Rabah Ben Yaou

5.2k citations

66 papers · 2.1k indexed · h-index 23

Molecular Biology top 5%
Cardiology and Cardiovascular Medicine top 5%
Cell Biology top 5%
Genetics top 5%
Cellular and Molecular Neuroscience top 10%

Co-authors: Gisèle Bonne Frans C. S. Ramaekers Christopher J. Hutchison Jos L. V. Broers A. Bertrand Anneke J. van der Kooi France Leturcq Marjolein Visser
Topics: Nuclear Structure and Function (37 papers)RNA Research and Splicing (33 papers)Muscle Physiology and Disorders (26 papers)
Cited by: Molecular Biology Cardiology and Cardiovascular Medicine Genetics
Journals: Physiological Reviews PLoS ONE Brain
Partner nations: France United Kingdom Italy

In The Last Decade

Rabah Ben Yaou

62 papers receiving 2.1k citations

Peers

Countries citing papers authored by Rabah Ben Yaou

Since Specialization

Citations

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

Fields of papers citing papers by Rabah Ben Yaou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rabah Ben Yaou. 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 Rabah Ben Yaou. The network helps show where Rabah Ben Yaou may publish in the future.

Co-authorship network of co-authors of Rabah Ben Yaou

This figure shows the co-authorship network connecting the top 25 collaborators of Rabah Ben Yaou. A scholar is included among the top collaborators of Rabah Ben Yaou 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 Rabah Ben Yaou. Rabah Ben Yaou 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	Preclinical Advances of Therapies for Laminopathies 2021 ·Journal of Clinical Medicine ·Louise Benarroch,(unknown),António Atalaia,Rabah Ben Yaou,Gisèle Bonne,A. Bertrand	7
2	Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular Dystrophy 2021 ·Journal of Neuromuscular Diseases ·Caroline Stalens,(unknown),Anthony Béhin,Rabah Ben Yaou,France Leturcq,Guillaume Bassez,Pascal Laforêt,Bertrand Fontaine,Stéphane Éderhy,Marion Masingue,(unknown),Sarah Louis,(unknown),Tanya Stojkovic,Denis Duboc,Karim Wahbi	2
3	Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery–Dreifuss Muscular Dystrophy 2020 ·Cells ·A. Bertrand,Astrid Brull,Fériel Azibani,Louise Benarroch,Khadija Chikhaoui,Colin L. Stewart,Ohad Medalia,Rabah Ben Yaou,Gisèle Bonne	26
4	Effects of Home Mechanical Ventilation on Left Ventricular Function in Sarcoglycanopathies (Limb Girdle Muscular Dystrophies) 2018 ·The American Journal of Cardiology ·Abdallah Fayssoil,Lee S. Nguyen,Adam Ogna,(unknown),Olivier Nardi,Pascal Laforêt,Bernard Clair,Hélène Prigent,Frédéric Lofaso,France Leturcq,Rabah Ben Yaou,Djillali Annane,David Orlikowski	2
5	Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype–genotype correlation 2018 ·Diabetes & Metabolism ·(unknown),Dominique Lacroix,Stéphanie Espiard,Sandro Ninni,François Brigadeau,Claude Kouakam,Pascal de Groote,(unknown),V. Tiffreau,Arnaud Jannin,L. Humbert,(unknown),Céline Tard,Rabah Ben Yaou,Nicolas Lamblin,Didier Klug,Pascale Richard,Corinne Vigouroux,Gisèle Bonne,Marie‐Christine Vantyghem	20
6	Left bundle branch block in Duchenne muscular dystrophy: Prevalence, genetic relationship and prognosis 2018 ·PLoS ONE ·Abdallah Fayssoil,Rabah Ben Yaou,Adam Ogna,Cendrine Chaffaut,(unknown),Olivier Nardi,Karim Wahbi,Denis Duboc,Frédéric Lofaso,Hélène Prigent,Bernard Clair,Pascal Crenn,Guillaume Nicolas,Pascal Laforêt,Anthony Béhin,Sylvie Chevret,David Orlikowski,Djillali Annane	8
7	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
8	Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation 2012 ·Human Molecular Genetics ·Christel Gentil,France Leturcq,Rabah Ben Yaou,Jean‐Claude Kaplan,Pascal Laforêt,I. Pénisson-Besnier,Caroline Espil‐Taris,Thomas Voït,Luis Garcı́a,France Piétri‐Rouxel	39
