Shin-Wen Chen
About
Shin-Wen Chen is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology.
According to data from OpenAlex, Shin-Wen Chen has authored 152 papers receiving a total of 747 indexed citations (citations by other indexed papers that have themselves been cited), including 119 papers in Pediatrics, Perinatology and Child Health, 116 papers in Genetics and 39 papers in Molecular Biology. Recurrent topics in Shin-Wen Chen's work include Prenatal Screening and Diagnostics (116 papers), Genomic variations and chromosomal abnormalities (95 papers) and Chromosomal and Genetic Variations (29 papers). Shin-Wen Chen is often cited by papers focused on Prenatal Screening and Diagnostics (116 papers), Genomic variations and chromosomal abnormalities (95 papers) and Chromosomal and Genetic Variations (29 papers). Shin-Wen Chen collaborates with scholars based in Taiwan and United Kingdom. Shin-Wen Chen's co-authors include Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Yen-Ni Chen, Chien-Wen Yang, Chen‐Chi Lee, Chen‐Wen Pan and Dai‐Dyi Town and has published in prestigious journals such as Taiwanese Journal of Obstetrics and Gynecology and Journal of Medical Ultrasound.
In The Last Decade
Shin-Wen Chen
136 papers receiving 695 citations
Peers
Shin-Wen Chen
Chen‐Wen Pan Taiwan
Chen‐Chi Lee Taiwan
Jun-Wei Su Taiwan
Steven L. Gersen United States
Nathalie Leporrier France
Emilia K. Bijlsma Netherlands
E. J. Maher United Kingdom
G. Lefort France
Celia Donaghue United Kingdom
Yvonne K. Kwok China
Citations per year, relative to Shin-Wen Chen Shin-Wen Chen (= 1×)
peers
Chen‐Wen Pan
Countries citing papers authored by Shin-Wen Chen
Since
Specialization
Citations
This map shows the geographic impact of Shin-Wen Chen'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 Shin-Wen Chen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shin-Wen Chen more than expected).
Fields of papers citing papers by Shin-Wen Chen
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Shin-Wen Chen. 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 Shin-Wen Chen. The network helps show where Shin-Wen Chen may publish in the future.
Co-authorship network of co-authors of Shin-Wen Chen
This figure shows the co-authorship network connecting the top 25 collaborators of Shin-Wen Chen. A scholar is included among the top collaborators of Shin-Wen Chen 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 Shin-Wen Chen. Shin-Wen Chen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2022). Prenatal diagnosis of mosaicism for trisomy 17 in a single colony at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 61(3). 558–559.
2.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2021). Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother. Taiwanese Journal of Obstetrics and Gynecology. 60(1). 165–168.
3.
Chen, Chih‐Ping, Tsang‐Ming Ko, Schu‐Rern Chern, et al.. (2021). Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus. Taiwanese Journal of Obstetrics and Gynecology. 60(3). 534–539.
4.
Chen, Chih‐Ping, Chia‐Hao Chan, Schu‐Rern Chern, et al.. (2021). Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome. Taiwanese Journal of Obstetrics and Gynecology. 60(1). 152–156.
5.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2020). Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 59(3). 440–442.
6.
Chen, Chih‐Ping, Te‐Yao Hsu, Tsang‐Ming Ko, et al.. (2020). Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 59(5). 728–735.
7.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2020). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 59(1). 130–134.
8.
Chen, Chih‐Ping, Liang‐Kai Wang, Schu‐Rern Chern, et al.. (2020). Prenatal diagnosis of mosaicism for double trisomies of trisomy 11 and trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 59(3). 443–445.
9.
Chen, Chih‐Ping, Liang‐Kai Wang, Schu‐Rern Chern, et al.. (2020). Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion. Taiwanese Journal of Obstetrics and Gynecology. 59(3). 432–436.
10.
Chen, Chih‐Ping, Tsang‐Ming Ko, Liang‐Kai Wang, et al.. (2019). Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization. Taiwanese Journal of Obstetrics and Gynecology. 58(5). 698–703.
11.
Chen, Chih‐Ping, Tsang‐Ming Ko, Chen‐Yu Chen, et al.. (2019). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3. Taiwanese Journal of Obstetrics and Gynecology. 58(6). 864–868.
12.
Chang, Sui‐Yuan, Chih‐Ping Chen, Ming-Huei Lin, et al.. (2018). Digynic triploidy in a fetus presenting with semilobar holoprosencephaly. Taiwanese Journal of Obstetrics and Gynecology. 57(6). 881–884.
13.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2017). Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect. Taiwanese Journal of Obstetrics and Gynecology. 56(4). 550–553.
14.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2017). Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones. Taiwanese Journal of Obstetrics and Gynecology. 56(6). 821–826.
15.
Chen, Chih‐Ping, Liang‐Kai Wang, Schu‐Rern Chern, et al.. (2017). Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1. Taiwanese Journal of Obstetrics and Gynecology. 56(3). 385–389.
16.
Chen, Chih‐Ping, Chen‐Ju Lin, Schu‐Rern Chern, et al.. (2017). Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome. Taiwanese Journal of Obstetrics and Gynecology. 56(2). 238–242.
17.
Chen, Chih‐Ping, Chang‐Sheng Yin, Liang‐Kai Wang, et al.. (2017). Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome. Taiwanese Journal of Obstetrics and Gynecology. 56(3). 390–393.
18.
Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2016). Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion. Taiwanese Journal of Obstetrics and Gynecology. 55(5). 705–711.
19.
Chen, Chih‐Ping, Chen‐Yu Chen, Schu‐Rern Chern, et al.. (2016). Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot. Taiwanese Journal of Obstetrics and Gynecology. 55(2). 270–274.
20.
Chen, Chih‐Ping, Shuan‐Pei Lin, Schu‐Rern Chern, et al.. (2016). Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome. Taiwanese Journal of Obstetrics and Gynecology. 55(5). 728–732.
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