Tsang‐Ming Ko

2.1k total citations
83 papers, 1.3k citations indexed

About

Tsang‐Ming Ko is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Tsang‐Ming Ko has authored 83 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 44 papers in Pediatrics, Perinatology and Child Health and 25 papers in Molecular Biology. Recurrent topics in Tsang‐Ming Ko's work include Prenatal Screening and Diagnostics (41 papers), Genomic variations and chromosomal abnormalities (27 papers) and Hemoglobinopathies and Related Disorders (13 papers). Tsang‐Ming Ko is often cited by papers focused on Prenatal Screening and Diagnostics (41 papers), Genomic variations and chromosomal abnormalities (27 papers) and Hemoglobinopathies and Related Disorders (13 papers). Tsang‐Ming Ko collaborates with scholars based in Taiwan, United States and China. Tsang‐Ming Ko's co-authors include Hsiao‐Lin Hwa, Li‐Hui Tseng, Fon‐Jou Hsieh, Chien‐Hao Huang, Chih‐Ping Chen, Wayseen Wang, Tzu‐Yao Lee, Schu‐Rern Chern, Wuh‐Liang Hwu and Chung‐Hsiung Chen and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Obstetrics and Gynecology and The Journal of Pediatrics.

In The Last Decade

Tsang‐Ming Ko

80 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tsang‐Ming Ko Taiwan 18 483 463 409 363 150 83 1.3k
Patricia A. Ward United States 25 1.0k 2.2× 1.2k 2.7× 627 1.5× 101 0.3× 161 1.1× 65 2.5k
P. Sistonen Finland 25 643 1.3× 906 2.0× 111 0.3× 144 0.4× 250 1.7× 52 2.2k
Jacqueline A. Hobbs United States 17 658 1.4× 661 1.4× 85 0.2× 99 0.3× 72 0.5× 32 1.7k
Kiyonori Miura Japan 24 1.2k 2.4× 633 1.4× 727 1.8× 44 0.1× 252 1.7× 132 2.5k
Jean Amos United States 11 565 1.2× 418 0.9× 95 0.2× 123 0.3× 93 0.6× 24 1.3k
Ikuko Teshima Canada 23 731 1.5× 797 1.7× 292 0.7× 112 0.3× 139 0.9× 61 1.5k
J. Hundrieser Germany 20 342 0.7× 397 0.9× 131 0.3× 234 0.6× 188 1.3× 55 1.3k
E.W. Lovrien United States 23 805 1.7× 585 1.3× 164 0.4× 124 0.3× 108 0.7× 58 1.6k
Erik Iwarsson Sweden 21 507 1.0× 516 1.1× 614 1.5× 144 0.4× 150 1.0× 49 1.4k
Frank Majewski Germany 16 579 1.2× 755 1.6× 271 0.7× 157 0.4× 200 1.3× 26 1.3k

Countries citing papers authored by Tsang‐Ming Ko

Since Specialization
Citations

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

Fields of papers citing papers by Tsang‐Ming Ko

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tsang‐Ming Ko. 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 Tsang‐Ming Ko. The network helps show where Tsang‐Ming Ko may publish in the future.

Co-authorship network of co-authors of Tsang‐Ming Ko

This figure shows the co-authorship network connecting the top 25 collaborators of Tsang‐Ming Ko. A scholar is included among the top collaborators of Tsang‐Ming Ko 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 Tsang‐Ming Ko. Tsang‐Ming Ko 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, 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
2.
Milligan, John N., Jessica L. Larson, Stela Filipovic-Sadic, et al.. (2021). Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants. Journal of Molecular Diagnostics. 23(6). 753–764. 6 indexed citations
3.
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
4.
Chen, Chih‐Ping, Tsang‐Ming Ko, Yi‐Yung Chen, et al.. (2020). Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome. Taiwanese Journal of Obstetrics and Gynecology. 59(5). 754–757. 13 indexed citations
5.
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
6.
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.
7.
Brandão, Andreia, Ken Eng, Teresa Rito, et al.. (2016). Quantifying the legacy of the Chinese Neolithic on the maternal genetic heritage of Taiwan and Island Southeast Asia. Human Genetics. 135(4). 363–376. 30 indexed citations
8.
Chen, Chih‐Ping, Liang‐Kai Wang, Tsang‐Ming Ko, et al.. (2014). Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Taiwanese Journal of Obstetrics and Gynecology. 53(2). 248–251. 9 indexed citations
9.
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
10.
Chen, Chih‐Ping, Tsang‐Ming Ko, Yi‐Ning Su, et al.. (2012). Prenatal diagnosis of mosaic tetrasomy 18p. Taiwanese Journal of Obstetrics and Gynecology. 51(4). 625–629. 15 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.
Hwa, Hsiao‐Lin, et al.. (2010). Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan. International Journal of Legal Medicine. 124(4). 295–300. 12 indexed citations
13.
Hwa, Hsiao‐Lin, Chien‐Hao Huang, Chung‐Hsiung Chen, et al.. (2008). Small Mutations of the DMD Gene in Taiwanese Families. Journal of the Formosan Medical Association. 107(6). 463–469. 6 indexed citations
14.
Hwa, Hsiao‐Lin, et al.. (2007). Multiplex Ligation-dependent Probe Amplification Identification of Deletions and Duplications of the Duchenne Muscular Dystrophy Gene in Taiwanese Subjects. Journal of the Formosan Medical Association. 106(5). 339–346. 33 indexed citations
15.
Huang, Chien‐Hao, et al.. (2007). Copy number analysis of survival motor neuron genes by multiplex ligation-dependent probe amplification. Genetics in Medicine. 9(4). 241–248. 51 indexed citations
16.
Hwa, Hsiao‐Lin, Ming‐Fang Yen, Fon-Jou Hsieh, Tsang‐Ming Ko, & Chien‐Jen Chen. (2004). Evaluation of second trimester maternal serum screening for Down’s Syndrome using the Spiegelhalter-Knill-Jones (S-KJ) approach. Journal of Perinatal Medicine. 32(5). 407–12. 5 indexed citations
17.
Ko, Tsang‐Ming, et al.. (1999). Molecular genetic study of Pompe disease in Chinese patients in Taiwan. Human Mutation. 13(5). 380–384. 53 indexed citations
18.
Chen, Chi‐An, Yen‐Hui Chen, Tzer-Ming Chen, et al.. (1994). Infrequent mutation in tumor suppressor gene p53 in gestational trophoblastic neoplasia. Carcinogenesis. 15(10). 2221–2223. 17 indexed citations
19.
Ko, Tsang‐Ming, et al.. (1992). Carrier detection and prenatal diagnosis of alpha-thalassemia of Southeast Asian deletion by polymerase chain reaction. Human Genetics. 88(3). 245–8. 44 indexed citations
20.
Ko, Tsang‐Ming, et al.. (1990). Early Amniocentesis for Prenatal Diagnosis. 1(2). 53–58. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Patricia A. Ward Breakdown of academic impact, for papers by P. Sistonen Breakdown of academic impact, for papers by Jacqueline A. Hobbs Breakdown of academic impact, for papers by Kiyonori Miura Breakdown of academic impact, for papers by Jean Amos Breakdown of academic impact, for papers by Ikuko Teshima Breakdown of academic impact, for papers by J. Hundrieser Breakdown of academic impact, for papers by E.W. Lovrien Breakdown of academic impact, for papers by Erik Iwarsson Breakdown of academic impact, for papers by Frank Majewski
Rankless by CCL
2026