Peih-Shan Wu

2.1k total citations
193 papers, 1.3k citations indexed

About

Peih-Shan Wu is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Peih-Shan Wu has authored 193 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Genetics, 144 papers in Pediatrics, Perinatology and Child Health and 60 papers in Molecular Biology. Recurrent topics in Peih-Shan Wu's work include Genomic variations and chromosomal abnormalities (142 papers), Prenatal Screening and Diagnostics (141 papers) and Congenital heart defects research (39 papers). Peih-Shan Wu is often cited by papers focused on Genomic variations and chromosomal abnormalities (142 papers), Prenatal Screening and Diagnostics (141 papers) and Congenital heart defects research (39 papers). Peih-Shan Wu collaborates with scholars based in Taiwan, Canada and United States. Peih-Shan Wu's co-authors include Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Shin-Wen Chen, Jun-Wei Su, Fang-Tzu Wu, Chen‐Chi Lee, Chien-Wen Yang, Chen‐Wen Pan and Lifeng Chen and has published in prestigious journals such as The Journal of Immunology, Molecular Biology of the Cell and Gene.

In The Last Decade

Peih-Shan Wu

175 papers receiving 1.2k citations

Peers

Countries citing papers authored by Peih-Shan Wu

Since Specialization

Citations

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

Fields of papers citing papers by Peih-Shan Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peih-Shan Wu. 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 Peih-Shan Wu. The network helps show where Peih-Shan Wu may publish in the future.

Co-authorship network of co-authors of Peih-Shan Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Peih-Shan Wu. A scholar is included among the top collaborators of Peih-Shan Wu 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 Peih-Shan Wu. Peih-Shan Wu 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

#	Work	Indexed citations
1	Prenatal diagnosis of a de novo 17q25.3 microdeletion encompassing RAC3 and CSNK1D in a fetus associated with partial agenesis of the corpus callosum, small brain volume, micrognathia and total anomalous pulmonary venous return 2025 ·Taiwanese Journal of Obstetrics and Gynecology ·(unknown), Liang‐Kai Wang, Fang-Tzu Wu, (unknown), Peih-Shan Wu, (unknown)	0
2	Genetic counseling of prenatally detected familial 15q13.2q13.3 microdeletion encompassing CHRNA7 and OTUD7A with asymptomatic carriers in the family 2025 ·Taiwanese Journal of Obstetrics and Gynecology ·(unknown), Fang-Tzu Wu, (unknown), Peih-Shan Wu, Wayseen Wang	1
3	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 2024 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Fang-Tzu Wu, Sui‐Yuan Chang, Peih-Shan Wu, (unknown), Meng‐Shan Lee, (unknown), Wayseen Wang	0
4	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 2024 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Fang-Tzu Wu, Sui‐Yuan Chang, Peih-Shan Wu, (unknown), Chen‐Chi Lee, (unknown), Meng‐Shan Lee, (unknown), Wayseen Wang	1
5	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 2023 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Te‐Yao Hsu, Schu‐Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, (unknown), Chen‐Chi Lee, Wen-Lin Chen, Wayseen Wang	7
6	Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother 2021 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Chen‐Yu Chen, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang	3
7	Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus 2021 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Tsang‐Ming Ko, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, (unknown), Dai‐Dyi Town, Lifeng Chen, Wayseen Wang	3
8	Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome 2020 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Chen‐Yu Chen, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, (unknown), Wayseen Wang	12
9	Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis 2020 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Te‐Yao Hsu, Tsang‐Ming Ko, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, (unknown), Chen‐Chi Lee, Chen‐Wen Pan, Wayseen Wang	6
10	Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization 2019 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Tsang‐Ming Ko, Liang‐Kai Wang, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, (unknown), Wayseen Wang	2
11	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 2019 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Tsang‐Ming Ko, Chen‐Yu Chen, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen‐Wen Pan, Wayseen Wang	0
12	Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect 2017 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, (unknown), Chen‐Yu Chen, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, (unknown), Chen‐Chi Lee, Chien-Wen Yang, Wayseen Wang	11
13	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 2017 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Chen‐Yu Chen, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, (unknown), (unknown), Chien-Wen Yang, Haiyong Chen, Wayseen Wang	6
14	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 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, (unknown), (unknown), Schu‐Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen‐Chi Lee, Dai‐Dyi Town, Meng‐Shan Lee, Chien-Wen Yang, Wayseen Wang	17
15	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 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Chen‐Yu Chen, (unknown), (unknown), Schu‐Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Haiyong Chen, Chien-Wen Yang, Wayseen Wang	5
16	Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome 2016 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Shuan‐Pei Lin, Schu‐Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen‐Chi Lee, Dai‐Dyi Town, Chien-Wen Yang, Wayseen Wang	9
17	Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects 2014 ·Taiwanese Journal of Obstetrics and Gynecology ·(unknown), Chih‐Ping Chen, Liang‐Kai Wang, Tsang‐Ming Ko, Tung‐Yao Chang, Schu‐Rern Chern, Peih-Shan Wu, Yuting Chen, Sui‐Yuan Chang	9
18	Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta 2013 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, (unknown), Chen‐Ju Lin, (unknown), (unknown), Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang	3
19	Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review 2013 ·Genomics ·Chih‐Ping Chen, (unknown), Yi‐Ning Su, (unknown), (unknown), Schu‐Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen‐Chi Lee, Lifeng Chen, Wayseen Wang	7
20	Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 2012 ·Taiwanese Journal of Obstetrics and Gynecology ·Chih‐Ping Chen, Ming Chen, Schu‐Rern Chern, Peih-Shan Wu, Shun‐Ping Chang, (unknown), Yu-Ting Chen, Lifeng Chen, Jun-Wei Su, (unknown), (unknown), Wayseen Wang	8

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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