Dai‐Dyi Town

800 total citations
51 papers, 380 citations indexed

About

Dai‐Dyi Town is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Plant Science. According to data from OpenAlex, Dai‐Dyi Town has authored 51 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Pediatrics, Perinatology and Child Health, 42 papers in Genetics and 16 papers in Plant Science. Recurrent topics in Dai‐Dyi Town's work include Prenatal Screening and Diagnostics (42 papers), Genomic variations and chromosomal abnormalities (37 papers) and Chromosomal and Genetic Variations (16 papers). Dai‐Dyi Town is often cited by papers focused on Prenatal Screening and Diagnostics (42 papers), Genomic variations and chromosomal abnormalities (37 papers) and Chromosomal and Genetic Variations (16 papers). Dai‐Dyi Town collaborates with scholars based in Taiwan. Dai‐Dyi Town's co-authors include Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Chen‐Chi Lee, Peih-Shan Wu, Shin-Wen Chen, Jun-Wei Su, Fang-Tzu Wu, Chen‐Wen Pan and Chien-Wen Yang and has published in prestigious journals such as Gene, Ultrasound in Obstetrics and Gynecology and Prenatal Diagnosis.

In The Last Decade

Dai‐Dyi Town

50 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dai‐Dyi Town Taiwan	12	279	279	78	73	64	51	380
Chen‐Wen Pan Taiwan	14	418 1.5×	438 1.6×	136 1.7×	98 1.3×	124 1.9×	68	593
N. Morichon-Delvallez France	12	143 0.5×	320 1.1×	173 2.2×	74 1.0×	66 1.0×	26	418
Anne M. Bandholz United States	6	332 1.2×	355 1.3×	154 2.0×	20 0.3×	70 1.1×	8	515
Chen‐Chi Lee Taiwan	11	183 0.7×	230 0.8×	69 0.9×	62 0.8×	40 0.6×	23	270
Drew Duckett United Kingdom	9	128 0.5×	249 0.9×	142 1.8×	63 0.9×	36 0.6×	23	353
Celia Donaghue United Kingdom	14	437 1.6×	479 1.7×	155 2.0×	68 0.9×	46 0.7×	16	629
Fang-Tzu Wu Taiwan	10	336 1.2×	253 0.9×	109 1.4×	32 0.4×	102 1.6×	133	437
Yen-Ni Chen Taiwan	10	180 0.6×	210 0.8×	78 1.0×	49 0.7×	68 1.1×	41	301
Stéphane Serero France	8	110 0.4×	188 0.7×	133 1.7×	46 0.6×	43 0.7×	15	328
Regine Schubert Germany	13	232 0.8×	429 1.5×	214 2.7×	137 1.9×	21 0.3×	23	550

Countries citing papers authored by Dai‐Dyi Town

Since Specialization

Citations

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

Fields of papers citing papers by Dai‐Dyi Town

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dai‐Dyi Town. 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 Dai‐Dyi Town. The network helps show where Dai‐Dyi Town may publish in the future.

Co-authorship network of co-authors of Dai‐Dyi Town

This figure shows the co-authorship network connecting the top 25 collaborators of Dai‐Dyi Town. A scholar is included among the top collaborators of Dai‐Dyi Town 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 Dai‐Dyi Town. Dai‐Dyi Town 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, Tsang‐Ming Ko, Schu‐Rern Chern, et al.. (2021). Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus. Taiwanese Journal of Obstetrics and Gynecology. 60(3). 534–539. 3 indexed citations

Chen, Chih‐Ping, Chia‐Hao Chan, Schu‐Rern Chern, et al.. (2021). Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome. Taiwanese Journal of Obstetrics and Gynecology. 60(1). 152–156. 1 indexed citations

Chen, Chih‐Ping, Schu‐Rern Chern, Peih-Shan Wu, et al.. (2021). Prenatal diagnosis of a familial Y long-arm and chromosome 15 short-arm translocation inherited from a mother carrier. Taiwanese Journal of Obstetrics and Gynecology. 60(4). 781–783. 1 indexed citations

Chen, Chih‐Ping, et al.. (2021). Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association. Taiwanese Journal of Obstetrics and Gynecology. 60(2). 355–358. 2 indexed citations

Chen, Chih‐Ping, Schu‐Rern Chern, Liang‐Kai Wang, et al.. (2020). Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy. Taiwanese Journal of Obstetrics and Gynecology. 59(6). 938–940. 2 indexed citations

Chen, Chih‐Ping, Jui‐Der Liou, Kok‐Min Seow, et al.. (2020). Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results. Taiwanese Journal of Obstetrics and Gynecology. 59(5). 758–762.

Chen, Chih‐Ping, Schu‐Rern Chern, Shin-Wen Chen, et al.. (2019). Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 58(6). 852–854. 16 indexed citations

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

Chen, Chih‐Ping, Sui‐Yuan Chang, Liang‐Kai Wang, et al.. (2018). Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound. Taiwanese Journal of Obstetrics and Gynecology. 57(5). 730–733. 11 indexed citations

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, 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.

Chen, Chih‐Ping, Chen‐Ju Lin, Schu‐Rern Chern, et al.. (2014). Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2–q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome. Taiwanese Journal of Obstetrics and Gynecology. 53(4). 583–587. 10 indexed citations

13.

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

14.

Chen, Chih‐Ping, Tsang‐Ming Ko, Schu‐Rern Chern, et al.. (2013). Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review. Taiwanese Journal of Obstetrics and Gynecology. 52(3). 446–449. 18 indexed citations

15.

Chen, Chih‐Ping, Shuenn‐Dyh Chang, Yuting Chen, et al.. (2012). Mosaic isochromosome 20q detected at amniocentesis: A likely cell culture artifact. Taiwanese Journal of Obstetrics and Gynecology. 51(4). 663–665. 4 indexed citations

16.

Chen, Chih‐Ping, Yi‐Ning Su, Yi‐Yung Chen, et al.. (2012). Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 471–474. 4 indexed citations

17.

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

18.

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2012). Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Taiwanese Journal of Obstetrics and Gynecology. 51(2). 245–252. 3 indexed citations

19.

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2012). Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): Array comparative genomic hybridization characterization and literature review. Taiwanese Journal of Obstetrics and Gynecology. 51(4). 672–676. 1 indexed citations

20.

Chen, Chih‐Ping, Schu‐Rern Chern, Chen‐Chi Lee, et al.. (1999). Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2). Prenatal Diagnosis. 19(8). 783–786. 10 indexed citations

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