Gisèle Bonne

18.9k citations

203 papers · 11.4k indexed · 1 hit paper · h-index 55

Molecular Biology top 0.5%
Cardiology and Cardiovascular Medicine top 0.5%
Cell Biology top 0.5%
Genetics top 1%
Genetics top 5%

Co-authors: Howard J. Worman Ketty Schwartz Antoine Muchir Pascale Richard Rabah Ben Yaou Lucie Carrier Luciano Merlini Bernard Hainque
Topics: Nuclear Structure and Function (129 papers)RNA Research and Splicing (115 papers)Muscle Physiology and Disorders (42 papers)
Cited by: Cardiology and Cardiovascular Medicine Molecular Biology Cell Biology
Journals: Circulation Journal of Clinical Investigation Nature Genetics
Partner nations: France United States United Kingdom

In The Last Decade

Gisèle Bonne

194 papers receiving 11.3k citations

Hit Papers

align trajectories

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.

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1999 1.0k citations Gisèle Bonne, Henri-Marc Bécane et al. profile →

Peers

Countries citing papers authored by Gisèle Bonne

Since Specialization

Citations

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

Fields of papers citing papers by Gisèle Bonne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gisèle Bonne

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and Myoblasts 2023 ·Cells ·Louise Benarroch,(unknown),(unknown),Kamel Mamchaoui,(unknown),Anne Bigot,Vincent Mouly,Gisèle Bonne,A. Bertrand,Philippe Collas	3
2	A lamin A/C variant causing striated muscle disease provides insights into filament organization 2021 ·Journal of Cell Science ·Rafael Kronenberg‐Tenga,(unknown),Matthias Eibauer,Wei Wu,Ji‐Yeon Shin,Gisèle Bonne,Howard J. Worman,Ohad Medalia	19
3	Preclinical Advances of Therapies for Laminopathies 2021 ·Journal of Clinical Medicine ·Louise Benarroch,(unknown),António Atalaia,Rabah Ben Yaou,Gisèle Bonne,A. Bertrand	7
4	Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies 2020 ·Cells ·(unknown),A. Bertrand,(unknown),(unknown),(unknown),(unknown),Zofia T. Bilińska,Gisèle Bonne,Marie‐Andrée Akimenko,Frédérique Tesson	5
5	Consequences of Lmna Exon 4 Mutations in Myoblast Function 2020 ·Cells ·(unknown),Carolina Epifano,Fernando de Miguel,Albert G. Castaño,(unknown),Alberto Martín,(unknown),A. Bertrand,Gisèle Bonne,Javier Ramón‐Azcón,Miguel Ángel Rodríguez-Milla,Ignacío Pérez de Castro	6
6	Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth 2020 ·International Journal of Molecular Sciences ·Daniel J. Owens,(unknown),Sophie Moog,(unknown),Arnaud Ferry,Kamel Mamchaoui,Emmanuelle Lacène,Norma B. Romero,Astrid Brull,Gisèle Bonne,Gillian Butler‐Browne,Catherine Coirault	21
7	Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery–Dreifuss Muscular Dystrophy 2020 ·Cells ·A. Bertrand,Astrid Brull,Fériel Azibani,Louise Benarroch,Khadija Chikhaoui,Colin L. Stewart,Ohad Medalia,Rabah Ben Yaou,Gisèle Bonne	26
8	Novel role of Tieg1 in muscle metabolism and mitochondrial oxidative capacities 2019 ·Acta Physiologica ·(unknown),Jérôme Piquereau,Lydie Nadal‐Desbarats,Sandra Même,Maud Beuvin,Gisèle Bonne,Vladimir Veksler,Yann Le Fur,Philippe Pouletaut,William Même,Frédéric Szeremeta,Jean‐Marc Constans,Elizabeth S. Bruinsma,(unknown),Zeynab Najafova,Steven A. Johnsen,Malayannan Subramaniam,John R. Hawse,Sabine F. Bensamoun	16
9	The mammalian LINC complex component SUN1 regulates muscle regeneration by modulating drosha activity 2019 ·eLife ·Tsui-Han Loo,(unknown),Ruth Jinfen Chai,Mitsuteru Ito,Gisèle Bonne,Anne C. Ferguson‐Smith,Colin L. Stewart	11
10	SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells 2018 ·Scientific Reports ·Alexandre Janin,(unknown),Francesca Ratti,(unknown),A. Bertrand,(unknown),Emilie Chopin,Nathalie Streichenberger,Gisèle Bonne,Vincent Gache,Tatiana V. Cohen,Alexandre Méjat	5
