Jun Liao

821 citations
18 papers · 321 · h-index 8

Impact in

    • Pharmacogenetics and Drug Metabolism
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • RNA modifications and cancer 2
    • Epigenetics and DNA Methylation 1
    • Genomic variations and chromosomal abnormalities 4
    • Genomics and Rare Diseases 3
    • Genetics and Neurodevelopmental Disorders 1

Jun Liao

17 papers receiving 315 citations

Peers

Jun Liao
Comparison fields: 5 of 57
  • Pharmacology 77
  • Genetics 107
  • Cancer Research 52
  • Molecular Biology 147
  • Immunology and Allergy 11
Replace Jennifer M. Phillips with:
Jennifer M. Phillips United States
Sophie Pâquet France
Maxwell N. Skor United States
Peter Bazeley United States
Y. Lachance Canada
Michelle Wang United States
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Jucimara Colombo Brazil
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Citations per field
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Citations per year

Countries citing papers authored by Jun Liao

Since Specialization
Citations

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

Fields of papers citing papers by Jun Liao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jun Liao, 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 Jun Liao Line = papers co-authored together Jun Liao links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 2015111
2 201555
3 201446
4 201138
5 201313
6 202212
7 201912
8 20207
9 20146
10 20215
11 20155
12
Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project
20163
13 20223
14 20142
15 20121
16 20221
17 20241
18 20240

About Jun Liao

Jun Liao is a scholar working on Molecular Biology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Oncology, having authored 18 papers that have together received 321 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Cancer Genomics and Diagnostics (3 papers), Pharmacogenetics and Drug Metabolism (2 papers), RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Epigenetics and DNA Methylation (1 paper) and Pancreatic and Hepatic Oncology Research (1 paper). The work is most often cited by research in Pharmacology (77 citations), Genetics (107 citations), Cancer Research (52 citations), Molecular Biology (147 citations) and Immunology and Allergy (11 citations). Jun Liao has collaborated with scholars based in United States, Jordan and Brazil. Frequent co-authors include Urvashi Surti, Jie Hu, Ruth Kornreich, Malini Sathanoori, Lorraine H. Toji, Rachel Lorier, Suneeta Madan‐Khetarpal, Svetlana A. Yatsenko, Praful Aggarwal and Robin E. Everts. Their work appears in journals such as Prenatal Diagnosis, Journal of Molecular Diagnostics, Genome Medicine, Orphanet Journal of Rare Diseases and American Journal of Clinical Pathology.

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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