Patrick Vourc’h

7.8k citations

158 papers · 3.9k indexed · h-index 34

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research 87
- Neurological diseases and metabolism 26
- Parkinson's Disease Mechanisms and Treatments 18
Genetics top 1%
- Neurogenetic and Muscular Disorders Research 52
- Genetics and Neurodevelopmental Disorders 15
Developmental Neuroscience top 2%
Biological Psychiatry top 2%
Neurology top 2%
- Amyotrophic Lateral Sclerosis Research 87
- Neurological diseases and metabolism 26
- Parkinson's Disease Mechanisms and Treatments 18
Cognitive Neuroscience
- Autism Spectrum Disorder Research 12
Cellular and Molecular Neuroscience
- Nerve injury and regeneration 10
Molecular Biology
- Prion Diseases and Protein Misfolding 10

Co-authors: Christian Andrés Hélène Blasco Philippe Corcia Franck Patin Charlotte Veyrat‐Durebex Patrick Emond Denis Guilloteau Sylvie Chalon
Cited by: Neurology Genetics Developmental Neuroscience
Journals: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (12 papers)Molecular Neurobiology (7 papers)European Journal of Neurology (7 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Patrick Vourc’h

154 papers receiving 3.8k citations

Peers

Countries citing papers authored by Patrick Vourc’h

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Vourc’h

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patrick Vourc’h. 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 Patrick Vourc’h. The network helps show where Patrick Vourc’h may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Dynamic Expression of Genes Encoding Ubiquitin Conjugating Enzymes (E2s) During Neuronal Differentiation and Maturation: Implications for Neurodevelopmental Disorders and Neurodegenerative Diseases Genes ·Keerthivasan Thamotharan,Sylviane Marouillat,Bernard F. Vogelaar,Cindy Maurel,信成義仁,Hélène Blasco,Philippe Corcia,Frédéric Laumonnier,Christian Andrés,Patrick Vourc’h	2024	1
2	Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease International Journal of Molecular Sciences ·K.-J. Wolf,Élodie Richard,Sylviane Marouillat,Céline Brulard,Tarek Alouane,S. Beltran,Christian Andrés,Hélène Blasco,Philippe Corcia,Charlotte Veyrat‐Durebex,Patrick Vourc’h	2024	5
3	N-Terminal Fragments of TDP-43—In Vitro Analysis and Implication in the Pathophysiology of Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration Genes ·良平竹内,K.-J. Wolf,Élodie Richard,Débora Lanznaster,Sylviane Marouillat,Charlotte Veyrat‐Durebex,Christian Andrés,Philippe Corcia,Hélène Blasco,Patrick Vourc’h	2024	1
4	MTHFR Polymorphism in Congo Type 2 Diabetics: Prevalence of c.677CT and c.1298AC Mutations and Degenerative Complications ez Miguel Ángel Salceda Pérez,Maria Stefanova,Patricia Villamediana Monreal,Yong-Syu Lee,Patrick Vourc’h,camilawesner,Amanada V. Prascsak,L. Łankiewicz,Sekti Joko Sutono Islamanto,Christian Andrés,Dina Elkady	2024	0
5	The effect of pH alterations on TDP-43 in a cellular model of amyotrophic lateral sclerosis Biochemistry and Biophysics Reports ·Ю.М. Будолати,正弥熊倉,Minnie Ngaluafe,Patricia Villamediana Monreal,Sylviane Marouillat,Philippe Corcia,Patrick Vourc’h,Débora Lanznaster,Hélène Blasco	2024	1
6	PET Study of Microglial Activation in Kleine-Levin Syndrome Neurology Neuroimmunology & Neuroinflammation ·Lucie Barateau,Ann Laenen,KumarAdhikari,Michel Lecendreux,Sofiène Chenini,Nicolas Arlicot,Patrick Vourc’h,Amie L. Robison,Anne‐Sophie Salabert,Séverine Béziat,Isabelle Jaussent,Denis Mariano‐Goulart,Pierre Payoux,Yves Dauvilliers	2024	3
7	Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders Frontiers in Neuroscience ·Claudinei da Rosa,Tore Väunngårrd,Patrick Vourc’h,Médéric Jeanne,Frédéric Laumonnier	2023	12
8	Implication of Central Nervous System Barrier Impairment in Amyotrophic Lateral Sclerosis: Gender-Related Difference in Patients International Journal of Molecular Sciences ·Patricia Villamediana Monreal,Patrick Vourc’h,M. Aleksić,Isabelle Benz‐de Bretagne,Éric Piver,Christian Andrés,Philippe Corcia,Charlotte Veyrat‐Durebex,Hélène Blasco	2023	7
9	Evaluation of arterial blood gas parameters as prognostic markers in amyotrophic lateral sclerosis European Journal of Neurology ·Patricia Villamediana Monreal,Е. Камиока,鑫戴,Julie Morel,Patrick Vourc’h,Christian Andrés,Philippe Corcia,Hélène Blasco	2023	3
10	French National Protocol for genetic of amyotrophic lateral sclerosis Revue Neurologique ·Philippe Corcia,Patrick Vourc’h,E Bernard,Julien Cassereau,Philippe Codron,Marie‐Céline Fleury,Nathalie Guy,Kévin Mouzat,D.K. Flock,Marie‐Hélène Soriani,Philippe Couratier	2023	1
