Lucie Guyant‐Maréchal

3.8k citations

31 papers · 1.0k indexed · h-index 15

Impact in

Neurology top 5%
- Neurological diseases and metabolism
- Cerebrovascular and genetic disorders
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases

Papers in

Neurology 11
- Neurological diseases and metabolism 4
- Neurological disorders and treatments 4
- Parkinson's Disease Mechanisms and Treatments 4
Cellular and Molecular Neuroscience 10
- Genetic Neurodegenerative Diseases 8

Co-authors: Didier Hannequin Dominique Campion A. Laquérrière Elisabeth Tournier‐Lasserve Thierry Frébourg David Maltête L. Cabrejo Anne Vital
Journals: Brain (3 papers)Neurology (3 papers)Acta Neuropathologica (1 paper)Movement Disorders (1 paper)European Journal of Medical Genetics (1 paper)
Partner nations: France Australia United Kingdom

In The Last Decade

Lucie Guyant‐Maréchal

29 papers receiving 992 citations

Peers

Countries citing papers authored by Lucie Guyant‐Maréchal

Since Specialization

Citations

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

Fields of papers citing papers by Lucie Guyant‐Maréchal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucie Guyant‐Maréchal. 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 Lucie Guyant‐Maréchal. The network helps show where Lucie Guyant‐Maréchal may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Development of an Objective Structured Clinical Examination (OSCE) to evaluate the diagnosis announcement of chronic neurological disease by residents in neurology Revue Neurologique ·Lou Grangeon, David Wallon, Bertrand Bourre, 伸一冨岡, E. Guégan-Massardier, Lucie Guyant‐Maréchal, A. Liard, Vanda Machado, David Maltête	2024	1
2	An Atypical Case of Head Tremor and Extensive White Matter in an Adult Female Caused by 3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency Diagnostics ·Tomas Cunha, G. Montuori, RUGGERO BONORA, Yuh-Jye Lee, Lucie Guyant‐Maréchal, Cécile Acquaviva, Mir Mazedur Rahaman, Soumeya Bekri, Ivana Dabaj, Abdellah Tebani	2021	1
3	A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies European Journal of Medical Genetics ·Louis Viollet, Kathryn J. Swoboda, Rong Mao, Hunter Best, Lucas Makuch, Annick Toutain, Lucie Guyant‐Maréchal, Agnieszka Sallinen, Karima Ghorab, Marie Anne Barthez, Jean Michel Pedespan, X. Hernandoréna, Anne‐Sophie Lia, Jean‐François Deleuze, Cécile Masson, Isabelle Nelson, Juliette Nectoux, Yue Si	2020	5
4	Giant axonal neuropathy: a multicenter retrospective study with genotypic spectrum expansion Neurogenetics ·Andoni Echaniz‐Laguna, Jean‐Marie Cuisset, Lucie Guyant‐Maréchal, Patrick Aubourg, Laurent Kremer, Dept . Ilmu, Alain Verloès, Carolina Saori Yamashita, Sanjay Kumar, Bruno Francou, Philippe Latour	2019	10
5	Novel VCP mutations expand the mutational spectrum of frontotemporal dementia Neurobiology of Aging ·Dario Saracino, Fabienne Clot, Agnès Camuzat, Vincent Anquetil, Didier Hannequin, Lucie Guyant‐Maréchal, Mira Didic, Léna Guillot‐Noël, Daisy Rinaldi, Morwena Latouche, Sylvie Forlani, Xiao Hui CHEN, Cinzia Coppola, Giuseppe Di Iorio, 史子杉本, E. Le Guern, Alexis Brice, 梶原博	2018	21
6	Morphological features in juvenile Huntington disease associated with cerebellar atrophy — magnetic resonance imaging morphometric analysis Pediatric Radiology ·C.K.Teom, Gaël Nicolas, Alice Goldenberg, Catherine Vanhulle, V. A. Gurov, Shilah Olson, М. С. Ковальчук, Isabelle Michelet, Lucie Guyant‐Maréchal, Didier Devys, Emmanuel Gérardin, Amina Kator, P.-H. Vivier	2018	10
7	Tubular aggregate myopathy with features of Stormorken disease due to a new STIM1 mutation Neuromuscular Disorders ·Jean‐Baptiste Noury, Johann Böhm, Purnima Mishra, Lucie Guyant‐Maréchal, Anne‐Laure Bédat‐Millet, Kris Needham, Robert‐Yves Carlier, Edoardo Malfatti, Norma B. Romero, Tanya Stojkovic	2016	31
8	Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack Neurophysiologie Clinique ·Nathalie Chastan, Axel Lebas, Tiara Amelia Putri, D. Parain, Lucie Guyant‐Maréchal	2016	11
9	HeterozygousHTRA1mutations are associated with autosomal dominant cerebral small vessel disease Brain ·Edgard Verdura, Dominique Hervé, Eva Scharrer, Maria del Mar Amador, Lucie Guyant‐Maréchal, Anne Philippi, Astrid Corlobé, Françoise Bergametti, Steven Gazal, SEDKI NAWEL, Nathalie Beaufort, Sumit Singh Sonker, Tim Wu, Martin Dichgans, Hugues Chabriat, Christof Haffner, Elisabeth Tournier‐Lasserve	2015	123
