Pascale Richard

12.0k citations

168 papers · 6.6k indexed · 1 hit paper · h-index 42

Cardiology and Cardiovascular Medicine top 0.2%
Molecular Biology top 2%
Cell Biology top 2%
Epidemiology top 5%
Genetics top 2%

Co-authors: Bernard Hainque Ketty Schwartz Gisèle Bonne Philippe Charron Lucie Carrier Michel Komajda Richard Isnard Olivier Dubourg
Topics: Cardiomyopathy and Myosin Studies (70 papers)Muscle Physiology and Disorders (39 papers)Nuclear Structure and Function (37 papers)
Cited by: Cardiology and Cardiovascular Medicine Molecular Biology Developmental Neuroscience
Journals: Nucleic Acids Research Circulation Nature Genetics
Partner nations: France Italy Germany

In The Last Decade

Pascale Richard

159 papers receiving 6.5k 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.

Hypertrophic Cardiomyopathy

2003 925 citations Pascale Richard, Philippe Charron et al. profile →

Peers

Countries citing papers authored by Pascale Richard

Since Specialization

Citations

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

Fields of papers citing papers by Pascale Richard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascale Richard

This figure shows the co-authorship network connecting the top 25 collaborators of Pascale Richard. A scholar is included among the top collaborators of Pascale Richard 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 Pascale Richard. Pascale Richard 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	Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy 2024 ·Clinical Genetics ·Flavie Ader,Guillaume Jedraszak,Alexandre Janin,Clarisse Billon,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Cécile Cazeneuve,Philippe Charron,Gilles Millat,Pascale Richard,(unknown)	4
2	Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies 2023 ·Cells ·Nathalie Vadrot,Flavie Ader,Maryline Moulin,(unknown),Françoise Chapon,Estelle Gandjbakhch,Fabien Labombarda,Pascale Maragnès,Patricia Réant,Caroline Rooryck,Vincent Probst,Erwan Donal,Pascale Richard,Ana Ferreiro,Brigitte Buendia	4
3	DNA ‐pools targeted‐sequencing as a robust cost‐effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis 2023 ·Clinical Genetics ·Claire Perret,Carole Proust,Ulrike Esslinger,Flavie Ader,Jan Haas,(unknown),Richard Isnard,Pascale Richard,David‐Alexandre Trégouët,Philippe Charron,François Cambien,Eric Villard	1
4	A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency 2020 ·Annals of Clinical and Translational Neurology ·Aurélien Perrin,Corinne Métay,Marcello Villanova,Robert‐Yves Carlier,Elena Pegoraro,Raúl Juntas‐Morales,Tanya Stojkovic,Isabelle Richard,Pascale Richard,Norma B. Romero,Henk Granzier,M. Kœnig,Edoardo Malfatti,Mireille Cossée	9
5	FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations 2020 ·Archives of Cardiovascular Diseases Supplements ·Flavie Ader,Pascal de Groote,Patricia Réant,(unknown),Caroline Rambaud,Diala Khraiche,(unknown),(unknown),(unknown),Laurent Gouya,Xavier Jeunemaı̂tre,Lionel Van Maldergem,Eric Villard,Philippe Charron,Pascale Richard	7
6	FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations 2019 ·Clinical Genetics ·Flavie Ader,Pascal de Groote,Patricia Réant,Caroline Rooryck,Delphine Dupin‐Deguine,Caroline Rambaud,Diala Khraiche,Claire Perret,(unknown),Michèle Mathieu‐Dramard,Marion Gérard,(unknown),Laurent Gouya,Xavier Jeunemaı̂tre,Lionel Van Maldergem,Albert Hagège,Eric Villard,Philippe Charron,Pascale Richard	57
7	0178 : Global and regional echocardiographic strain to assess early phase of hypertrophic cardiomyopathy due to sarcomeric mutations 2016 ·Archives of Cardiovascular Diseases Supplements ·Guillaume Baudry,Nicolas Mansencal,(unknown),Pascale Richard,Richard Isnard,Olivier Dubourg,(unknown),Philippe Charron	2
8	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