11	Taking Advantages of Blood–Brain or Spinal Cord Barrier Alterations or Restoring Them to Optimize Therapy in ALS? Journal of Personalized Medicine ·Patricia Villamediana Monreal,Ю.М. Будолати,Débora Lanznaster,Jean‐Michel Escoffre,Philippe Corcia,Patrick Vourc’h,Christian Andrés,Charlotte Veyrat‐Durebex,Hélène Blasco	2022	10
12	Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral Sclerosis Biomedicines ·Débora Lanznaster,Clément Bruno,Jérôme Bourgeais,Patrick Emond,Ilyess Zemmoura,Antoine Lefèvre,Pascal Reynier,Sébastien Eymieux,Emmanuelle Blanchard,Patrick Vourc’h,Christian Andrés,Diana del Castillo Cortázar,Olivier Hérault,Luc Favard,Philippe Corcia,Hélène Blasco	2022	11
13	Some CSF Kynurenine Pathway Intermediates Associated with Disease Evolution in Amyotrophic Lateral Sclerosis Biomolecules ·Patricia Villamediana Monreal,Felix Krüger,Patrick Emond,Isabelle Benz‐de Bretagne,Antoine Lefèvre,佐野浩彬,Charlotte Veyrat‐Durebex,Patrick Vourc’h,Christian Andrés,Philippe Corcia,Hélène Blasco	2021	13
14	Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders Molecular Genetics & Genomic Medicine ·Nicholas Gravbrot,Walid Hleihel,Sylviane Marouillat,Αθηνά Χρήστος Μπαλάσκα,Marie‐Laure Vuillaume,Michel Soufia,Patrick Vourc’h,Frédéric Laumonnier,Christian Andrés	2019	12
15	Ductal adenocarcinoma of the prostate: Clinical and biological profiles The Prostate ·Armelle Vinceneux,F. Bruyère,O. Haillot,T. Charles,Alexandre de la Taille,Laurent Salomon,Yves Allory,Idir Ouzaïd,Laurence Choudat,Morgan Rouprêt,Éva Compérat,Nadine Houédé,Jean‐Baptiste Beauval,Patrick Vourc’h,Gaëlle Fromont	2017	24
16	Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism Psychiatric Genetics ·Lorener Brayboy,V. N. Gutman,Sylviane Marouillat,Joëlle Malvy,茂美岩田,Annick Toutain,Keerthivasan Thamotharan,闫英敏,Hélène Bénédetti,Frédéric Laumonnier,Catherine Barthélémy,Frédérique Bonnet‐Brilhault,Christian Andrés,Patrick Vourc’h	2015	18
17	Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis Molecular Neurobiology ·Charlotte Veyrat‐Durebex,Philippe Corcia,Éric Piver,David Devos,Bernard F. Vogelaar,Flore Gouel,Patrick Vourc’h,Patrick Emond,Frédéric Laumonnier,Lydie Nadal‐Desbarats,Gordon Gilbert,Christian Andrés,Hélène Blasco	2015	38
18	The BDNF Val66Met polymorphism is associated with escitalopram response in depressed patients Psychopharmacology ·Wissam El‐Hage,Patrick Vourc’h,Philippe Gaillard,Julie Léger,Catherine Belzung,Yadira Ibargüen-Vargas,Christian Andrés,Vincent Camus	2014	22
19	Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis Journal of the Neurological Sciences ·Hélène Blasco,Patrick Vourc’h,Yann Nadjar,C. Wen Wang,Gordon Gilbert,차현숙,William Camu,Julien Praline,Vincent Meininger,Christian Andrés,Philippe Corcia	2011	28
20	Correction:¹H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis PLoS ONE ·Hélène Blasco,Philippe Corcia,Caroline Moreau,І. І. Ярема,Cecilia Boggio,Patrick Vourc’h,Patrick Emond,Gordon Gilbert,Pierre‐François Pradat,Julien Praline,David Devos,Lydie Nadal‐Desbarats,Christian Andrés	2010	26

About Patrick Vourc’h

Patrick Vourc’h is a scholar working on Neurology, Genetics and Neurology, having authored 158 papers that have together received 3.9k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (87 papers), Neurogenetic and Muscular Disorders Research (52 papers), Neurological diseases and metabolism (26 papers), Parkinson's Disease Mechanisms and Treatments (18 papers), Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (12 papers), Nerve injury and regeneration (10 papers) and Prion Diseases and Protein Misfolding (10 papers). The work is most often cited by research in Neurology (1.4k citations), Genetics (875 citations) and Developmental Neuroscience (269 citations). Patrick Vourc’h has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Christian Andrés, Hélène Blasco, Philippe Corcia, Franck Patin, Charlotte Veyrat‐Durebex, Patrick Emond, Denis Guilloteau, Sylvie Chalon, Lydie Nadal‐Desbarats and Jean‐Michel Halimi. Their work appears in journals such as Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Molecular Neurobiology, European Journal of Neurology, International Journal of Molecular Sciences and Journal of the Neurological Sciences.

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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