Stéphanie Bauché

2.0k total citations
20 papers, 271 citations indexed

About

Stéphanie Bauché is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Stéphanie Bauché has authored 20 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Neurology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Stéphanie Bauché's work include Ion channel regulation and function (11 papers), Myasthenia Gravis and Thymoma (8 papers) and Cellular transport and secretion (5 papers). Stéphanie Bauché is often cited by papers focused on Ion channel regulation and function (11 papers), Myasthenia Gravis and Thymoma (8 papers) and Cellular transport and secretion (5 papers). Stéphanie Bauché collaborates with scholars based in France, United Kingdom and Tunisia. Stéphanie Bauché's co-authors include B. Eymard, Daniel Hantaı̈, Jeanine Koenig, Jean‐Paul Leroy, Martine Verdière‐Sahuqué, Frédéric Chevessier, Marion Paturneau-Jouas, Pascale Richard, Karen Gaudon and Emmanuel Fournier and has published in prestigious journals such as Scientific Reports, The Journal of Pathology and Journal of Medical Genetics.

In The Last Decade

Stéphanie Bauché

19 papers receiving 263 citations

Peers

Countries citing papers authored by Stéphanie Bauché

Since Specialization

Citations

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

Fields of papers citing papers by Stéphanie Bauché

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Bauché

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphanie Bauché. A scholar is included among the top collaborators of Stéphanie Bauché 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 Stéphanie Bauché. Stéphanie Bauché 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	New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome 2023 ·Scientific Reports ·(unknown), (unknown), Nicolas Wolff, (unknown), Damien Sternberg, (unknown), (unknown), Anthony Béhin, (unknown), Thierry Maisonobe, Marie‐Christine Nouguès, Arnaud Isapof, Bertrand Fontaine, (unknown), B. Eymard, Laure Strochlic, Stéphanie Bauché	2
2	Pathogenic DPAGT1 variants in limb‐girdle congenital myasthenic syndrome (LG‐CMS) associated with tubular aggregates and ORAI1 hypoglycosylation 2023 ·Neuropathology and Applied Neurobiology ·(unknown), Stéphanie Bauché, (unknown), Damien Sternberg, A. Seferian, Edoardo Malfatti, (unknown), C. Labasse, Frédéric Chevessier, Pierre G. Carlier, B. Eymard, Norma B. Romero, Jocelyn Laporte, Laurent Servais, Teresa Gidaro, Johann Böhm	5
3	The cell polarity protein Vangl2 in the muscle shapes the neuromuscular synapse by binding to and regulating the tyrosine kinase MuSK 2022 ·Science Signaling ·(unknown), (unknown), (unknown), Stéphanie Bauché, (unknown), Nathalie Sans, Mireille Montcouquiol, Jordi Molgó, Muriel Amar, Arnaud Ferry, (unknown), Andrée Rouche, Dominique Langui, (unknown), Bertrand Fontaine, (unknown), Laure Strochlic	6
4	Diagnostic yield of a practical electrodiagnostic protocol discriminating between different congenital myasthenic syndromes 2022 ·Neuromuscular Disorders ·Tanya Stojkovic, (unknown), (unknown), (unknown), Anthony Béhin, Sarah Léonard-Louis, Guillaume Bassez, Stéphanie Bauché, (unknown), Pascale Richard, Damien Sternberg, B. Eymard, Emmanuel Fournier, (unknown)	1
5	Regulation of mammalian neuromuscular junction formation and maintenance by Wnt signaling 2018 ·Current Opinion in Physiology ·(unknown), (unknown), Stéphanie Bauché, Bertrand Fontaine, Claire Legay, Laure Strochlic	10
6	Congenital Myasthenic Syndromes or Inherited Disorders of Neuromuscular Transmission: Recent Discoveries and Open Questions 2017 ·Journal of Neuromuscular Diseases ·Sophie Nicole, Yoshiteru Azuma, Stéphanie Bauché, B. Eymard, Hanns Lochmüller, Clarke R. Slater	24
