Natacha Broucqsault

478 total citations
15 papers, 261 citations indexed

About

Natacha Broucqsault is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Natacha Broucqsault has authored 15 papers receiving a total of 261 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in Natacha Broucqsault's work include Chronic Lymphocytic Leukemia Research (4 papers), Muscle Physiology and Disorders (4 papers) and Lymphoma Diagnosis and Treatment (3 papers). Natacha Broucqsault is often cited by papers focused on Chronic Lymphocytic Leukemia Research (4 papers), Muscle Physiology and Disorders (4 papers) and Lymphoma Diagnosis and Treatment (3 papers). Natacha Broucqsault collaborates with scholars based in France, Singapore and United States. Natacha Broucqsault's co-authors include Frédérique Magdinier, Karine Nguyen, Nicolas Lévy, Shahram Attarian, Camille Dion, Stéphane Roche, Marc Bartoli, Julia Morere, Jérôme D. Robin and Rafaëlle Bernard and has published in prestigious journals such as Blood, Neurology and Scientific Reports.

In The Last Decade

Natacha Broucqsault

15 papers receiving 257 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Natacha Broucqsault France 9 184 98 43 40 32 15 261
Maryam Sedghi Iran 11 176 1.0× 39 0.4× 9 0.2× 80 2.0× 32 1.0× 46 338
Nicole Hellbach Germany 7 171 0.9× 55 0.6× 9 0.2× 33 0.8× 20 0.6× 7 237
Robea Ballo South Africa 7 137 0.7× 39 0.4× 10 0.2× 79 2.0× 45 1.4× 19 281
Noriko Ide-Iwata United States 4 181 1.0× 29 0.3× 21 0.5× 19 0.5× 18 0.6× 5 263
Marian James United Kingdom 6 278 1.5× 15 0.2× 18 0.4× 29 0.7× 42 1.3× 9 360
Valentina Potrich Italy 5 306 1.7× 130 1.3× 9 0.2× 15 0.4× 18 0.6× 6 372
Silvia Stringara Italy 8 183 1.0× 15 0.2× 80 1.9× 22 0.6× 24 0.8× 9 349
Rosamaria Silipigni Italy 10 144 0.8× 50 0.5× 6 0.1× 79 2.0× 16 0.5× 35 264
Kanchan Sarda India 11 123 0.7× 60 0.6× 64 1.5× 92 2.3× 55 1.7× 13 334
Paula Fraczek United States 6 310 1.7× 61 0.6× 7 0.2× 20 0.5× 10 0.3× 10 365

Countries citing papers authored by Natacha Broucqsault

Since Specialization
Citations

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

Fields of papers citing papers by Natacha Broucqsault

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natacha Broucqsault

This figure shows the co-authorship network connecting the top 25 collaborators of Natacha Broucqsault. A scholar is included among the top collaborators of Natacha Broucqsault 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 Natacha Broucqsault. Natacha Broucqsault is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Van‐Gils, Julien, Stéphane Claverol, Caroline Tokarski, et al.. (2024). Transcriptome and acetylome profiling identify crucial steps of neuronal differentiation in Rubinstein-Taybi syndrome. Communications Biology. 7(1). 1331–1331. 2 indexed citations
2.
Caron, Leslie, Claire El Yazidi, Natacha Broucqsault, et al.. (2022). Mesenchymal stem cells derived from patients with premature aging syndromes display hallmarks of physiological aging. Life Science Alliance. 5(12). e202201501–e202201501. 6 indexed citations
3.
Broucqsault, Natacha, Nathalie Streichenberger, Véronique Manel, et al.. (2021). Facioscapulohumeral dystrophy weakened sarcomeric contractility is mimicked in induced pluripotent stem cells‐derived innervated muscle fibres. Journal of Cachexia Sarcopenia and Muscle. 13(1). 621–635. 8 indexed citations
4.
Broucqsault, Natacha, Karine Nguyen, Shifeng Xue, et al.. (2021). AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome. Biomedicines. 9(7). 751–751. 4 indexed citations
5.
Broucqsault, Natacha, et al.. (2020). Production of Innervated Skeletal Muscle Fibers Using Human Induced Pluripotent Stem Cells. Methods in molecular biology. 2454. 231–239. 3 indexed citations
6.
Badja, Cherif, Natacha Broucqsault, Camille Dion, et al.. (2020). Multilineage Differentiation for Formation of Innervated Skeletal Muscle Fibers from Healthy and Diseased Human Pluripotent Stem Cells. Cells. 9(6). 1531–1531. 36 indexed citations
7.
Broucqsault, Natacha, Julia Morere, Camille Dion, et al.. (2019). Analysis of the 4q35 chromatin organization reveals distinct long-range interactions in patients affected with Facio-Scapulo-Humeral Dystrophy. Scientific Reports. 9(1). 10327–10327. 12 indexed citations
8.
Roche, Stéphane, Camille Dion, Natacha Broucqsault, et al.. (2019). Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism. Neurology Genetics. 5(6). e372–e372. 16 indexed citations
9.
Herbaux, Charles, Elisabeth Bertrand, Guillemette Marot, et al.. (2016). BACH2 promotes indolent clinical presentation in Waldenström macroglobulinemia. Oncotarget. 8(34). 57451–57459. 1 indexed citations
10.
Roche, Stéphane, Camille Dion, Natacha Broucqsault, et al.. (2014). Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers. Neurology. 83(8). 733–742. 66 indexed citations
11.
Boussouar, Amina, Caroline Barette, Robert Nadon, et al.. (2013). Acacetin and Chrysin, Two Polyphenolic Compounds, Alleviate Telomeric Position Effect in Human Cells. Molecular Therapy — Nucleic Acids. 2. e116–e116. 15 indexed citations
12.
Broucqsault, Natacha, Julia Morere, Julie Dumonceaux, et al.. (2013). Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy. Human Molecular Genetics. 22(20). 4206–4214. 44 indexed citations
13.
Poulain, Stéphanie, Christophe Roumier, Sylvie Galiègue‐Zouitina, et al.. (2013). Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemia. American Journal of Hematology. 88(11). 948–954. 29 indexed citations
14.
Poulain, Stéphanie, Esteban Braggio, Christophe Roumier, et al.. (2011). High-Throughput Genomic Analysis in Waldenström's Macroglobulinemia. Clinical Lymphoma Myeloma & Leukemia. 11(1). 106–108. 18 indexed citations
15.
Poulain, Stéphanie, Natacha Broucqsault, Salomon Manier, et al.. (2010). A20 Gene Deregulation In Waldenstrom's Macroglobulinemia.. Blood. 116(21). 3628–3628. 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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