Wayseen Wang
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 303
- Genomic variations and chromosomal abnormalities 239
- Genetic Syndromes and Imprinting 61
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 25
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- Prenatal Screening and Diagnostics 283
- Fetal and Pediatric Neurological Disorders 28
- Co-authors
- Chih‐Ping Chen (251 shared papers)Schu‐Rern Chern (251 shared papers)Peih-Shan Wu (187 shared papers)Chen‐Chi Lee (104 shared papers)Jun-Wei Su (72 shared papers)Shin-Wen Chen (146 shared papers)Chen‐Wen Pan (65 shared papers)Fuu‐Jen Tsai (41 shared papers)
- Journals
- Prenatal Diagnosis (38 papers)Taiwanese Journal of Obstetrics and Gynecology (307 papers)Gene (19 papers)Fertility and Sterility (7 papers)European Journal of Medical Genetics (3 papers)
- Partner nations
- TaiwanCanadaUnited States
In The Last Decade
Wayseen Wang
373 papers receiving 2.9k citations
Peers
Comparison fields: 5 of 82
- Pediatrics, Perinatology and Child Health 1.9k
- Genetics 2.1k
- Developmental Biology 84
- Urology 92
- Surgery 624
Countries citing papers authored by Wayseen Wang
This map shows the geographic impact of Wayseen Wang'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 Wayseen Wang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wayseen Wang more than expected).
Fields of papers citing papers by Wayseen Wang
This network shows the impact of papers produced by Wayseen Wang. 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 Wayseen Wang. The network helps show where Wayseen Wang may publish in the future.
Co-authors
The 25 scholars most cited alongside Wayseen Wang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 399 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 49 | |
| 2 | 2001 | 49 | |
| 3 | 2006 | 42 | |
| 4 | 1998 | 41 | |
| 5 | 2006 | 33 | |
| 6 | 2002 | 32 | |
| 7 | 2005 | 32 | |
| 8 | 2004 | 32 | |
| 9 | 2013 | 31 | |
| 10 | 2016 | 30 | |
| 11 | 2008 | 28 | |
| 12 | 2001 | 28 | |
| 13 | 2011 | 28 | |
| 14 | 2013 | 27 | |
| 15 | 2002 | 26 | |
| 16 | 2005 | 26 | |
| 17 | 2010 | 25 | |
| 18 | 2012 | 25 | |
| 19 | 2011 | 24 | |
| 20 | 2006 | 24 |
About Wayseen Wang
Wayseen Wang is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Surgery and Plant Science, having authored 399 papers that have together received 3.1k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (283 papers), Genomic variations and chromosomal abnormalities (239 papers), Chromosomal and Genetic Variations (69 papers), Congenital Anomalies and Fetal Surgery (68 papers), Genetic Syndromes and Imprinting (61 papers), Congenital heart defects research (52 papers), Fetal and Pediatric Neurological Disorders (28 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (25 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.9k citations), Genetics (2.1k citations), Developmental Biology (84 citations), Urology (92 citations) and Surgery (624 citations). Wayseen Wang has collaborated with scholars based in Taiwan, Canada and United States. Frequent co-authors include Chih‐Ping Chen, Schu‐Rern Chern, Peih-Shan Wu, Chen‐Chi Lee, Jun-Wei Su, Shin-Wen Chen, Chen‐Wen Pan, Fuu‐Jen Tsai, Fang-Tzu Wu and Wenlin Chen. Their work appears in journals such as Prenatal Diagnosis, Taiwanese Journal of Obstetrics and Gynecology, Gene, Fertility and Sterility and European Journal of Medical Genetics.
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.