A Barois

688 total citations
14 papers, 180 citations indexed

About

A Barois is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, A Barois has authored 14 papers receiving a total of 180 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Neurology, 4 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in A Barois's work include Neurogenetic and Muscular Disorders Research (3 papers), Myasthenia Gravis and Thymoma (2 papers) and Neurological and metabolic disorders (2 papers). A Barois is often cited by papers focused on Neurogenetic and Muscular Disorders Research (3 papers), Myasthenia Gravis and Thymoma (2 papers) and Neurological and metabolic disorders (2 papers). A Barois collaborates with scholars based in France, Lebanon and United States. A Barois's co-authors include M Goulon, P Gajdos, Valérie Delague, Jacques Raphael, Rima Nabbout, Cécile Masson, Pascale Richard, Andoni Urtizberea, D. Brunel and M Prieur and has published in prestigious journals such as Neurology, Journal of Medical Genetics and American Journal of Medical Genetics.

In The Last Decade

A Barois

14 papers receiving 172 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
A Barois France 7 81 77 45 29 26 14 180
J. Puech France 6 58 0.7× 29 0.4× 34 0.8× 14 0.5× 42 1.6× 8 299
Elly F. Ippel Netherlands 9 139 1.7× 49 0.6× 96 2.1× 15 0.5× 18 0.7× 10 254
Mark Busby United Kingdom 4 139 1.7× 65 0.8× 106 2.4× 19 0.7× 18 0.7× 6 224
Monia Hammer United States 8 111 1.4× 46 0.6× 71 1.6× 19 0.7× 42 1.6× 12 213
Daniela Bernardo Italy 6 72 0.9× 68 0.9× 47 1.0× 29 1.0× 14 0.5× 13 146
R. Mercelis Belgium 11 252 3.1× 19 0.2× 54 1.2× 73 2.5× 22 0.8× 15 301
Rahul Lakshmanan Australia 7 54 0.7× 44 0.6× 22 0.5× 8 0.3× 18 0.7× 20 161
Eugenia Borgione Italy 8 81 1.0× 22 0.3× 27 0.6× 18 0.6× 8 0.3× 19 125
Melissa Barghigiani Italy 8 125 1.5× 38 0.5× 147 3.3× 12 0.4× 34 1.3× 18 204
Fabrizia Stregapede Italy 9 83 1.0× 43 0.6× 90 2.0× 41 1.4× 22 0.8× 17 205

Countries citing papers authored by A Barois

Since Specialization
Citations

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

Fields of papers citing papers by A Barois

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Barois

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

All Works

14 of 14 papers shown
1.
Maystadt, Isabelle, Mohammed Zarhrate, B. Estournet, et al.. (2006). A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36. Neurology. 67(1). 120–124. 8 indexed citations
2.
Ioos, Christine, A Barois, Pascale Richard, et al.. (2004). Congenital Myasthenic Syndrome due to Rapsyn Deficiency: Three Cases with Arthrogryposis and Bulbar Symptoms. Neuropediatrics. 35(4). 246–249. 19 indexed citations
3.
Delague, Valérie, et al.. (2000). Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?. American Journal of Medical Genetics. 92(2). 117–121. 38 indexed citations
4.
Guicheney, Pascale, Yi He, Corinne Cruaud, et al.. (1998). PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy.. Journal of Medical Genetics. 35(3). 211–217. 45 indexed citations
5.
Fauroux, Brigitte, et al.. (1993). [Respiratory form mof myasthenia gravis].. PubMed. 49(7). 633–5. 1 indexed citations
6.
Boyer, François, Patrice Nordmann, & A Barois. (1992). [Whooping cough with Bordetella parapertussis isolation in an HIV positive child].. PubMed. 49(3). 197–8. 1 indexed citations
7.
Estournet, B., C Duyckaerts, C. Marsac, et al.. (1991). [Familial mitochondrial encephalopathy. A clinicopathologic study].. PubMed. 147(6-7). 491–6. 2 indexed citations
8.
Raphael, Jacques, Cécile Masson, D. Brunel, et al.. (1986). [The Landry-Guillain-Barré syndrome. Study of prognostic factors in 223 cases].. PubMed. 142(6-7). 613–24. 36 indexed citations
9.
Barois, A, et al.. (1978). [Diagnostic problems posed by a case of bird breeder's lung].. PubMed. 129(2). 129–35. 1 indexed citations
10.
Couturier, J, Alain Aurias, M Prieur, & A Barois. (1977). [Partial trisomy for the long arm of chromosome 2 due to malsegregation of a maternal insertion : ins(6;2)(p22;q24q34)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 20(1). 52–5. 12 indexed citations
11.
Goulon, M, et al.. (1975). [Dysautonomia in acute primary polyradiculoneuritis].. PubMed. 131(2). 95–119. 8 indexed citations
12.
Escourolle, R, et al.. (1969). [Endogenous pellagra without hyperaminoaciduria].. PubMed. 120(3). 149–58. 1 indexed citations
13.
Goulon, M, et al.. (1968). [Norman type congenital atrophy of the granular layer. Observation of 2 sisters; neuro-pathological examination of a case].. PubMed. 118(1). 87–8. 2 indexed citations
14.
Goulon, M, et al.. (1968). [Primary atrophy of the granular layer of the cerebellum as described by R. M. Norman. Study of 2 cases].. PubMed. 76(35). 1691–4. 6 indexed citations

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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