P. Byrne

1.1k total citations
18 papers, 547 citations indexed

About

P. Byrne is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, P. Byrne has authored 18 papers receiving a total of 547 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 10 papers in Neurology and 6 papers in Molecular Biology. Recurrent topics in P. Byrne's work include Hereditary Neurological Disorders (11 papers), Neurological diseases and metabolism (10 papers) and Endoplasmic Reticulum Stress and Disease (4 papers). P. Byrne is often cited by papers focused on Hereditary Neurological Disorders (11 papers), Neurological diseases and metabolism (10 papers) and Endoplasmic Reticulum Stress and Disease (4 papers). P. Byrne collaborates with scholars based in Ireland, United Kingdom and United States. P. Byrne's co-authors include Michael Hutchinson, Paul McMonagle, Nollaig A. Parfrey, Stewart Webb, Peter Sanders, Jianping Lu, Kirby Snell, Brendan Fitzgerald, Paola S. Denora and James McRedmond and has published in prestigious journals such as Neurology, Biochemical Journal and Biochemical and Biophysical Research Communications.

In The Last Decade

P. Byrne

18 papers receiving 541 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. Byrne Ireland 12 373 250 140 128 120 18 547
Andrzej Kochański Poland 14 490 1.3× 184 0.7× 287 2.0× 62 0.5× 126 1.1× 73 706
Alleene V. Strickland United States 7 256 0.7× 113 0.5× 185 1.3× 52 0.4× 105 0.9× 7 417
Simone M. Sauter Germany 9 279 0.7× 170 0.7× 111 0.8× 116 0.9× 114 0.9× 11 465
Tarik Hamadouche France 15 410 1.1× 177 0.7× 221 1.6× 48 0.4× 163 1.4× 19 630
Yujiro Higuchi Japan 13 381 1.0× 161 0.6× 206 1.5× 41 0.3× 84 0.7× 53 551
David S. Lynch United Kingdom 13 145 0.4× 210 0.8× 346 2.5× 75 0.6× 30 0.3× 30 578
Paola S. Denora Italy 10 353 0.9× 241 1.0× 89 0.6× 146 1.1× 83 0.7× 12 491
Maria Schabhüttl Austria 9 202 0.5× 101 0.4× 162 1.2× 67 0.5× 132 1.1× 9 382
Dagmara Kabzińska Poland 13 329 0.9× 140 0.6× 210 1.5× 48 0.4× 73 0.6× 50 482
Julianne Aebischer France 9 82 0.2× 65 0.3× 249 1.8× 184 1.4× 37 0.3× 11 493

Countries citing papers authored by P. Byrne

Since Specialization
Citations

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

Fields of papers citing papers by P. Byrne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Byrne

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

All Works

18 of 18 papers shown
1.
Byrne, P., et al.. (2015). Different expression levels of spartin cause broad spectrum of cellular consequences in human neuroblastoma cells. Cell Biology International. 39(9). 1007–1015. 6 indexed citations
2.
Byrne, P.. (2012). Training medical students on rare disorders. Orphanet Journal of Rare Diseases. 7(Suppl 2). A15–A15. 15 indexed citations
3.
McRedmond, James, et al.. (2009). Identification of novel spartin‐interactors shows spartin is a multifunctional protein. Journal of Neurochemistry. 111(4). 1022–1030. 24 indexed citations
4.
Murphy, Sinéad M., Gráinne S. Gorman, Christian Beetz, et al.. (2009). Dementia in SPG4 hereditary spastic paraplegia. Neurology. 73(5). 378–384. 36 indexed citations
5.
Hanein, Sylvain, Elodie Martin, Amir Boukhris, et al.. (2008). Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome. The American Journal of Human Genetics. 82(4). 992–1002. 148 indexed citations
6.
Lu, Jianping, et al.. (2006). The hereditary spastic paraplegia protein spartin localises to mitochondria. Journal of Neurochemistry. 98(6). 1908–1919. 39 indexed citations
7.
8.
McMonagle, Paul, P. Byrne, & Michael Hutchinson. (2004). Further evidence of dementia in SPG4 -linked autosomal dominant hereditary spastic paraplegia. Neurology. 62(3). 407–410. 34 indexed citations
9.
Johnsson, Anders, et al.. (2001). Identification of gene clusters differentially expressed during the cellular injury responses (CIR) to cisplatin. British Journal of Cancer. 85(8). 1206–1210. 8 indexed citations
10.
Byrne, P., Stewart Webb, Paul McMonagle, et al.. (2001). SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q. Neurology. 56(9). 1230–1233. 50 indexed citations
11.
Snell, Keith, et al.. (2000). The genetic organization and protein crystallographic structure of human serine hydroxymethyltransferase. Advances in Enzyme Regulation. 40(1). 353–403. 11 indexed citations
12.
Byrne, P., et al.. (2000). Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p. Neurology. 54(7). 1510–1517. 35 indexed citations
13.
McMonagle, Paul, P. Byrne, Brendan Fitzgerald, et al.. (2000). Phenotype of AD-HSP due to mutations in the SPAST gene. Neurology. 55(12). 1794–1800. 30 indexed citations
14.
Byrne, P., et al.. (1998). Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance. European Journal of Human Genetics. 6(3). 275–282. 20 indexed citations
15.
Byrne, P., Janet Shipley, Karen J. Chave, Peter Sanders, & Keith Snell. (1996). Characterisation of a human serine hydroxymethyltransferase pseudogene and its localisation to 1p32.3–33. Human Genetics. 97(3). 340–344. 10 indexed citations
16.
Byrne, P., Peter Sanders, & Kirby Snell. (1995). Translational Control of Mammalian Serine Hydroxymethyltransferase Expression. Biochemical and Biophysical Research Communications. 214(2). 496–502. 11 indexed citations
17.
Byrne, P., Peter Sanders, & Keith Snell. (1993). Comparisons of nucleotide and protein sequences for mammalian serine hydroxymethyltransferase. Biochemical Society Transactions. 21(1). 36S–36S. 1 indexed citations
18.
Byrne, P., Peter Sanders, & Kirby Snell. (1992). Nucleotide sequence and expression of a cDNA encoding rabbit liver cytosolic serine hydroxymethyltransferase. Biochemical Journal. 286(1). 117–123. 24 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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