Daniel Rochefort

5.0k citations
45 papers · 2.4k · 1 hit paper · h-index 24

Impact in

  • Neurology top 2%
    • Amyotrophic Lateral Sclerosis Research
    • Parkinson's Disease Mechanisms and Treatments
  • Genetics top 2%
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders

Papers in

    • RNA regulation and disease 6
    • Muscle Physiology and Disorders 6
    • Parkinson's Disease Mechanisms and Treatments 9
    • Amyotrophic Lateral Sclerosis Research 7

Daniel Rochefort

44 papers receiving 2.3k citations

Hit Papers

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy 1998 · 583 citations
5830+9+18Years since publication100200300400500

Peers

Daniel Rochefort
Comparison fields: 5 of 103
  • Neurology 724
  • Genetics 449
  • Cellular and Molecular Neuroscience 759
  • Neurology 185
  • Molecular Biology 1.4k
Replace Hussein Daoud with:
Hussein Daoud Canada
Kevin L. Seburn United States
Klaus Wagner Austria
Carmen Cifuentes-Díaz France
Bernard Brais Canada
Erica Korb United States
Mackenzie W. Amoroso United States
Gert‐Jan B. van Ommen Netherlands
Esther de Graaff Netherlands
Lawrence T. Reiter United States
Daniel Rochefort relative to Hussein Daoud Canada Hussein Daoud's profile →
Citations per field
00.5×1.5×2.2×
Hussein Daoud · 1×
Citations per year

Countries citing papers authored by Daniel Rochefort

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Rochefort

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
Hit paper breakdown →
1998583
2 2009314
3 2010170
4 2010128
5 2013119
6 2014101
7 200197
8 200881
9 200348
10 201945
11 201243
12 201641
13 200541
14 201241
15 201339
16 200339
17 200336
18 202333
19 200732
20 199532

About Daniel Rochefort

Daniel Rochefort is a scholar working on Molecular Biology, Neurology, Cellular and Molecular Neuroscience, Genetics and Genetics, having authored 45 papers that have together received 2.4k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (9 papers), Genetic Neurodegenerative Diseases (8 papers), Amyotrophic Lateral Sclerosis Research (7 papers), Neurogenetic and Muscular Disorders Research (7 papers), RNA regulation and disease (6 papers), Muscle Physiology and Disorders (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Restless Legs Syndrome Research (4 papers). The work is most often cited by research in Neurology (724 citations), Genetics (449 citations), Cellular and Molecular Neuroscience (759 citations), Neurology (185 citations) and Molecular Biology (1.4k citations). Daniel Rochefort has collaborated with scholars based in Canada, France and United States. Frequent co-authors include Guy A. Rouleau, Patrick A. Dion, Bernard Brais, Jean‐Pierre Bouchard, Pierre Drapeau, Johanna M. Rommens, Ya‐Gang Xie, François Codère, F.M.S. Tomé and Michel Fardeau. Their work appears in journals such as Human Molecular Genetics, Genomics, European Journal of Human Genetics, Scientific Reports and Movement Disorders.

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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