Chupong Ittiwut

901 total citations
53 papers, 496 citations indexed

About

Chupong Ittiwut is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Chupong Ittiwut has authored 53 papers receiving a total of 496 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 23 papers in Genetics and 8 papers in Immunology. Recurrent topics in Chupong Ittiwut's work include Metabolism and Genetic Disorders (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (5 papers). Chupong Ittiwut is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (5 papers). Chupong Ittiwut collaborates with scholars based in Thailand, United States and Netherlands. Chupong Ittiwut's co-authors include Vorasuk Shotelersuk, Kanya Suphapeetiporn, Apiwat Mutirangura, Chureerat Phokaew, Rungnapa Ittiwut, Chatchawit Aporntewan, Jittima Piriyapongsa, Chumpol Ngamphiw, Sissades Tongsima and Joel Gelernter and has published in prestigious journals such as PLoS ONE, Scientific Reports and The Lancet Oncology.

In The Last Decade

Chupong Ittiwut

50 papers receiving 487 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chupong Ittiwut Thailand 14 261 151 60 50 45 53 496
Rehab Ali Qatar 14 286 1.1× 212 1.4× 62 1.0× 51 1.0× 36 0.8× 21 554
Geetha Anand United Kingdom 13 303 1.2× 105 0.7× 77 1.3× 58 1.2× 36 0.8× 34 565
Noora Shahbeck Qatar 11 193 0.7× 143 0.9× 104 1.7× 62 1.2× 48 1.1× 14 426
Gözde Yeşil Türkiye 15 290 1.1× 205 1.4× 30 0.5× 30 0.6× 88 2.0× 78 679
Konstantinos Douroudis United Kingdom 15 245 0.9× 171 1.1× 44 0.7× 100 2.0× 28 0.6× 27 567
Deborah L. Renaud United States 11 233 0.9× 79 0.5× 88 1.5× 51 1.0× 25 0.6× 41 470
Khalid Al‐Thihli Oman 13 219 0.8× 116 0.8× 135 2.3× 33 0.7× 58 1.3× 50 456
Fuad Al Mutairi Saudi Arabia 16 342 1.3× 225 1.5× 195 3.3× 48 1.0× 70 1.6× 47 674
Bret L. Bostwick United States 9 225 0.9× 215 1.4× 35 0.6× 35 0.7× 29 0.6× 17 414
Kei Shioda Japan 14 274 1.0× 82 0.5× 18 0.3× 74 1.5× 40 0.9× 25 517

Countries citing papers authored by Chupong Ittiwut

Since Specialization
Citations

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

Fields of papers citing papers by Chupong Ittiwut

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chupong Ittiwut

This figure shows the co-authorship network connecting the top 25 collaborators of Chupong Ittiwut. A scholar is included among the top collaborators of Chupong Ittiwut 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 Chupong Ittiwut. Chupong Ittiwut 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.
Chen, Huey‐Ling, et al.. (2024). Novel PLEC variants associated with infantile cholestasis. Clinical Genetics. 106(6). 769–775.
2.
Ittiwut, Rungnapa, et al.. (2024). Molecular profiles and long-term outcomes of Thai children with hepatic glycogen storage disease in Thailand. World Journal of Clinical Pediatrics. 13(4). 100493–100493. 1 indexed citations
3.
Ittiwut, Chupong, et al.. (2023). Utilisation of exome sequencing for muscular disorders in Thai paediatric patients: diagnostic yield and mutational spectrum. Scientific Reports. 13(1). 1376–1376. 1 indexed citations
4.
Ittiwut, Chupong, Rungnapa Ittiwut, Chalurmpon Srichomthong, et al.. (2023). Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis. Scientific Reports. 13(1). 805–805. 4 indexed citations
5.
Moonla, Chatphatai, Rungnapa Ittiwut, Chupong Ittiwut, et al.. (2023). Genetic variations of type 2 and type 3 von Willebrand diseases in Thailand. Journal of Clinical Pathology. 78(1). 57–63.
6.
Ittiwut, Chupong, Rungnapa Ittiwut, Tetsuro Matsuhashi, et al.. (2023). Genetic, metabolic and clinical delineation of an MRPS23-associated mitochondrial disorder. Scientific Reports. 13(1). 22005–22005. 2 indexed citations
7.
Caengprasath, Natarin, et al.. (2023). Nine patients with KCNQ2-related neonatal seizures and functional studies of two missense variants. Scientific Reports. 13(1). 3328–3328. 6 indexed citations
8.
Rojnueangnit, Kitiwan, et al.. (2022). Genetic diagnosis for adult patients at a genetic clinic. Molecular Case Studies. 8(7). a006235–a006235. 1 indexed citations
9.
Caengprasath, Natarin, et al.. (2022). Severe coarctation of the aorta, developmental delay, and multiple dysmorphic features in a child with SMAD6 and SMARCA4 variants. European Journal of Medical Genetics. 65(11). 104601–104601. 1 indexed citations
10.
Rojnueangnit, Kitiwan, Duangrurdee Wattanasirichaigoon, Chalurmpon Srichomthong, et al.. (2021). Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand. Clinical Genetics. 100(1). 100–105. 14 indexed citations
11.
Suratannon, Narissara, Chupong Ittiwut, Rungnapa Ittiwut, et al.. (2021). Phenotypic heterogeneity and genotypic spectrum of inborn errors of immunity identified through whole exome sequencing in a Thai patient cohort. Pediatric Allergy and Immunology. 33(1). e13701–e13701. 2 indexed citations
12.
Ittiwut, Chupong, et al.. (2020). Nagashima-Type Palmoplantar Keratosis with Compound Heterozygous Mutations in SERPINB7. Case Reports in Dermatology. 12(3). 241–248. 2 indexed citations
13.
Rojnueangnit, Kitiwan, Sookkasem Khositseth, Chupong Ittiwut, et al.. (2020). Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency. European Journal of Medical Genetics. 63(12). 104086–104086. 12 indexed citations
14.
Phokaew, Chureerat, et al.. (2020). A case of GABRA5-related developmental and epileptic encephalopathy with response to a combination of antiepileptic drugs and a GABAering agent. Brain and Development. 42(7). 546–550. 3 indexed citations
15.
Chongsrisawat, Voranush, et al.. (2018). The phenotypic and mutational spectrum of Thai female patients with ornithine transcarbamylase deficiency. Gene. 679. 377–381. 14 indexed citations
16.
Ittiwut, Chupong, et al.. (2017). Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand. BMC Medical Genetics. 18(1). 102–102. 14 indexed citations
17.
Ittiwut, Chupong, et al.. (2016). Novel Mutations, Including a Large Deletion in the ARSB Gene, Causing Mucopolysaccharidosis Type VI. Genetic Testing and Molecular Biomarkers. 21(1). 58–62. 9 indexed citations
18.
Ittiwut, Rungnapa, et al.. (2016). Variants of the CDH1 (E-Cadherin) Gene Associated with Oral Clefts in the Thai Population. Genetic Testing and Molecular Biomarkers. 20(7). 406–409. 8 indexed citations
19.
Ittiwut, Chupong, Bao‐Zhu Yang, Henry R. Kranzler, et al.. (2011). GABRG1andGABRA2Variation Associated with Alcohol Dependence in African Americans. Alcoholism Clinical and Experimental Research. 36(4). 588–593. 32 indexed citations
20.
Manchana, Tarinee, Chupong Ittiwut, Apiwat Mutirangura, & John J. Kavanagh. (2010). Targeted therapies for rare gynaecological cancers. The Lancet Oncology. 11(7). 685–693. 26 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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