Vicharn Panich
Impact in
- Genetics top 5%
- Hemoglobinopathies and Related Disorders
- Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 8
- Hemoglobinopathies and Related Disorders 8
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Neonatal Health and Biochemistry 5
- Prenatal Screening and Diagnostics 3
- Co-authors
- M Pornpatkul (7 shared papers)S Na-Nakorn (4 shared papers)Prawase Wasi (1 shared paper)S. Pootrakul (1 shared paper)Chamnong Nopparatana (4 shared papers)P Wasi (2 shared papers)Yasuyuki Fukumaki (4 shared papers)Pensri Pootrakul (1 shared paper)
In The Last Decade
Vicharn Panich
19 papers receiving 380 citations
Peers
Comparison fields: 5 of 50
- Genetics 266
- Hematology 175
- Pediatrics, Perinatology and Child Health 142
- Clinical Biochemistry 23
- Physiology 63
Countries citing papers authored by Vicharn Panich
This map shows the geographic impact of Vicharn Panich'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 Vicharn Panich with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vicharn Panich more than expected).
Fields of papers citing papers by Vicharn Panich
This network shows the impact of papers produced by Vicharn Panich. 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 Vicharn Panich. The network helps show where Vicharn Panich may publish in the future.
Co-authors
The 25 scholars most cited alongside Vicharn Panich, 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 | 1969 | 176 | |
| 2 | The problem of thalassemia in Thailand. | 1992 | 33 |
| 3 | 1981 | 26 | |
| 4 | 1973 | 23 | |
| 5 | 1992 | 20 | |
| 6 | 1980 | 20 | |
| 7 | 1996 | 19 | |
| 8 | The spectrum of beta-thalassemia mutations in southern Thailand. | 1995 | 18 |
| 9 | 1972 | 18 | |
| 10 | 1980 | 9 | |
| 11 | 1999 | 9 | |
| 12 | 1986 | 9 | |
| 13 | 1974 | 8 | |
| 14 | Alpha-thalassemia incidence in southern Thailand by restriction endonuclease analysis of globin DNA from placental blood at Songklanagarind Hospital. | 1997 | 8 |
| 15 | 1980 | 8 | |
| 16 | 1974 | 7 | |
| 17 | Hereditary elliptocytosis (the first report in Thailand) in association with erythrocyte glucose-6-phosphate dehydrogenase deficiency and hemoglobin E. | 1970 | 4 |
| 18 | 1973 | 3 | |
| 19 | Difference between G-6-PD B and Mahidol: differential stimulation by magnesium chloride. | 1973 | 1 |
| 20 | 1999 | 0 |
About Vicharn Panich
Vicharn Panich is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology and Hematology, having authored 20 papers that have together received 419 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (8 papers), Neonatal Health and Biochemistry (5 papers), Iron Metabolism and Disorders (3 papers), Erythrocyte Function and Pathophysiology (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Genetics (266 citations), Hematology (175 citations), Pediatrics, Perinatology and Child Health (142 citations), Clinical Biochemistry (23 citations) and Physiology (63 citations). Vicharn Panich has collaborated with scholars based in Thailand, Japan and Australia. Frequent co-authors include M Pornpatkul, S Na-Nakorn, Prawase Wasi, S. Pootrakul, Chamnong Nopparatana, P Wasi, Yasuyuki Fukumaki, Pensri Pootrakul, Vannarat Saechan and Vichai Laosombat. Their work appears in journals such as Human Genetics, American Journal of Hematology, Annals of Human Genetics, Human Heredity and Annals of the New York Academy of Sciences.
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.