Fernande Freyermuth

2.2k citations
10 papers · 1.6k · 1 hit paper · h-index 9

Impact in

  • Neurology top 2%
    • Amyotrophic Lateral Sclerosis Research
  • Genetics top 5%
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders

Papers in

Fernande Freyermuth

10 papers receiving 1.6k citations

Fernande Freyermuth's Hit Papers

Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration 2019 · 419 citations
4190+2+4Years since publication100200300400

Peers

Fernande Freyermuth
Comparison fields: 5 of 63
  • Neurology 573
  • Genetics 368
  • Cellular and Molecular Neuroscience 472
  • Molecular Biology 1.2k
  • Aging 14
Replace Mário Gomes-Pereira with:
Mário Gomes-Pereira France
Niels Henning Skotte Canada
Jonathan W. Artates United States
Tammy S. Reid United States
Amar N. Kar United States
Crystal N. Doty Canada
Yalda Sedaghat United States
Rahul Kanadia United States
Lindsey R. Hayes United States
Sharan Paul United States
Fernande Freyermuth relative to Mário Gomes-Pereira France Mário Gomes-Pereira's profile →
Citations per field
00.5×1.5×1.9×
Mário Gomes-Pereira · 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

10 of 10 papers shown
#Work
1
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration
Hit paper breakdown →
2019419
2 2018377
3 2011236
4 2013210
5 2016164
6 2018112
7 201864
8 201427
9 201726
10 20227

About Fernande Freyermuth

Fernande Freyermuth is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics, having authored 10 papers that have together received 1.6k indexed citations. Recurring topics across this work include RNA Research and Splicing (6 papers), Genetic Neurodegenerative Diseases (4 papers), Amyotrophic Lateral Sclerosis Research (3 papers), RNA regulation and disease (2 papers), Cardiomyopathy and Myosin Studies (2 papers), RNA modifications and cancer (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Neurology (573 citations), Genetics (368 citations), Cellular and Molecular Neuroscience (472 citations), Molecular Biology (1.2k citations) and Aging (14 citations). Fernande Freyermuth has collaborated with scholars based in United States, France and Japan. Frequent co-authors include Clotilde Lagier‐Tourenne, Nicolas Charlet‐Berguerand, Takuya Ohkubo, Ze’ev Melamed, John Ravits, Sandrine Da Cruz, Don W. Cleveland, Ouyang Zhang, Ying Sun and Kevin Drenner. Their work appears in journals such as Nature Communications, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Cell Reports, Cell and Nature Structural & Molecular 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.

Explore authors with similar magnitude of impact