Yaping Yang

8.5k citations
35 papers · 843 · h-index 17

Impact in

  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Epigenetics and DNA Methylation
    • RNA modifications and cancer
    • Congenital heart defects research

Papers in

    • Genomics and Rare Diseases 14
    • Genetics and Neurodevelopmental Disorders 9
    • Genomic variations and chromosomal abnormalities 8
    • RNA modifications and cancer 4
    • Congenital heart defects research 3

Yaping Yang

34 papers receiving 826 citations

Peers

Yaping Yang
Comparison fields: 5 of 96
  • Genetics 440
  • Molecular Biology 485
  • Genetics 54
  • Clinical Biochemistry 33
  • Reproductive Medicine 37
Replace Takahito Wada with:
Takahito Wada Japan
Karen Buysse Belgium
Irene Madrigal Spain
Athel Hockey Australia
Ahmet Okay Çağlayan Türkiye
Marianna Baybis United States
Zöe Powis United States
Rocío G. Urdinguio Spain
Miriam S. Reuter Germany
Andrew F. Stewart United States
Yaping Yang relative to Takahito Wada Japan Takahito Wada's profile →
Citations per field
00.5×3.4×
Takahito Wada · 1×
Citations per year

Countries citing papers authored by Yaping Yang

Since Specialization
Citations

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

Fields of papers citing papers by Yaping Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2013210
2 2013102
3 200869
4 200853
5 201349
6 201040
7 201233
8 201629
9 201621
10 202220
11 201619
12 201319
13 201418
14 201918
15 202117
16 201816
17 201516
18 201014
19 201912
20 202111

About Yaping Yang

Yaping Yang is a scholar working on Genetics, Molecular Biology, Cancer Research, Neurology and Oncology, having authored 35 papers that have together received 843 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA modifications and cancer (4 papers), Cancer Genomics and Diagnostics (3 papers), Congenital heart defects research (3 papers), Metabolism and Genetic Disorders (3 papers) and Botulinum Toxin and Related Neurological Disorders (2 papers). The work is most often cited by research in Genetics (440 citations), Molecular Biology (485 citations), Genetics (54 citations), Clinical Biochemistry (33 citations) and Reproductive Medicine (37 citations). Yaping Yang has collaborated with scholars based in United States, China and United Kingdom. Frequent co-authors include Karen W. Gripp, Arthur L. Beaudet, Lorraine Potocki, Fan Xia, Mark A. McElwain, C. Thomas Caskey, Manuel L. Gonzalez‐Garay, Christian P. Schaaf, Radoje Drmanac and Brock A. Peters. Their work appears in journals such as Human Mutation, Journal of Clinical Oncology, Genome Medicine, Cancer Research and Nature Genetics.

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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