Chen‐Chi Lee

2.1k total citations
116 papers, 929 citations indexed

About

Chen‐Chi Lee is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Chen‐Chi Lee has authored 116 papers receiving a total of 929 indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Pediatrics, Perinatology and Child Health, 95 papers in Genetics and 38 papers in Molecular Biology. Recurrent topics in Chen‐Chi Lee's work include Prenatal Screening and Diagnostics (97 papers), Genomic variations and chromosomal abnormalities (80 papers) and Chromosomal and Genetic Variations (24 papers). Chen‐Chi Lee is often cited by papers focused on Prenatal Screening and Diagnostics (97 papers), Genomic variations and chromosomal abnormalities (80 papers) and Chromosomal and Genetic Variations (24 papers). Chen‐Chi Lee collaborates with scholars based in Taiwan, Canada and Belgium. Chen‐Chi Lee's co-authors include Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Peih-Shan Wu, Chen‐Wen Pan, Wenlin Chen, Shin-Wen Chen, Dai‐Dyi Town, Chin‐Yuan Tzen and Jun-Wei Su and has published in prestigious journals such as Gene, Fertility and Sterility and Genomics.

In The Last Decade

Chen‐Chi Lee

107 papers receiving 824 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Chen‐Chi Lee Taiwan 17 673 550 285 185 176 116 929
Shin-Wen Chen Taiwan 12 511 0.8× 548 1.0× 180 0.6× 166 0.9× 77 0.4× 152 747
Chen‐Wen Pan Taiwan 14 438 0.7× 418 0.8× 136 0.5× 124 0.7× 98 0.6× 68 593
Jun-Wei Su Taiwan 14 472 0.7× 353 0.6× 197 0.7× 106 0.6× 99 0.6× 75 658
G. Lefort France 16 377 0.6× 290 0.5× 189 0.7× 58 0.3× 217 1.2× 34 632
Judy Chernos Canada 15 521 0.8× 286 0.5× 375 1.3× 97 0.5× 132 0.8× 38 859
G. L. Terzoli Italy 10 397 0.6× 517 0.9× 237 0.8× 146 0.8× 143 0.8× 14 843
Michele Clemens United States 15 394 0.6× 157 0.3× 298 1.0× 123 0.7× 54 0.3× 25 625
Frederick W. Luthardt United States 17 318 0.5× 191 0.3× 387 1.4× 89 0.5× 99 0.6× 28 890
E. J. Maher United Kingdom 8 440 0.7× 342 0.6× 173 0.6× 66 0.4× 129 0.7× 11 613
Cheryl DeScipio United States 15 334 0.5× 404 0.7× 337 1.2× 84 0.5× 67 0.4× 18 834

Countries citing papers authored by Chen‐Chi Lee

Since Specialization
Citations

This map shows the geographic impact of Chen‐Chi Lee'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‐Chi Lee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chen‐Chi Lee more than expected).

Fields of papers citing papers by Chen‐Chi Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chen‐Chi Lee. 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‐Chi Lee. The network helps show where Chen‐Chi Lee may publish in the future.

Co-authorship network of co-authors of Chen‐Chi Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Chen‐Chi Lee. A scholar is included among the top collaborators of Chen‐Chi Lee 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 Chen‐Chi Lee. Chen‐Chi Lee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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.
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Chen, Chih‐Ping, Te‐Yao Hsu, Schu‐Rern Chern, et al.. (2023). Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with a negative NIPT result, cytogenetic discrepancy in various tissues, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome. Taiwanese Journal of Obstetrics and Gynecology. 62(4). 582–585. 7 indexed citations
4.
Wu, Fang-Tzu, Chih‐Ping Chen, Shin-Wen Chen, et al.. (2023). Concomitance of 47,XXY, a balanced reciprocal translocation of t(4;17)(q12;q11.2) encompassing SPINK2 at 4q12 and NOS at 17q11.2 and an AZFa sY86 deletion in an infertile male. Taiwanese Journal of Obstetrics and Gynecology. 62(2). 336–342.
5.
Chen, Chih‐Ping, Fang-Tzu Wu, Peih-Shan Wu, et al.. (2023). Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome. Taiwanese Journal of Obstetrics and Gynecology. 62(6). 891–895. 4 indexed citations
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. 6 indexed citations
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. 2 indexed citations
8.
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. 2 indexed citations
9.
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. 11 indexed citations
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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. 9 indexed citations
12.
Lin, Chen‐Ju, Chih‐Ping Chen, Shu‐Chin Chien, et al.. (2014). Chromosomal deletions detected at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 53(1). 62–67. 2 indexed citations
13.
Chen, Chih‐Ping, Shuan‐Pei Lin, Schu‐Rern Chern, et al.. (2014). A 1.37-Mb 12p11.22–p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation. Taiwanese Journal of Obstetrics and Gynecology. 53(1). 74–78. 5 indexed citations
14.
Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2013). Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review. Genomics. 102(4). 265–269. 7 indexed citations
15.
Chen, Chih‐Ping, Shuenn‐Dyh Chang, Ho‐Yen Chueh, et al.. (2012). Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 475–480. 7 indexed citations
16.
Chen, Chih‐Ping, Yi‐Ning Su, Pei‐Chen Wu, et al.. (2011). Rapid Aneuploidy Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes in a Pregnancy With Fetal Nuchal Edema and Mild Ascites. Journal of Medical Ultrasound. 19(2). 64–67. 5 indexed citations
17.
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Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2011). Prenatal diagnosis of mosaic trisomy 9. Taiwanese Journal of Obstetrics and Gynecology. 50(4). 549–553. 10 indexed citations
19.
Chen, Chih‐Ping, et al.. (2006). Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation. Fertility and Sterility. 86(5). 1514.e1–1514.e2. 5 indexed citations
20.
Liu, Yichun, Ming‐Liang Lee, Chih‐Ping Chen, et al.. (1997). Inversion and Enlargement of the Heterochromatin Region of Chromosome No.9 among Taiwanese. 9(3). 159–167. 2 indexed citations

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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