Chen‐Chi Lee

571 total citations
23 papers, 270 citations indexed

About

Chen‐Chi Lee is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Chen‐Chi Lee has authored 23 papers receiving a total of 270 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 20 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Chen‐Chi Lee's work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (20 papers) and Chromosomal and Genetic Variations (5 papers). Chen‐Chi Lee is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (20 papers) and Chromosomal and Genetic Variations (5 papers). Chen‐Chi Lee collaborates with scholars based in Taiwan and Belgium. Chen‐Chi Lee's co-authors include Wayseen Wang, Schu‐Rern Chern, Chih‐Ping Chen, Fuu‐Jen Tsai, Pei-Chen Wu, Yi‐Ning Su, Chen‐Wen Pan, Yu-Ting Chen, Chin‐Yuan Tzen and Tung‐Yao Chang and has published in prestigious journals such as Prenatal Diagnosis, European Journal of Medical Genetics and Taiwanese Journal of Obstetrics and Gynecology.

In The Last Decade

Chen‐Chi Lee

23 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chen‐Chi Lee Taiwan	11	230	183	69	62	40	23	270
Dai‐Dyi Town Taiwan	12	279 1.2×	279 1.5×	78 1.1×	73 1.2×	64 1.6×	51	380
Yen-Ni Chen Taiwan	10	210 0.9×	180 1.0×	78 1.1×	49 0.8×	68 1.7×	41	301
Francesca Dulcetti Italy	10	203 0.9×	301 1.6×	83 1.2×	29 0.5×	28 0.7×	12	387
Cathy Sullivan United States	5	174 0.8×	170 0.9×	72 1.0×	38 0.6×	13 0.3×	7	276
Constance J. Sandlin United States	8	316 1.4×	239 1.3×	132 1.9×	138 2.2×	63 1.6×	10	397
Matthew Hoi Kin Chau Hong Kong	13	250 1.1×	271 1.5×	93 1.3×	32 0.5×	38 0.9×	28	387
Núria Clusellas Spain	9	195 0.8×	189 1.0×	100 1.4×	59 1.0×	62 1.6×	14	319
P Balícek Czechia	10	217 0.9×	130 0.7×	113 1.6×	101 1.6×	34 0.8×	27	296
M. Crocker United Kingdom	9	183 0.8×	68 0.4×	88 1.3×	52 0.8×	15 0.4×	16	245
Françoise Girard‐Lemaire France	8	140 0.6×	98 0.5×	81 1.2×	21 0.3×	31 0.8×	12	194

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

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20 of 20 papers shown

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2011). Inv dup del(9p): Prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwanese Journal of Obstetrics and Gynecology. 50(1). 67–73. 13 indexed citations

Chen, Chih‐Ping, Pei‐Ying Ling, Yi‐Ning Su, et al.. (2011). A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. Taiwanese Journal of Obstetrics and Gynecology. 50(4). 492–498. 5 indexed citations

Chen, Chih‐Ping, Pei-Chen Wu, Schu‐Rern Chern, et al.. (2011). Unbalanced reciprocal translocations at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 50(1). 48–57. 17 indexed citations

Chen, Chih‐Ping, C.-C. Chiang, Yi‐Ning Su, et al.. (2011). Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 50(2). 245–248. 7 indexed citations

Chen, Chih‐Ping, Yi‐Ning Su, Fuu‐Jen Tsai, et al.. (2011). Partial monosomy 13q (13q21.32→qter) and partial trisomy 8p (8p12→pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization. Taiwanese Journal of Obstetrics and Gynecology. 50(2). 205–211. 5 indexed citations

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2011). De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure. Taiwanese Journal of Obstetrics and Gynecology. 50(3). 339–344. 12 indexed citations

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. 2 indexed citations

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2010). Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses. Taiwanese Journal of Obstetrics and Gynecology. 49(3). 341–350. 49 indexed citations

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2010). Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings. Taiwanese Journal of Obstetrics and Gynecology. 49(4). 473–480. 7 indexed citations

10.

Chen, Chih‐Ping, Yung‐Ting Kuo, Shuan-Pei Lin, et al.. (2010). Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization. Taiwanese Journal of Obstetrics and Gynecology. 49(3). 327–332. 16 indexed citations

11.

Chen, Chih‐Ping, Ming Chen, Tsang‐Ming Ko, et al.. (2010). Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 8. Taiwanese Journal of Obstetrics and Gynecology. 49(4). 500–505. 14 indexed citations

12.

Chen, Chih‐Ping, Yi‐Ning Su, Fuu‐Jen Tsai, et al.. (2010). Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated With a Reciprocal Translocation Involving Chromosomes 17 And 18. Taiwanese Journal of Obstetrics and Gynecology. 49(2). 188–191. 7 indexed citations

13.

Chen, Chih‐Ping, Pei-Chen Wu, Yi‐Ning Su, et al.. (2010). Balanced Reciprocal Translocations Detected at Amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 49(4). 455–467. 12 indexed citations

14.

Chen, Chih‐Ping, Schu‐Rern Chern, Fuu‐Jen Tsai, et al.. (2009). Trisomy 13 Mosaicism Associated With Cyclopia and Cystic Hygroma. Taiwanese Journal of Obstetrics and Gynecology. 48(4). 434–436. 6 indexed citations

15.

Chen, Chih‐Ping, Schu‐Rern Chern, Pei-Chen Wu, et al.. (2009). Unbalanced and Balanced Acrocentric Rearrangements Involving Chromosomes Other Than Chromosome 21 at Amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 48(4). 389–399. 5 indexed citations

16.

Chen, Chih‐Ping, Schu‐Rern Chern, Fuu‐Jen Tsai, et al.. (2009). Down Syndrome Due to Unbalanced Homologous Acrocentric Rearrangements and its Recurrence in Subsequent Pregnancies: Prenatal Diagnosis by Amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 48(4). 403–407. 6 indexed citations

17.

Chen, Chih‐Ping, Shuan-Pei Lin, Fuu‐Jen Tsai, et al.. (2008). A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay. European Journal of Medical Genetics. 51(4). 368–372. 18 indexed citations

18.

Chen, Chih-Ping, et al.. (2004). Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature. Prenatal Diagnosis. 24(10). 767–773. 15 indexed citations

19.

Chen, Chih‐Ping, Schu‐Rern Chern, Chen‐Chi Lee, et al.. (2004). Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4. Prenatal Diagnosis. 24(1). 38–44. 7 indexed citations

20.

Chen, Chih‐Ping, Schu‐Rern Chern, Tung‐Yao Chang, et al.. (2003). Prenatal diagnosis of de novo terminal deletion of chromosome 7q. Prenatal Diagnosis. 23(5). 375–379. 10 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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