7	Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome 2013 ·Neuromuscular Disorders ·Stéphanie Bauché, Delphine Boërio, Claire-Sophie Davoine, Véronique Bernard, Morgane Stum, (unknown), Michel Fardeau, Norma B. Romero, Bertrand Fontaine, Jeanine Koenig, Daniel Hantaı̈, Antoine Guéguen, Emmanuel Fournier, B. Eymard, Sophie Nicole	14
8	Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations 2011 ·Neuromuscular Disorders ·I. Wargon, Pascale Richard, Thierry Küntzer, Damien Sternberg, Shahriar Nafissi, Karen Gaudon, (unknown), Stéphanie Bauché, Daniel Hantaı̈, Emmanuel Fournier, B. Eymard, Tanya Stojkovic	56
9	Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing 2010 ·Journal of Medical Genetics ·Karen Gaudon, I. Pénisson-Besnier, B. Chabrol, Françoise Bouhour, L. Demay, Asma Ammar, Stéphanie Bauché, Christophe Vial, Gaël Nicolas, B. Eymard, Daniel Hantaı̈, Pascale Richard	9
10	Principaux mécanismes impliqués dans la transmission synaptique au sein de l’appareil neuromusculaire 2009 ·Neurochirurgie ·(unknown), Michel Wager, K. Buffenoir, Stéphanie Bauché, Jean‐Philippe Giot, J. M. Maixent, Philippe Rigoard	2
11	Modalités et outils d’observation de la jonction neuromusculaire 2009 ·Neurochirurgie ·Philippe Rigoard, K. Buffenoir, Stéphanie Bauché, (unknown), Jeanine Koenig, Daniel Hantaı̈, Jean‐Philippe Giot, F. Seguin, Caroline Huzé, Laurent Schaeffer, J. M. Maixent	0
12	Architecture moléculaire du réticulum sarcoplasmique et son rôle dans le couplage excitation-contraction 2009 ·Neurochirurgie ·Philippe Rigoard, K. Buffenoir, Michel Wager, Stéphanie Bauché, Jean‐Philippe Giot, F. Lapierre	1
13	Remaniements expérimentaux et pathologiques de la jonction neuromusculaire 2009 ·Neurochirurgie ·Jeanine Koenig, Stéphanie Bauché, Asma Ammar, Delphine Nicolle, Philippe Rigoard, B. Eymard, Daniel Hantaı̈	2
14	Organisation anatomique et physiologique du nerf périphérique 2009 ·Neurochirurgie ·Philippe Rigoard, K. Buffenoir, Michel Wager, Stéphanie Bauché, Jean‐Philippe Giot, Roger Robert, F. Lapierre	20
15	Formation et régénération synaptique 2009 ·Neurochirurgie ·(unknown), (unknown), K. Buffenoir, Jean‐Philippe Giot, Michel Wager, Stéphanie Bauché, F. Lapierre, Philippe Rigoard	5
16	Le support anatomique de la contraction musculaire 2009 ·Neurochirurgie ·Philippe Rigoard, Stéphanie Bauché, K. Buffenoir, Jean‐Philippe Giot, (unknown), M. Scépi, (unknown), F. Lapierre, Michel Wager	3
17	A synonymous CHRNE mutation responsible for an aberrant splicing leading to congenital myasthenic syndrome 2007 ·Neuromuscular Disorders ·Pascale Richard, Karen Gaudon, Emmanuel Fournier, C. Ellen Jackson, Stéphanie Bauché, (unknown), Jeanine Koenig, Bernard Échenne, Daniel Hantaı̈, B. Eymard	18
18	The origin of tubular aggregates in human myopathies 2005 ·The Journal of Pathology ·Frédéric Chevessier, Stéphanie Bauché, Jean‐Paul Leroy, Jeanine Koenig, Marion Paturneau-Jouas, B. Eymard, Daniel Hantaı̈, Martine Verdière‐Sahuqué	64
19	CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia 2002 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Claudine Laurent, Dana Niehaus, Stéphanie Bauché, Douglas F. Levinson, Stéphane Soubigou, (unknown), Michael R. Hayden, (unknown), Robin Emsley, Jean‐François Deleuze, Jacques Mallet	11
20	Identifying and characterizing a five‐gene cluster of ATP‐binding cassette transporters mapping to human chromosome 17q24: a new subgroup within the ABCA subfamily 2001 ·Isabelle Arnould, Lynn M. Schriml, Catherine Prades, (unknown), Thomas D. Schneider, (unknown), Cendrine Lemoine, (unknown), Catherine Devaud, Laurent Naudin, Stéphanie Bauché, (unknown), Tarmo Annilo, Rando Allikmets, Bert Gold, Patrice Denèfle, Marie Rosier, Michael Dean	18

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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