Emmanuelle Lacène

2.7k total citations
32 papers, 1.5k citations indexed

About

Emmanuelle Lacène is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Emmanuelle Lacène has authored 32 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 11 papers in Cardiology and Cardiovascular Medicine and 9 papers in Cell Biology. Recurrent topics in Emmanuelle Lacène's work include Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (10 papers) and Nuclear Structure and Function (8 papers). Emmanuelle Lacène is often cited by papers focused on Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (10 papers) and Nuclear Structure and Function (8 papers). Emmanuelle Lacène collaborates with scholars based in France, Germany and Italy. Emmanuelle Lacène's co-authors include Norma B. Romero, Jocelyn Laporte, Michel Fardeau, Marc Bitoun, Pascale Guicheney, B. Eymard, Gisèle Bonne, Guy Brochier, Pascal Laforêt and Maud Beuvin and has published in prestigious journals such as Nature Genetics, The Journal of Cell Biology and Brain.

In The Last Decade

Emmanuelle Lacène

29 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emmanuelle Lacène France 17 1.3k 415 370 356 212 32 1.5k
Rabah Ben Yaou France 23 1.8k 1.4× 562 1.4× 309 0.8× 223 0.6× 173 0.8× 66 2.1k
Gianina Ravenscroft Australia 25 1.1k 0.9× 628 1.5× 239 0.6× 367 1.0× 313 1.5× 94 1.5k
Marco Savarese Finland 20 983 0.8× 477 1.1× 166 0.4× 271 0.8× 224 1.1× 72 1.3k
Suzanne Lillis United Kingdom 13 609 0.5× 388 0.9× 143 0.4× 198 0.6× 138 0.7× 21 829
Fédérica Piccolo United States 10 897 0.7× 238 0.6× 259 0.7× 126 0.4× 409 1.9× 21 969
S. Britton United Kingdom 6 914 0.7× 240 0.6× 189 0.5× 104 0.3× 227 1.1× 9 1.0k
Hisaomi Kawai Japan 17 575 0.5× 174 0.4× 148 0.4× 92 0.3× 224 1.1× 45 932
Vishram Kedar United States 12 1.1k 0.9× 313 0.8× 255 0.7× 46 0.1× 204 1.0× 16 1.4k
Laurence Suel France 16 652 0.5× 162 0.4× 258 0.7× 61 0.2× 166 0.8× 18 741
Nuria Muelas Spain 18 422 0.3× 148 0.4× 106 0.3× 160 0.4× 370 1.7× 50 922

Countries citing papers authored by Emmanuelle Lacène

Since Specialization
Citations

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

Fields of papers citing papers by Emmanuelle Lacène

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuelle Lacène

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuelle Lacène. A scholar is included among the top collaborators of Emmanuelle Lacène 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 Emmanuelle Lacène. Emmanuelle Lacène 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.
Hentschel, Andreas, Emmanuelle Lacène, Guy Brochier, et al.. (2025). Glycogenosis type XI, a rare association between muscle and skin manifestations - the contribution of proteomics for the understanding of the underlying myopathology. Journal of Neuromuscular Diseases. 12(2). 271–278. 1 indexed citations
2.
Bui, Mai Thao, Gorka Fernández‐Eulate, Teresinha Evangelista, et al.. (2024). Relevance of muscle biopsies in the neonatal and early infantile period: a 52 years retrospective study in the gene-sequencing era. Acta Neuropathologica Communications. 12(1). 191–191. 1 indexed citations
3.
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Vassilopoulos, Stéphane, Anthony Béhin, Céline Tard, et al.. (2023). Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort. European Journal of Neurology. 30(8). 2506–2517. 4 indexed citations
6.
Meyer, Nancy, René P. Zahedi, Teresinha Evangelista, et al.. (2022). FYCO1 Increase and Effect of Arimoclomol–Treatment in Human VCP–Pathology. Biomedicines. 10(10). 2443–2443. 2 indexed citations
7.
Owens, Daniel J., Sophie Moog, Arnaud Ferry, et al.. (2020). Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth. International Journal of Molecular Sciences. 22(1). 306–306. 21 indexed citations
8.
Carvalho, Alzira Alves de Siqueira, Emmanuelle Lacène, Beatriz da Costa Aguiar Alves, et al.. (2019). mRna Expression Genes Associated To Myofibrillar Myopathies – Preliminary Study (P5.4-015). Neurology. 92(15_supplement). 1 indexed citations
9.
Lainé, Jeanne, Gilles Moulay, Michaël Trichet, et al.. (2019). Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle. Molecular Biology of the Cell. 30(5). 579–590. 36 indexed citations
10.
Garibaldi, Matteo, John Rendu, Julie Brocard, et al.. (2019). ‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies. Acta Neuropathologica Communications. 7(1). 3–3. 33 indexed citations
11.
Malfatti, Edoardo, Johann Böhm, Emmanuelle Lacène, Norma B. Romero, & Jocelyn Laporte. (2015). A premature stop codon in MYO18B is associated with severe nemaline myopathy with cardiomyopathy. Neuromuscular Disorders. 25. S186–S186. 6 indexed citations
12.
Malfatti, Edoardo, Johann Böhm, Emmanuelle Lacène, et al.. (2015). A Premature Stop Codon in MYO18B is Associated with Severe Nemaline Myopathy with Cardiomyopathy. Journal of Neuromuscular Diseases. 2(3). 219–227. 67 indexed citations
13.
Wanschitz, Julia, O. Dubourg, Emmanuelle Lacène, et al.. (2012). Expression of myogenic regulatory factors and myo-endothelial remodeling in sporadic inclusion body myositis. Neuromuscular Disorders. 23(1). 75–83. 31 indexed citations
14.
Claeys, Kristl G., Jean‐Jacques Martin, Emmanuelle Lacène, et al.. (2010). DNAJB2 Expression in Normal and Diseased Human and Mouse Skeletal Muscle. American Journal Of Pathology. 176(6). 2901–2910. 18 indexed citations
15.
Hernández‐Laín, Aurelio, Isabelle Husson, Nicole Monnier, et al.. (2010). de novo RYR1 heterozygous mutation (I4898T) causing lethal core–rod myopathy in twins. European Journal of Medical Genetics. 54(1). 29–33. 38 indexed citations
16.
Allamand, Valérie, Corine Gartioux, Emmanuelle Lacène, et al.. (2007). C.O.3 Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophy. Neuromuscular Disorders. 17(9-10). 833–833. 1 indexed citations
17.
Auré, Karine, et al.. (2006). Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation. Brain. 129(5). 1249–1259. 62 indexed citations
18.
Bevilacqua, Jorge A., Marc Bitoun, Svetlana Maugenre, et al.. (2006). G.P.8 11 Towards the identification of new morphological subtypes of congenital myopathy. Neuromuscular Disorders. 16(9-10). 709–710. 1 indexed citations
19.
Laforêt, Pascal, Pascale Richard, Mina Ait Saïd, et al.. (2006). A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis. Neuromuscular Disorders. 16(3). 178–182. 41 indexed citations
20.
Arimura, Takuro, A. Leclerc, Catherine Massart, et al.. (2004). Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Human Molecular Genetics. 14(1). 155–169. 258 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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