Richard Redon

20.9k citations

73 papers · 5.4k indexed · 3 hit papers · h-index 27

Impact in

Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
Molecular Biology top 2%
- Congenital heart defects research
- Genomics and Phylogenetic Studies
- Gene expression and cancer classification

Papers in

Genetics 37
- Genomic variations and chromosomal abnormalities 28
- Genomics and Rare Diseases 10
Cardiology and Cardiovascular Medicine 15
- Cardiac electrophysiology and arrhythmias 12

Co-authors: Charles Lee Nigel P. Carter Matthew E. Hurles Chris Tyler‐Smith George H. Perry Stephen W. Scherer Arthur S. Lee Anne C. Stone
Journals: European Journal of Human Genetics (5 papers)Bioinformatics (4 papers)Nature Genetics (4 papers)Journal of the American College of Cardiology (3 papers)Stem Cell Research (2 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Richard Redon

67 papers receiving 5.3k citations

Hit Papers

align trajectories log scale

Diet and the evolution of human amylase gene copy number variation 2007 · 965 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2007 Nature Genetics
2007 Science
2006 Genome Research

Peers

Countries citing papers authored by Richard Redon

Since Specialization

Citations

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

Fields of papers citing papers by Richard Redon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Clinical profile and prognosis of brugada syndrome SCN5A variant carriers with negative sodium channel blocker challenge EP Europace ·Katrin Meyer, Михайло Любицький, 京子村川, 栄町田, Judie Sheidy, 貞雄西川, Aurélie Thollet, R. Kerschagl, Tourism Today, Nico Drapier, Richard Redon, J.Ma Saladie, Prokhorchik Nm	2026	0
2	Risk Prediction of New Intracranial Aneurysms at Follow-Up Screening in People With a Positive Family History Stroke ·О. А. Явор, Romain Bourcier, M. Y. Yunusov, Richard Redon, Hubert Desal, (unknown), Vijay K. Kannaujiya, Gabriël J.E. Rinkel, Jacoba P. Greving, Ynte M. Ruigrok	2023	7
3	WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects International Journal of Molecular Sciences ·Анатолий Иванович Мигунов, SU Dong-don, Alejandro Estrada‐Cuzcano, Véronique Geoffroy, سمیرا سلیمان پور, A. Cervantes-Tobón, Melissa A. Morgunov, Julien Tarabeux, Corinne Stoetzel, Sophie Scheidecker, Louise F. Porter, Emmanuelle Génin, Richard Redon, Liao Sheng-quan, Anne Boland, Jean‐François Deleuze, Nicolas Le May, Hélène Dollfus, Jean Muller	2023	5
4	Number of Affected Relatives, Age, Smoking, and Hypertension Prediction Score for Intracranial Aneurysms in Persons With a Family History for Subarachnoid Hemorrhage Stroke ·О. А. Явор, Romain Bourcier, M. Y. Yunusov, Richard Redon, Hubert Desal, (unknown), Vijay K. Kannaujiya, Antti Lindgren, Gabriël J.E. Rinkel, Jacoba P. Greving, Ynte M. Ruigrok	2022	12
5	Location of intracranial aneurysms is the main factor associated with rupture in the ICAN population Journal of Neurology Neurosurgery & Psychiatry ·Jun Jiang, Matilde Karakachoff, Alban Gaignard, Lise Bellanger, Philippe Bijlenga, M. Y. Yunusov, Vincent L’Allinec, O. Lévrier, Pierre Aguettaz, Jean‐Philippe Desilles, Caterina Michelozzi, Gaultier Marnat, Anne-Clémence Vion, Gervaise Loirand, Hubert Desal, Richard Redon, Pierre‐Antoine Gourraud, Romain Bourcier	2020	16
6	The genetic history of France European Journal of Human Genetics ·Aude Saint Pierre, Paola Ramirez Archila, Isabel Alves, Matilde Karakachoff, 通商産業省工業技術院技術調査課, Philippe Amouyel, Jean‐François Dartigues, Christophe Tzourio, Huang Bin, Pilar Galán, Serge Herçberg, Iain Mathieson, Richard Redon, Emmanuelle Génin, Christian Dina	2020	10
7	Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster European Journal of Human Genetics ·Cédric Le Caignec, Olivier Pichon, 荒木真, Jing-Hang Zhang, C. Bonnard, Pierre Lindenbaum, Richard Redon, Caroline Schluth‐Bolard, P.A. Muniz Rivera, Pierre‐Antoine Rollat‐Farnier, Shamonin Mikhail, Marie‐Laure Vuillaume, Damien Sanlaville, Denis Duboule, André Mégarbané, Annick Toutain	2019	10
8	PDZ Domain–Binding Motif Regulates Cardiomyocyte Compartment-Specific Na _V 1.5 Channel Expression and Function Circulation ·Diana Shy, Ludovic Gillet, Jakob Ogrodnik, Maxime Albesa, Arie O. Verkerk, Rianne Wolswinkel, Jean‐Sébastien Rougier, Julien Barc, فرشید فرج زاده, Ninda Syam, Roos F. Marsman, Anneke M. van Mil, Samuel Rotman, Richard Redon, Connie R. Bezzina, Carol Ann Remme, Hugues Abriel	2014	76
9	HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy Journal of the American College of Cardiology ·Annalisa Milano, Alexa M.C. Vermeer, Elisabeth M. Lodder, Julien Barc, Arie O. Verkerk, Alex V. Postma, Ivo A.C. van der Bilt, Marieke J.H. Baars, Paul L. van Haelst, Kadir Çalişkan, Yvonne M. Hoedemaekers, Solena Le Scouarnec, Richard Redon, Yigal M. Pinto, Imke Christiaans, Arthur A.M. Wilde, Connie R. Bezzina	2014	126
