Verayuth Praphanphoj
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- Congenital heart defects research 4
- Biochemical and Molecular Research 2
- Genetics 11
- Genomic variations and chromosomal abnormalities 7
- Craniofacial Disorders and Treatments 2
- Forensic and Genetic Research 1
- Co-authors
- Michael T. Geraghty (3 shared papers)George H. Thomas (2 shared papers)Piranit Nik Kantaputra (3 shared papers)Rachaneekorn Tammachote (1 shared paper)Carmel Toomes (1 shared paper)Michael J. Dixon (1 shared paper)Barbara K. Goodman (1 shared paper)Stephen J. Gould (1 shared paper)
- Journals
- Scientific Reports (1 paper)Journal of Inherited Metabolic Disease (1 paper)European Journal of Human Genetics (1 paper)FEBS Journal (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- ThailandUnited StatesGermany
In The Last Decade
Verayuth Praphanphoj
20 papers receiving 323 citations
Peers
Comparison fields: 5 of 83
- Genetics 138
- Developmental Biology 9
- Behavioral Neuroscience 13
- Clinical Biochemistry 21
- Molecular Biology 181
Countries citing papers authored by Verayuth Praphanphoj
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
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-authors
The 25 scholars most cited alongside Verayuth Praphanphoj, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 44 | |
| 2 | 2015 | 35 | |
| 3 | 2008 | 34 | |
| 4 | 2000 | 29 | |
| 5 | 2001 | 26 | |
| 6 | 2013 | 25 | |
| 7 | 2010 | 24 | |
| 8 | 2003 | 18 | |
| 9 | 2014 | 17 | |
| 10 | 2004 | 17 | |
| 11 | 2006 | 16 | |
| 12 | 2011 | 11 | |
| 13 | 2011 | 6 | |
| 14 | 2016 | 6 | |
| 15 | 2006 | 5 | |
| 16 | 2025 | 4 | |
| 17 | 2015 | 4 | |
| 18 | 2016 | 3 | |
| 19 | 2016 | 3 | |
| 20 | 2021 | 1 |
About Verayuth Praphanphoj
Verayuth Praphanphoj is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Social Psychology, having authored 20 papers that have together received 328 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (4 papers), Chromosomal and Genetic Variations (3 papers), Craniofacial Disorders and Treatments (2 papers), Autism Spectrum Disorder Research (2 papers), Prenatal Screening and Diagnostics (2 papers), Biochemical and Molecular Research (2 papers) and Forensic and Genetic Research (1 paper). The work is most often cited by research in Genetics (138 citations), Developmental Biology (9 citations), Behavioral Neuroscience (13 citations), Clinical Biochemistry (21 citations) and Molecular Biology (181 citations). Verayuth Praphanphoj has collaborated with scholars based in Thailand, United States and Germany. Frequent co-authors include Michael T. Geraghty, George H. Thomas, Piranit Nik Kantaputra, Rachaneekorn Tammachote, Carmel Toomes, Michael J. Dixon, Barbara K. Goodman, Stephen J. Gould, Katherine A. Sacksteder and Pranoot Tanpaiboon. Their work appears in journals such as Scientific Reports, Journal of Inherited Metabolic Disease, European Journal of Human Genetics, FEBS Journal and Molecular Genetics and Metabolism.
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.