Dominique Récan

4.0k citations

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

Molecular Biology top 5%
Genetics top 5%
Cardiology and Cardiovascular Medicine top 10%
Endocrinology, Diabetes and Metabolism top 5%
Reproductive Medicine top 5%

Co-authors: Jean‐Claude Kaplan Anthony P. Monaco Ann P. Walker Hans Peter Schwarz Alfons Meindl Barbara Bardoni Elena Zanaria Tim M. Strom
Topics: Muscle Physiology and Disorders (18 papers)RNA Research and Splicing (10 papers)Nuclear Structure and Function (8 papers)
Cited by: Genetics Reproductive Medicine Molecular Biology
Journals: Nature Cell Nucleic Acids Research
Partner nations: France United States United Kingdom

In The Last Decade

Dominique Récan

33 papers receiving 1.6k 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.

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

1994 549 citations Ann P. Walker, Dominique Récan et al. profile →

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 of co-authors of Dominique Récan

This figure shows the co-authorship network connecting the top 25 collaborators of Dominique Récan. A scholar is included among the top collaborators of Dominique Récan 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 Dominique Récan. Dominique Récan 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	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 2006 ·Neuromuscular Disorders ·Yanyan Hu,France Leturcq,D. Héron,Delphine Logeart‐Avramoglou,S. Llense,Jamel Chelly,Dominique Récan,(unknown),(unknown),B. Eymard	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 2006 ·Human Mutation ·(unknown),(unknown),S. Llense,(unknown),Dominique Récan,Cécile Peccate,Arthur H.M. Burghes,Christophe Béroud,Luis Garcı́a,Jean‐Claude Kaplan,Jamel Chelly,France Leturcq	95
3	X‐linked Emery–Dreifuss muscular dystrophy and vacuoles: An immunohistochemical characterization 2005 ·Muscle & Nerve ·Carmen Paradas,Celedonio Márquez,Eduard Gallardo,Noemí de Luna,(unknown),Dominique Récan,(unknown),Isabel Illa	6
4	The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre 2004 ·Neuromuscular Disorders ·Sylvie Tuffery‐Giraud,(unknown),(unknown),Bernard Échenne,J. Cuisset,François Rivier,Mireille Cossée,Christophe Philippe,Nicole Monnier,Éric Bieth,Dominique Récan,(unknown),(unknown),(unknown),Sue Malcolm,Mireille Claustres	34
5	Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicine 2003 ·Neuromuscular Disorders ·Jon Andoni Urtizberea,(unknown),Elizabeth Vroom,Dominique Récan,(unknown)	9
6	Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature 2003 ·Annales de Génétique ·N. Bouayed Abdelmoula,Marie‐France Portnoï,Leila Keskes,Dominique Récan,Ali Bahloul,T. Boudawara,Saad Ali,Tarek Rebaï	29
7	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
8	Limb-girdle muscular dystrophy with calpain deficiency(LGMD 2A) in Croatia: a survey in a small rural community 2002 ·Neuromuscular Disorders ·(unknown),(unknown),(unknown),Dominique Récan,(unknown),(unknown),Kristina Potočki,(unknown)	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 2002 ·Neuromuscular Disorders ·Gisèle Bonne,(unknown),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	21
10	A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism 2000 ·Journal of Clinical Investigation ·Antoine Tabarin,John C. Achermann,Dominique Récan,(unknown),Xavier Bertagna,Sophie Christin‐Maître,Masafumi Ito,J. Larry Jameson,Philippe Bouchard	133
11	Early presentation of X-linked Emery–Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy 1998 ·Neuromuscular Disorders ·Francesco Muntoni,(unknown),Caroline A. Sewry,S. Manilal,Dominique Récan,S. Llense,Jacqueline Taylor,Glenn E. Morris,Victor Dubowitz	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 1997 ·Neuromuscular Disorders ·Norma B. Romero,Dominique Récan,Odile Rigal,France Leturcq,S. Llense,(unknown),Nathalie Deburgrave,(unknown),(unknown),Jean‐Claude Kaplan	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 1994 ·European Journal of Human Genetics ·Emmanuelle Plassart,J Reboul,(unknown),Dominique Récan,Philippe Millasseau,B. Eymard,Jean Pelletier,C. Thomas,Françoise Chapon,Claude Desnuelle,Christian Confavreux,B Bady,(unknown),Gilbert Lenoir,G Serratrice,Michel Fardeau,Bertrand Fontaine	42
14	Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X‐chromosome inactivation 1994 ·American Journal of Medical Genetics ·(unknown),Christophe Philippe,M. Chery,Hélène Gilgenkrantz,F. Tomé,H. Barry Collin,(unknown),Dominique Récan,Odile Broux,Michel Fardeau,J.‐C. Kaplan,S Gilgenkrantz	32
15	Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin. 1993 ·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	60
16	A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes 1992 ·Human Molecular Genetics ·Ann P. Walker,Jamel Chelly,Donald R. Love,(unknown),Dominique Récan,Jean-Louis Chaussain,Christine A. Oley,J. M. Connor,John R. Yates,David A. Price,Maurice Super,Armand Bottani,(unknown),(unknown),Kay E. Davies,Anthony P. Monaco	33
17	Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization? 1992 ·Journal of Clinical Investigation ·Dominique Récan,Philippe Chafey,France Leturcq,Jean‐Philippe Hugnot,(unknown),F. Tomé,H. Barry Collin,Dávid Simon,P Czernichow,L. V. B. Nicholson	46
18	A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD) 1991 ·Nucleic Acids Research ·Jean‐Philippe Hugnot,Dominique Récan,Marc Jeanpierre,J.‐C. Kaplan,Aslıhan Tolun	16
19	Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients. 1991 ·Journal of Clinical Investigation ·Jamel Chelly,Hélène Gilgenkrantz,Jean‐Philippe Hugnot,G. Hamard,(unknown),Dominique Récan,Saïd Akli,(unknown),A Kahn,J.‐C. Kaplan	46
20	Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies 1990 ·Cell ·(unknown),Hélène Gilgenkrantz,(unknown),Ghislaine Hamard,Philippe Chafey,Dominique Récan,(unknown),Albert de la Chapelle,(unknown),Ieke B. Ginjaar,(unknown),F. Tomé,Axel Kahn,(unknown)	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) and Nuclear Structure and Function (8 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 Nature, Cell and Nucleic Acids Research.

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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