This map shows the geographic impact of E. Andermann'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 E. Andermann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Andermann more than expected).
This network shows the impact of papers produced by E. Andermann. 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 E. Andermann. The network helps show where E. Andermann may publish in the future.
Co-authorship network of co-authors of E. Andermann
This figure shows the co-authorship network connecting the top 25 collaborators of E. Andermann.
A scholar is included among the top collaborators of E. Andermann 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 E. Andermann. E. Andermann is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
20 of 20 papers shown
1.
Rubboli, Guido, Silvana Franceschetti, Laura Canafoglia, et al.. (2010). CLINICAL AND NEUROPHYSIOLOGICAL FEATURES OF PROGRESSIVE MYOCLONUS EPILEPSY ( PME) ASSOCIATED WITH SCARB2 MUTATIONS WITHOUT RENAL FAILURE. Epilepsia. 51. 23–23.2 indexed citations
Andermann, Frédérick, Anna Jansen, Abdullah Al‐Asmi, & E. Andermann. (2005). Epilepsy in neuroacanthocytosis. Movement Disorders. 20. 1680–1680.2 indexed citations
4.
Jansen, Anna, Őzgür Sancak, Daniela D’Agostino, et al.. (2005). Mild Epilepsy Phenotype in TSC2 Patients with Codon 905 Mutations. Epilepsia. 46. 52–52.2 indexed citations
Mulley, John C., Bree Hodgson, Bronwyn E. Grinton, et al.. (2003). Sodium channel alpha-1 subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms. The American Journal of Human Genetics. 73(5).11 indexed citations
7.
Andermann, F., Daniele D’Agostino, Alexandre Bastos, et al.. (2003). Posterior quadrantic dysplasia or hemi-hemime galencephaly: A surgical approach to a characteristic brain malformation. Epilepsia. 44. 89.3 indexed citations
8.
Picard, Fabienne, et al.. (2001). Benign nocturnal alternating hemiplegia of childhood: six patients and long-term follow-up.. Neurourology and Urodynamics. 23(8). 1491–1493.
Hart, Y, E. Andermann, & Hannah M. Mitchison. (1994). Genetic heterogeneity in juvenile NCL. The American Journal of Human Genetics. 55.2 indexed citations
Hechtman, Peter, Feige Kaplan, Janet K. Bayleran, et al.. (1990). More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians.. PubMed. 47(5). 815–22.45 indexed citations
Andermann, Frédérick, Paul R. Kileny, J. A. Watt, et al.. (1984). XIX Canadian Congress of Neurological Sciences. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 11(2). 318–320.1 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.