Stéphanie Baulac

10.6k total citations · 2 hit papers
81 papers, 4.7k citations indexed

About

Stéphanie Baulac is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Stéphanie Baulac has authored 81 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 37 papers in Psychiatry and Mental health and 36 papers in Molecular Biology. Recurrent topics in Stéphanie Baulac's work include Epilepsy research and treatment (37 papers), Genetics and Neurodevelopmental Disorders (31 papers) and Neuroscience and Neuropharmacology Research (23 papers). Stéphanie Baulac is often cited by papers focused on Epilepsy research and treatment (37 papers), Genetics and Neurodevelopmental Disorders (31 papers) and Neuroscience and Neuropharmacology Research (23 papers). Stéphanie Baulac collaborates with scholars based in France, United States and Switzerland. Stéphanie Baulac's co-authors include Michel Baulac, Alexis Brice, Éric Leguern, Gilles Huberfeld, Eric Leguern, Isabelle Gourfinkel‐An, Elise Marsan, Isabelle An-Gourfinkel, Miriam H. Meisler and Roberto Bruzzone and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Stéphanie Baulac

77 papers receiving 4.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

2000 739 citations Stéphanie Baulac, Gilles Huberfeld et al. profile →
First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

2001 574 citations Stéphanie Baulac, Gilles Huberfeld et al. profile →

Peers

Countries citing papers authored by Stéphanie Baulac

Since Specialization

Citations

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

Fields of papers citing papers by Stéphanie Baulac

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Baulac

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphanie Baulac. A scholar is included among the top collaborators of Stéphanie Baulac 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 Baulac. Stéphanie Baulac 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	Single-cell genotyping and transcriptomic profiling of mosaic focal cortical dysplasia 2025 ·Nature Neuroscience ·Sara Baldassari, Esther Klingler, (unknown), (unknown), (unknown), Sergi Roig‐Puiggros, Sara Bizzotto, J. Couturier, Alice Gilbert, (unknown), Théo Ribierre, Eleonora Aronica, Homa Adle‐Biassette, Mathilde Chipaux, Denis Jabaudon, Stéphanie Baulac	4
2	WONOEP appraisal: Modeling early onset epilepsies 2024 ·Epilepsia ·(unknown), Christopher A. Reid, Stéphane Auvin, Peter L. Carlen, Andrew J. Cole, (unknown), (unknown), Solomon L. Moshé, Raman Sankar, Terence J. O’Brien, Stéphanie Baulac, David C. Henshall, Özlem Akman, Aristea S. Galanopoulou	0
3	Somatic variant analysis of resected brain tissue in epilepsy surgery patients 2024 ·Epilepsia ·(unknown), Bobby P.C. Koeleman, Eva H. Brilstra, Floor E. Jansen, Sara Baldassari, Mathilde Chipaux, Nam Suk Sim, Ara Ko, Hoon‐Chul Kang, Ingmar Blümcke, Dennis Lal, Stéphanie Baulac, Jeong Ho Lee, Eleonora Aronica, Kees P. J. Braun	6
4	WONOEP 2022: Neurotechnology for the diagnosis of epilepsy 2024 ·Epilepsia ·Konrad Wagstyl, Katja Kobow, Pablo M. Casillas‐Espinosa, Andrew J. Cole, Diego Jiménez‐Jiménez, Hiroki Nariai, Stéphanie Baulac, Terence J. O’Brien, David C. Henshall, Özlem Akman, Raman Sankar, Aristea S. Galanopoulou, Stéphane Auvin	3
5	mTOR-therapy and targeted treatment opportunities in mTOR-related epilepsies associated with cortical malformations 2023 ·Revue Neurologique ·Stéphane Auvin, Stéphanie Baulac	11
6	Targeted suppression of mTORC2 reduces seizures across models of epilepsy 2023 ·Nature Communications ·(unknown), (unknown), Alexandre Bacq, Juan A. Osés-Prieto, Stefka Tyanova, (unknown), (unknown), (unknown), Hongyi Zhou, Paymaan Jafar‐Nejad, Alma L. Burlingame, Jeffrey L. Noebels, Stéphanie Baulac, Mauro Costa‐Mattioli	9
