Sai Chen

2.1k citations
26 papers · 1.2k · 1 hit paper · h-index 12

Impact in

  • Genetics top 5%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genetic Associations and Epidemiology 9
    • Genomics and Rare Diseases 3
    • Genetic Mapping and Diversity in Plants and Animals 3
    • Cancer Genomics and Diagnostics 1

Sai Chen

26 papers receiving 1.2k citations

Sai Chen's Hit Papers

Discovery of common and rare genetic risk variants for colorectal cancer 2018 · 388 citations
3880+2+5Years since publication100200300

Peers

Sai Chen
Comparison fields: 5 of 90
  • Genetics 444
  • Cancer Research 128
  • Cellular and Molecular Neuroscience 164
  • Pathology and Forensic Medicine 141
  • Molecular Biology 492
Replace Mahmoud Shekari Khaniani with:
Mahmoud Shekari Khaniani Iran
Marita Hernández Spain
Jennifer B. Nixon United States
Guy Fuhrmann France
Jürgen Hescheler Germany
Wenting Yang China
Su Ryeon Seo South Korea
Mitsuhiro Kondo Japan
Ning An China
Shan Ma China
Sai Chen relative to Mahmoud Shekari Khaniani Iran Mahmoud Shekari Khaniani's profile →
Citations per field
00.5×2×3×4.1×
Mahmoud Shekari Khaniani · 1×
Citations per year

Countries citing papers authored by Sai Chen

Since Specialization
Citations

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

Fields of papers citing papers by Sai Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Discovery of common and rare genetic risk variants for colorectal cancer
Hit paper breakdown →
2018388
2 2019241
3 2019128
4 2020127
5 201661
6 201343
7 201941
8 201636
9 202230
10 201825
11 201720
12 201820
13 202111
14 20209
15 20259
16 20177
17 20226
18 20206
19 20256
20 20235

About Sai Chen

Sai Chen is a scholar working on Genetics, Cancer Research, Molecular Biology, Pathology and Forensic Medicine and Oncology, having authored 26 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (9 papers), RNA modifications and cancer (4 papers), Genomics and Phylogenetic Studies (3 papers), Genomics and Rare Diseases (3 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers), Genetic factors in colorectal cancer (2 papers), Bioinformatics and Genomic Networks (2 papers) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Genetics (444 citations), Cancer Research (128 citations), Cellular and Molecular Neuroscience (164 citations), Pathology and Forensic Medicine (141 citations) and Molecular Biology (492 citations). Sai Chen has collaborated with scholars based in United States, China and Australia. Frequent co-authors include Egor Dolzhenko, David Bentley, Michael A. Eberle, Peter Krusche, Melanie Kirsche, Michael C. Schatz, Felix Schlesinger, Rachel M. Sherman, Fritz Joachim Sedlazeck and Xiaofang Yi. Their work appears in journals such as Journal of Controlled Release, Frontiers in Genetics, PLoS Genetics, Genome biology and Bioinformatics.

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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