Y. Agid

1.0k total citations
5 papers, 148 citations indexed

About

Y. Agid is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Y. Agid has authored 5 papers receiving a total of 148 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cellular and Molecular Neuroscience, 3 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Y. Agid's work include Hereditary Neurological Disorders (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Neurological diseases and metabolism (2 papers). Y. Agid is often cited by papers focused on Hereditary Neurological Disorders (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Neurological diseases and metabolism (2 papers). Y. Agid collaborates with scholars based in France, Brazil and Cuba. Y. Agid's co-authors include Alexis Brice, Giovanni Stévanin, Géraldine Cancel‐Tassin, Alexandra Dürr, Hervé Chneiweiss, Christiane Penet, Olivier Dubourg, N. Ravisé, P. Bouché and N. Abbas and has published in prestigious journals such as Annals of Neurology, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Y. Agid

5 papers receiving 145 citations

Peers

Countries citing papers authored by Y. Agid

Since Specialization

Citations

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

Fields of papers citing papers by Y. Agid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Y. Agid

This figure shows the co-authorship network connecting the top 25 collaborators of Y. Agid. A scholar is included among the top collaborators of Y. Agid 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 Y. Agid. Y. Agid is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

#	Work	Indexed citations
1	Charcot‐Marie‐Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families 1997 ·Human Mutation ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Y. Agid, Alexis Brice	6
2	A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2? 1996 ·Human Molecular Genetics ·(unknown), (unknown), N. Ravisé, Judith Lopes, (unknown), (unknown), N. Abbas, P. Bouché, Y. Agid, Alexis Brice	27
3	Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease 1995 ·Journal of Medical Genetics ·Giovanni Stévanin, (unknown), Géraldine Cancel‐Tassin, N. Abbas, Alexandra Dürr, (unknown), Y. Agid, (unknown), Alexis Brice	16
4	Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations 1995 ·Annals of Neurology ·Olivier Dubourg, Alexandra Dürr, Géraldine Cancel‐Tassin, Giovanni Stévanin, Christiane Penet, Y. Agid, Alexis Brice, Hervé Chneiweiss	62
5	Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP) 1994 ·Cytogenetic and Genome Research ·E. Le Guern, (unknown), Michel Gugenheim, Riadh Gouider, (unknown), N. Ravisé, Pierre‐Marie Gonnaud, (unknown), P. Bouché, G Chazot, Y. Agid, A. Vandenberghe, Alexis Brice	37

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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