Schu‐Rern Chern
About
Schu‐Rern Chern is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology.
According to data from OpenAlex, Schu‐Rern Chern has authored 354 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 276 papers in Genetics, 257 papers in Pediatrics, Perinatology and Child Health and 111 papers in Molecular Biology. Recurrent topics in Schu‐Rern Chern's work include Prenatal Screening and Diagnostics (251 papers), Genomic variations and chromosomal abnormalities (220 papers) and Chromosomal and Genetic Variations (64 papers). Schu‐Rern Chern is often cited by papers focused on Prenatal Screening and Diagnostics (251 papers), Genomic variations and chromosomal abnormalities (220 papers) and Chromosomal and Genetic Variations (64 papers). Schu‐Rern Chern collaborates with scholars based in Taiwan, Canada and United States. Schu‐Rern Chern's co-authors include Chih‐Ping Chen, Wayseen Wang, Peih-Shan Wu, Chen‐Chi Lee, Shin-Wen Chen, Jun-Wei Su, Chen‐Wen Pan, Fuu‐Jen Tsai, Dai‐Dyi Town and Wenlin Chen and has published in prestigious journals such as International Journal of Molecular Sciences, Clinical Chemistry and Gene.
In The Last Decade
Schu‐Rern Chern
334 papers receiving 2.8k citations
Peers
Schu‐Rern Chern
Helen Stewart United Kingdom
Sandra A. Farrell Canada
I. Liebaers Belgium
Beata Nowakowska Poland
Tiong Yang Tan Australia
Éric Bieth France
Charles Hanson Sweden
Güven Lüleci Türkiye
W.G. Kearns United States
Citations per year, relative to Schu‐Rern Chern Schu‐Rern Chern (= 1×)
peers
Helen Stewart
Countries citing papers authored by Schu‐Rern Chern
Since
Specialization
Citations
This map shows the geographic impact of Schu‐Rern Chern'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 Schu‐Rern Chern with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Schu‐Rern Chern more than expected).
Fields of papers citing papers by Schu‐Rern Chern
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Schu‐Rern Chern. 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 Schu‐Rern Chern. The network helps show where Schu‐Rern Chern may publish in the future.
Co-authorship network of co-authors of Schu‐Rern Chern
This figure shows the co-authorship network connecting the top 25 collaborators of Schu‐Rern Chern. A scholar is included among the top collaborators of Schu‐Rern Chern 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 Schu‐Rern Chern. Schu‐Rern Chern is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Chen, Chih‐Ping, Jian‐Pei Huang, Liang‐Kai Wang, et al.. (2025). Concomitant omphalocele, craniorachischisis and ectopic cordis associated with trisomy 18 diagnosed in first trimester. Taiwanese Journal of Obstetrics and Gynecology. 64(2). 353–356.
2.
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.
3.
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.
4.
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.
5.
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.
6.
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.
7.
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.
8.
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.
9.
Chen, Chih‐Ping, Yi‐Ning Su, Ming-Huei Lin, et al.. (2014). Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia. Taiwanese Journal of Obstetrics and Gynecology. 53(1). 68–73.
10.
Chen, Chih‐Ping, Liang‐Kai Wang, Tsang‐Ming Ko, et al.. (2014). Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Taiwanese Journal of Obstetrics and Gynecology. 53(2). 248–251.
11.
Chen, Chih‐Ping, Chen‐Ju Lin, Schu‐Rern Chern, et al.. (2013). Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta. Taiwanese Journal of Obstetrics and Gynecology. 52(2). 303–305.
12.
Chen, Chih‐Ping, Yuh‐Ming Hwu, Chen‐Yu Chen, et al.. (2013). Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization, and embryo transfer. Taiwanese Journal of Obstetrics and Gynecology. 52(4). 611–612.
13.
Chen, Chih‐Ping, Tung‐Yao Chang, Wan‐Yuo Guo, et al.. (2013). Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy. Taiwanese Journal of Obstetrics and Gynecology. 52(3). 415–419.
14.
Chen, Chih‐Ping, et al.. (2013). Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis. Taiwanese Journal of Obstetrics and Gynecology. 52(4). 607–610.
15.
Chen, Chih‐Ping, Schu‐Rern Chern, Shing‐Jyh Chang, et al.. (2012). Placenta proteome analysis from Down syndrome pregnancies for biomarker discovery. Molecular BioSystems. 8(9). 2360–2372.
16.
Chen, Chih‐Ping, Yi‐Ning Su, Shun-Long Weng, et al.. (2012). Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 481–484.
17.
Chen, Chih‐Ping, Yi‐Ning Su, Tung‐Yao Chang, et al.. (2012). Osteogenesis imperfecta type I: Second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father. Taiwanese Journal of Obstetrics and Gynecology. 51(2). 276–279.
18.
Chen, Chih‐Ping, Ming Chen, Schu‐Rern Chern, et al.. (2012). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 411–417.
19.
Chen, Chih‐Ping, Schu‐Rern Chern, Chen‐Yu Chen, et al.. (2011). Double aneuploidy with Edwards–Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb. Taiwanese Journal of Obstetrics and Gynecology. 50(4). 479–484.
20.
Chen, Chih‐Ping, Schu‐Rern Chern, Pei-Chen Wu, et al.. (2010). Unbalanced and Balanced Heterologous Acrocentric Rearrangements Involving Chromosome 21 at Amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 49(1). 62–68.
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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