9	PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy –Consequences in Clinical Diagnosis and Genetic Counselling 2015 ·Journal of Neuromuscular Diseases ·Pascale Richard,Capucine Trollet,Teresa Gidaro,L. Demay,Guy Brochier,Edoardo Malfatti,(unknown),Michel Fardeau,(unknown),Norma B. Romero,(unknown),(unknown),(unknown),(unknown),B. Eymard	15
10	Syndromes myasthéniques congénitaux — L’expérience française 2014 ·Bulletin de l Académie Nationale de Médecine ·B. Eymard,Daniel Hantaı̈,Emmanuel Fournier,Sophie Nicole,Damien Sternberg,Pascale Richard,Michel Fardeau	1
11	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
12	Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study 2009 ·Acta Neuropathologica ·Kristl G. Claeys,Peter F. M. van der Ven,Anthony Béhin,Tanya Stojkovic,B. Eymard,O. Dubourg,Pascal Laforêt,Georgine Faulkner,Pascale Richard,Patrick Vicart,Norma B. Romero,G. Stoltenburg,Bjarne Udd,Michel Fardeau,Thomas Voït,Dieter O. Fürst	54
13	Desminopathies : What can we learn from a long term follow-up? 2008 ·Neuromuscular Disorders ·Anthony Béhin,T. Stojkovic,Kristl G. Claeys,Karim Wahbi,D Duboc,Henri Marc Bécane,O. Dubourg,Thierry Maisonobe,G. Stoltenburg,(unknown),Pascale Richard,(unknown),(unknown),B. Eymard	0
14	Severe MDC1A Congenital Muscular Dystrophy Due to a Splicing Mutation in the LAMA2 Gene Resulting in Exon Skipping and Significant Decrease of mRNA Level 2007 ·Genetic Testing ·(unknown),(unknown),Chahnez Triki,Madeleine Morinière,Ahmed Rebaï,Pascale Richard,Pascale Guicheney,Faouzi Baklouti,Faiza Fakhfakh	11
15	G.P.5.01 Inflammatory or ‘congenital myopathy’ type findings in muscle biopsies of patients with LMNA mutations 2007 ·Neuromuscular Disorders ·Fabiana Lubieniecki,Soledad Monges,Alberto Dubrovsky,(unknown),Víctor Ruggieri,Fábio Barroso,Graciela Espada,(unknown),(unknown),Pascale Richard,Gisèle Bonne,Norma B. Romero,Pascale Guicheney,(unknown),A.L. Taratuto	2
16	C.O.3 Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophy 2007 ·Neuromuscular Disorders ·Valérie Allamand,Corine Gartioux,Emmanuelle Lacène,Jeanne Lainé,C. Ledeuil,Susana Quijano‐Roy,S. Makri,Louis Viollet,Pierre‐Yves Jeannet,(unknown),(unknown),Pascale Richard,B. Estournet,Norma B. Romero,Pascale Guicheney	1
17	La dystrophie musculaire des ceintures autosomique dominante associée à des troubles de la conduction cardiaque (LGMD1B). Description de 8 nouvelles familles avec mutations du gène LMNA 2005 ·Revue Neurologique ·Rabah Ben Yaou,Henri Marc Bécane,L. Demay,Pascal Laforêt,Didier Hannequin,(unknown),Valérie Drouin‐Garraud,Xavier Ferrer,J.M. Mussini,(unknown),P. Petiot,I. Pénisson-Besnier,Nathalie Streichenberger,Annick Toutain,Pascale Richard,B. Eymard,Gisèle Bonne	12
18	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
19	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
20	Relationship between Hp<sup>1</sup><sup>s</sup> and Hp<sup>2</sup> Gene Frequencies among Human Populations 1978 ·Human Heredity ·J. Constans,Pascale Richard,M. Viau	7

About Pascale Richard

Pascale Richard is a scholar working on Cardiology and Cardiovascular Medicine, Genetics and Molecular Biology, having authored 168 papers that have together received 6.6k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (70 papers), Muscle Physiology and Disorders (39 papers) and Nuclear Structure and Function (37 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (4.3k citations), Molecular Biology (3.9k citations) and Developmental Neuroscience (209 citations). Pascale Richard has collaborated with scholars based in France, Italy and Germany. Frequent co-authors include Bernard Hainque, Ketty Schwartz, Gisèle Bonne, Philippe Charron, Lucie Carrier, Michel Komajda, Richard Isnard, Olivier Dubourg, Michel Desnos and Pascale Guicheney. Their work appears in journals such as Nucleic Acids Research, Circulation 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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