Sandrine Tardieu

1.8k citations

25 papers · 985 indexed · h-index 17

Cellular and Molecular Neuroscience top 2%
Molecular Biology
Neurology top 5%
Neurology top 5%
Cell Biology

Co-authors: Alexis Brice Éric Leguern Riadh Gouider P. Bouché Thierry Maisonobe Nazha Birouk Yves Agid O. Dubourg
Topics: Hereditary Neurological Disorders (17 papers)Genetic Neurodegenerative Diseases (8 papers)Neurological diseases and metabolism (5 papers)
Cited by: Cellular and Molecular Neuroscience Neurology
Journals: The Journal of Clinical Endocrinology & Metabolism Neurology Human Molecular Genetics
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 of co-authors of Sandrine Tardieu

This figure shows the co-authorship network connecting the top 25 collaborators of Sandrine Tardieu. A scholar is included among the top collaborators of Sandrine Tardieu 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 Sandrine Tardieu. Sandrine Tardieu 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	Charcot-Marie-Tooth Disease Type 2A 2014 ·JAMA Neurology ·Francesco Bombelli,Tanya Stojkovic,O. Dubourg,Andoni Echaniz‐Laguna,Sandrine Tardieu,(unknown),Patrizia Amati‐Bonneau,Philippe Latour,(unknown),Cécile Cazeneuve,Alexis Brice,Éric Leguern	95
2	Characteristics of clinical and electrophysiological pattern of Charcot‐Marie‐Tooth 4C 2012 ·Journal of the Peripheral Nervous System ·Marion Yger,Tanya Stojkovic,Sandrine Tardieu,Thierry Maisonobe,Alexis Brice,Andoni Echaniz‐Laguna,Yves Alembik,(unknown),Cécile Cazeneuve,Éric Leguern,O. Dubourg	34
3	Detection of genomic rearrangements by DHPLC: A prospective study of 90 patients with inherited peripheral neuropathies associated with 17p11.2 rearrangements 2005 ·American Journal of Medical Genetics Part A ·(unknown),Sandrine Tardieu,Christel Depienne,Merle Ruberg,Alexis Brice,O. Dubourg,Éric Leguern	7
4	Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene 2003 ·Clinical Neurophysiology ·Tanya Stojkovic,J. de Sèze,Olivier Dubourg,Marie‐Christine Arné‐Bes,Sandrine Tardieu,J C Hache,Patrick Vermersch	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 2003 ·American Journal of Medical Genetics Part A ·N. Ravisé,O. Dubourg,Sandrine Tardieu,(unknown),(unknown),Philippe Coullin,Merle Ruberg,Martin Catala,(unknown),Alexis Brice,Éric Leguern	4
6	[Review of quality of life instruments used in end-stage renal disease]. 2003 ·PubMed ·Stéphanie Gentile,(unknown),(unknown),Sandrine Tardieu,B Devictor,Bertrand Dussol,J.P. Daurès,Yvon Berland,Roland Sambuc	17
7	A Comprehensive Endocrine Description of Kennedy’s Disease Revealing Androgen Insensitivity Linked to CAG Repeat Length 2002 ·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	124
8	The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders 2001 ·Journal of Neurology ·Véronique Pingault,Nadège Bondurand,C. Le Caignec,Sandrine Tardieu,N Lemort,O. Dubourg,E. Le Guern,M. Goossens,Odile Boespflug‐Tanguy	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 2001 ·Neuromuscular Disorders ·O. Dubourg,Sandrine Tardieu,Nazha Birouk,Riadh Gouider,Juliane Léger,Thierry Maisonobe,Alexis Brice,P. Bouché,Éric Leguern	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 2000 ·European Journal of Human Genetics ·Rafaëlle Bernard,Véronique Labelle,(unknown),Sandrine Tardieu,Jean‐Philippe Azulay,Perrine Malzac,Jean-François Mattéi,Éric Leguern,Nicole Philip,Nicolas Lévy	3
11	Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion 1999 ·Neurology ·(unknown),Sandrine Tardieu,Riadh Gouider,Nazha Birouk,Thierry Maisonobe,O. Dubourg,Alexis Brice,Éric Leguern,P. Bouché	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 1999 ·Human Molecular Genetics ·Judith Lopes,Sandrine Tardieu,Kaisa Silander,Ian P. Blair,A. Vandenberghe,Francesc Palau,Merle Ruberg,Alexis Brice,(unknown)	47
13	X-linked Charcot-Marie-Tooth disease with connexin 32 mutations 1998 ·Neurology ·Nazha Birouk,Éric Leguern,Thierry Maisonobe,H Rouger,Riadh Gouider,Sandrine Tardieu,Michel Gugenheim,(unknown),J.M. Léger,Yves Agid,Alexis Brice,P. Bouché	133
14	Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families 1997 ·Human Mutation ·H Rouger,Éric Leguern,Nazha Birouk,Riadh Gouider,Sandrine Tardieu,Emmanuelle Plassart,Michel Gugenheim,(unknown),J.P. Louboutin,P. Bouché,Yves Agid,Alexis Brice	51
15	Allelic association at the D14S43 locus in early onset Alzheimer's disease 1995 ·American Journal of Medical Genetics ·Alexis Brice,Sandrine Tardieu,Dominique Campion,E. Le Guern,María Martínez,Alexandre Carpentier,Christiane Penet,Bruno Dubois,(unknown),Jacques Mallet,Didier Hannequin,Françoise Clerget‐Darpoux,Yves Agid	3
16	Evidence for apolipoprotein E ϵ4 association in early‐onset Alzheimer's patients with late‐onset relatives 1995 ·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	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 1995 ·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	15
18	A large pedigree with early-onset Alzheimer's disease 1995 ·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	39
19	[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]. 1995 ·PubMed ·Didier Hannequin,Dominique Campion,Sandrine Tardieu,(unknown),(unknown),Bénédicte Dubois,Françoise Clerget‐Darpoux,Yves Agid,Alexis Brice	2
20	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies 1994 ·Neurology ·Riadh Gouider,Éric Leguern,Jean‐François Emile,Sandrine Tardieu,(unknown),(unknown),J. Weissenbach,Yves Agid,P. Bouché,Alexis Brice	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) and Neurological diseases and metabolism (5 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.

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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