Pascale Guicheney

22.7k citations

237 papers · 12.0k · 3 hit papers · h-index 58

Impact in

Cardiology and Cardiovascular Medicine top 0.2%
- Cardiac electrophysiology and arrhythmias
- Cardiomyopathy and Myosin Studies
- Cardiac Arrhythmias and Treatments
Molecular Biology top 0.5%
- Muscle Physiology and Disorders
- Ion channel regulation and function

Papers in

Molecular Biology 165
- Muscle Physiology and Disorders 71
- Ion channel regulation and function 58
- Nuclear Structure and Function 24
- Receptor Mechanisms and Signaling 20
Cardiology and Cardiovascular Medicine 93
- Cardiac electrophysiology and arrhythmias 63
- Cardiomyopathy and Myosin Studies 35

Co-authors: Isabelle Denjoy (50 shared papers)Michel Fardeau (25 shared papers)Ketty Schwartz (10 shared papers)Norma B. Romero (32 shared papers)Marc Bitoun (23 shared papers)B. Estournet (21 shared papers)Nathalie Neyroud (19 shared papers)Valérie Allamand (14 shared papers)
Journals: Neuromuscular Disorders (29 papers)Annals of Neurology (11 papers)Circulation (10 papers)Journal of Hypertension (10 papers)European Journal of Human Genetics (6 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Pascale Guicheney

232 papers receiving 11.8k citations

Pascale Guicheney's Hit Papers

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A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy 1998 · 866 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1998 Nature Genetics
1997 Nature Genetics
1995 Nature Genetics

