L. Demay

1.3k total citations
18 papers, 661 citations indexed

About

L. Demay is a scholar working on Molecular Biology, Cell Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, L. Demay has authored 18 papers receiving a total of 661 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 4 papers in Cell Biology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in L. Demay's work include Nuclear Structure and Function (9 papers), RNA Research and Splicing (8 papers) and Ion channel regulation and function (4 papers). L. Demay is often cited by papers focused on Nuclear Structure and Function (9 papers), RNA Research and Splicing (8 papers) and Ion channel regulation and function (4 papers). L. Demay collaborates with scholars based in France, Tunisia and Italy. L. Demay's co-authors include Pascale Richard, Gisèle Bonne, Pascale Guicheney, P Coumel, Isabelle Denjoy, Bernard Hainque, Claire Donger, Luciano Merlini, Ketty Schwartz and Nathalie Neyroud and has published in prestigious journals such as Circulation, Circulation Research and Neurology.

In The Last Decade

L. Demay

18 papers receiving 653 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L. Demay France 13 596 301 78 58 42 18 661
S. White Australia 5 311 0.5× 289 1.0× 93 1.2× 73 1.3× 108 2.6× 5 374
E. Hammouda France 4 1.1k 1.8× 260 0.9× 148 1.9× 62 1.1× 99 2.4× 4 1.1k
S.M. Dorosz Australia 4 342 0.6× 324 1.1× 102 1.3× 95 1.6× 107 2.5× 6 421
Pascale Sébillon France 8 467 0.8× 454 1.5× 51 0.7× 37 0.6× 27 0.6× 10 628
Jenni Laitila Finland 9 226 0.4× 225 0.7× 88 1.1× 36 0.6× 92 2.2× 18 313
Ana Domazetovska Australia 9 231 0.4× 205 0.7× 87 1.1× 43 0.7× 68 1.6× 13 293
William Wallefeld Australia 6 266 0.4× 258 0.9× 78 1.0× 44 0.8× 91 2.2× 11 333
Xavière Lornage France 10 186 0.3× 105 0.3× 28 0.4× 54 0.9× 40 1.0× 19 243
Satu Sandell Finland 10 232 0.4× 114 0.4× 41 0.5× 89 1.5× 56 1.3× 21 313
Josine M. de Winter Netherlands 11 283 0.5× 255 0.8× 62 0.8× 41 0.7× 96 2.3× 16 328

Countries citing papers authored by L. Demay

Since Specialization
Citations

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

Fields of papers citing papers by L. Demay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Demay

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

All Works

18 of 18 papers shown
1.
Richard, Pascale, Capucine Trollet, Teresa Gidaro, et al.. (2015). PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling. Journal of Neuromuscular Diseases. 2(2). 175–180. 15 indexed citations
2.
Sabatelli, Patrizia, Silvia Castagnaro, Francesca Tagliavini, et al.. (2014). Aggresome–Autophagy Involvement in a Sarcopenic Patient with Rigid Spine Syndrome and a p.C150R Mutation in FHL1 Gene. Frontiers in Aging Neuroscience. 6. 215–215. 16 indexed citations
3.
Gaudon, Karen, I. Pénisson-Besnier, B. Chabrol, et al.. (2010). Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing. Journal of Medical Genetics. 47(12). 795–796. 9 indexed citations
4.
Lilienbaum, Alain, Sabrina Batonnet‐Pichon, Francine Bruston, et al.. (2010). Desmin myopathy with severe cardiomyopathy in a Uruguayan family due to a codon deletion in a new location within the desmin 1A rod domain. Neuromuscular Disorders. 20(3). 178–187. 27 indexed citations
5.
Makri, S., Nigel F. Clarke, Pascale Richard, et al.. (2008). Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy. Neuromuscular Disorders. 19(1). 26–28. 15 indexed citations
6.
Yaou, Rabah Ben, Annick Toutain, Takuro Arimura, et al.. (2007). Multitissular involvement in a family with LMNA and EMD mutations. Neurology. 68(22). 1883–1894. 45 indexed citations
7.
Yaou, Rabah Ben, Lucie Gueneau, L. Demay, et al.. (2006). Heart involvement in lamin A/C related diseases.. PubMed. 99(9). 848–55. 17 indexed citations
8.
Gueneau, Lucie, Rabah Ben Yaou, L. Demay, et al.. (2006). G.P.4.09 Looking for a third gene causing Emery-Dreifuss muscular dystrophy: Lessons and perspectives. Neuromuscular Disorders. 16(9-10). 677–678. 3 indexed citations
9.
10.
Lampe, AK, Michelle Eagle, L. Demay, et al.. (2005). Bethlem myopathy, autosomal dominant and X-linked Emery Dreifuss muscular dystrophy - comparison of contractural phenotypes. 1 indexed citations
11.
Yaou, Rabah Ben, Antoine Muchir, Takuro Arimura, et al.. (2005). Genetics of Laminopathies. Novartis Foundation symposium. 264. 81–97. 21 indexed citations
12.
Mercuri, Eugenio, Maja Poppe, Rosaline C. M. Quinlivan, et al.. (2004). Extreme Variability of Phenotype in Patients With an Identical Missense Mutation in the Lamin A/C Gene. Archives of Neurology. 61(5). 690–690. 85 indexed citations
13.
Bonne, Gisèle, Rabah Ben Yaou, L. Demay, et al.. (2002). Clinical analysis of 32 patients carrying R453W LMNA mutation. UCL Discovery (University College London). 2 indexed citations
14.
Vytopil, Michal, Enzo Ricci, Antonio Dello Russo, et al.. (2002). Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy. Neuromuscular Disorders. 12(10). 958–963. 42 indexed citations
15.
Kooi, Anneke J. van der, Gisèle Bonne, B. Eymard, et al.. (2002). Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy. Neurology. 59(4). 620–623. 104 indexed citations
16.
Lupoglazoff, Jean‐Marc, Isabelle Denjoy, Myriam Berthet, et al.. (2001). Notched T Waves on Holter Recordings Enhance Detection of Patients With LQT2 ( HERG ) Mutations. Circulation. 103(8). 1095–1101. 74 indexed citations
17.
Neyroud, Nathalie, Pascale Richard, Nicolas Vignier, et al.. (1999). Genomic Organization of the KCNQ1 K + Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome. Circulation Research. 84(3). 290–297. 90 indexed citations
18.
Berthet, Myriam, Isabelle Denjoy, Claire Donger, et al.. (1999). C-terminal HERG Mutations. Circulation. 99(11). 1464–1470. 83 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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