Sandra Duqué

2.0k citations
24 papers · 1.5k · h-index 14

Impact in

  • Genetics top 1%
    • Neurogenetic and Muscular Disorders Research
    • Virus-based gene therapy research
    • RNA modifications and cancer
    • RNA Interference and Gene Delivery
    • CRISPR and Genetic Engineering
    • Muscle Physiology and Disorders
    • RNA Research and Splicing

Papers in

    • RNA modifications and cancer 7
    • RNA Research and Splicing 3
    • CRISPR and Genetic Engineering 2
    • RNA Interference and Gene Delivery 2
    • Neurogenetic and Muscular Disorders Research 13
    • Virus-based gene therapy research 6

Sandra Duqué

23 papers receiving 1.5k citations

Peers

Sandra Duqué
Comparison fields: 5 of 84
  • Genetics 693
  • Genetics 573
  • Molecular Biology 1.0k
  • Developmental Neuroscience 52
  • Cellular and Molecular Neuroscience 203
Replace Curtis M. Chan with:
Curtis M. Chan United States
Emily Nurre United States
Thibaut Marais France
Yves De Repentigny Canada
S Malcolm United Kingdom
María Morell Spain
Bernhard Laggerbauer Germany
Lucy E. Walmsley United Kingdom
Francesco Lotti United States
Matthew Murtha United States
Sandra Duqué relative to Curtis M. Chan United States Curtis M. Chan's profile →
Citations per field
00.5×1.5×2.0×
Curtis M. Chan · 1×
Citations per year

Countries citing papers authored by Sandra Duqué

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Duqué

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2009404
2 2011256
3 2010236
4 2013105
5 2014105
6 200762
7 201762
8 201359
9 200743
10 201842
11 201337
12 202116
13 201116
14 199916
15 201312
16 201610
17 201710
18 20189
19 20129
20 20203

About Sandra Duqué

Sandra Duqué is a scholar working on Molecular Biology, Genetics, Genetics, Surgery and Neurology, having authored 24 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (13 papers), RNA modifications and cancer (7 papers), Virus-based gene therapy research (6 papers), Congenital Anomalies and Fetal Surgery (5 papers), RNA Research and Splicing (3 papers), Amyotrophic Lateral Sclerosis Research (2 papers), CRISPR and Genetic Engineering (2 papers) and RNA Interference and Gene Delivery (2 papers). The work is most often cited by research in Genetics (693 citations), Genetics (573 citations), Molecular Biology (1.0k citations), Developmental Neuroscience (52 citations) and Cellular and Molecular Neuroscience (203 citations). Sandra Duqué has collaborated with scholars based in United States, France and Belgium. Frequent co-authors include Martine Barkats, Thibaut Marais, Béatrice Joussemet, Marie‐Anne Colle, Philippe Moullier, John C. Fyfe, Laurence Dubreil, Christel Rivière, Anne‐Marie Douar and Stéphanie Astord. Their work appears in journals such as Molecular Therapy, Human Molecular Genetics, Natural Product Communications, PLoS ONE and Human Gene Therapy.

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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