11	Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy 2017 ·Molecular Therapy — Nucleic Acids ·Fériel Azibani,Astrid Brull,Ludovic Arandel,Maud Beuvin,Isabelle Nelson,Arnaud Jollet,(unknown),Bernard Prudhon,Sofia Benkhelifa‐Ziyyat,Marc Bitoun,Stéphanie Lorain,Gisèle Bonne,A. Bertrand	32
12	Lamins and nesprin-1 mediate inside-out mechanical coupling in muscle cell precursors through FHOD1 2017 ·Scientific Reports ·Christine Schwartz,Martina Fischer,Kamel Mamchaoui,Anne Bigot,(unknown),Claude Verdier,Alain Duperray,R. Michel,Ian Holt,Thomas Voit,(unknown),Gisèle Bonne,Catherine Coirault	38
13	Proceso histórico-pedagógico de las bibliotecas escolares en Cuba en el período 1960-2010 2016 ·SHILAP Revista de lepidopterología ·(unknown),Gisèle Bonne	0
14	Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related Diseases 2015 ·Journal of Neuromuscular Diseases ·Isabelle Nelson,(unknown),(unknown),France Leturcq,Henri-Marc Bécane,Dominique Babuty,Annick Toutain,Christophe Béroud,Pascale Richard,Norma B. Romero,B. Eymard,Rabah Ben Yaou,Gisèle Bonne	26
15	Myoblasts and Embryonic Stem Cells Differentially Engraft in a Mouse Model of Genetic Dilated Cardiomyopathy 2013 ·Molecular Therapy ·Cyril Catelain,(unknown),(unknown),Nathalie Mougenot,Adeline Jacquet,(unknown),Erica Yada,Michel Pucéat,Marc Fiszman,Gillian Butler‐Browne,Gisèle Bonne,Jean‐Thomas Vilquin	6
16	A Novel Genetic Variant in the Transcription Factor Islet-1 Exerts Gain of Function on Myocyte Enhancer Factor 2C Promoter Activity 2012 ·European Journal of Heart Failure ·Felix W. Friedrich,Gilles Dilanian,(unknown),Denise Juhr,Lucie Gueneau,Philippe Charron,Véronique Fressart,Jean‐Thomas Vilquin,Richard Isnard,Laurent Gouya,Pascale Richard,Naima Hammoudi,Michel Komajda,Gisèle Bonne,Thomas Eschenhagen,Olivier Dubourg,Eric Villard,Lucie Carrier	21
17	Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy 2009 ·The Journal of Cell Biology ·Alexandre Méjat,V. Decostre,Juan Li,(unknown),Akanchha Kesari,Daniel Hantaı̈,Colin L. Stewart,Xiao Xiao,Eric P. Hoffman,Gisèle Bonne,Tom Misteli	96
18	AB26-1 2006 ·Heart Rhythm ·Frédéric Anselme,(unknown),Jop H. van Berlo,Gisèle Bonne,Arnaud Savouré,Rabah Ben Yaou,J. Peter van Tintelen,Henri-Marc Bécane,Maarten P. van den Berg,Pascal Laforêt,Alain Cribier,(unknown),Denis Duboc	1
19	Clinical analysis of 32 patients carrying R453W LMNA mutation 2002 ·UCL Discovery (University College London) ·Gisèle Bonne,Rabah Ben Yaou,L. Demay,Pascale Richard,B. Eymard,J. Andoni Urtizberea,D Duboc,F. Muntoni,M Wehnert,(unknown),Luciano Merlini,(unknown),M. Visser,Dominique Récan,Kevin J. Schwartz	2
20	Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy. 1999 ·PubMed ·Pascale Richard,Richard Isnard,Lucie Carrier,Olivier Dubourg,(unknown),(unknown),Gisèle Bonne,Françoise Gary,Philippe Charron,(unknown),Michel Komajda,K Schwartz,Bernard Hainque	60

About Gisèle Bonne

Gisèle Bonne is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology, having authored 203 papers that have together received 11.4k indexed citations. Recurring topics across this work include Nuclear Structure and Function (129 papers), RNA Research and Splicing (115 papers) and Muscle Physiology and Disorders (42 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (3.3k citations), Molecular Biology (9.3k citations) and Cell Biology (1.6k citations). Gisèle Bonne has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Howard J. Worman, Ketty Schwartz, Antoine Muchir, Pascale Richard, Rabah Ben Yaou, Lucie Carrier, Luciano Merlini, Bernard Hainque, Denis Duboc and Shaïda Varnous. Their work appears in journals such as Circulation, Journal of Clinical Investigation and Nature Genetics.

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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