Alexis Brice

115.8k citations

548 papers · 35.8k indexed · 13 hit papers · h-index 88

Impact in

Neurology top 0.01%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Neurological disorders and treatments
Cellular and Molecular Neuroscience top 0.01%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Nuclear Receptors and Signaling

Papers in

Cellular and Molecular Neuroscience 347
- Genetic Neurodegenerative Diseases 204
- Hereditary Neurological Disorders 110
- Nuclear Receptors and Signaling 58
Neurology 252
- Parkinson's Disease Mechanisms and Treatments 174
- Neurological diseases and metabolism 131
- Neurological disorders and treatments 65

Co-authors: Alexandra Dürr Giovanni Stévanin Yves Agid Suzanne Lesage Olga Corti Éric Leguern Géraldine Cancel‐Tassin Pablo Ibáñez
Journals: Neurology (49 papers)Annals of Neurology (25 papers)Movement Disorders (21 papers)Neurobiology of Aging (19 papers)Brain (18 papers)
Partner nations: France United States Germany

In The Last Decade

Alexis Brice

540 papers receiving 35.1k citations

Hit Papers

13 papers align trajectories log scale

G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome 2013 · 531 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2013 Annals of Neurology
2011 The Lancet
2009 Human Molecular Genetics
2005 Nature Genetics
2004 The Lancet
2003 Science
2001 Nature Genetics
2000 Nature Genetics
1999 The American Journal of Human Genetics
1997 Nature Genetics
1996 Nature Genetics
1996 New England Journal of Medicine
1995 Nature

