Laurence Reutenauer

2.5k citations

20 papers · 1.9k indexed · h-index 18

Molecular Biology top 5%
Cellular and Molecular Neuroscience top 1%
Cell Biology top 5%
Neurology top 5%
Nutrition and Dietetics top 5%

Co-authors: Hélène Puccio Michel Kœnig Jean‐Louis Mandel Alain Martelli Marie Wattenhofer‐Donzé Stéphane Schmucker Nadia Messaddeq Céline Moutou
Topics: Mitochondrial Function and Pathology (18 papers)Genetic Neurodegenerative Diseases (17 papers)Endoplasmic Reticulum Stress and Disease (7 papers)
Cited by: Cellular and Molecular Neuroscience Biochemistry Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nature Medicine Nature Genetics
Partner nations: France United States Italy

In The Last Decade

Laurence Reutenauer

20 papers receiving 1.8k citations

Peers

Countries citing papers authored by Laurence Reutenauer

Since Specialization

Citations

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

Fields of papers citing papers by Laurence Reutenauer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurence Reutenauer

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Reutenauer. A scholar is included among the top collaborators of Laurence Reutenauer 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 Laurence Reutenauer. Laurence Reutenauer 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	Mitochondrial dysfunction and calcium dysregulation in COQ8A-ataxia Purkinje neurons are rescued by CoQ10 treatment 2023 ·Brain ·(unknown),(unknown),(unknown),Laurence Reutenauer,(unknown),Bianca Habermann,Hélène Puccio	18
2	High Levels of Frataxin Overexpression Lead to Mitochondrial and Cardiac Toxicity in Mouse Models 2020 ·Molecular Therapy — Methods & Clinical Development ·Brahim Belbellaa,Laurence Reutenauer,Nadia Messaddeq,Laurent Monassier,Hélène Puccio	46
3	Rapid and Complete Reversal of Sensory Ataxia by Gene Therapy in a Novel Model of Friedreich Ataxia 2018 ·Molecular Therapy ·Françoise Piguet,(unknown),(unknown),Laurence Reutenauer,(unknown),Hélène Puccio	82
4	Correction of half the cardiomyocytes fully rescue Friedreich ataxia mitochondrial cardiomyopathy through cell-autonomous mechanisms 2018 ·Human Molecular Genetics ·Brahim Belbellaa,Laurence Reutenauer,Laurent Monassier,Hélène Puccio	24
5	54. Prevention of Sensory Ataxia in a Novel Mouse Model of Friedreich Ataxia Using Gene Therapy Approach 2016 ·Molecular Therapy ·Françoise Piguet,(unknown),(unknown),Laurence Reutenauer,Hélène Puccio	4
6	Iron Regulatory Protein 1 Sustains Mitochondrial Iron Loading and Function in Frataxin Deficiency 2015 ·Cell Metabolism ·Alain Martelli,Stéphane Schmucker,Laurence Reutenauer,Jacques R.R. Mathieu,Carole Peyssonnaux,Zoubida Karim,Hervé Puy,Bruno Galy,Matthias W. Hentze,Hélène Puccio	61
7	Prevention and reversal of severe mitochondrial cardiomyopathy by gene therapy in a mouse model of Friedreich's ataxia 2014 ·Nature Medicine ·(unknown),Brahim Belbellaa,Laurent Monassier,Laurence Reutenauer,Nadia Messaddeq,Nathalie Cartier,Ronald G. Crystal,Patrick Aubourg,Hélène Puccio	172
8	Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia 2012 ·Disease Models & Mechanisms ·Aurore Hick,Marie Wattenhofer‐Donzé,Satyan Chintawar,Philippe Tropel,Jodie P. Simard,(unknown),David Gall,Laurie Lambot,(unknown),Laurence Reutenauer,Myriam Rai,Marius Teletin,Nadia Messaddeq,Serge N. Schiffmann,Stéphane Viville,Christopher E. Pearson,Massimo Pandolfo,Hélène Puccio	120
9	Clinical data and characterization of the liver conditional mouse model exclude neoplasia as a non-neurological manifestation associated with Friedreich's ataxia 2012 ·Disease Models & Mechanisms ·Alain Martelli,Lisa S. Friedman,Laurence Reutenauer,Nadia Messaddeq,Susan Perlman,David R. Lynch,(unknown),Jörg B. Schulz,Massimo Pandolfo,Hélène Puccio	31
