Fengxia Yao

506 citations
30 papers · 355 · h-index 11

Impact in

    • Muscle Physiology and Disorders
    • Sexual Differentiation and Disorders
    • Retinal Development and Disorders
    • Genomic variations and chromosomal abnormalities

Papers in

    • Sexual Differentiation and Disorders 6
    • Retinal Development and Disorders 5
    • Muscle Physiology and Disorders 3
    • CRISPR and Genetic Engineering 2
    • Glycogen Storage Diseases and Myoclonus 2

Fengxia Yao

27 papers receiving 348 citations

Peers

Fengxia Yao
Comparison fields: 5 of 47
  • Molecular Biology 194
  • Genetics 77
  • Pediatrics, Perinatology and Child Health 45
  • Clinical Biochemistry 13
  • Ophthalmology 15
Replace Miguel Angel Alcántara‐Ortigoza with:
Miguel Angel Alcántara‐Ortigoza Mexico
Joshua Hoffman United States
Uta Burck Germany
Carlos F. Knopf Israel
Sami Alkayyali Sweden
Kei Fukuda Japan
Shaoyan Chang China
Wenxia Han China
Sumaya Alkanderi United Kingdom
Yousheng Yan China
Fengxia Yao relative to Miguel Angel Alcántara‐Ortigoza Mexico Miguel Angel Alcántara‐Ortigoza's profile →
Citations per field
00.5×2×3×
Miguel Angel Alcántara‐Ortigoza · 1×
Citations per year

Countries citing papers authored by Fengxia Yao

Since Specialization
Citations

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

Fields of papers citing papers by Fengxia Yao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201358
2 201241
3 201228
4 201226
5 201922
6 201717
7 201314
8 201913
9 201613
10 201112
11 200912
12 202010
13 202210
14 201610
15 20239
16 20178
17 20217
18
[An analysis of mutations causing Gaucher disease in Chinese population].
20096
19 20236
20 20216

About Fengxia Yao

Fengxia Yao is a scholar working on Molecular Biology, Rheumatology, Physiology, Genetics and Cell Biology, having authored 30 papers that have together received 355 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (6 papers), Retinal Development and Disorders (5 papers), Lysosomal Storage Disorders Research (5 papers), Muscle Physiology and Disorders (3 papers), CRISPR and Genetic Engineering (2 papers), Glycogen Storage Diseases and Myoclonus (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Molecular Biology (194 citations), Genetics (77 citations), Pediatrics, Perinatology and Child Health (45 citations), Clinical Biochemistry (13 citations) and Ophthalmology (15 citations). Fengxia Yao has collaborated with scholars based in China, United States and Denmark. Frequent co-authors include Zhengqing Qiu, Qinjie Tian, Ruifang Sui, Yi Dai, Shangzhi Huang, Weimin Zhang, Shuyang Zhang, Min Wei, Hung Tseng and Jinsong Gao. Their work appears in journals such as Experimental Eye Research, European Journal of Human Genetics, PLoS ONE, Documenta Ophthalmologica and Frontiers in 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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