Verayuth Praphanphoj

765 total citations
20 papers, 328 citations indexed

About

Verayuth Praphanphoj is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Verayuth Praphanphoj has authored 20 papers receiving a total of 328 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Verayuth Praphanphoj's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (4 papers) and Chromosomal and Genetic Variations (3 papers). Verayuth Praphanphoj is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (4 papers) and Chromosomal and Genetic Variations (3 papers). Verayuth Praphanphoj collaborates with scholars based in Thailand, United States and Germany. Verayuth Praphanphoj's co-authors include Michael T. Geraghty, George H. Thomas, Piranit Nik Kantaputra, Rachaneekorn Tammachote, Barbara K. Goodman, Carmel Toomes, Michael J. Dixon, Stephen J. Gould, Katherine A. Sacksteder and Pranoot Tanpaiboon and has published in prestigious journals such as PLoS ONE, Scientific Reports and Journal of Dental Research.

In The Last Decade

Verayuth Praphanphoj

20 papers receiving 323 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Verayuth Praphanphoj Thailand 12 181 138 35 32 28 20 328
C. Nowak Germany 13 144 0.8× 88 0.6× 28 0.8× 9 0.3× 28 1.0× 41 369
Tipu Sultan Pakistan 12 135 0.7× 59 0.4× 23 0.7× 21 0.7× 20 0.7× 52 393
Xiaonan Du China 8 161 0.9× 87 0.6× 10 0.3× 10 0.3× 27 1.0× 23 333
Asude Durmaz Türkiye 11 100 0.6× 92 0.7× 11 0.3× 19 0.6× 45 1.6× 60 334
Rini Pauly United States 9 171 0.9× 90 0.7× 7 0.2× 14 0.4× 15 0.5× 31 335
Ramin Badii Qatar 12 161 0.9× 123 0.9× 8 0.2× 36 1.1× 17 0.6× 21 394
S.A. Guttormsen United States 12 125 0.7× 182 1.3× 23 0.7× 14 0.4× 17 0.6× 25 436
Sorina Mihaela Papuc Romania 10 166 0.9× 116 0.8× 8 0.2× 36 1.1× 37 1.3× 29 327
Daniel Amsallem France 10 173 1.0× 222 1.6× 19 0.5× 6 0.2× 29 1.0× 21 335
Naghmeh Dorrani United States 12 314 1.7× 367 2.7× 31 0.9× 12 0.4× 37 1.3× 20 518

