Sandrine Tardieu

1.8k citations

25 papers · 985 indexed · h-index 17

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders 17
- Genetic Neurodegenerative Diseases 8
Neurology top 5%
- Neurological diseases and metabolism 5
- Botulinum Toxin and Related Neurological Disorders 5
- Peripheral Neuropathies and Disorders 2
Neurology top 5%
- Neurological diseases and metabolism 5
- Botulinum Toxin and Related Neurological Disorders 5
- Peripheral Neuropathies and Disorders 2
Genetics top 10%
Cell Biology
- Cellular transport and secretion 2
Physiology
- Alzheimer's disease research and treatments 4
Molecular Biology
- RNA regulation and disease 3

Co-authors: Alexis Brice Éric Leguern Riadh Gouider P. Bouché Thierry Maisonobe Nazha Birouk Yves Agid O. Dubourg
Cited by: Cellular and Molecular Neuroscience Neurology
Journals: The Journal of Clinical Endocrinology & Metabolism (1 paper)Neurology (5 papers)Human Molecular Genetics (2 papers)
Partner nations: France Australia Switzerland

In The Last Decade

Sandrine Tardieu

25 papers receiving 959 citations

Peers

Countries citing papers authored by Sandrine Tardieu

Since Specialization

Citations

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

Fields of papers citing papers by Sandrine Tardieu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Charcot-Marie-Tooth Disease Type 2A JAMA Neurology ·Francesco Bombelli,Tanya Stojkovic,O. Dubourg,Andoni Echaniz‐Laguna,Sandrine Tardieu,Kathy Larcher,Patrizia Amati‐Bonneau,Philippe Latour,Odile Vignal,Cécile Cazeneuve,Alexis Brice,Éric Leguern	2014	95
2	Characteristics of clinical and electrophysiological pattern of Charcot‐Marie‐Tooth 4C Journal of the Peripheral Nervous System ·Marion Yger,Tanya Stojkovic,Sandrine Tardieu,Thierry Maisonobe,Alexis Brice,Andoni Echaniz‐Laguna,Yves Alembik,Samantha Girard,Cécile Cazeneuve,Éric Leguern,O. Dubourg	2012	34
3	Detection of genomic rearrangements by DHPLC: A prospective study of 90 patients with inherited peripheral neuropathies associated with 17p11.2 rearrangements American Journal of Medical Genetics Part A ·Mourad Naïmi,Sandrine Tardieu,Christel Depienne,Merle Ruberg,Alexis Brice,O. Dubourg,Éric Leguern	2005	7
4	Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene Clinical Neurophysiology ·Tanya Stojkovic,J. de Sèze,Olivier Dubourg,Marie‐Christine Arné‐Bes,Sandrine Tardieu,J C Hache,Patrick Vermersch	2003	31
5	Rapid detection of 17p11.2 rearrangements by FISH without cell culture (direct FISH, DFISH): A prospective study of 130 patients with inherited peripheral neuropathies American Journal of Medical Genetics Part A ·N. Ravisé,O. Dubourg,Sandrine Tardieu,Françoise Aurias,Monique Mercadiel,Philippe Coullin,Merle Ruberg,Martin Catala,Sylvie Lesourd,Alexis Brice,Éric Leguern	2003	4
6	[Review of quality of life instruments used in end-stage renal disease]. PubMed ·Stéphanie Gentile,Jean-Christophe Delarozière,Carme Sánchez Fernández,Sandrine Tardieu,B Devictor,Bertrand Dussol,J.P. Daurès,Yvon Berland,Roland Sambuc	2003	17
7	A Comprehensive Endocrine Description of Kennedy’s Disease Revealing Androgen Insensitivity Linked to CAG Repeat Length The Journal of Clinical Endocrinology & Metabolism ·S. Dejager,Hélène Bry‐Gauillard,Éric Bruckert,B. Eymard,François Salachas,Eric Leguern,Sandrine Tardieu,Rita Chadarévian,P. Giral,G Turpin	2002	124
8	The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders Journal of Neurology ·Véronique Pingault,Nadège Bondurand,C. Le Caignec,Sandrine Tardieu,N Lemort,O. Dubourg,E. Le Guern,M. Goossens,Odile Boespflug‐Tanguy	2001	21
9	The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity Neuromuscular Disorders ·O. Dubourg,Sandrine Tardieu,Nazha Birouk,Riadh Gouider,Juliane Léger,Thierry Maisonobe,Alexis Brice,P. Bouché,Éric Leguern	2001	36