Peers

Countries citing papers authored by Pascale Guicheney

Since Specialization

Citations

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

Fields of papers citing papers by Pascale Guicheney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Pascale Guicheney, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Pascale Guicheney Line = papers co-authored together Pascale Guicheney links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 237 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy Nature Genetics ·Patrick Vicart, Anne Caron, Pascale Guicheney, Zhenlin Li, Marie-Christine Prévost, Armelle Faure, Danielle Château, Françoise Chapon, Fernando Tomé, Jean-Marie Dupret, Denise Paulin, Michel Fardeau Hit paper breakdown →	1998	866
2	A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome Nature Genetics ·Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy, Michel Leibovici, Claire Donger, Jacques Barhanin, Sabine Fauré, Françoise Gary, P Coumel, Christine Petit, Ketty Schwartz, Pascale Guicheney Hit paper breakdown →	1997	659
3	Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy Nature Genetics ·A. Leclerc, Xu Zhang, Haluk Topaloğlu, Corinne Cruaud, Frédérique Tesson, Jean Weissenbach, F.M.S. Tomé, Ketty Schwartz, Michel Fardeau, Karl Tryggvason, Pascale Guicheney Hit paper breakdown →	1995	506
4	Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan The American Journal of Human Genetics ·Martin Brockington, Derek J. Blake, Paola Prandini, S. Brown, Silvia Torelli, Matthew A. Benson, Chris P. Ponting, B. Estournet, Norma B. Romero, Eugenio Mercuri, Thomas Voit, Caroline A. Sewry, Pascale Guicheney, Francesco Muntoni	2001	452
5	Mutations in dynamin 2 cause dominant centronuclear myopathy Nature Genetics ·Marc Bitoun, Svetlana Maugenre, Pierre‐Yves Jeannet, Emmanuelle Lacène, Xavier Ferrer, Pascal Laforêt, Jean‐Jacques Martin, Jocelyn Laporte, Hanns Lochmüller, Alan H. Beggs, Michel Fardeau, B. Eymard, Norma B. Romero, Pascale Guicheney	2005	315
6	Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia Circulation ·Meiso Hayashi, Isabelle Denjoy, Fabrice Extramiana, Alice Maltret, Nathalie Roux Buisson, Jean‐Marc Lupoglazoff, Didier Klug, Miyuki Hayashi, Seiji Takatsuki, E Villain, J Kamblock, A. Messali, Pascale Guicheney, Joël Lunardi, Antoine Leenhardt	2009	314
7	Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia Circulation Research ·Alex V. Postma, Isabelle Denjoy, Theo M. Hoorntje, Jean‐Marc Lupoglazoff, Antoine Da Costa, Pascale Sébillon, Marcel M. A. M. Mannens, Arthur A.M. Wilde, Pascale Guicheney	2002	302
8	KVLQT1 C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome Circulation ·Claire Donger, Isabelle Denjoy, Myriam Berthet, Nathalie Neyroud, Corinne Cruaud, Mohammed Bennaceur, G Chivoret, Ketty Schwartz, P Coumel, Pascale Guicheney	1997	247
9	Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies The American Journal of Human Genetics ·Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau, Behzad Moghadaszadeh, Nathalie Goemans, Carsten G. Bönnemann, Heinz Jungbluth, Volker Straub, Marcello Villanova, Jean‐Paul Leroy, Norma B. Romero, Jean‐Jacques Martin, Francesco Muntoni, Thomas Voit, B. Estournet, Pascale Richard, Michel Fardeau, Pascale Guicheney	2002	234
10	Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome Nature Genetics ·Behzad Moghadaszadeh, Nathalie Petit, Céline Jaillard, Martin Brockington, Susana Quijano Roy, Luciano Merlini, Norma B. Romero, B. Estournet, Isabelle Desguerre, Denys Chaigne, Francesco Muntoni, Haluk Topaloğlu, Pascale Guicheney	2001	229
11	SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome Circulation Cardiovascular Genetics ·Vincent Probst, Arthur A.M. Wilde, Julien Barc, Frédéric Sacher, Dominique Babuty, Philippe Mabo, Jacques Mansourati, Solena Le Scouarnec, Florence Kyndt, Cédric Le Caignec, Pascale Guicheney, Laëtitia Gouas, Juliette Albuisson, Paola G. Meregalli, Hervé Le Marec, Hanno L. Tan, Jean‐Jacques Schott	2009	211
12	Phenotypic spectrum associated with mutations in the fukutin‐related protein gene Annals of Neurology ·Eugenio Mercuri, Martin Brockington, Volker Straub, Susana Quijano‐Roy, Yeliz Yuva, Ralf Herrmann, S. Brown, Silvia Torelli, Victor Dubowitz, Derek J. Blake, Norma B. Romero, B. Estournet, Caroline A. Sewry, Pascale Guicheney, Thomas Voit, Francesco Muntoni	2003	172
13	Hydroquinidine therapy in Brugada syndrome Journal of the American College of Cardiology ·Jean‐Sylvain Hermida, Isabelle Denjoy, J. Clerc, Fabrice Extramiana, G Jarry, Paul Milliez, Pascale Guicheney, S Di Fusco, Jean-Luc Rey, B Cauchemez, Antoine Leenhardt	2004	167
14	Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1) Neuromuscular Disorders ·Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh, Nathalie Petit, Martin Brockington, Serena J. Counsell, Pascale Guicheney, Francesco Muntoni, Luciano Merlini	2002	160
15	C‐terminal titin deletions cause a novel early‐onset myopathy with fatal cardiomyopathy Annals of Neurology ·Virginie Carmignac, Mustafa A. Salih, Susana Quijano‐Roy, Sylvie Marchand, Molham M. Al Rayess, Maowia M. Mukhtar, Jon Andoni Urtizberea, Siegfried Labeit, Pascale Guicheney, France Leturcq, Mathias Gautel, Michel Fardeau, Kevin P. Campbell, Isabelle Richard, B. Estournet, Ana Ferreiro	2007	156
16	Brugada syndrome and fever: Genetic and molecular characterization of patients carrying mutations Cardiovascular Research ·Dagmar I. Keller, Jean‐Sébastien Rougier, Jan Kučera, N. Benammar, Véronique Fressart, Pascale Guicheney, A Mádle, Menachem Fromer, Jürg Schläpfer, Hugues Abriel	2005	153
17	A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Annals of Neurology ·Ana Ferreiro, Nicole Monnier, Norma B. Romero, Jean‐Paul Leroy, Carsten G. Bönnemann, Charles‐Antoine Haenggeli, Volker Straub, W Voss, Y. Nivoche, Heinz Jungbluth, Arnaud Lemainque, Thomas Voit, Joël Lunardi, Michel Fardeau, Pascale Guicheney	2002	137
18	Desmin‐related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene Annals of Neurology ·Ana Ferreiro, Chantal Ceuterick‐de Groote, Jared J. Marks, Nathalie Goemans, Gudrun Schreiber, F. Hanefeld, Michel Fardeau, Jean‐Jacques Martin, Hans H. Goebel, Pascale Richard, Pascale Guicheney, Carsten G. Bönnemann	2004	134
19	Molecular Basis of Familial Cardiomyopathies Circulation ·Ketty Schwartz, Lucie Carrier, Pascale Guicheney, Michel Komajda	1995	133
20	Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic) The American Journal of Human Genetics ·Claire Donger, Éric Krejci, Adolf Pou Serradell, B. Eymard, Suzanne Bon, Sophie Nicole, Danielle Château, Françoise Gary, Michel Fardeau, Jean Massoulié, Pascale Guicheney	1998	125

About Pascale Guicheney

Pascale Guicheney is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Cell Biology, Cellular and Molecular Neuroscience and Physiology, having authored 237 papers that have together received 12.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (71 papers), Cardiac electrophysiology and arrhythmias (63 papers), Ion channel regulation and function (58 papers), Cardiomyopathy and Myosin Studies (35 papers), Nuclear Structure and Function (24 papers), Receptor Mechanisms and Signaling (20 papers), Cellular transport and secretion (20 papers) and Genetic Neurodegenerative Diseases (18 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (5.6k citations), Molecular Biology (9.0k citations), Cell Biology (1.9k citations), Cellular and Molecular Neuroscience (1.8k citations) and Immunology and Allergy (547 citations). Pascale Guicheney has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Isabelle Denjoy, Michel Fardeau, Ketty Schwartz, Norma B. Romero, Marc Bitoun, B. Estournet, Nathalie Neyroud, Valérie Allamand, Haluk Topaloğlu and Frédérique Tesson. Their work appears in journals such as Neuromuscular Disorders, Annals of Neurology, Circulation, Journal of Hypertension and European Journal of Human 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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Pascale Guicheney

Pascale Guicheney's Hit Papers

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About Pascale Guicheney

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