9	Cardioembolic stroke prompting diagnosis of LMNA‐associated Emery–Dreifuss muscular dystrophy 2011 ·Muscle & Nerve ·(unknown),Rabah Ben Yaou,(unknown),(unknown),Pascale Richard,Gisèle Bonne	7
10	Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation 2011 ·European Journal of Human Genetics ·Rabah Ben Yaou,Claire Navarro,Susana Quijano-Roy,A. Bertrand,Catherine Massart,Annachiara De Sandre‐Giovannoli,Juan Cadiñanos,Kamel Mamchaoui,Gillian Butler‐Browne,B. Estournet,Pascale Richard,A Barois,Nicolas Lévy,Gisèle Bonne	36
11	Laminopathies : un seul gène, de nombreuses pathologies 2011 ·Biologie Aujourd hui ·A. Bertrand,Khadija Chikhaoui,Rabah Ben Yaou,Gisèle Bonne	3
12	Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern 2010 ·Neuromuscular Disorders ·Nicolas Deconinck,Élisabeth Dion,Rabah Ben Yaou,Ana Ferreiro,B. Eymard,Laura Briñas,C. Payán,Thomas Voït,Pascale Guicheney,Pascale Richard,Valérie Allamand,Gisèle Bonne,Tanya Stojkovic	20
13	G.P.9.10 Clinical development of the French UMD–DMD database 2007 ·Neuromuscular Disorders ·Véronique Humbertclaude,Sylvie Tuffery‐Giraud,Rabah Ben Yaou,Dalil Hamroun,Philippe Khau Van Kien,France Leturcq,(unknown),(unknown),Christophe Béroud	1
14	AB26-1 2006 ·Heart Rhythm ·Frédéric Anselme,(unknown),Jop H. van Berlo,Gisèle Bonne,Arnaud Savouré,Rabah Ben Yaou,J. Peter van Tintelen,Henri-Marc Bécane,Maarten P. van den Berg,Pascal Laforêt,Alain Cribier,(unknown),Denis Duboc	1
15	Nuclear Lamins: Laminopathies and Their Role in Premature Ageing 2006 ·Physiological Reviews ·Jos L. V. Broers,Frans C. S. Ramaekers,Gisèle Bonne,Rabah Ben Yaou,Christopher J. Hutchison	449
16	Cardiac and Pulmonary Investigations in Bethlem Myopathy 2006 ·Archives of Neurology ·Anneke J. van der Kooi,Willem G. de Voogt,Enrico Bertini,Luciano Merlini,(unknown),Rabah Ben Yaou,(unknown),Marianne de Visser	29
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	Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death? 2004 ·Journal of Molecular Medicine ·Jop H. van Berlo,Willem G. de Voogt,Anneke J. van der Kooi,J. Peter van Tintelen,Gisèle Bonne,Rabah Ben Yaou,Denis Duboc,Tom Rossenbacker,Hein Heidbüchel,Marjolein Visser,Harry J.G.M. Crijns,Yigal M. Pinto	301
19	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
20	Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC International Workshop, 23–24 November 2001, Naarden, The Netherlands 2002 ·Neuromuscular Disorders ·Guglielmina Pepe,Enrico Bertini,Paolo Bonaldo,Kate Bushby,Betti Giusti,Marjolein Visser,Pascale Guicheney,Giovanna Lattanzi,Luciano Merlini,Francesco Muntoni,Ichizo Nishino,Ikuya Nonaka,Rabah Ben Yaou,Patrizia Sabatelli,Caroline A. Sewry,Haluk Topaloğlu,Anneke J. van der Kooi	67

About Rabah Ben Yaou

Rabah Ben Yaou is a scholar working on Developmental Biology, Cell Biology and Molecular Biology, having authored 66 papers that have together received 2.1k indexed citations. Recurring topics across this work include Nuclear Structure and Function (37 papers), RNA Research and Splicing (33 papers) and Muscle Physiology and Disorders (26 papers). The work is most often cited by research in Molecular Biology (1.8k citations), Cardiology and Cardiovascular Medicine (562 citations) and Genetics (223 citations). Rabah Ben Yaou has collaborated with scholars based in France, United Kingdom and Italy. Frequent co-authors include Gisèle Bonne, Frans C. S. Ramaekers, Christopher J. Hutchison, Jos L. V. Broers, A. Bertrand, Anneke J. van der Kooi, France Leturcq, Marjolein Visser, Willem G. de Voogt and Denis Duboc. Their work appears in journals such as Physiological Reviews, PLoS ONE 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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