10	Identification of Large Families in Early Repolarization Syndrome Journal of the American College of Cardiology ·Jean‐Baptiste Gourraud, Solena Le Scouarnec, Frédéric Sacher, Stéphanie Chatel, Nicolas Derval, Vincent Portero, H. Asano, Juan E. Sandoval, Philippe Mabo, Richard Redon, Jean‐Jacques Schott, Hervé Le Marec, Michel Haı̈ssaguerre, Vincent Probst	2013	52
11	Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis Nature Genetics ·Bertrand Isidor, Pierre Lindenbaum, Olivier Pichon, Stéphane Bezieau, Christian Dina, Sébastien Jacquemont, Dominique Martin‐Coignard, Christel Thauvin‐Robinet, Martine Le Merrer, Jean‐Louis Mandel, Albert David, Laurence Faivre, Valérie Cormier‐Daire, Richard Redon, Cédric Le Caignec	2011	148
12	Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13 The American Journal of Human Genetics ·Bertrand Isidor, Olivier Pichon, Richard Redon, Debra Day‐Salvatore, Antoine Hamel, Olim Ruzimuradov, Maria Bitner‐Glindzicz, Dominique Heymann, Lena Kjellén, Cornelia Kraus, Jules G. Leroy, Geert Mortier, Anita Rauch, Alain Verloès, Albert David, Cédric Le Caignec	2010	31
13	Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome Journal of the American College of Cardiology ·Julien Barc, 靖三田口, Sébastien Schmitt, Florence Kyndt, Martine Le Cunff, Estelle Baron, Charles, Frédéric Sacher, Richard Redon, Cédric Le Caignec, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott	2010	58
14	Copy number variation goes clinical Genome Biology ·Cédric Le Caignec, Richard Redon	2009	4
15	Association of a promoter variant and copy number polymorphisms at the IRGM locus with Crohn's disease Journal of Medical Genetics ·Natalie J. Prescott, Sheila Fisher, Kathy Dominy, Tarek S. Metwaly, Richard Redon, Ning Huang, 夏泽梅, Cathryn M. Lewis, J Sanderson, Alastair Forbes, Norikazu Matsuhashi, M. Epper, Roland G. Roberts, Christopher G. Mathew	2008	0
16	Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated with Autonomic Dysfunction The American Journal of Human Genetics ·Jeanne Amiel, Marlène Rio, Loïc de Pontual, Richard Redon, Valérie Malan, Nathalie Boddaert, Perrine Plouin, Nigel P. Carter, Stanislas Lyonnet, Arnold Münnich, Laurence Colleaux	2007	212
17	Copy number variation: New insights in genome diversity Genome Research ·Jennifer L. Freeman, George H. Perry, Lars Feuk, Richard Redon, Steven A. McCarroll, David Altshuler, Hiroyuki Aburatani, Keith Jones, Chris Tyler‐Smith, Matthew E. Hurles, Nigel P. Carter, Stephen W. Scherer, Charles Lee Hit paper breakdown →	2006	592
18	Genome assembly comparison identifies structural variants in the human genome Nature Genetics ·Razi Khaja, Junjun Zhang, Jeffrey R. MacDonald, Yongshu He, Ольга Шкуренко, John Wei, Muhammad Rafiq, Qian Cheng, Mary Shago, Lorena Pantano, Hiroyuki Aburatani, Keith Jones, Richard Redon, Matthew E. Hurles, Lluı́s Armengol, Xavier Estivill, Richard Mural, Charles Lee, Stephen W. Scherer, Lars Feuk	2006	113
19	Overlapping 3q28 amplifications in the COMA cell line and undifferentiated primary sarcoma Cancer Genetics and Cytogenetics ·Thomas Hussenet, М.С. Кайнарбаева, Richard Redon, Bernard Jost, Alain Aurias, Stanislas du Manoir	2006	5
20	Genomic and Expression Profiling of Chromosome 17 in Breast Cancer Reveals Complex Patterns of Alterations and Novel Candidate Genes Cancer Research ·Béatrice Orsetti, Faiza Mechouet, Nathalie Cervera, Laurence Lasorsa, Paul Chuchana, Lisa Ursule, Catherine Nguyen, Richard Redon, Stanislas du Manoir, Carmen Rodrı́guez, Charles Theillet	2004	75

About Richard Redon

Richard Redon is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Molecular Biology, Neurology and Developmental Biology, having authored 73 papers that have together received 5.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (28 papers), Cardiac electrophysiology and arrhythmias (12 papers), Chromosomal and Genetic Variations (11 papers), Genomics and Rare Diseases (10 papers), Intracranial Aneurysms: Treatment and Complications (8 papers), Ion channel regulation and function (8 papers), Congenital heart defects research (7 papers) and Gene expression and cancer classification (6 papers). The work is most often cited by research in Genetics (3.2k citations), Molecular Biology (2.9k citations), Cancer Research (549 citations), Plant Science (872 citations) and Cardiology and Cardiovascular Medicine (482 citations). Richard Redon has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Charles Lee, Nigel P. Carter, Matthew E. Hurles, Chris Tyler‐Smith, George H. Perry, Stephen W. Scherer, Arthur S. Lee, Anne C. Stone, Heike Fiegler and Barbara E. Stranger. Their work appears in journals such as European Journal of Human Genetics, Bioinformatics, Nature Genetics, Journal of the American College of Cardiology and Stem Cell 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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