John Rendu

2.3k citations

48 papers · 944 indexed · h-index 16

Impact in

Reproductive Medicine top 5%
- Sperm and Testicular Function
Nephrology top 10%
- Renal Diseases and Glomerulopathies

Papers in ⓘ

Cell Biology 12
- Cellular transport and secretion 10
Genetics 7
- Neurogenetic and Muscular Disorders Research 5

Co-authors: Julien Fauré (28 shared papers)Charles Coutton (5 shared papers)Joël Lunardi (7 shared papers)Thomas Karaouzène (1 shared paper)Denise Escalier (1 shared paper)Sandra Yassine (1 shared paper)Raoudha Zouari (1 shared paper)Julie Delaroche (1 shared paper)
Journals: Neuromuscular Disorders (5 papers)Human Molecular Genetics (3 papers)Human Mutation (3 papers)Acta Neuropathologica Communications (2 papers)Journal of Neuromuscular Diseases (2 papers)
Partner nations: France United States Italy

In The Last Decade

John Rendu

42 papers receiving 934 citations

Peers

Countries citing papers authored by John Rendu

Since Specialization

Citations

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

Fields of papers citing papers by John Rendu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella The American Journal of Human Genetics ·Mariem Ben Khelifa, Charles Coutton, Raoudha Zouari, Thomas Karaouzène, John Rendu, Marie Bidart, Sandra Yassine, Virginie Pierre, Julie Delaroche, Sylviane Hennebicq, Didier Grünwald, Denise Escalier, Karine Pernet-Gallay, Pierre‐Simon Jouk, Nicolas Thierry‐Mieg, Aminata Touré, Christophe Arnoult, Pierre F. Ray	2013	298
2	From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes Human Mutation ·Haifa Hichri, John Rendu, Nicole Monnier, Charles Coutton, Olivier Dorseuil, Rosa Vargas Poussou, Geneviève Baujat, Anne Blanchard, François Nobili, Bruno Ranchin, Michel Remesy, Rémi Salomon, Véronique Satre, Joël Lunardi	2010	102
3	Phospholipase A2 Receptor–Related Membranous Nephropathy and Mannan-Binding Lectin Deficiency Journal of the American Society of Nephrology ·Stéphane Bally, Hanna Dêbiec, D. Ponard, Frédérique Dijoud, John Rendu, Julien Fauré, Pierre Ronco, Chantal Dumestre‐Pérard	2016	76
4	Muscle weakness inTPM3-myopathy is due to reduced Ca²⁺-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres Human Molecular Genetics ·Michaela Yuen, Sandra T. Cooper, Steven B. Marston, Kristen L. Nowak, Elyshia McNamara, Nancy Mokbel, Biljana Ilkovski, Gianina Ravenscroft, John Rendu, Josine M. de Winter, Lars Klinge, Alan H. Beggs, Kathryn N. North, Coen A. C. Ottenheijm, Nigel F. Clarke	2015	37
5	‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies Acta Neuropathologica Communications ·Matteo Garibaldi, John Rendu, Julie Brocard, Emmanuelle Lacène, Julien Fauré, Guy Brochier, Maud Beuvin, C. Labasse, A. Madelaine, Edoardo Malfatti, Jorge A. Bevilacqua, Fabiana Lubieniecki, Soledad Monges, Ana Lía Taratuto, Jocelyn Laporte, Isabelle Marty, Giovanni Antonini, Norma B. Romero	2019	33
6	Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome Acta Neurologica Scandinavica ·Nanna Witting, Pascal Laforêt, Nicol C. Voermans, Nathalie Roux-Buisson, Flavie Bompaire, John Rendu, Morten Dunø, François Feillet, Erik‐Jan Kamsteeg, Nanna Scharff Poulsen, Julia R. Dahlqvist, Norma B. Romero, Julien Fauré, John Vissing, Anthony Béhin	2017	31
7	OCRL-mutated fibroblasts from patients with Dent-2 disease exhibit INPP5B-independent phenotypic variability relatively to Lowe syndrome cells Human Molecular Genetics ·Rodrick Montjean, Rifdat Aoidi, P. Desbois, J. Rucci, Michaël Trichet, Rémi Salomon, John Rendu, Julien Fauré, Joël Lunardi, Gérard Gâcon, Pierre Billuart, Olivier Dorseuil	2014	30
8	Added Value of Next-Generation Sequencing for Multilocus Sequence Typing Analysis of aPneumocystis jiroveciiPneumonia Outbreak1 Emerging infectious diseases ·Éléna Charpentier, Cécile Garnaud, C. Wintenberger, Sébastien Bailly, Jean‐Benjamin Murat, John Rendu, Patricia Pavèse, Thibault Drouet, Caroline Augier, Paolo Malvezzi, Anne Thiebaut‐Bertrand, Marie‐Reine Mallaret, Olivier Épaulard, Muriel Cornet, Sylvie Larrat, Danièle Maubon	2017	29
9	Ornithine Transcarbamylase – From Structure to Metabolism: An Update Frontiers in Physiology ·Morgane Couchet, C. Breuillard, Christelle Corne, John Rendu, Béatrice Morio, Uwe Schlattner, Christophe Moinard	2021	28
10	Exon Skipping as a Therapeutic Strategy Applied to an RYR1 Mutation with Pseudo-Exon Inclusion Causing a Severe Core Myopathy Human Gene Therapy ·John Rendu, Julie Brocard, Éric Denarier, Nicole Monnier, France Piétri‐Rouxel, Cyriaque Beley, Nathalie Roux-Buisson, Brigitte Gilbert‐Dussardier, Marie José Perez, Norma B. Romero, Luis Garcı́a, Joël Lunardi, Julien Fauré, Anne Fourest‐Lieuvin, Isabelle Marty	2013	28
