indexed citations
3.
Munkongdee, Thongperm, et al.. (2021). Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at Gγ-globin gene promoter. Scientific Reports. 11(1). 8552–8552. 6 indexed citations
4.
Munkongdee, Thongperm, Ping Chen, Pranee Winichagoon, Suthat Fucharoen, & Kittiphong Paiboonsukwong. (2020). Update in Laboratory Diagnosis of Thalassemia. Frontiers in Molecular Biosciences. 7. 74–74. 88 indexed citations
5.
Munkongdee, Thongperm, Kanet Wongravee, Orapan Sripichai, et al.. (2020). Visual genotyping of thalassemia by using pyrrolidinyl peptide nucleic acid probes immobilized on carboxymethylcellulose-modified paper and enzyme-induced pigmentation. Microchimica Acta. 187(4). 238–238. 18 indexed citations
6.
Pata, Supansa, et al.. (2019). Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion. Biological Procedures Online. 21(1). 15–15. 1 indexed citations
7.
Tangprasittipap, Amornrat, Thongperm Munkongdee, Saovaros Svasti, et al.. (2017). Establishment of MUi009 – A human induced pluripotent stem cells from a 32 year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2. Stem Cell Research. 20. 80–83. 2 indexed citations
8.
Sripichai, Orapan, et al.. (2017). Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE disease. International Journal of Hematology. 107(3). 297–310. 15 indexed citations
9.
Kampuansai, Jatupol, Daoroong Kangwanpong, Thongperm Munkongdee, et al.. (2017). A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand. Scientific Reports. 7(1). 4690–4690. 10 indexed citations
10.
Munkongdee, Thongperm, Punnee Butthep, Pranee Winichagoon, et al.. (2016). Molecular Epidemiology of Hemoglobinopathies in Cambodia. Hemoglobin. 40(3). 163–167. 18 indexed citations
11.
Tubsuwan, Alisa, Thongperm Munkongdee, Natee Jearawiriyapaisarn, et al.. (2011). Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of βE pre‐mRNA splicing determine disease severity. British Journal of Haematology. 154(5). 635–643. 16 indexed citations
12.
Munkongdee, Thongperm, et al.. (2010). Rapid Diagnosis of α-Thalassemia by Melting Curve Analysis. Journal of Molecular Diagnostics. 12(3). 354–358. 16 indexed citations
13.
Munkongdee, Thongperm, et al.. (2010). Quantitative analysis of Hb Bart’s in cord blood by capillary electrophoresis system. Annals of Hematology. 90(7). 741–746. 20 indexed citations
14.
Nuinoon, Manit, Wattanan Makarasara, Taisei Mushiroda, et al.. (2009). A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E. Human Genetics. 127(3). 303–314. 146 indexed citations
15.
Tayapiwatana, Chatchai, Thanusak Tatu, Sawitree Chiampanichayakul, et al.. (2009). Simple method for screening of α-thalassaemia 1 carriers. International Journal of Hematology. 89(5). 559–567. 23 indexed citations
16.
Svasti, Saovaros, Orapan Sripichai, Thongperm Munkongdee, et al.. (2008). Association of SNP in exon 1 of HBS1L with hemoglobin F level in β0-thalassemia/hemoglobin E. International Journal of Hematology. 88(4). 357–361. 15 indexed citations
17.
Sripichai, Orapan, Wattanan Makarasara, Thongperm Munkongdee, et al.. (2008). A scoring system for the classification of β‐thalassemia/Hb E disease severity. American Journal of Hematology. 83(6). 482–484. 106 indexed citations
18.
Winichagoon, Pranee, et al.. (2008). Rapid diagnosis of thalassemias and other hemoglobinopathies by capillary electrophoresis system. Translational research. 152(4). 178–184. 48 indexed citations
19.
Sripichai, Orapan, Thongperm Munkongdee, Chutima Kumkhaek, et al.. (2007). Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease. Annals of Hematology. 87(5). 375–379. 40 indexed citations
20.
Sripichai, Orapan, Johanna L. Whitacre, Thongperm Munkongdee, et al.. (2005). Genetic Analysis of Candidate Modifier Polymorphisms in Hb E‐β0‐Thalassemia Patients. Annals of the New York Academy of Sciences. 1054(1). 433–438. 15 indexed citations

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