10	Mammalian Frataxin: An Essential Function for Cellular Viability through an Interaction with a Preformed ISCU/NFS1/ISD11 Iron-Sulfur Assembly Complex 2011 ·PLoS ONE ·Stéphane Schmucker,Alain Martelli,Florent Colin,Adeline Page,Marie Wattenhofer‐Donzé,Laurence Reutenauer,Hélène Puccio	192
11	Limitations in a frataxin knockdown cell model for Friedreich ataxia in a high-throughput drug screen 2009 ·BMC Neurology ·Nadège Calmels,H. Seznec,Pascal Villa,Laurence Reutenauer,Marcel Hibert,Jacques Haiech,Pierre Rustin,Michel Kœnig,Hélène Puccio	13
12	The First Cellular Models Based on Frataxin Missense Mutations That Reproduce Spontaneously the Defects Associated with Friedreich Ataxia 2009 ·PLoS ONE ·Nadège Calmels,Stéphane Schmucker,Marie Wattenhofer‐Donzé,Alain Martelli,(unknown),Laurence Reutenauer,Nadia Messaddeq,Cécile Bouton,Michel Kœnig,Hélène Puccio	46
13	Frataxin is essential for extramitochondrial Fe–S cluster proteins in mammalian tissues 2007 ·Human Molecular Genetics ·Alain Martelli,Marie Wattenhofer‐Donzé,Stéphane Schmucker,(unknown),Laurence Reutenauer,Hélène Puccio	104
14	Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cells 2005 ·Human Molecular Genetics ·Robert Schoenfeld,Eleonora Napoli,Alice Wong,(unknown),Laurence Reutenauer,Dexter Morin,Alan R. Buckpitt,Franco Taroni,Bo Lönnerdal,Michael Ristow,Hélène Puccio,Gino Cortopassi	92
15	Friedreich ataxia: the oxidative stress paradox 2004 ·Human Molecular Genetics ·H. Seznec,Delphine Simon,Cécile Bouton,Laurence Reutenauer,(unknown),Paweł Golik,Vincent Procaccio,Manisha Patel,Jean‐Claude Drapier,Michel Kœnig,Hélène Puccio	181
16	Ataxia with Isolated Vitamin E Deficiency: Heterogeneity of Mutations and Phenotypic Variability in a Large Number of Families 1998 ·The American Journal of Human Genetics ·L Cavalier,Karim Ouahchi,Herbert J. Kayden,(unknown),Laurence Reutenauer,Jean‐Louis Mandel,Michel Kœnig	211
17	Evolution of the Friedreich’s ataxia trinucleotide repeat expansion: Founder effect and premutations 1997 ·Proceedings of the National Academy of Sciences ·Mireille Cossée,M. Schmitt,Victoria Campuzano,Laurence Reutenauer,Céline Moutou,Jean‐Louis Mandel,Michel Kœnig	245
18	Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear family 1995 ·Human Molecular Genetics ·Nathalie Nadal,Marie-Odile Rolland,Christine Tranchant,Laurence Reutenauer,Gàbor Gyapay,Jean‐Marie Warter,Jean‐Louis Mandel,M. Kœnig	17
19	Familial isolated vitamin E deficiency. Extensive study of a large family with a 5‐year therapeutic follow‐up 1994 ·Journal of Inherited Metabolic Disease ·Jeanne Amiel,Jean‐Claude Mazière,Isabel Beucler,(unknown),Laurence Reutenauer,(unknown),(unknown),Carlo V. Feo,P. Landrieu	30
20	Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping 1993 ·Nature Genetics ·Christiane Ben Hamida,Nathalie Doerflinger,Samir Belal,(unknown),Laurence Reutenauer,Colette Dib,Gàbor Gyapay,Alain Vignal,Denis Le Paslier,Daniel Cohen,Massimo Pandolfo,Vahe Mokini,Giuseppe Novelli,F. Hentati,M. Ben Hamida,Jean‐Louis Mandel,Michel Kœnig	163

About Laurence Reutenauer

Laurence Reutenauer is a scholar working on Cellular and Molecular Neuroscience, Clinical Biochemistry and Cell Biology, having authored 20 papers that have together received 1.9k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (18 papers), Genetic Neurodegenerative Diseases (17 papers) and Endoplasmic Reticulum Stress and Disease (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.2k citations), Biochemistry (178 citations) and Molecular Biology (1.5k citations). Laurence Reutenauer has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Hélène Puccio, Michel Kœnig, Jean‐Louis Mandel, Alain Martelli, Marie Wattenhofer‐Donzé, Stéphane Schmucker, Nadia Messaddeq, Céline Moutou, M. Schmitt and Victoria Campuzano. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Nature Genetics.

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