11	Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunction Skeletal Muscle ·Muriel Sébastien, Benoı̂t Giannesini, Perrine Aubin, Julie Brocard, Mathilde Chivet, Laura Pietrangelo, Simona Boncompagni, Christophe Bosc, Jacques Brocard, John Rendu, Sylvie Gory‐Fauré, Annie Andrieux, Anne Fourest‐Lieuvin, Julien Fauré, Isabelle Marty	2018	19
12	Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity European Radiology ·Mickaël Tordjman, Ivana Dabaj, Pascal Laforêt, Adrien Felter, Ana Ferreiro, Moustafa Biyoukar, Bruno Law-Ye, Edmar Zanoteli, Claudia Castiglioni, John Rendu, Christophe Béroud, Alexandre Chamouni, Pascale Richard, D. Mompoint, Susana Quijano‐Roy, Robert‐Yves Carlier	2018	19
13	Role of Triadin in the Organization of Reticulum Membrane at the Muscle Triad Journal of Cell Science ·Anne Fourest‐Lieuvin, John Rendu, Alexis Osseni, Karine Pernet-Gallay, Daniela Rossi, Sarah Oddoux, Julie Brocard, Vincenzo Sorrentino, Isabelle Marty, Julien Fauré	2012	19
14	The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease Human Molecular Genetics ·Laurianne Davignon, Claire Chauveau, Cédric Julien, C. Dill, Isabelle Duband‐Goulet, Éva Cabet, Brigitte Buendia, Alain Lilienbaum, John Rendu, Marie Christine Minot, Agnès Guichet, Valérie Allamand, Nathalie Vadrot, Julien Fauré, Sylvie Odent, Leïla Lazaro, Jean Paul Leroy, Pascale Marcorelles, O. Dubourg, Ana Ferreiro	2016	17
15	Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 Protein Journal of Neuromuscular Diseases ·Marine Cacheux, Ariane Blum, Muriel Sébastien, Anne‐Sophie Wozny, Julie Brocard, Kamel Mamchaoui, Vincent Mouly, Nathalie Roux-Buisson, John Rendu, Nicole Monnier, R Krivosic, Paul D. Allen, Arnaud Lacour, Joël Lunardi, Julien Fauré, Isabelle Marty	2015	16
16	In vivo RyR1 reduction in muscle triggers a core-like myopathy Acta Neuropathologica Communications ·Laurent Pelletier, Anne Petiot, Julie Brocard, Benoı̂t Giannesini, Diane Giovannini, Colline Sanchez, Lauriane Travard, Mathilde Chivet, Mathilde Beaufils, Candice Kutchukian, David Bendahan, Daniel Metzger, Clara Franzini Armstrong, Norma B. Romero, John Rendu, Vincent Jacquemond, Julien Fauré, Isabelle Marty	2020	15
17	Development of a multiplex ligation-dependent probe amplification (MLPA) assay for quantification of the OCRL1 gene Clinical Biochemistry ·Charles Coutton, Nicole Monnier, John Rendu, Joël Lunardi	2010	14
18	Mild clinical presentation in KLHL40-related nemaline myopathy (NEM 8) Neuromuscular Disorders ·A. Seferian, Edoardo Malfatti, Caroline Bosson, Laurent Pelletier, Jessica Taytard, V. Forin, Teresa Gidaro, E. Gargaun, Pierre Carlier, Julien Fauré, Norma B. Romero, John Rendu, Laurent Servais	2016	14
19	Functional Characterization and Rescue of a Deep Intronic Mutation inOCRLGene Responsible for Lowe Syndrome Human Mutation ·John Rendu, Rodrick Montjean, Charles Coutton, Mohnish Suri, Gaëtan Chicanne, Anne Petiot, Julie Brocard, Didier Grünwald, France Piétri‐Rouxel, Bernard Payrastre, Joël Lunardi, Olivier Dorseuil, Isabelle Marty, Julien Fauré	2016	13
20	Functional analysis reveals splicing mutations of the CASQ2 gene in patients with CPVT: implication for genetic counselling and clinical management Human Mutation ·Nathalie Roux-Buisson, John Rendu, Isabelle Denjoy, Pascale Guicheney, Alice Goldenberg, Nadine David, Laurence Faivre, Olivier Barthez, Gian Antonio Danieli, Isabelle Marty, Joël Lunardi, Julien Fauré	2011	10

About John Rendu

John Rendu is a scholar working on Cell Biology, Genetics, Cardiology and Cardiovascular Medicine, Molecular Biology and Clinical Biochemistry, having authored 48 papers that have together received 944 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (14 papers), Cellular transport and secretion (10 papers), Cardiomyopathy and Myosin Studies (9 papers), Ion channel regulation and function (8 papers), Genetic Neurodegenerative Diseases (6 papers), Nuclear Structure and Function (5 papers), CRISPR and Genetic Engineering (5 papers) and Neurogenetic and Muscular Disorders Research (5 papers). The work is most often cited by research in Reproductive Medicine (204 citations), Nephrology (87 citations), Cell Biology (167 citations), Genetics (279 citations) and Genetics (85 citations). John Rendu has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Julien Fauré, Charles Coutton, Joël Lunardi, Thomas Karaouzène, Denise Escalier, Sandra Yassine, Raoudha Zouari, Julie Delaroche, Pierre F. Ray and Aminata Touré. Their work appears in journals such as Neuromuscular Disorders, Human Molecular Genetics, Human Mutation, Acta Neuropathologica Communications and Journal of Neuromuscular Diseases.

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.

Explore authors with similar magnitude of impact