Fernande Freyermuth

2.2k citations
7 papers · 1.0k · 1 hit paper · h-index 7

Impact in

  • Genetics top 5%
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders
  • Neurology top 5%
    • Amyotrophic Lateral Sclerosis Research

Papers in

Fernande Freyermuth

7 papers receiving 1.0k citations

Fernande Freyermuth's Hit Papers

Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration 2019 · 368 citations
3680+2+4Years since publication100200300

Peers

Fernande Freyermuth
Comparison fields: 5 of 53
  • Genetics 249
  • Neurology 349
  • Cellular and Molecular Neuroscience 321
  • Molecular Biology 744
  • Genetics 164
Replace Niels H. Skotte with:
Niels H. Skotte Denmark
Sharan Paul United States
Ricardos Tabet France
Warunee Dansithong United States
S. H. Subramony United States
Constantin d’Ydewalle Belgium
Jonathan W. Artates United States
Rahul Kanadia United States
Crystal N. Doty Canada
Hongru Zhou China
Fernande Freyermuth relative to Niels H. Skotte Denmark Niels H. Skotte's profile →
Citations per field
00.5×1.7×
Niels H. Skotte · 1×
Citations per year

Countries citing papers authored by Fernande Freyermuth

Since Specialization
Citations

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

Fields of papers citing papers by Fernande Freyermuth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

7 of 7 papers shown
#Work
1
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration
Hit paper breakdown →
2019368
2 2011234
3 2013206
4 2018100
5 201861
6 201426
7 201724

About Fernande Freyermuth

Fernande Freyermuth is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Cardiology and Cardiovascular Medicine and Genetics, having authored 7 papers that have together received 1.0k indexed citations. Recurring topics across this work include RNA Research and Splicing (5 papers), Genetic Neurodegenerative Diseases (3 papers), Amyotrophic Lateral Sclerosis Research (2 papers), Cardiomyopathy and Myosin Studies (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), Muscle Physiology and Disorders (1 paper) and RNA regulation and disease (1 paper). The work is most often cited by research in Genetics (249 citations), Neurology (349 citations), Cellular and Molecular Neuroscience (321 citations), Molecular Biology (744 citations) and Genetics (164 citations). Fernande Freyermuth has collaborated with scholars based in United States, France and Japan. Frequent co-authors include Nicolas Charlet‐Berguerand, Clotilde Lagier‐Tourenne, Ricardos Tabet, John Ravits, Moira A. McMahon, Frank Rigo, Kevin Drenner, Ouyang Zhang, Ze’ev Melamed and Takuya Ohkubo. Their work appears in journals such as Nature Communications, Nature Structural & Molecular Biology, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Nature Neuroscience and Cell Reports.

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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