Chien-Wen Yang
About
Chien-Wen Yang is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology.
According to data from OpenAlex, Chien-Wen Yang has authored 49 papers receiving a total of 424 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 23 papers in Pediatrics, Perinatology and Child Health and 18 papers in Molecular Biology. Recurrent topics in Chien-Wen Yang's work include Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (22 papers) and Congenital heart defects research (11 papers). Chien-Wen Yang is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (22 papers) and Congenital heart defects research (11 papers). Chien-Wen Yang collaborates with scholars based in Taiwan, United States and Australia. Chien-Wen Yang's co-authors include Wayseen Wang, Peih-Shan Wu, Chih‐Ping Chen, Schu‐Rern Chern, Shin-Wen Chen, Yen-Ni Chen, Wen‐Chi Chang, Chi-Nga Chow, Chen‐Chi Lee and Chen‐Wen Pan and has published in prestigious journals such as Nucleic Acids Research, Journal of Experimental Botany and Journal of the American Society of Nephrology.
In The Last Decade
Chien-Wen Yang
45 papers receiving 374 citations
Peers
Chien-Wen Yang
Pei-Chen Wu Taiwan
Jeong‐Mook Lim South Korea
Tiziana Marsella Italy
J. J. P. Schrander Netherlands
G Mundel Israel
Chunyu Luo China
Baosheng Zhu China
Y. Hillion France
L. Giglio Italy
Semra Gürsoy Türkiye
Citations per year, relative to Chien-Wen Yang Chien-Wen Yang (= 1×)
peers
Pei-Chen Wu
Countries citing papers authored by Chien-Wen Yang
Since
Specialization
Citations
This map shows the geographic impact of Chien-Wen Yang'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 Chien-Wen Yang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chien-Wen Yang more than expected).
Fields of papers citing papers by Chien-Wen Yang
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Chien-Wen Yang. 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 Chien-Wen Yang. The network helps show where Chien-Wen Yang may publish in the future.
Co-authorship network of co-authors of Chien-Wen Yang
This figure shows the co-authorship network connecting the top 25 collaborators of Chien-Wen Yang. A scholar is included among the top collaborators of Chien-Wen Yang 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 Chien-Wen Yang. Chien-Wen Yang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Chen, Chih‐Ping, Sui‐Yuan Chang, Liang‐Kai Wang, et al.. (2018). Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound. Taiwanese Journal of Obstetrics and Gynecology. 57(5). 730–733.
2.
Chen, Chih‐Ping, Sui‐Yuan Chang, Yen-Ni Chen, et al.. (2018). Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound. Taiwanese Journal of Obstetrics and Gynecology. 57(5). 739–744.
3.
Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2018). Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability. Taiwanese Journal of Obstetrics and Gynecology. 57(4). 578–582.
4.
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.
5.
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.
6.
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.
7.
Chen, Chih‐Ping, Liang‐Kai Wang, Pei‐Chen Wu, et al.. (2017). Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound. Taiwanese Journal of Obstetrics and Gynecology. 56(1). 102–105.
8.
Chen, Chih‐Ping, Jian‐Pei Huang, Schu‐Rern Chern, et al.. (2017). Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 56(4). 569–570.
9.
Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2017). Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1. Taiwanese Journal of Obstetrics and Gynecology. 56(6). 847–851.
10.
Chen, Chih‐Ping, Tsang‐Ming Ko, Yi‐Yung Chen, et al.. (2017). Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 56(6). 836–839.
11.
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.
12.
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.
13.
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.
14.
Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2016). Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome. Taiwanese Journal of Obstetrics and Gynecology. 55(6). 902–903.
15.
Chen, Chih‐Ping, Shuan‐Pei Lin, Schu‐Rern Chern, et al.. (2016). Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability. Taiwanese Journal of Obstetrics and Gynecology. 55(6). 856–860.
16.
Chen, Chih‐Ping, Chen‐Ju Lin, Schu‐Rern Chern, et al.. (2016). Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication. Taiwanese Journal of Obstetrics and Gynecology. 55(4). 596–601.
17.
Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2016). Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome. Taiwanese Journal of Obstetrics and Gynecology. 55(6). 900–901.
18.
Chen, Chih‐Ping, Chen‐Ju Lin, Schu‐Rern Chern, et al.. (2014). Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2–q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome. Taiwanese Journal of Obstetrics and Gynecology. 53(4). 583–587.
19.
Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2014). Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister–Killian syndrome. Taiwanese Journal of Obstetrics and Gynecology. 53(4). 566–571.
20.
Tseng, Yu‐Chee, Fang–Jing Wu, Chi-Fu Huang, et al.. (2009). A Wireless Human Motion Capturing System for Home Rehabilitation. 359–360.
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.
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