Peers

Countries citing papers authored by Alexis Brice

Since Specialization

Citations

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

Fields of papers citing papers by Alexis Brice

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores npj Parkinson s Disease ·Johann Faouzi, Manuela Tan, Fanny Casse, Suzanne Lesage, Christelle Tesson, Alexis Brice, Graziella Mangone, Louise‐Laure Mariani, Hirotaka Iwaki, Olivier Colliot, Lasse Pihlstrøm, Jean‐Christophe Corvol	2024	5
2	The Whole-Exome Sequencing of a Cohort of 19 Families with Adolescent Idiopathic Scoliosis (AIS): Candidate Pathways Genes ·Laura Marie-Hardy, Thomas Courtin, Hugues Pascal‐Moussellard, S. Zakine, Alexis Brice	2023	0
3	Differences in Survival across Monogenic Forms of Parkinson's Disease Annals of Neurology ·Aymeric Lanore, Fanny Casse, Christelle Tesson, Thomas Courtin, Poornima Jayadev Menon, Sara Sambin, Graziella Mangone, Louise‐Laure Mariani, Suzanne Lesage, Alexis Brice, Alexis Elbaz, Jean‐Christophe Corvol	2023	6
4	Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia Brain ·Raquel Real, Alejandro Martínez-Carrasco, Regina H. Reynolds, Michael Lawton, Manuela Tan, Maryam Shoai, Jean‐Christophe Corvol, Mina Ryten, Catherine Bresner, Leon Hubbard, Alexis Brice, Suzanne Lesage, Johann Faouzi, Alexis Elbaz, Fanny Artaud, Nigel Williams, (unknown), Yoav Ben‐Shlomo, Donald G. Grosset, John Hardy, Huw R. Morris	2022	31
5	Mutation analysis of Parkinson's disease genes in a Russian data set Neurobiology of Aging ·Anton Emelyanov, Tatiana Usenko, Christelle Tesson, Konstantin Senkevich, Михаил Николаев, Irina Miliukhina, Alena E. Kopytova, Alla Timofeeva, Andrey F. Yakimovsky, Suzanne Lesage, Alexis Brice, Sofya Pchelina	2018	38
6	Dopaminergic denervation severity depends on COMT Val158Met polymorphism in Parkinson's disease Parkinsonism & Related Disorders ·Julia Muellner, Iman Gharrad, Marie‐Odile Habert, Aurélie Kas, Jean‐Baptiste Martini, Florence Cormier‐Dequaire, Khadija Tahiri, Marie Vidailhet, Niklaus Meier, Alexis Brice, Michael Schuepbach, Alain Mallet, Andreas Hartmann, Jean‐Christophe Corvol	2015	16
7	Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD Human Molecular Genetics ·Serena Lattante, Hortense de Calbiac, Isabelle Le Ber, Alexis Brice, Sorana Ciura, Edor Kabashi	2014	67
8	Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers Neurology ·Mathieu Anheim, Alexis Elbaz, Suzanne Lesage, Alexandra Dürr, Christel Condroyer, François Viallet, Pierre Pollak, Bernard Bonaïti, Catherine Bonaïti‐Pellié, Alexis Brice	2012	183
9	A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations Journal of Nuclear Medicine ·Maria-João Ribeiro, Stéphane Thobois, Ebba Lohmann, Sophie Tézenas du Montcel, Suzanne Lesage, Antoine Pélissolo, Bruno Dubois, Luc Mallet, Pierre Pollak, Yves Agid, Emmanuel Broussolle, Alexis Brice, Philippe Rémy, (unknown)	2009	29
10	CNS aquaporin-4 autoimmunity in children Neurology ·Paris Pierre, ́-Salpe ˆtrie `, ́-Salpe ˆtrie `, Chu Mustapha, Alexis Brice, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2008	5
11	Are parkin patients particularly suited for deep‐brain stimulation? Movement Disorders ·Ebba Lohmann, Marie‐Laure Welter, Valérie Fraix, Paul Krack, Suzanne Lesage, Sophie Lainé, Marie‐Laure Tanguy, Jean‐Luc Houéto, Valérie Mesnage, Pierre Pollak, Alexandra Dürr, Yves Agid, Alexis Brice, (unknown)	2008	29
12	Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Stephan Klebe, Alexandra Dürr, Naïma Bouslam, Djamel Grid, Caroline Paternotte, Christel Depienne, Sylvain Hanein, Ahmed Bouhouche, Nizar Elleuch, Hamid Azzedine, Sandrine Poëa‐Guyon, Sylvie Forlani, Elodie Denis, Céline Charon, Jamïlé Hazan, Alexis Brice, Giovanni Stévanin	2007	14
13	A Conditional Pan-NeuronalDrosophilaModel of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes Journal of Neuroscience ·Morwena Latouche, Christelle Lasbleiz, Elodie Martin, Véronique Monnier, Thomas Debeir, Annick Mouatt‐Prigent, Marie‐Paule Muriel, Lydie Morel, Merle Ruberg, Alexis Brice, Giovanni Stévanin, Hervé Tricoire	2007	70
14	Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa Brain ·Pablo Ibáñez, Suzanne Lesage, Ebba Lohmann, Stéphane Thobois, Giuseppe De Michele, Michel Borg, Yves Agid, Alexandra Dürr, Alexis Brice	2006	123
15	[Clinical and genetic analysis of juvenile parkinsonism in Russia]. PubMed ·Zagorovskaia Tb, С. Н. Иллариошкин, Slominskiĭ Pa, Ivanova-Smolenskaia Ia, Markova Ed, Limborskaia Sa, Levin Os, Miloserdova Ov, Proskokova Tn, Bagyeva BKh, Alexis Brice	2004	5
16	Recent advances in hereditary spastic paraplegia Current Opinion in Neurology ·Chantal Tallaksen, Alexandra Dürr, Alexis Brice	2001	61
17	Levodopa-responsive dystonia Brain ·Jean‐Pol Tassin, Alexandra Dürr, Muriel Bonnet, Roger Gil, Marie Vidailhet, Christoph B. Lücking, Jean-Yves Goas, Franck Durif, Myriem Abada, Bernard Échenne, Jacques Motté, A Lagueny, Lucette Lacomblez, Pierre Jedynak, Barbara Bartholomé, Yves Agid, Alexis Brice	2000	123
18	Clinical and genetic aspects of spinocerebellar degeneration Current Opinion in Neurology ·Alexandra Dürr, Alexis Brice	2000	26
19	The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus. PubMed ·Gilles David, Paola Giunti, N. Abbas, P. Coullin, Giovanni Stévanin, Wagner Horta, Robert M. Gemmill, J. Weissenbach, Nicholas Wood, Susana Cunha, Harry A. Drabkin, A E Harding, Yves Agid, Alexis Brice	1996	52
20	No evidence for association of familial Parkinson's disease with CAG repeat expansion Neurology ·R. Carrero-Valenzuela, K Lindblad, Haydeh Payami, William G. Johnson, Martin Schalling, Edward S. Stenroos, S. Shattuc, John G. Nutt, Alexis Brice, M. Litt	1995	22

About Alexis Brice

Alexis Brice is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Molecular Biology and Physiology, having authored 548 papers that have together received 35.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (204 papers), Parkinson's Disease Mechanisms and Treatments (174 papers), Mitochondrial Function and Pathology (138 papers), Neurological diseases and metabolism (131 papers), Hereditary Neurological Disorders (110 papers), Neurological disorders and treatments (65 papers), Alzheimer's disease research and treatments (59 papers) and Nuclear Receptors and Signaling (58 papers). The work is most often cited by research in Neurology (16.2k citations), Cellular and Molecular Neuroscience (18.9k citations), Neurology (6.7k citations), Molecular Biology (16.9k citations) and Physiology (6.1k citations). Alexis Brice has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Alexandra Dürr, Giovanni Stévanin, Yves Agid, Suzanne Lesage, Olga Corti, Suzanne Lesage, Éric Leguern, Géraldine Cancel‐Tassin, Pablo Ibáñez and Didier Hannequin. Their work appears in journals such as Neurology, Annals of Neurology, Movement Disorders, Neurobiology of Aging and Brain.

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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