Linyan Meng

3.3k citations
16 papers · 1.1k · 1 hit paper · h-index 10

Impact in

    • Cancer-related molecular mechanisms research
  • Genetics top 5%
    • Genetic Syndromes and Imprinting
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genetic Syndromes and Imprinting 6
    • Genomics and Rare Diseases 4
    • Neurogenetic and Muscular Disorders Research 2
    • Genetics and Neurodevelopmental Disorders 2
    • Epigenetics and DNA Methylation 3
    • Mitochondrial Function and Pathology 2
    • RNA regulation and disease 2

Linyan Meng

16 papers receiving 1.1k citations

Linyan Meng's Hit Papers

Towards a therapy for Angelman syndrome by targeting a long non-coding RNA 2014 · 378 citations
3780+4+8Years since publication100200300

Peers

Linyan Meng
Comparison fields: 5 of 93
  • Cancer Research 244
  • Genetics 445
  • Cognitive Neuroscience 207
  • Molecular Biology 610
  • Clinical Psychology 131
Replace Jacqueline Hewitt with:
Jacqueline Hewitt Australia
Tessel E. Galesloot Netherlands
Michael Harbord Australia
Sarah M. Nikkel Canada
Yanchun Bao United Kingdom
Julie‐Anne Little United Kingdom
Teresa Wong United States
Kandamurugu Manickam United States
Hamdi Mbarek Netherlands
Alicia Hurtado Spain
Linyan Meng relative to Jacqueline Hewitt Australia Jacqueline Hewitt's profile →
Citations per field
00.5×6.2×
Jacqueline Hewitt · 1×
Citations per year

Countries citing papers authored by Linyan Meng

Since Specialization
Citations

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

Fields of papers citing papers by Linyan Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

16 of 16 papers shown
#Work
1
Towards a therapy for Angelman syndrome by targeting a long non-coding RNA
Hit paper breakdown →
2014378
2 2007174
3 2007159
4 2012148
5 2013118
6 201531
7 201615
8 201915
9 202314
10
Estimating Car Insurance Premia: a Case Study in High-Dimensional Data Inference
200112
11 20218
12 20207
13 20216
14 20223
15 20163
16 20251

About Linyan Meng

Linyan Meng is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Cellular and Molecular Neuroscience, having authored 16 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), Genomics and Rare Diseases (4 papers), Prenatal Screening and Diagnostics (3 papers), Epigenetics and DNA Methylation (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Mitochondrial Function and Pathology (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Cancer Research (244 citations), Genetics (445 citations), Cognitive Neuroscience (207 citations), Molecular Biology (610 citations) and Clinical Psychology (131 citations). Linyan Meng has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Arthur L. Beaudet, Richard Person, C. Frank Bennett, Amanda J. Ward, Frank Rigo, Seung Chun, Éric Fombonne, Vicky Tagalakis, Laurie H. Plotnick and Xun Zhang. Their work appears in journals such as Human Mutation, Human Molecular Genetics, The Journal of Pediatrics, Frontiers in Genetics and PLoS 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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