Wayseen Wang

6.7k total citations
399 papers, 3.1k citations indexed

About

Wayseen Wang is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Wayseen Wang has authored 399 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 303 papers in Genetics, 292 papers in Pediatrics, Perinatology and Child Health and 115 papers in Molecular Biology. Recurrent topics in Wayseen Wang's work include Prenatal Screening and Diagnostics (283 papers), Genomic variations and chromosomal abnormalities (239 papers) and Chromosomal and Genetic Variations (69 papers). Wayseen Wang is often cited by papers focused on Prenatal Screening and Diagnostics (283 papers), Genomic variations and chromosomal abnormalities (239 papers) and Chromosomal and Genetic Variations (69 papers). Wayseen Wang collaborates with scholars based in Taiwan, Canada and United States. Wayseen Wang's co-authors include Chih‐Ping Chen, Schu‐Rern Chern, Peih-Shan Wu, Chen‐Chi Lee, Jun-Wei Su, Shin-Wen Chen, Chen‐Wen Pan, Fuu‐Jen Tsai, Fang-Tzu Wu and Wenlin Chen and has published in prestigious journals such as Clinical Chemistry, Gene and Fertility and Sterility.

In The Last Decade

Wayseen Wang

373 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wayseen Wang Taiwan	23	2.1k	1.9k	914	624	435	399	3.1k
Dominic McMullan United Kingdom	21	848 0.4×	801 0.4×	550 0.6×	231 0.4×	59 0.1×	41	1.7k
Philippos C. Patsalis Cyprus	27	1.2k 0.6×	705 0.4×	1.0k 1.1×	79 0.1×	266 0.6×	100	2.0k
Arabella Smith Australia	22	1.2k 0.5×	591 0.3×	605 0.7×	182 0.3×	103 0.2×	119	1.8k
Edith Coonen Netherlands	33	1.2k 0.6×	2.8k 1.5×	825 0.9×	330 0.5×	231 0.5×	69	3.5k
Isabel Lorda‐Sánchez Spain	23	759 0.4×	689 0.4×	558 0.6×	130 0.2×	163 0.4×	67	1.4k
Sioban SenGupta United Kingdom	23	471 0.2×	1.1k 0.6×	494 0.5×	203 0.3×	77 0.2×	49	1.8k
Peter Miny Germany	21	629 0.3×	844 0.5×	437 0.5×	203 0.3×	65 0.1×	88	1.5k
Beata Nowakowska Poland	21	741 0.3×	218 0.1×	563 0.6×	242 0.4×	197 0.5×	87	1.5k
Svetlana Rechitsky United States	28	669 0.3×	1.4k 0.8×	637 0.7×	387 0.6×	40 0.1×	100	2.1k
Boris G. Kousseff United States	25	785 0.4×	276 0.1×	603 0.7×	307 0.5×	134 0.3×	83	1.6k

Countries citing papers authored by Wayseen Wang

Since Specialization

Citations

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

Fields of papers citing papers by Wayseen Wang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wayseen Wang. 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 Wayseen Wang. The network helps show where Wayseen Wang may publish in the future.

Co-authorship network of co-authors of Wayseen Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Wayseen Wang. A scholar is included among the top collaborators of Wayseen Wang 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 Wayseen Wang. Wayseen Wang 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, 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.

Wu, Fang-Tzu, et al.. (2025). Genetic counseling of prenatally detected familial 15q13.2q13.3 microdeletion encompassing CHRNA7 and OTUD7A with asymptomatic carriers in the family. Taiwanese Journal of Obstetrics and Gynecology. 64(2). 361–363. 1 indexed citations

Chen, Chih‐Ping, Fang-Tzu Wu, Sui‐Yuan Chang, et al.. (2024). Low-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, positive non-invasive prenatal testing for trisomy 14, perinatal progressive decrease of the trisomy 14 cell line and a favorable fetal outcome. Taiwanese Journal of Obstetrics and Gynecology. 63(5). 755–758.

Chen, Chih‐Ping, Fang-Tzu Wu, Sui‐Yuan Chang, et al.. (2024). Mosaic distal 13q duplication due to mosaic unbalanced translocation of 46,XY,der(14)t(13;14)(q32.2;p13)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes. Taiwanese Journal of Obstetrics and Gynecology. 63(5). 750–754. 1 indexed citations

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. 1 indexed citations

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 indexed citations

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. 12 indexed citations

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. 2 indexed citations

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.

10.

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. 17 indexed citations

11.

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. 5 indexed citations

12.

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. 3 indexed citations

13.

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. 2 indexed citations

14.

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. 9 indexed citations

15.

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. 9 indexed citations

16.

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. 2 indexed citations

17.

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. 6 indexed citations

18.

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

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.

Chen, Chih‐Ping, Jin‐Chung Shih, Jui‐Hsing Chang, Yi‐Hui Lin, & Wayseen Wang. (2003). Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence. Prenatal Diagnosis. 23(6). 515–518. 13 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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