A. Saporta

904 citations
14 papers · 639 · h-index 10

Impact in

    • Hereditary Neurological Disorders
    • Genetic Neurodegenerative Diseases
  • Neurology top 10%
    • Neurological diseases and metabolism
    • Botulinum Toxin and Related Neurological Disorders
    • Peripheral Neuropathies and Disorders

Papers in

A. Saporta

14 papers receiving 625 citations

Peers

A. Saporta
Comparison fields: 5 of 65
  • Cellular and Molecular Neuroscience 381
  • Neurology 110
  • Neurology 148
  • Psychiatry and Mental health 84
  • Pediatrics, Perinatology and Child Health 57
Replace Hana Ošlejšková with:
Hana Ošlejšková Czechia
David A. Ruhl United States
Christine Burness United Kingdom
Joseph Jankovic United States
Francesca Talpo Italy
P. Riguzzi Italy
Sigrid Reuter Germany
Nikos Makris United States
Alicia Semaka Canada
M. Harold Fogelson United States
A. Saporta relative to Hana Ošlejšková Czechia Hana Ošlejšková's profile →
Citations per field
00.5×4.3×
Hana Ošlejšková · 1×
Citations per year

Countries citing papers authored by A. Saporta

Since Specialization
Citations

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

Fields of papers citing papers by A. Saporta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

14 of 14 papers shown
#Work
1 2011387
2 200952
3 200950
4 201228
5 201927
6 202222
7 201119
8 200917
9 201917
10
Strategy for genetic testing in Charcot-Marie-disease.
201111
11 20224
12 20223
13 20241
14 20211

About A. Saporta

A. Saporta is a scholar working on Cellular and Molecular Neuroscience, Psychiatry and Mental health, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Public Health, Environmental and Occupational Health, having authored 14 papers that have together received 639 indexed citations. Recurring topics across this work include Epilepsy research and treatment (3 papers), Hereditary Neurological Disorders (3 papers), Cerebrospinal fluid and hydrocephalus (2 papers), Spinal Dysraphism and Malformations (2 papers), Autism Spectrum Disorder Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Fetal and Pediatric Neurological Disorders (1 paper) and Neurosurgical Procedures and Complications (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (381 citations), Neurology (110 citations), Neurology (148 citations), Psychiatry and Mental health (84 citations) and Pediatrics, Perinatology and Child Health (57 citations). A. Saporta has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Shawna Feely, Carly E. Siskind, Michael E. Shy, Lindsey J. Miller, Harry T. Chugani, Otto Muzik, Benjamin J. Wilson, Michael E. Behen, Csaba Juhász and Aashit Shah. Their work appears in journals such as Journal of Alzheimer s Disease, Annals of Neurology, Epilepsia, Journal of Child Neurology and Alzheimer s & Dementia.

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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