Chen‐Wen Pan
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
-
- Prenatal Screening and Diagnostics 35
- Genetics 42
- Genomic variations and chromosomal abnormalities 37
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetic Syndromes and Imprinting 2
- Co-authors
- Chih‐Ping Chen (72 shared papers)Wayseen Wang (71 shared papers)Schu‐Rern Chern (62 shared papers)Peih-Shan Wu (38 shared papers)Chen‐Chi Lee (22 shared papers)Shin-Wen Chen (33 shared papers)Jun-Wei Su (11 shared papers)Fang-Tzu Wu (28 shared papers)
- Journals
- Taiwanese Journal of Obstetrics and Gynecology (61 papers)Prenatal Diagnosis (5 papers)Gene (4 papers)European Journal of Medical Genetics (1 paper)American Journal of Medical Genetics Part A (2 papers)
- Partner nations
- Taiwan
In The Last Decade
Chen‐Wen Pan
69 papers receiving 672 citations
Peers
Comparison fields: 5 of 36
- Pediatrics, Perinatology and Child Health 395
- Genetics 357
- Developmental Biology 18
- Surgery 95
- Obstetrics and Gynecology 15
Countries citing papers authored by Chen‐Wen Pan
This map shows the geographic impact of Chen‐Wen Pan'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 Chen‐Wen Pan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chen‐Wen Pan more than expected).
Fields of papers citing papers by Chen‐Wen Pan
This network shows the impact of papers produced by Chen‐Wen Pan. 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 Chen‐Wen Pan. The network helps show where Chen‐Wen Pan may publish in the future.
Co-authors
The 25 scholars most cited alongside Chen‐Wen Pan, 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 74 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 55 | |
| 2 | 2006 | 43 | |
| 3 | 2004 | 35 | |
| 4 | 1998 | 29 | |
| 5 | 2012 | 28 | |
| 6 | 2005 | 27 | |
| 7 | 2002 | 24 | |
| 8 | 2016 | 24 | |
| 9 | 2011 | 19 | |
| 10 | 2016 | 18 | |
| 11 | 2020 | 18 | |
| 12 | 2013 | 18 | |
| 13 | 2012 | 15 | |
| 14 | 2010 | 14 | |
| 15 | 2013 | 14 | |
| 16 | 2013 | 13 | |
| 17 | 2017 | 13 | |
| 18 | 2023 | 13 | |
| 19 | 2017 | 12 | |
| 20 | 2001 | 11 |
About Chen‐Wen Pan
Chen‐Wen Pan is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Molecular Biology and Plant Science, having authored 74 papers that have together received 717 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Prenatal Screening and Diagnostics (35 papers), Congenital heart defects research (5 papers), Congenital Anomalies and Fetal Surgery (5 papers), Chromosomal and Genetic Variations (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetic Syndromes and Imprinting (2 papers) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (395 citations), Genetics (357 citations), Developmental Biology (18 citations), Surgery (95 citations) and Obstetrics and Gynecology (15 citations). Chen‐Wen Pan has collaborated with scholars based in Taiwan. Frequent co-authors include Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Peih-Shan Wu, Chen‐Chi Lee, Shin-Wen Chen, Jun-Wei Su, Fang-Tzu Wu, Fuu‐Jen Tsai and Pei-Chen Wu. Their work appears in journals such as Taiwanese Journal of Obstetrics and Gynecology, Prenatal Diagnosis, Gene, European Journal of Medical Genetics and American Journal of Medical Genetics Part A.
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.