Kathrin Meyer

7.5k citations
94 papers · 5.8k · 2 hit papers · h-index 28

Impact in

  • Genetics top 0.5%
    • Neurogenetic and Muscular Disorders Research
    • Virus-based gene therapy research
  • Neurology top 0.5%
    • Amyotrophic Lateral Sclerosis Research

Papers in

    • Neurogenetic and Muscular Disorders Research 40
    • Virus-based gene therapy research 9
    • Genetics and Neurodevelopmental Disorders 8
    • Amyotrophic Lateral Sclerosis Research 16

Kathrin Meyer

92 papers receiving 5.7k citations

Kathrin Meyer's Hit Papers

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy 2017 · 1.8k citations
1.8k0+5+10Years since publication50010001.5k

Peers

Kathrin Meyer
Comparison fields: 5 of 125
  • Genetics 2.2k
  • Neurology 1.5k
  • Developmental Neuroscience 253
  • Neurology 504
  • Molecular Biology 2.9k
Replace Lyndsey Braun with:
Lyndsey Braun United States
Carlos J. Miranda United States
Kevin D. Foust United States
Shibi B. Likhite United States
Stephen J. Kolb United States
Annie Laquerrière France
Perry B. Shieh United States
Kathy Keyvani Germany
Imaharu Nakano Japan
Ubaldo Del Carro Italy
Kathrin Meyer relative to Lyndsey Braun United States Lyndsey Braun's profile →
Citations per field
00.5×1.6×
Lyndsey Braun · 1×
Citations per year

Countries citing papers authored by Kathrin Meyer

Since Specialization
Citations

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

Fields of papers citing papers by Kathrin Meyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 94 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
Hit paper breakdown →
20171824
2
Astrocytes from familial and sporadic ALS patients are toxic to motor neurons
Hit paper breakdown →
2011661
3 2016326
4 2013296
5 2014240
6 2008236
7 2013175
8 2011158
9 2016156
10 2014116
11 2016115
12 2017104
13 200981
14 200877
15 200773
16 201865
17 201365
18 201047
19 201646
20 202242

About Kathrin Meyer

Kathrin Meyer is a scholar working on Genetics, Neurology, Molecular Biology, Genetics and Developmental Neuroscience, having authored 94 papers that have together received 5.8k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (40 papers), RNA modifications and cancer (20 papers), Amyotrophic Lateral Sclerosis Research (16 papers), CRISPR and Genetic Engineering (15 papers), Virus-based gene therapy research (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), RNA regulation and disease (8 papers) and RNA Research and Splicing (7 papers). The work is most often cited by research in Genetics (2.2k citations), Neurology (1.5k citations), Developmental Neuroscience (253 citations), Neurology (504 citations) and Molecular Biology (2.9k citations). Kathrin Meyer has collaborated with scholars based in United States, Switzerland and United Kingdom. Frequent co-authors include Brian K. Kaspar, Shibi B. Likhite, Laura Ferraiuolo, Anne Frances Mannion, Haiko Sprott, Arthur H.M. Burghes, Carlos J. Miranda, Lyndsey Braun, Kevin D. Foust and Pamela J. Shaw. Their work appears in journals such as Molecular Therapy, Neurology, Molecular Therapy — Methods & Clinical Development, Molecular Genetics and Metabolism and RNA Biology.

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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