7	Detection of brain somatic mutations in focal cortical dysplasia during epilepsy presurgical workup 2023 ·Brain Communications ·(unknown), Mathilde Chipaux, Sarah Ferrand‐Sorbets, Emmanuel Raffo, Christine Bulteau, Sarah Rosenberg, (unknown), Georg Dorfmüller, Homa Adle‐Biassette, Sara Baldassari, Stéphanie Baulac	19
8	Cardiac Investigations in Sudden Unexpected Death in DEPDC5‐Related Epilepsy 2021 ·Annals of Neurology ·Alexandre Bacq, Delphine Roussel, (unknown), Sara Zagaglia, (unknown), Théo Ribierre, Homa Adle‐Biassette, Cécile Marchal, Mélanie Jennesson, Isabelle An, Fabienne Picard, Vincent Navarro, Sanjay M. Sisodiya, Stéphanie Baulac	17
9	Detection of Brain Somatic Mutations in Cerebrospinal Fluid from Refractory Epilepsy Patients 2021 ·Annals of Neurology ·Seyeon Kim, Sara Baldassari, Nam Suk Sim, Mathilde Chipaux, Georg Dorfmüller, Dong Seok Kim, Won Seok Chang, Valérie Taly, Jeong Ho Lee, Stéphanie Baulac	38
10	Depdc5 knockdown causes mTOR‐dependent motor hyperactivity in zebrafish 2018 ·Annals of Clinical and Translational Neurology ·Hortense de Calbiac, (unknown), Elise Marsan, Hervé Tostivint, (unknown), Saeko Ishida, Éric Leguern, Stéphanie Baulac, Raul C. Mureșan, Edor Kabashi, Sorana Ciura	38
11	The Nogo Receptor Ligand LGI1 Regulates Synapse Number and Synaptic Activity in Hippocampal and Cortical Neurons 2018 ·eNeuro ·Rhalena A. Thomas, Julien Gibon, Carol X.‐Q. Chen, Sabrina Chierzi, Vincent Soubannier, Stéphanie Baulac, Philippe Séguéla, Keith K. Murai, Philip Barker	13
12	DEPDC5-Related Epilepsy 2016 ·Stéphanie Baulac, Sarah Weckhuysen	5
13	mTOR signaling pathway genes in focal epilepsies 2016 ·Progress in brain research ·Stéphanie Baulac	56
14	Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations 2013 ·Epilepsy Research ·Lynette G. Sadleir, (unknown), E Chabrol, (unknown), Eric Leguern, (unknown), (unknown), Susannah T. Bellows, Samuel F. Berkovic, Ingrid E. Scheffer, Stéphanie Baulac	11
15	A rat model for LGI1-related epilepsies 2012 ·Human Molecular Genetics ·Stéphanie Baulac, Saeko Ishida, Tomoji Mashimo, (unknown), (unknown), Mitsuru Kuwamura, Yukihiro Ohno, Akiko Takizawa, (unknown), Masatsugu Ueda, Akio Ikeda, Éric Leguern, Ryōsuke Takahashi, Tadao Serikawa	31
16	Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice 2010 ·Brain ·E Chabrol, Vincent Navarro, Giovanni Provenzano, Ivan Cohen, Céline Dinocourt, Sophie Rivaud-Péchoux, Desdemona Fricker, Michel Baulac, Richard Miles, Éric Leguern, Stéphanie Baulac	95
17	Increased DJ-1 expression under oxidative stress and in Alzheimer's disease brains 2009 ·Molecular Neurodegeneration ·Stéphanie Baulac, (unknown), Jennifer M. Strahle, Ting Yang, Matthew S. Goldberg, Jie Shen, Michael G. Schlossmacher, Cynthia A. Lemere, Qun Lu, Weiming Xia	60
18	A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes 2009 ·Epilepsy Research ·Julitta de Bellescize, (unknown), E Chabrol, Nathalie André‐Obadia, Alexis Arzimanoglou, Éric Leguern, Stéphanie Baulac, Alain Calender, Philippe Ryvlin, Gaëtan Lesca	16
19	GABA_AReceptor γ2 Subunit Mutations Linked to Human Epileptic Syndromes Differentially Affect Phasic and Tonic Inhibition 2007 ·Journal of Neuroscience ·Emmanuel Eugène, Christel Depienne, Stéphanie Baulac, Michel Baulac, Jean‐Marc Fritschy, E. Le Guern, Richard Miles, Jean Christophe Poncer	67
20	Fever, genes, and epilepsy 2004 ·The Lancet Neurology ·Stéphanie Baulac, Isabelle Gourfinkel‐An, Rima Nabbout, Gilles Huberfeld, José M. Serratosa, Eric Leguern, Michel Baulac	129

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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