Philippe Latour

4.2k citations

103 papers · 2.5k indexed · h-index 28

Impact in

Cellular and Molecular Neuroscience top 1%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 2%
- Neurological diseases and metabolism
- Peripheral Neuropathies and Disorders
- Botulinum Toxin and Related Neurological Disorders

Papers in

Cellular and Molecular Neuroscience 72
- Hereditary Neurological Disorders 70
- Genetic Neurodegenerative Diseases 23
Neurology 20
- Neurological diseases and metabolism 19
- Botulinum Toxin and Related Neurological Disorders 13
- Peripheral Neuropathies and Disorders 10

Co-authors: Sergio R. Acchiardo Linda W. Moore Marie T. Vanier A. Vandenberghe Tanya Stojkovic Antoon Vandenberghe Andoni Echaniz‐Laguna Françoise Chapon
Journals: Neuromuscular Disorders (13 papers)Journal of the Peripheral Nervous System (9 papers)Human Mutation (6 papers)Journal of Neurology Neurosurgery & Psychiatry (4 papers)Neurogenetics (4 papers)
Partner nations: France United States Spain

In The Last Decade

Philippe Latour

99 papers receiving 2.4k citations

Peers

Countries citing papers authored by Philippe Latour

Since Specialization

Citations

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

Fields of papers citing papers by Philippe Latour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Severe Respiratory and Swallowing Disorders in Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease Type 1 Neurology Genetics ·Richard Hymans, Philippe Latour, Gabriela Marcon, В. С. Паршин, Mohammed El Amine Bechar, Norma B. Romero, Emmanuelle Lacène, Teresinha Evangelista, Tanya Stojkovic	2024	0
2	Clinical and electrophysiological characteristics of women with X‐linked Charcot–Marie–Tooth disease European Journal of Neurology ·Cristian Guillermo Quilumba-Sanchez, Nathalie Bonello‐Palot, Yann Péréon, Andoni Echaniz‐Laguna, Jean‐Philippe Camdessanché, Tahani Salem Alharbi, Jean‐Baptiste Chanson, Helle Vesti, Laurent Magy, Julien Cassereau, Pascal Cintas, (unknown), Perrine Devic, Sarah Louis, Tanja Hadzhiolova, Émilien Delmont, Emmanuelle Salort‐Campana, Françoise Bouhour, Philippe Latour, Tanya Stojkovic, Shahram Attarian	2023	1
3	Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: a national French retrospective study Orphanet Journal of Rare Diseases ·П. А. Злобин, Volodymyr Voytenko, Anaïs Brassier, Pierre Broué, Claude Cancés, B. Chabrol, Didier Eyer, F. Labarthe, Philippe Latour, Thierry Levade, Samia Pichard, Caroline Sevin, Marie T. Vanier, Bénédicte Héron	2023	7
4	HINT1 neuropathy: Expanding the genotype and phenotype spectrum Clinical Genetics ·程克波, Emmanuelle Salort‐Campana, Amandine Boyer, Florence Esselin, Ulrike Walther‐Louvier, Giorgia Querin, Philippe Latour, Anne‐Sophie Lia, Corinne Magdelaine, Max Dewhurst, Anthony Béhin, Valérie Delague, Nicolas Lévy, Tanya Stojkovic, Shahram Attarian, Patricia Fank	2022	3
5	Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy Brain ·Arnaud Jacquier, Conrad Buschkiel, Fanny Fontaine, Kristiningrum Kristin, Nicolas Lacoste, J. K. Sharma, Valérie Risson, Christine Maleske, Andrea Ginepri, Thomas Simonet, Philippe Latour, Tanya Stojkovic, Juliette Piard, S Palsbo, Gaëtan Lesca, Françoise Bouhour, Stéphane Allouche, Hélène Puccio, Antoine Pégat, Laurent Schaeffer	2022	11
6	Expanding the phenotypic variability of MORC2 gene mutations: From Charcot‐Marie‐Tooth disease to late‐onset pure motor neuropathy Human Mutation ·Arnaud Jacquier, J. K. Sharma, Ari Klapholz, Nicolas Lacoste, Valérie Risson, Christine Maleske, Philippe Latour, Aleksandra Nadaj‐Pakleza, Tanya Stojkovic, Laurent Schaeffer	2022	6
7	Strategy for genetic analysis in hereditary neuropathy Revue Neurologique ·Hailiang Zhang, Gorka Fernández‐Eulate, Rabab Debs, Céline Tard, Céline Labeyrie, Ė. M. Murzaev, Claire‐Marie Dhaenens, Julio Cesar Sánchez-Redondo, Philippe Latour, Tanya Stojkovic	2022	6
8	CMT2N-causing aminoacylation domain mutants enable Nrp1 interaction with AlaRS Proceedings of the National Academy of Sciences ·Litao Sun, Na Wei, Bernhard Kuhle, David Blocquel, Scott J. Novick, Żaneta Matuszek, Huihao Zhou, Weiwei He, Алёшечкин П. А., Thomas G. Weber, Rita Horváth, Philippe Latour, Tao Pan, Paul Schimmel, Patrick R. Griffin, Xiang‐Lei Yang	2021	19
9	Ustekinumab in bio-naïve and bio-failure Crohn's disease patients: Results from a « real-life » monocentric cohort. Digestive and Liver Disease ·Leticia Monin, Séverine Dubois, Cathérine Reenaers, Catherine Van Kemseke, Philippe Latour, Benchimol Maíra, Sophie Vieujean, Laurence Seidel, Édouard Louis	2020	15