10	Juvenile Huntington disease in an 18-month-old boy revealed by global developmental delay and reduced cerebellar volume American Journal of Medical Genetics Part A ·Gaël Nicolas, Didier Devys, Alice Goldenberg, David Maltête, Catherine Hervé, Didier Hannequin, Lucie Guyant‐Maréchal	2011	43
11	Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias Movement Disorders ·尚田頭, Perrine Charles, Pascale Ribaı̈, Cyril Goizet, Cécilia Marelli, J.B. Yang, Chrysostomos Soultanidis, Lucie Guyant‐Maréchal, N. Vandenberghe, Mathieu Anheim, David Devos, Léorah Freeman, Isabelle Le Ber, Karine Nguyen, Maya Tchikviladzé, Pierre Labauge, Didier Hannequin, Alexis Brice, Alexandra Dürr, Sophie Tézenas du Montcel	2011	19
12	Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementia The British Journal of Psychiatry ·Leonia Moreira Trajano, Didier Hannequin, Olivier Martinaud, 勇治阿部, Lucie Guyant‐Maréchal, Isabelle Le Ber, Dominique Campion	2010	32
13	Démences du sujet jeune : démarche diagnostique Revue Neurologique ·Didier Hannequin, Lucie Guyant‐Maréchal, Isabelle Le Ber, David Wallon, Dominique Campion, F. Sedel	2009	2
14	Dissections artérielles cervicales multiples chez deux frères : dysplasie fibro-musculaire ou maladie du tissu conjonctif ? Revue Neurologique ·В. Н. Ломасов, Aude Triquenot-Bagan, Y. D. Yu, Emmanuel Gérardin, A. Laquérrière, Didier Hannequin, Lucie Guyant‐Maréchal	2008	0
15	Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment Brain ·Sophie Tézenas du Montcel, Perrine Charles, Pascale Ribaı̈, Cyril Goizet, Chrysostomos Soultanidis, Pierre Labauge, Lucie Guyant‐Maréchal, Sylvie Forlani, C Jauffret, N. Vandenberghe, Karine Nguyen, Isabelle Le Ber, David Devos, J.B. Yang, Mario‐Ubaldo Manto, François Tison, Didier Hannequin, Merle Ruberg, Alexis Brice, Alexandra Dürr	2008	67
16	Génétique de la maladie d’Alzheimer : formes autosomiques dominantes Revue Neurologique ·Lucie Guyant‐Maréchal, Dominique Campion, Didier Hannequin	2008	6
17	Nephroangiosclerosis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Is NOTCH3 Mutation the Common Culprit? American Journal of Kidney Diseases ·Dominique Guerrot, Arnaud François, Jean‐Jacques Boffa, Min Li, M. Hanoy, B. Legallicier, Aude Triquenot-Bagan, Lucie Guyant‐Maréchal, Annie Laquerrière, 李崇世, Pierre Ronco, M. Godin	2008	10
18	Phenotype associated with APP duplication in five families Brain ·L. Cabrejo, Lucie Guyant‐Maréchal, A. Laquérrière, Martine Vercelletto, S. M. Dzyadookh, C. Thomas-Antérion, Christophe Verny, Franck Letournel, Florence Pasquier, Anne Vital, Frédéric Checler, Thierry Frébourg, Dominique Campion, Didier Hannequin	2006	218
19	Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family Acta Neuropathologica ·Olivier Martinaud, A. Laquérrière, Lucie Guyant‐Maréchal, Puspayanti Puspayanti, Pierre Véra, Nicolas Sergeant, A. Camuzat, Philippe Bourgeois, J J Hauw, Dominique Campion, Didier Hannequin	2005	18
20	Movement disorders and Creutzfeldt-Jakob disease: A review Parkinsonism & Related Disorders ·David Maltête, Lucie Guyant‐Maréchal, B Mihout, Didier Hannequin	2005	49

About Lucie Guyant‐Maréchal

Lucie Guyant‐Maréchal is a scholar working on Neurology, Neurology, Cellular and Molecular Neuroscience, Family Practice and Psychiatry and Mental health, having authored 31 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (5 papers), Neurological diseases and metabolism (4 papers), Alzheimer's disease research and treatments (4 papers), Neurological disorders and treatments (4 papers), Parkinson's Disease Mechanisms and Treatments (4 papers), Migraine and Headache Studies (3 papers) and Cholesterol and Lipid Metabolism (3 papers). The work is most often cited by research in Neurology (233 citations), Neurology (421 citations), Cellular and Molecular Neuroscience (282 citations), Psychiatry and Mental health (209 citations) and Physiology (289 citations). Lucie Guyant‐Maréchal has collaborated with scholars based in France, Australia and United Kingdom. Frequent co-authors include Didier Hannequin, Dominique Campion, A. Laquérrière, Elisabeth Tournier‐Lasserve, Thierry Frébourg, David Maltête, L. Cabrejo, Anne Vital, C. Thomas-Antérion and Martine Vercelletto. Their work appears in journals such as Brain, Neurology, Acta Neuropathologica, Movement Disorders and European Journal of Medical Genetics.

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