Véronique Bolduc

2.0k total citations
19 papers, 492 citations indexed

About

Véronique Bolduc is a scholar working on Molecular Biology, Genetics and Immunology and Allergy. According to data from OpenAlex, Véronique Bolduc has authored 19 papers receiving a total of 492 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Immunology and Allergy. Recurrent topics in Véronique Bolduc's work include Muscle Physiology and Disorders (9 papers), Cell Adhesion Molecules Research (5 papers) and RNA Research and Splicing (5 papers). Véronique Bolduc is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Cell Adhesion Molecules Research (5 papers) and RNA Research and Splicing (5 papers). Véronique Bolduc collaborates with scholars based in United States, United Kingdom and Canada. Véronique Bolduc's co-authors include Bernard Brais, Lambert Busque, Pierre Chagnon, Claude Bélisle, Sylvie Provost, Yves Robitaille, Carsten G. Bönnemann, Marjolein Visser, Isabelle Richard and I. Mahjneh and has published in prestigious journals such as Journal of Clinical Investigation, Brain and The American Journal of Human Genetics.

In The Last Decade

Véronique Bolduc

17 papers receiving 483 citations

Peers

Véronique Bolduc
Patrick Frosk Canada
Leïla Lazaro France
Jaya Punetha United States
Lanying Song United States
Ke-Yu Deng China
Burcu Balcı-Hayta Türkiye
Dwi U. Kemaladewi Netherlands
Shehla Mohammed United Kingdom
Steven E. Boyden United States
Marjon A. van Slegtenhorst Netherlands
Patrick Frosk Canada
Véronique Bolduc
Citations per year, relative to Véronique Bolduc Véronique Bolduc (= 1×) peers Patrick Frosk

Countries citing papers authored by Véronique Bolduc

Since Specialization
Citations

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

Fields of papers citing papers by Véronique Bolduc

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Véronique Bolduc

This figure shows the co-authorship network connecting the top 25 collaborators of Véronique Bolduc. A scholar is included among the top collaborators of Véronique Bolduc based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Véronique Bolduc. Véronique Bolduc is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Brull, Astrid, et al.. (2024). Optimized allele-specific silencing of the dominant-negative COL6A1 G293R substitution causing collagen VI-related dystrophy. Molecular Therapy — Nucleic Acids. 35(2). 102178–102178. 8 indexed citations
2.
Bolduc, Véronique, et al.. (2024). Consistent Delivery of Adeno-Associated Virus via Lateral Tail-Vein Injection in Adult Mice. Journal of Visualized Experiments.
3.
Bolduc, Véronique, et al.. (2024). Allele-specific CRISPR-Cas9 editing inactivates a single nucleotide variant associated with collagen VI muscular dystrophy. Molecular Therapy — Nucleic Acids. 35(3). 102269–102269. 3 indexed citations
4.
Mörgelin, Matthias, Véronique Bolduc, Francesco Muntoni, et al.. (2023). The UCMD-Causing COL6A1 ( c . 930 + 189 C > T ) Intron Mutation Leads to the Secretion and Aggregation of Single Mutated Collagen VI α1 Chains. Human Mutation. 2023. 1–16.
5.
Bönnemann, Carsten G., et al.. (2022). Exon-Skipping for a Pathogenic COL6A1 Variant in Ullrich Congenital Muscular Dystrophy. Methods in molecular biology. 2587. 387–407. 1 indexed citations
6.
Bolduc, Véronique, Katie M. Minor, Ying Hu, et al.. (2020). Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs. Neuromuscular Disorders. 30(5). 360–367. 11 indexed citations
7.
Bolduc, Véronique, et al.. (2020). Exon-Skipping Oligonucleotides Restore Functional Collagen VI by Correcting a Common COL6A1 Mutation in Ullrich CMD. Molecular Therapy — Nucleic Acids. 21. 205–216. 19 indexed citations
8.
Hu, Ying, Payam Mohassel, Sandra Donkervoort, et al.. (2019). Identification of a Novel Deep Intronic Mutation in CAPN3 Presenting a Promising Target for Therapeutic Splice Modulation. Journal of Neuromuscular Diseases. 6(4). 475–483. 6 indexed citations
9.
Foley, A. Reghan, Sandra Donkervoort, Véronique Bolduc, et al.. (2017). A common COL6A1 deep-intronic pseudo-exon inserting mutation causes a distinct phenotype of Ullrich congenital muscular dystrophy. Neuromuscular Disorders. 27. S106–S106. 1 indexed citations
10.
11.
Srour, Myriam, Jeremy Schwartzentruber, Véronique Bolduc, et al.. (2014). Mutations in riboflavin transporter present with severe sensory loss and deafness in childhood. Muscle & Nerve. 50(5). 775–779. 20 indexed citations
12.
Bolduc, Véronique, Yaqun Zou, Dayoung Ko, & Carsten G. Bönnemann. (2014). siRNA-mediated Allele-specific Silencing of a COL6A3 Mutation in a Cellular Model of Dominant Ullrich Muscular Dystrophy. Molecular Therapy — Nucleic Acids. 3. e147–e147. 22 indexed citations
13.
Bolduc, Véronique, Gareth Marlow, Kym M. Boycott, et al.. (2010). Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies. The American Journal of Human Genetics. 86(2). 213–221. 195 indexed citations
14.
Srour, Myriam, Véronique Bolduc, Velina Guergueltcheva, et al.. (2010). DOK7 mutations presenting as a proximal myopathy in French Canadians. Neuromuscular Disorders. 20(7). 453–457. 18 indexed citations
15.
Bolduc, Véronique, Pierre Chagnon, Sylvie Provost, et al.. (2007). No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans. Journal of Clinical Investigation. 118(1). 333–341. 88 indexed citations
16.
17.
Jarry, Julien, Véronique Bolduc, Yves Robitaille, et al.. (2006). A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12. Brain. 130(2). 368–380. 38 indexed citations
18.
Chagnon, Pierre, et al.. (2005). Age-associated skewing of X-inactivation ratios of blood cells in normal females: a candidate-gene analysis approach. Experimental Hematology. 33(10). 1209–1214. 26 indexed citations
19.
Foley, A. Reghan, Payam Mohassel, Sandra Donkervoort, Véronique Bolduc, & Carsten G. Bönnemann. (1993). Collagen VI-Related Dystrophies. 1 indexed citations

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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