10	Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death Acta Neuropathologica Communications ·Arnaud Jacquier, Cécile Delorme, Edwige Belotti, Blair R. McMurren, Guilhem Solé, O. Dubourg, Amber Tannehill, Claude-Alain Maurage, Valérie Castellani, Adriana Rebelo, Alexander J. Abrams, Stephan Züchner, Tanya Stojkovic, Laurent Schaeffer, Philippe Latour	2017	18
11	LC-MS/MS multiplex analysis of lysosphingolipids in plasma and amniotic fluid: A novel tool for the screening of sphingolipidoses and Niemann-Pick type C disease PLoS ONE ·Magali Pettazzoni, Roseline Froissart, Cécile Pagan, Marie T. Vanier, Pilar Perez Lloret, Philippe Latour, Nathalie Guffon, Alain Fouilhoux, Piérola Dorado, Thierry Levade, Christine Vianey‐Saban, Monique Piraud, David Cheillan	2017	49
12	Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses Journal of Neurology Neurosurgery & Psychiatry ·Yusuf A. Rajabally, David Adams, Philippe Latour, Shahram Attarian	2016	47
13	Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C Orphanet Journal of Rare Diseases ·Bénédicte Héron, Vassili Valayannopoulos, Julien Baruteau, B. Chabrol, Hélène Ogier, Philippe Latour, Dries Dobbelaere, Didier Eyer, F. Labarthe, Hélène Maurey, Jean‐Marie Cuisset, Marina Monteiro, Frédéric Sedel, Marie T. Vanier	2012	64
14	Induction of Multi-Functional T Cells in a Phase I Clinical Trial of Dendritic Cell Immunotherapy in Hepatitis C Virus Infected Individuals PLoS ONE ·Shuo Li, Stuart K. Roberts, Magdalena Plebanski, Maëlenn Gouillou, Tim Spelman, Philippe Latour, David C. Jackson, Lorena E. Brown, Rosemary L. Sparrow, H. Miles Prince, Derek N.J. Hart, Bruce E. Loveland, Eric J. Gowans	2012	9
15	U1 snRNA mis-binding: a new cause of CMT1B Neurogenetics ·Camila Cano Caporale, Philippe Latour, Véronique Bonnet, Shahram Attarian, Pierre Labauge, Nathalie Bonello‐Palot, Rafaëlle Bernard, Gilles Millat, Robert Rousson, Dominique Bozon	2009	16
16	NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement Neuromuscular Disorders ·Andoni Echaniz‐Laguna, Bertrand Degos, Céline Bonnet, Philippe Latour, Tarik Hamadouche, Nicolas Lévy, Bruno Leheup	2006	36
17	Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot–Marie–Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE Neuromuscular Disorders ·Katell Beauvais, A. Furby, Philippe Latour	2005	22
18	Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene Neuromuscular Disorders ·Tanya Stojkovic, Philippe Latour, 广忠张, J. de Sèze, Jean‐François Hurtevent, Antoon Vandenberghe, Patrick Vermersch	2004	34
19	[Recurrent facial nerve paralysis in hereditary neuropathy with liability to pressure palsy]. PubMed ·A. Drouet, L. Guilloton, Philippe Latour, C Ribot	2000	5
20	New Mutations in the X-Linked Form of Charcot-Marie-Tooth Disease European Neurology ·Philippe Latour, Johanna Carolina Sanchez Tuta, Catherine Ressot, Андрей Михайлович Куликов, J.‐C. Antoine, Patrick Calvas, Françoise Chapon, Lia Agustine Chandra, B. Sung, Franck Sturtz, M. Boucherat, G Chazot, André Dautigny, Danielle Pham-Dinh, Antoon Vandenberghe	1997	13

About Philippe Latour

Philippe Latour is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Cell Biology and Physiology, having authored 103 papers that have together received 2.5k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (70 papers), Genetic Neurodegenerative Diseases (23 papers), Neurological diseases and metabolism (19 papers), Botulinum Toxin and Related Neurological Disorders (13 papers), Lysosomal Storage Disorders Research (13 papers), Peripheral Neuropathies and Disorders (10 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Cellular Mechanics and Interactions (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Neurology (407 citations), Nephrology (276 citations), Neurology (541 citations) and Physiology (559 citations). Philippe Latour has collaborated with scholars based in France, United States and Spain. Frequent co-authors include Sergio R. Acchiardo, Linda W. Moore, Marie T. Vanier, A. Vandenberghe, Tanya Stojkovic, Antoon Vandenberghe, Andoni Echaniz‐Laguna, Françoise Chapon, Patrick Vermersch and Xavier Ferrer. Their work appears in journals such as Neuromuscular Disorders, Journal of the Peripheral Nervous System, Human Mutation, Journal of Neurology Neurosurgery & Psychiatry and Neurogenetics.

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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