A Barois

688 citations
14 papers · 180 indexed · h-index 7
Topics
Neurogenetic and Muscular Disorders Research (3 papers)Myasthenia Gravis and Thymoma (2 papers)Neurological and metabolic disorders (2 papers)

In The Last Decade

A Barois

14 papers receiving 172 citations

Peers

A Barois
Comparison fields: 5 of 47
  • Molecular Biology 81
  • Neurology 77
  • Cellular and Molecular Neuroscience 45
  • Clinical Biochemistry 29
  • Cell Biology 26
Replace Mark Busby with:
Mark Busby United Kingdom
Eugenia Borgione Italy
Melissa Barghigiani Italy
James M. Polke United Kingdom
Emmanuelle Lagrue France
Giacomo Garone Italy
Yi‐Chun Lu Taiwan
Daniela Bernardo Italy
Fabrizia Stregapede Italy
Marina Michelson Israel
A Barois relative to Mark Busby United Kingdom Mark Busby's profile →
Citations per field
00.5×1.5×
Mark Busby · 1×
Citations per year

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
#WorkIndexed citations
1 8
2 19
3 38
4 45
5
[Respiratory form mof myasthenia gravis].
1
6
[Whooping cough with Bordetella parapertussis isolation in an HIV positive child].
1
7
[Familial mitochondrial encephalopathy. A clinicopathologic study].
2
8
[The Landry-Guillain-Barré syndrome. Study of prognostic factors in 223 cases].
36
9
[Diagnostic problems posed by a case of bird breeder's lung].
1
10
[Partial trisomy for the long arm of chromosome 2 due to malsegregation of a maternal insertion : ins(6;2)(p22;q24q34)].
12
11
[Dysautonomia in acute primary polyradiculoneuritis].
8
12
[Endogenous pellagra without hyperaminoaciduria].
1
13
[Norman type congenital atrophy of the granular layer. Observation of 2 sisters; neuro-pathological examination of a case].
2
14
[Primary atrophy of the granular layer of the cerebellum as described by R. M. Norman. Study of 2 cases].
6

About A Barois

A Barois is a scholar working on Neurology, Clinical Biochemistry and Genetics, having authored 14 papers that have together received 180 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (3 papers), Myasthenia Gravis and Thymoma (2 papers) and Neurological and metabolic disorders (2 papers). The work is most often cited by research in Neurology (77 citations), Clinical Biochemistry (29 citations) and Immunology and Allergy (18 citations). A Barois has collaborated with scholars based in France, United States and Lebanon. Frequent co-authors include M Goulon, P Gajdos, Andoni Urtizberea, Pascale Richard, Rima Nabbout, D. Brunel, Valérie Delague, Jacques Raphael, Cécile Masson and Daniel Hantaı̈. Their work appears in journals such as Neurology, Journal of Medical Genetics and American Journal of Medical Genetics.

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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