10	Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A European Journal of Human Genetics ·Rafaëlle Bernard,Véronique Labelle,Philippe Nègre,Sandrine Tardieu,Jean‐Philippe Azulay,Perrine Malzac,Jean-François Mattéi,Éric Leguern,Nicole Philip,Nicolas Lévy	2000	3
11	Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion Neurology ·Philippe Mouton,Sandrine Tardieu,Riadh Gouider,Nazha Birouk,Thierry Maisonobe,O. Dubourg,Alexis Brice,Éric Leguern,P. Bouché	1999	120
12	Homologous DNA Exchanges in Humans Can Be Explained by the Yeast Double-Strand Break Repair Model: A Study of 17p11.2 Rearrangements Associated with CMT1A and HNPP Human Molecular Genetics ·Judith Lopes,Sandrine Tardieu,Kaisa Silander,Ian P. Blair,A. Vandenberghe,Francesc Palau,Merle Ruberg,Alexis Brice,E. LeGuern	1999	47
13	X-linked Charcot-Marie-Tooth disease with connexin 32 mutations Neurology ·Nazha Birouk,Éric Leguern,Thierry Maisonobe,H Rouger,Riadh Gouider,Sandrine Tardieu,Michel Gugenheim,M. C. Routon,J.M. Léger,Yves Agid,Alexis Brice,P. Bouché	1998	133
14	Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families Human Mutation ·H Rouger,Éric Leguern,Nazha Birouk,Riadh Gouider,Sandrine Tardieu,Emmanuelle Plassart,Michel Gugenheim,J-M Vallat,J.P. Louboutin,P. Bouché,Yves Agid,Alexis Brice	1997	51
15	Allelic association at the D14S43 locus in early onset Alzheimer's disease American Journal of Medical Genetics ·Alexis Brice,Sandrine Tardieu,Dominique Campion,E. Le Guern,María Martínez,Alexandre Carpentier,Christiane Penet,Bruno Dubois,Michel Bellis,Jacques Mallet,Didier Hannequin,Françoise Clerget‐Darpoux,Yves Agid	1995	3
16	Evidence for apolipoprotein E ϵ4 association in early‐onset Alzheimer's patients with late‐onset relatives American Journal of Medical Genetics ·Jordi Pérez‐Tur,Dominique Campion,María Martínez,Alexis Brice,Sandrine Tardieu,Didier Hannequin,Yves Agid,André Delacourte,Françoise Clerget‐Darpoux,Marie‐Christine Chartier‐Harlin	1995	24
17	Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases Human Molecular Genetics ·Éric Leguern,Riadh Gouider,Judith Lopes,N. Abbas,Michel Gugenheim,Sandrine Tardieu,N. Ravisé,J.-M. Léger,Jean‐Michel Vallat,P. Bouché,Yves Agid,Alexis Brice	1995	15
18	A large pedigree with early-onset Alzheimer's disease Neurology ·Dominique Campion,Alexis Brice,Didier Hannequin,Sandrine Tardieu,Bruno Dubois,Alphonse Calenda,E Brun,Christiane Penet,J Tayot,María Martínez,M. Bellis,Jacques Mallet,Yves Agid,Françoise Clerget‐Darpoux	1995	39
19	[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]. PubMed ·Didier Hannequin,Dominique Campion,Sandrine Tardieu,P Auzou,Marco Martínez,Bénédicte Dubois,Françoise Clerget‐Darpoux,Yves Agid,Alexis Brice	1995	2
20	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies Neurology ·Riadh Gouider,Éric Leguern,Jean‐François Emile,Sandrine Tardieu,F. Cabon,M. Samid,J. Weissenbach,Yves Agid,P. Bouché,Alexis Brice	1994	33

About Sandrine Tardieu

Sandrine Tardieu is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 25 papers that have together received 985 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (17 papers), Genetic Neurodegenerative Diseases (8 papers), Neurological diseases and metabolism (5 papers), Botulinum Toxin and Related Neurological Disorders (5 papers), Alzheimer's disease research and treatments (4 papers), RNA regulation and disease (3 papers), Peripheral Neuropathies and Disorders (2 papers) and Cellular transport and secretion (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (720 citations), Neurology (261 citations) and Neurology (300 citations). Sandrine Tardieu has collaborated with scholars based in France, Australia and Switzerland. Frequent co-authors include Alexis Brice, Éric Leguern, Riadh Gouider, P. Bouché, Thierry Maisonobe, Nazha Birouk, Yves Agid, O. Dubourg, Michel Gugenheim and H Rouger. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and Human Molecular Genetics.

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