Irène Boccaccio

2.7k total citations · 1 hit paper
13 papers, 2.0k citations indexed

About

Irène Boccaccio is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Irène Boccaccio has authored 13 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Irène Boccaccio's work include Nuclear Structure and Function (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Hereditary Neurological Disorders (3 papers). Irène Boccaccio is often cited by papers focused on Nuclear Structure and Function (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Hereditary Neurological Disorders (3 papers). Irène Boccaccio collaborates with scholars based in France, United States and Lebanon. Irène Boccaccio's co-authors include Nicolas Lévy, Annachiara De Sandre‐Giovannoli, Claire Navarro, Rafaëlle Bernard, Pierre Cau, Martine Le Merrer, Arnold Münnich, Colin L. Stewart, Stanislas Lyonnet and Jeanne Amiel and has published in prestigious journals such as Science, Journal of Biological Chemistry and The American Journal of Human Genetics.

In The Last Decade

Irène Boccaccio

13 papers receiving 2.0k citations

Hit Papers

Lamin A Truncation in Hut... 2003 2026 2010 2018 2003 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Lamin A Truncation in Hutchinson-Gilford Progeria
    2003 1.1k citations Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard et al. Science profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Irène Boccaccio France 9 1.7k 282 204 130 124 13 2.0k
Neil Dear United Kingdom 9 664 0.4× 281 1.0× 250 1.2× 113 0.9× 90 0.7× 11 1.2k
Catherine Creppe Belgium 13 844 0.5× 257 0.9× 107 0.5× 65 0.5× 221 1.8× 17 1.2k
Muriel Vernet France 15 980 0.6× 407 1.4× 176 0.9× 61 0.5× 138 1.1× 20 1.4k
Rener Xu China 16 1.5k 0.9× 464 1.6× 124 0.6× 100 0.8× 130 1.0× 20 1.7k
Wendy Bushell United Kingdom 4 877 0.5× 160 0.6× 318 1.6× 99 0.8× 121 1.0× 4 1.3k
Lynne V. Mayne United Kingdom 20 2.1k 1.2× 90 0.3× 414 2.0× 127 1.0× 83 0.7× 33 2.3k
A. Cohen France 17 1.4k 0.8× 184 0.7× 250 1.2× 115 0.9× 106 0.9× 28 1.7k
Bennett H. Penn United States 9 1.5k 0.9× 104 0.4× 262 1.3× 108 0.8× 155 1.3× 12 1.6k
Zohra Rahmani France 16 880 0.5× 255 0.9× 512 2.5× 72 0.6× 69 0.6× 26 1.6k
Akiko Yanagiya Canada 19 1.1k 0.6× 67 0.2× 116 0.6× 130 1.0× 126 1.0× 31 1.5k

Countries citing papers authored by Irène Boccaccio

Since Specialization
Citations

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

Fields of papers citing papers by Irène Boccaccio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irène Boccaccio

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

All Works

13 of 13 papers shown
1.
Hamadouche, Tarik, Yannick Poitelon, Emmanuelle Génin, et al.. (2008). Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa. Annals of Human Genetics. 72(5). 590–597. 21 indexed citations
2.
Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H. The American Journal of Human Genetics. 81(1). 1–16. 117 indexed citations
3.
Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H. Neuromuscular Disorders. 17(9-10). 767–767. 3 indexed citations
4.
Navarro, Claire, Irène Boccaccio, Catherine Badens, et al.. (2006). P.I.3 Recent advances in defective prelamin A associated syndromes. Neuromuscular Disorders. 16(9-10). 682–682. 1 indexed citations
5.
Navarro, Claire, Juan Cadiñanos, Annachiara De Sandre‐Giovannoli, et al.. (2005). Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors. Human Molecular Genetics. 14(11). 1503–1513. 217 indexed citations
6.
Navarro, Claire, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, et al.. (2004). Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy. Human Molecular Genetics. 13(20). 2493–2503. 266 indexed citations
7.
Lévy, Nicolas, Claire Navarro, Irène Boccaccio, et al.. (2003). Functional exploration of A type lamins and associated proteins in patients affected with Hutchinson-Gilford progeria syndrome caused by G608G mutation in LMNA. The American Journal of Human Genetics. 73(5). 554. 1 indexed citations
8.
Sandre‐Giovannoli, Annachiara De, Rafaëlle Bernard, Pierre Cau, et al.. (2003). Lamin A Truncation in Hutchinson-Gilford Progeria. Science. 300(5628). 2055–2055. 1084 indexed citations breakdown →
9.
Syin, Chiang, Daniel Parzy, François Traincard, et al.. (2001). The H89 cAMP‐dependent protein kinase inhibitor blocks Plasmodium falciparum development in infected erythrocytes. European Journal of Biochemistry. 268(18). 4842–4849. 80 indexed citations
10.
Boccaccio, Irène, Heather R. Glatt-Deeley, Françoise Watrin, et al.. (1999). The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region. Human Molecular Genetics. 8(13). 2497–2505. 151 indexed citations
11.
Dorin, Dominique, Pietro Alano, Irène Boccaccio, et al.. (1999). An Atypical Mitogen-activated Protein Kinase (MAPK) Homologue Expressed in Gametocytes of the Human Malaria Parasite Plasmodium falciparum. Journal of Biological Chemistry. 274(42). 29912–29920. 89 indexed citations
12.
Boccaccio, Irène, et al.. (1996). Unexpected Inheritance of the(CGG)(n) Trinucleotide Expansion in aFragile X Syndrome Family. European Journal of Human Genetics. 4(1). 8–12. 9 indexed citations
13.
Voelckel, Marie‐Antoinette, et al.. (1991). Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter Syndrome. American Journal of Medical Genetics. 38(2-3). 374–377. 3 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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