Yingjun Xie

818 citations
65 papers · 543 · h-index 13

Impact in

Papers in

    • CRISPR and Genetic Engineering 8
    • Congenital heart defects research 7
    • Genomic variations and chromosomal abnormalities 19
    • Genetics and Neurodevelopmental Disorders 8
    • Genomics and Rare Diseases 7
    • Genetic Syndromes and Imprinting 6

Yingjun Xie

59 papers receiving 537 citations

Peers

Yingjun Xie
Comparison fields: 5 of 79
  • Genetics 128
  • Pediatrics, Perinatology and Child Health 138
  • Aging 10
  • Genetics 157
  • Hematology 56
Replace Maria Serafina Ristaldi with:
Maria Serafina Ristaldi Italy
Amal Y. Kentab Saudi Arabia
Sara Hardy United States
Kelly J. Lehman United States
Zhengjun Jia China
Jan-Maarten Cobben Netherlands
LaDonna Immken United States
Christalena Sofocleous Greece
Franklin Quan United States
Mansour Djedaini France
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Citations per field
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Maria Serafina Ristaldi · 1×
Citations per year

Countries citing papers authored by Yingjun Xie

Since Specialization
Citations

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

Fields of papers citing papers by Yingjun Xie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 65 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201852
2 201935
3 201635
4 201724
5 202220
6 201620
7 201618
8 202216
9 201916
10 202015
11 201514
12 201714
13 202112
14 202112
15 201712
16 202112
17 202311
18 201811
19 201410
20 202110

About Yingjun Xie

Yingjun Xie is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Plant Science, having authored 65 papers that have together received 543 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (11 papers), CRISPR and Genetic Engineering (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (7 papers), Genomics and Rare Diseases (7 papers), Genetic Syndromes and Imprinting (6 papers) and Chromosomal and Genetic Variations (6 papers). The work is most often cited by research in Genetics (128 citations), Pediatrics, Perinatology and Child Health (138 citations), Aging (10 citations), Genetics (157 citations) and Hematology (56 citations). Yingjun Xie has collaborated with scholars based in China, France and Singapore. Frequent co-authors include Xiaofang Sun, Bing Song, Ding Wang, Yexing Xian, Zhanhui Ou, Hongning Xie, Yu‐Chang Chen, Linhuan Huang, Yi Yang and Diyu Chen. Their work appears in journals such as Stem Cell Research, Frontiers in Pediatrics, Frontiers in Genetics, Prenatal Diagnosis and Journal of Cellular and Molecular Medicine.

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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