Tsang‐Ming Ko

2.2k citations
86 papers · 1.5k · h-index 20

Impact in

  • Genetics top 2%
    • Neurogenetic and Muscular Disorders Research
    • Hemoglobinopathies and Related Disorders
    • Forensic and Genetic Research
    • Genomic variations and chromosomal abnormalities
    • Hearing, Cochlea, Tinnitus, Genetics

Papers in

    • Genomic variations and chromosomal abnormalities 19
    • Hemoglobinopathies and Related Disorders 13
    • Forensic and Genetic Research 8
    • Neurogenetic and Muscular Disorders Research 5
    • Prenatal Screening and Diagnostics 25
    • Fetal and Pediatric Neurological Disorders 6

Tsang‐Ming Ko

82 papers receiving 1.4k citations

Peers

Tsang‐Ming Ko
Comparison fields: 5 of 94
  • Genetics 360
  • Sensory Systems 95
  • Pediatrics, Perinatology and Child Health 339
  • Genetics 410
  • Hepatology 67
Replace Päivi Lahermo with:
Päivi Lahermo Finland
Jacqueline A. Hobbs United States
P. Sistonen Finland
Sajid Malik Pakistan
Annette Lee United States
E Bois France
Pierangela Castorina Italy
Corinne D. Boehm United States
Bettina Bessières France
S A Al-Awadi Kuwait
Tsang‐Ming Ko relative to Päivi Lahermo Finland Päivi Lahermo's profile →
Citations per field
00.5×5×10×16.8×
Päivi Lahermo · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Tsang‐Ming Ko, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tsang‐Ming Ko Line = papers co-authored together Tsang‐Ming Ko links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 86 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2017122
2 2001110
3 2003102
4 198491
5 199162
6 199955
7 201655
8 200755
9 199450
10 199244
11 199940
12 200733
13 201827
14 198822
15 199522
16 199822
17 199320
18 201320
19 199120
20 198719

About Tsang‐Ming Ko

Tsang‐Ming Ko is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Epidemiology, having authored 86 papers that have together received 1.5k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (19 papers), Hemoglobinopathies and Related Disorders (13 papers), Forensic and Genetic Research (8 papers), Fetal and Pediatric Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers), Molecular Biology Techniques and Applications (5 papers) and Parvovirus B19 Infection Studies (4 papers). The work is most often cited by research in Genetics (360 citations), Sensory Systems (95 citations), Pediatrics, Perinatology and Child Health (339 citations), Genetics (410 citations) and Hepatology (67 citations). Tsang‐Ming Ko has collaborated with scholars based in Taiwan, United States and China. Frequent 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 Yuh‐Jyh Jong. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, International Journal of Legal Medicine, Taiwanese Journal of Obstetrics and Gynecology and Journal of Evaluation in Clinical Practice.

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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