Countries citing papers authored by Verayuth Praphanphoj

Since Specialization
Citations

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

Fields of papers citing papers by Verayuth Praphanphoj

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verayuth Praphanphoj

This figure shows the co-authorship network connecting the top 25 collaborators of Verayuth Praphanphoj. A scholar is included among the top collaborators of Verayuth Praphanphoj 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 Verayuth Praphanphoj. Verayuth Praphanphoj 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.
Kittichotirat, Weerayuth, Kanthida Kusonmano, Chinae Thammarongtham, et al.. (2025). Characterization of gut microbiota on gender and age groups bias in Thai patients with autism spectrum disorder. Scientific Reports. 15(1). 2587–2587. 4 indexed citations
2.
Vatanavicharn, Nithiwat, et al.. (2021). Bilateral squamosal synostosis: unusual presentation of chromosome 1p12–1p13.3 deletion. Illustrative case. Journal of Neurosurgery Case Lessons. 1(3). CASE20102–CASE20102. 1 indexed citations
3.
4.
Sutapun, Boonsong, et al.. (2016). Fabrication of protein microarrays for alpha fetoprotein detection by using a rapid photo-immobilization process. Sensing and Bio-Sensing Research. 7. 95–99. 6 indexed citations
5.
Praphanphoj, Verayuth, et al.. (2016). Proteolytic activity of Crocodylus porosus transthyretin protease and role of the terminal polypeptide sequences. ScienceAsia. 42(3). 190–190. 3 indexed citations
6.
Tammachote, Rachaneekorn, et al.. (2015). Glucocorticoid receptor gene (NR3C1) promoter is hypermethylated in Thai females with major depressive disorder. Genetics and Molecular Research. 14(4). 19071–19079. 35 indexed citations
7.
Srikhirin, Toemsak, et al.. (2015). Hepatocellular Carcinoma Biomarker Detection by Surface Plasmon Resonance Sensor. Advanced materials research. 1131. 84–87. 4 indexed citations
8.
Praphanphoj, Verayuth, et al.. (2014). A Case with a Ring Chromosome 13 in a Cohort of 203 Children with Non-Syndromic Autism and Review of the Cytogenetic Literature. Cytogenetic and Genome Research. 144(1). 1–8. 17 indexed citations
9.
Wangkumhang, Pongsakorn, Philip J. Shaw, Kridsadakorn Chaichoompu, et al.. (2013). Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure. PLoS ONE. 8(11). e79522–e79522. 25 indexed citations
10.
Tongkobpetch, Siraprapa, Verayuth Praphanphoj, Charan Mahatumarat, et al.. (2011). PTPRF is disrupted in a patient with syndromic amastia. BMC Medical Genetics. 12(1). 46–46. 11 indexed citations
11.
Praphanphoj, Verayuth, et al.. (2011). Effect of the N‐terminal sequence on the binding affinity of transthyretin for human retinol‐binding protein. FEBS Journal. 278(18). 3337–3347. 6 indexed citations
12.
Klopocki, Eva, Bianca P. Hennig, Verayuth Praphanphoj, et al.. (2010). Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q. European Journal of Human Genetics. 18(12). 1310–1314. 24 indexed citations
13.
Kantaputra, Piranit Nik, Isabelle Milétich, H.‐J. Lüdecke, et al.. (2008). Tricho-Rhino-Phalangeal Syndrome with Supernumerary Teeth. Journal of Dental Research. 87(11). 1027–1031. 34 indexed citations
14.
Kantaputra, Piranit Nik, et al.. (2006). Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: Association with an 18p11.3 deletion. American Journal of Medical Genetics Part A. 140A(23). 2598–2602. 16 indexed citations
15.
Kongruttanachok, Narisorn, et al.. (2006). Tetralogy of Fallot with absent pulmonary valve in a de novo derivative chromosome 9 with duplication of 9p13 → 9pter and deletion of 9q34.3. American Journal of Medical Genetics Part A. 140A(18). 1981–1987. 5 indexed citations
16.
Kantaputra, Piranit Nik, et al.. (2004). Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome. American Journal of Medical Genetics Part A. 130A(2). 181–190. 17 indexed citations
17.
Al‐Hassnan, Zuhair N., SA Boyadjiev, Verayuth Praphanphoj, et al.. (2003). The relationship of plasma glutamine to ammonium and of glycine to acid–base balance in propionic acidaemia. Journal of Inherited Metabolic Disease. 26(1). 89–91. 18 indexed citations
18.
Praphanphoj, Verayuth, Katherine A. Sacksteder, Stephen J. Gould, George H. Thomas, & Michael T. Geraghty. (2001). Identification of the α-Aminoadipic Semialdehyde Dehydrogenase-Phosphopantetheinyl Transferase Gene, the Human Ortholog of the Yeast LYS5 Gene. Molecular Genetics and Metabolism. 72(4). 336–342. 26 indexed citations
19.
Praphanphoj, Verayuth, et al.. (2000). Cryptic subtelomeric translocations in the 22q13 deletion syndrome. Journal of Medical Genetics. 37(1). 58–61. 29 indexed citations
20.
Praphanphoj, Verayuth, Barbara K. Goodman, George H. Thomas, et al.. (2000). Molecular Cytogenetic Evaluation in a Patient with a Translocation (3;21) Associated with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome (BPES). Genomics. 65(1). 67–69. 44 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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