Dominique Récan

4.0k citations

33 papers · 1.6k indexed · 1 hit paper · h-index 20

Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
Reproductive Medicine top 5%
Molecular Biology top 5%
- Muscle Physiology and Disorders 18
- RNA Research and Splicing 10
- Nuclear Structure and Function 8
- RNA regulation and disease 6
Endocrinology, Diabetes and Metabolism top 5%
Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 5
Physiology
- Adipose Tissue and Metabolism 3
Biomaterials
- Silk-based biomaterials and applications 3

Co-authors: Jean‐Claude Kaplan Anthony P. Monaco Ann P. Walker Hans Peter Schwarz Alfons Meindl Barbara Bardoni Elena Zanaria Tim M. Strom
Cited by: Genetics Reproductive Medicine Molecular Biology
Journals: Neuromuscular Disorders (9 papers)Journal of Clinical Investigation (4 papers)European Journal of Human Genetics (2 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Dominique Récan

33 papers receiving 1.6k citations

Hit Papers

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Peers

Countries citing papers authored by Dominique Récan

Since Specialization

Citations

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

Fields of papers citing papers by Dominique Récan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Dominique Récan, 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 Dominique Récan Line = papers co-authored together Dominique Récan links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	G.P.6 02 Somatic and germinal mosaicism of an out-of-frame deletion in the dystrophin gene in an adult male patient with predominant dilated cardiomyopathy Neuromuscular Disorders ·Yanyan Hu,France Leturcq,D. Héron,Delphine Logeart‐Avramoglou,S. Llense,Jamel Chelly,Dominique Récan,H. P. Hobik,M. I. Faddeeva,B. Eymard	2006	1
2	Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene Human Mutation ·Purushothaman Pichandi,S. V. Neklyudov,S. Llense,M. Akhtar,Dominique Récan,Cécile Peccate,Arthur H.M. Burghes,Christophe Béroud,Luis Garcı́a,Jean‐Claude Kaplan,Jamel Chelly,France Leturcq	2006	95
3	X‐linked Emery–Dreifuss muscular dystrophy and vacuoles: An immunohistochemical characterization Muscle & Nerve ·Carmen Paradas,Celedonio Márquez,Eduard Gallardo,Noemí de Luna,Prapasri Siri,Dominique Récan,V. Chiappori,Isabel Illa	2005	6
4	The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre Neuromuscular Disorders ·Sylvie Tuffery‐Giraud,H Dafina,Mounica Gowda KN,Bernard Échenne,J. Cuisset,François Rivier,Mireille Cossée,Christophe Philippe,Nicole Monnier,Éric Bieth,Dominique Récan,Rao Hui-qin,Lanhao Li,Azriel Auqi Attarsyah,Sue Malcolm,Mireille Claustres	2004	34
5	Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicine Neuromuscular Disorders ·Jon Andoni Urtizberea,W Petrie Watson,Elizabeth Vroom,Dominique Récan,Y. Zhang	2003	9
6	Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature Annales de Génétique ·N. Bouayed Abdelmoula,Marie‐France Portnoï,Leila Keskes,Dominique Récan,Ali Bahloul,T. Boudawara,Saad Ali,Tarek Rebaï	2003	29
7	Clinical analysis of 32 patients carrying R453W LMNA mutation 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,Dina Rahmadani,Luciano Merlini,Syntia Regina Rodrigues SOUZA,M. Visser,Dominique Récan,Kevin J. Schwartz	2002	2
8	Limb-girdle muscular dystrophy with calpain deficiency(LGMD 2A) in Croatia: a survey in a small rural community Neuromuscular Disorders ·Fiorella E. Carpio-Oviedo,M. S. Gehlan,ナオミチオギワラ,Dominique Récan,Yingying Pei,Rachel Heiblim,Kristina Potočki,Jihye Noh	2002	1
9	82nd ENMC international workshop, 5th international Emery–Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15–16 September 2000, Naarden, The Netherlands Neuromuscular Disorders ·Gisèle Bonne,Netta-Leena Nuotio,Marianne de Visser,Denis Duboc,Luciano Merlini,Glenn E. Morris,Francesco Muntoni,Dominique Récan,Caroline A. Sewry,Stefano Squarzoni,Colin L. Stewart,Beril Talim,Anneke J. van der Kooi,Howard J. Worman,Ketty Schwartz	2002	21
10	A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism Journal of Clinical Investigation ·Antoine Tabarin,John C. Achermann,Dominique Récan,Fredrik Mogensen,Xavier Bertagna,Sophie Christin‐Maître,Masafumi Ito,J. Larry Jameson,Philippe Bouchard	2000	133
