Thomas Bourinaris

653 total citations
10 papers, 86 citations indexed

About

Thomas Bourinaris is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology. According to data from OpenAlex, Thomas Bourinaris has authored 10 papers receiving a total of 86 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 5 papers in Neurology and 4 papers in Neurology. Recurrent topics in Thomas Bourinaris's work include Neurological diseases and metabolism (4 papers), Hereditary Neurological Disorders (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Thomas Bourinaris is often cited by papers focused on Neurological diseases and metabolism (4 papers), Hereditary Neurological Disorders (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Thomas Bourinaris collaborates with scholars based in United Kingdom, Greece and Cyprus. Thomas Bourinaris's co-authors include Henry Houlden, Stéphanie Efthymiou, Vincenzo Salpietro, Georgia Xiromerisiou, Ghazala Kaukab Raja, Andrew Singleton, Chrysoula Marogianni, Marianthi Arnaoutoglou, Alkyoni Athanasiou‐Fragkouli and Sarah Wiethoff and has published in prestigious journals such as Journal of the Neurological Sciences, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

Thomas Bourinaris

10 papers receiving 85 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Bourinaris United Kingdom 5 37 35 30 23 19 10 86
Kheireddin Mufti Canada 5 45 1.2× 34 1.0× 31 1.0× 18 0.8× 17 0.9× 10 81
Maria Elena Conidi Italy 6 17 0.5× 32 0.9× 38 1.3× 32 1.4× 24 1.3× 10 85
Alberto Rábano Spain 4 59 1.6× 42 1.2× 25 0.8× 53 2.3× 19 1.0× 5 116
Daniela Bernardo Italy 6 68 1.8× 47 1.3× 22 0.7× 72 3.1× 12 0.6× 13 146
Zoltán Grosz Hungary 8 33 0.9× 57 1.6× 44 1.5× 81 3.5× 20 1.1× 20 170
Fahri Küçükali Belgium 3 55 1.5× 17 0.5× 31 1.0× 62 2.7× 45 2.4× 8 123
Linn Öijerstedt Sweden 5 53 1.4× 13 0.4× 26 0.9× 42 1.8× 45 2.4× 14 124
Vincent Anquetil France 7 53 1.4× 16 0.5× 29 1.0× 96 4.2× 31 1.6× 14 165
Xena Flowers United States 6 41 1.1× 25 0.7× 14 0.5× 20 0.9× 29 1.5× 9 91
Liena E. O. Elsayed Sudan 6 14 0.4× 53 1.5× 31 1.0× 40 1.7× 6 0.3× 14 108

Countries citing papers authored by Thomas Bourinaris

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Bourinaris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Bourinaris

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

All Works

10 of 10 papers shown
1.
Xiromerisiou, Georgia, Thomas Bourinaris, Henry Houlden, et al.. (2021). SORL1 mutation in a Greek family with Parkinson's disease and dementia. Annals of Clinical and Translational Neurology. 8(10). 1961–1969. 4 indexed citations
2.
Bourinaris, Thomas, et al.. (2021). Allelic and phenotypic heterogeneity in Junctophillin-3 related neurodevelopmental and movement disorders. European Journal of Human Genetics. 29(6). 1027–1031. 3 indexed citations
3.
Ullah, Asmat, Thomas Bourinaris, Stéphanie Efthymiou, et al.. (2021). Tay-Sachs Disease: Two Novel Rare HEXA Mutations from Pakistan and Morocco. Klinische Pädiatrie. 233(5). 226–230. 7 indexed citations
4.
Bourinaris, Thomas, Damian Smedley, Valentina Cipriani, et al.. (2020). Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project. European Journal of Human Genetics. 28(12). 1763–1768. 11 indexed citations
5.
Efthymiou, Stéphanie, Thomas Bourinaris, Gerome Breen, et al.. (2020). Rare novel CYP2U1 and ZFYVE26 variants identified in two Pakistani families with spastic paraplegia. Journal of the Neurological Sciences. 411. 116669–116669. 10 indexed citations
6.
Rikos, Dimitrios, Chrysoula Marogianni, Thomas Bourinaris, et al.. (2020). Screening for the C9ORF72 Expansion in Greek Huntington Disease Phenocopies and Controls and Meta-analysis of Current Data. Tremor and Other Hyperkinetic Movements. 10(0). 5–5. 3 indexed citations
7.
Sokratous, Maria, Thomas Bourinaris, Chrysoula Marogianni, et al.. (2020). Prevalence of C9orf72 hexanucleotide repeat expansion in Greek patients with sporadic ALS. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 21(5-6). 470–472. 3 indexed citations
8.
Ilyas, Muhammad, Vincenzo Salpietro, Stéphanie Efthymiou, et al.. (2019). Identification of common genetic markers of paroxysmal neurological disorders using a network analysis approach. Neurological Sciences. 41(4). 851–857. 4 indexed citations
9.
Bourinaris, Thomas & Henry Houlden. (2018). C9orf72 and its Relevance in Parkinsonism and Movement Disorders: A Comprehensive Review of the Literature. Movement Disorders Clinical Practice. 5(6). 575–585. 29 indexed citations
10.
Bettencourt, Conceição, Vincenzo Salpietro, Stéphanie Efthymiou, et al.. (2017). Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia. Orphanet Journal of Rare Diseases. 12(1). 172–172. 12 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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