Virginie Carmignac

7.0k total citations
38 papers, 1.1k citations indexed

About

Virginie Carmignac is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Virginie Carmignac has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Virginie Carmignac's work include Muscle Physiology and Disorders (9 papers), Genetic Syndromes and Imprinting (8 papers) and Prenatal Screening and Diagnostics (5 papers). Virginie Carmignac is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Genetic Syndromes and Imprinting (8 papers) and Prenatal Screening and Diagnostics (5 papers). Virginie Carmignac collaborates with scholars based in France, Sweden and United Kingdom. Virginie Carmignac's co-authors include Madeleine Durbeej, Ana Ferreiro, Mathias Gautel, Ronan Quéré, Patricia Fauque, Céline Bruno, Cécile Choux, Paul Sagot, Linda Elowsson and Anna Vihola and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Virginie Carmignac

37 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Virginie Carmignac France 17 714 269 182 177 144 38 1.1k
Jaime Meléndez Chile 16 734 1.0× 387 1.4× 113 0.6× 278 1.6× 23 0.2× 25 1.3k
P. Gallano Spain 20 1.0k 1.4× 261 1.0× 287 1.6× 116 0.7× 158 1.1× 65 1.4k
Annalaura Torella Italy 18 697 1.0× 174 0.6× 286 1.6× 83 0.5× 71 0.5× 77 983
Ariana Kariminejad Iran 21 756 1.1× 57 0.2× 715 3.9× 284 1.6× 75 0.5× 100 1.5k
Carol A. Crowe United States 17 582 0.8× 79 0.3× 318 1.7× 100 0.6× 136 0.9× 28 904
Anas M. Alazami Saudi Arabia 22 857 1.2× 60 0.2× 584 3.2× 100 0.6× 128 0.9× 55 1.5k
Corinna Warburton Canada 13 649 0.9× 47 0.2× 179 1.0× 80 0.5× 72 0.5× 16 1.1k
Giuliano Giuseppe Stirparo United Kingdom 21 1.8k 2.5× 226 0.8× 179 1.0× 95 0.5× 87 0.6× 29 2.1k
Rannar Airik United States 21 1.3k 1.8× 177 0.7× 445 2.4× 87 0.5× 208 1.4× 32 1.5k
Judith A. Skinner United Kingdom 12 963 1.3× 117 0.4× 418 2.3× 74 0.4× 80 0.6× 15 1.1k

Countries citing papers authored by Virginie Carmignac

Since Specialization
Citations

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

Fields of papers citing papers by Virginie Carmignac

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Virginie Carmignac

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

All Works

20 of 20 papers shown
1.
Chevarin, Martin, Juliette Piard, Quentin Thomas, et al.. (2024). Allelic heterogeneity in a patient with postzygotic MTOR ‐related hypomelanosis of Ito with neurodevelopmental abnormalities. Clinical Genetics. 105(5). 581–583. 2 indexed citations
2.
Carmignac, Virginie, et al.. (2022). Becker’s Naevus Syndrome with Breast Aplasia Due to Postzygotic Mutation of ACTB. Acta Dermato Venereologica. 102. adv00806–adv00806.
3.
Theiler, Martin, Lisa Weibel, Stéphanie Christen‐Zaech, et al.. (2021). Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations. Journal of the European Academy of Dermatology and Venereology. 35(10). 2085–2090. 4 indexed citations
4.
Carmignac, Virginie, Arthur Sorlin, Yannis Duffourd, et al.. (2021). Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway. Ultrasound in Obstetrics and Gynecology. 59(4). 532–542. 7 indexed citations
5.
Gori, Ilaria, Roger George, Andrew G. Purkiss, et al.. (2021). Mutations in SKI in Shprintzen–Goldberg syndrome lead to attenuated TGF-β responses through SKI stabilization. eLife. 10. 18 indexed citations
6.
Agopiantz, Mikaël, Arthur Sorlin, P. Vabres, et al.. (2021). Fertility in McCune Albright syndrome female: A case study focusing on AMH as a marker of ovarian dysfunction and a literature review. Journal of Gynecology Obstetrics and Human Reproduction. 50(9). 102171–102171. 2 indexed citations
7.
Delplancq, Geoffroy, Antonio Vitobello, Sophie Nambot, et al.. (2020). Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 129–135. 15 indexed citations
8.
Uzan, Benjamin, Romain Aucagne, François Hermetet, et al.. (2019). T-cell acute lymphoblastic leukemia displays autocrine production of Interleukin-7. Oncogene. 38(48). 7357–7365. 12 indexed citations
9.
Thévenon, Julien, Laurence Duplomb, Shubha R. Phadke, et al.. (2016). Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia. Clinical Genetics. 90(6). 509–517. 18 indexed citations
10.
Bruno, Céline, Virginie Carmignac, Irène Netchine, et al.. (2015). Germline correction of an epimutation related to Silver-Russell syndrome. Human Molecular Genetics. 24(12). 3314–3321. 8 indexed citations
11.
Faivre, Laurence, Thomas Gautier, Jean‐Michel Petit, et al.. (2015). Insulin response dysregulation explains abnormal fat storage and increased risk of diabetes mellitus type 2 in Cohen Syndrome. Human Molecular Genetics. 24(23). 6603–6613. 22 indexed citations
12.
Gueneau, Lucie, Laurence Duplomb, Pierre Sarda, et al.. (2013). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. American Journal of Medical Genetics Part A. 164(2). 522–527. 11 indexed citations
13.
Elowsson, Linda, Harald Kirsebom, Virginie Carmignac, Bo Mattìasson, & Madeleine Durbeej. (2013). Evaluation of macroporous blood and plasma scaffolds for skeletal muscle tissue engineering. Biomaterials Science. 1(4). 402–402. 14 indexed citations
14.
Rauch, Uwe, Annelie Shami, Feng Zhang, et al.. (2012). Increased Neointimal Thickening in Dystrophin-Deficient mdx Mice. PLoS ONE. 7(1). e29904–e29904. 8 indexed citations
15.
Carmignac, Virginie & Madeleine Durbeej. (2011). Cell–matrix interactions in muscle disease. The Journal of Pathology. 226(2). 200–218. 73 indexed citations
16.
Carmignac, Virginie, Martina Svensson, Linda Elowsson, et al.. (2011). Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A. Human Molecular Genetics. 20(24). 4891–4902. 103 indexed citations
17.
Carmignac, Virginie, Ronan Quéré, & Madeleine Durbeej. (2010). Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice. Human Molecular Genetics. 20(3). 541–552. 54 indexed citations
18.
Åkerlund, Mikael, et al.. (2009). Laminin α1 domains LG4-5 are essential for the complete differentiation of visceral endoderm. Cell and Tissue Research. 338(1). 129–137. 3 indexed citations
19.
Bigotti, Maria Giulia, Virginie Carmignac, Johan Holmberg, et al.. (2008). Cib2 Binds Integrin α7Bβ1D and Is Reduced in Laminin α2 Chain-deficient Muscular Dystrophy. Journal of Biological Chemistry. 283(36). 24760–24769. 35 indexed citations
20.
Carmignac, Virginie, Mustafa A. Salih, Susana Quijano‐Roy, et al.. (2007). C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy. Annals of Neurology. 61(4). 340–351. 156 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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