11	Early presentation of X-linked Emery–Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy Neuromuscular Disorders ·Francesco Muntoni,Jesús Arango-Cano,Caroline A. Sewry,S. Manilal,Dominique Récan,S. Llense,Jacqueline Taylor,Glenn E. Morris,Victor Dubowitz	1998	27
12	A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystrophy: non-contiguous gene syndrome involving Becker muscular dystrophy and glycerol kinase loci Neuromuscular Disorders ·Norma B. Romero,Dominique Récan,Odile Rigal,France Leturcq,S. Llense,Emma Petherbridge,Nathalie Deburgrave,Carlo Notari,Jiazheng Tian,Jean‐Claude Kaplan	1997	7
13	Mutations in the Muscle SodiumChannel Gene (SCN4A) in 13 FrenchFamilies with Hyperkalemic PeriodicParalysis and ParamyotoniaCongenita: Phenotype to GenotypeCorrelations and Demonstration of thePredominance of Two Mutations European Journal of Human Genetics ·Emmanuelle Plassart,J Reboul,Pokusaev Bp,Dominique Récan,Philippe Millasseau,B. Eymard,Jean Pelletier,C. Thomas,Françoise Chapon,Claude Desnuelle,Christian Confavreux,B Bady,N. Hayashi,Gilbert Lenoir,G Serratrice,Michel Fardeau,Bertrand Fontaine	1994	42
14	Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X‐chromosome inactivation American Journal of Medical Genetics ·Souheila Cheriet,Christophe Philippe,M. Chery,Hélène Gilgenkrantz,F. Tomé,H. Barry Collin,G Hofmeister,Dominique Récan,Odile Broux,Michel Fardeau,J.‐C. Kaplan,S Gilgenkrantz	1994	32
15	Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. Journal of Clinical Investigation ·Kiichiro Matsumura,F.M.S. Tomé,Victor Ionâşescu,James M. Ervasti,Richard D. Anderson,Norma B. Romero,Dávid Simon,Dominique Récan,J.‐C. Kaplan,Michel Fardeau	1993	60
16	A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes Human Molecular Genetics ·Ann P. Walker,Jamel Chelly,Donald R. Love,Lisa Kasmer,Dominique Récan,Jean-Louis Chaussain,Christine A. Oley,J. M. Connor,John R. Yates,David A. Price,Maurice Super,Armand Bottani,MD. LITON RABBANI,Y. Zhang,Kay E. Davies,Anthony P. Monaco	1992	33
17	Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization? Journal of Clinical Investigation ·Dominique Récan,Philippe Chafey,France Leturcq,Jean‐Philippe Hugnot,とも子村上,F. Tomé,H. Barry Collin,Dávid Simon,P Czernichow,L. V. B. Nicholson	1992	46
18	A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD) Nucleic Acids Research ·Jean‐Philippe Hugnot,Dominique Récan,Marc Jeanpierre,J.‐C. Kaplan,Aslıhan Tolun	1991	16
19	Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients. Journal of Clinical Investigation ·Jamel Chelly,Hélène Gilgenkrantz,Jean‐Philippe Hugnot,G. Hamard,J Misković,Dominique Récan,Saïd Akli,Haardik Gupta,A Kahn,J.‐C. Kaplan	1991	46
20	Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies Cell ·M. Walsh,Hélène Gilgenkrantz,Jonah Gula,Ghislaine Hamard,Philippe Chafey,Dominique Récan,Misriyah Misriyah,Albert de la Chapelle,Ilaria Cinelli,Ieke B. Ginjaar,E. V. Belkina,F. Tomé,Axel Kahn,Y. Zhang	1990	141

About Dominique Récan

Dominique Récan is a scholar working on Molecular Biology, Genetics and Rehabilitation, having authored 33 papers that have together received 1.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (18 papers), RNA Research and Splicing (10 papers), Nuclear Structure and Function (8 papers), RNA regulation and disease (6 papers), Cardiomyopathy and Myosin Studies (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Adipose Tissue and Metabolism (3 papers) and Silk-based biomaterials and applications (3 papers). The work is most often cited by research in Genetics (700 citations), Reproductive Medicine (210 citations) and Molecular Biology (1.3k citations). Dominique Récan has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Jean‐Claude Kaplan, Anthony P. Monaco, Ann P. Walker, Hans Peter Schwarz, Alfons Meindl, Barbara Bardoni, Elena Zanaria, Tim M. Strom, Silvana Guioli and Françoise Muscatelli. Their work appears in journals such as Neuromuscular Disorders, Journal of Clinical Investigation, European Journal of Human Genetics, Human Molecular Genetics and Brain.

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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