Vivien J. Bubb

7.6k total citations · 1 hit paper
84 papers, 3.5k citations indexed

About

Vivien J. Bubb is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Vivien J. Bubb has authored 84 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 22 papers in Genetics and 16 papers in Cellular and Molecular Neuroscience. Recurrent topics in Vivien J. Bubb's work include Chromosomal and Genetic Variations (16 papers), RNA Research and Splicing (14 papers) and Amyotrophic Lateral Sclerosis Research (10 papers). Vivien J. Bubb is often cited by papers focused on Chromosomal and Genetic Variations (16 papers), RNA Research and Splicing (14 papers) and Amyotrophic Lateral Sclerosis Research (10 papers). Vivien J. Bubb collaborates with scholars based in United Kingdom, Australia and United States. Vivien J. Bubb's co-authors include Richard Schlegel, William C. Phelps, Peter M. Howley, Karl Münger, John P. Quinn, Melissa D. Conrad, George Fink, Anthony J. Harmar, G M Goodwin and S. Battersby and has published in prestigious journals such as Nature, The Lancet and Journal of Neuroscience.

In The Last Decade

Vivien J. Bubb

84 papers receiving 3.5k citations

Hit Papers

The E6 and E7 genes of the human papillomavirus type 16 t... 1989 2026 2001 2013 1989 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vivien J. Bubb United Kingdom 27 1.6k 1.1k 918 688 510 84 3.5k
Elizabeth M. Simpson Canada 31 3.3k 2.1× 494 0.4× 1.7k 1.8× 717 1.0× 594 1.2× 97 6.3k
William F. Goins United States 41 2.0k 1.3× 2.0k 1.8× 2.3k 2.6× 733 1.1× 961 1.9× 141 5.2k
Helen Lockstone United Kingdom 31 1.8k 1.1× 337 0.3× 563 0.6× 433 0.6× 171 0.3× 53 3.9k
Franz Rüschendorf Germany 40 2.3k 1.4× 250 0.2× 1.2k 1.3× 381 0.6× 277 0.5× 83 5.0k
Markus U. Ehrengruber Switzerland 32 1.8k 1.1× 344 0.3× 482 0.5× 381 0.6× 1.0k 2.0× 54 3.7k
Jonathan L. Rees United Kingdom 38 2.1k 1.3× 586 0.5× 967 1.1× 1.3k 1.8× 150 0.3× 89 6.1k
Kyung‐Il Park South Korea 30 725 0.5× 475 0.4× 338 0.4× 177 0.3× 531 1.0× 158 3.4k
Sérgio Rosemberg Brazil 30 948 0.6× 528 0.5× 234 0.3× 205 0.3× 302 0.6× 129 2.7k
Douglas J. Creedon United States 27 1.7k 1.0× 492 0.4× 207 0.2× 260 0.4× 1.3k 2.6× 53 4.2k
Gudrun Nürnberg Germany 44 2.9k 1.8× 226 0.2× 1.6k 1.7× 171 0.2× 451 0.9× 93 5.1k

Countries citing papers authored by Vivien J. Bubb

Since Specialization
Citations

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

Fields of papers citing papers by Vivien J. Bubb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vivien J. Bubb. 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 Vivien J. Bubb. The network helps show where Vivien J. Bubb may publish in the future.

Co-authorship network of co-authors of Vivien J. Bubb

This figure shows the co-authorship network connecting the top 25 collaborators of Vivien J. Bubb. A scholar is included among the top collaborators of Vivien J. Bubb 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 Vivien J. Bubb. Vivien J. Bubb 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.
Hughes, Lauren S., et al.. (2024). Exploring SVA Insertion Polymorphisms in Shaping Differential Gene Expressions in the Central Nervous System. Biomolecules. 14(3). 358–358. 4 indexed citations
2.
Hall, Ashley, Ben Middlehurst, Xylena Reed, et al.. (2024). A SINE-VNTR-Alu at the LRIG2 locus is associated with proximal and distal gene expression in CRISPR and population models. Scientific Reports. 14(1). 792–792. 1 indexed citations
3.
Pfaff, Abigail L., et al.. (2023). Reference LINE-1 insertion polymorphisms correlate with Parkinson’s disease progression and differential transcript expression in the PPMI cohort. Scientific Reports. 13(1). 13857–13857. 4 indexed citations
4.
Pfaff, Abigail L., Vivien J. Bubb, John P. Quinn, & Sulev Kõks. (2023). A Genome-Wide Screen for the Exonisation of Reference SINE-VNTR-Alus and Their Expression in CNS Tissues of Individuals with Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences. 24(14). 11548–11548. 6 indexed citations
5.
Kõks, Sulev, Abigail L. Pfaff, Vivien J. Bubb, & John P. Quinn. (2022). Longitudinal intronic RNA-Seq analysis of Parkinson’s disease patients reveals disease-specific nascent transcription. Experimental Biology and Medicine. 247(11). 945–957. 9 indexed citations
6.
Kõks, Sulev, et al.. (2022). Non-reference genome transposable elements (TEs) have a significant impact on the progression of the Parkinson’s disease. Experimental Biology and Medicine. 247(18). 1680–1690. 8 indexed citations
7.
Pfaff, Abigail L., et al.. (2022). Characterisation of the Function of a SINE-VNTR-Alu Retrotransposon to Modulate Isoform Expression at the MAPT Locus. Frontiers in Molecular Neuroscience. 15. 815695–815695. 10 indexed citations
8.
Kõks, Gea, Abigail L. Pfaff, Vivien J. Bubb, John P. Quinn, & Sulev Kõks. (2020). At the dawn of the transcriptomic medicine. Experimental Biology and Medicine. 246(3). 286–292. 13 indexed citations
9.
Hall, Ashley, Anni Moore, Dena Hernández, et al.. (2020). A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus. International Journal of Molecular Sciences. 21(22). 8486–8486. 6 indexed citations
10.
Billingsley, Kimberley J., Freddy Lättekivi, Anu Planken, et al.. (2019). Analysis of repetitive element expression in the blood and skin of patients with Parkinson’s disease identifies differential expression of satellite elements. Scientific Reports. 9(1). 4369–4369. 14 indexed citations
11.
Warburton, Alix, et al.. (2016). Novel brain expressed RNA identified at the MIR137 schizophrenia-associated locus. Schizophrenia Research. 184. 109–115. 14 indexed citations
12.
Warburton, Alix, Gerome Breen, Vivien J. Bubb, & John P. Quinn. (2015). A GWAS SNP for Schizophrenia Is Linked to the Internal MIR137 Promoter and Supports Differential Allele-Specific Expression. Schizophrenia Bulletin. 42(4). 1003–1008. 32 indexed citations
13.
Stevens, Hannah, David J. Hughes, Ren Sun, et al.. (2012). CTCF and Sp1 interact with the Murine gammaherpesvirus 68 internal repeat elements. Virus Genes. 45(2). 265–273. 3 indexed citations
14.
Haddley, K., et al.. (2011). Activity-Dependent Neuroprotective Protein Modulates Its Own Gene Expression. Journal of Molecular Neuroscience. 46(1). 33–39. 18 indexed citations
15.
Stevens, Hannah, Carolyn E. FISKERSTRAND, Vivien J. Bubb, Robert Dalziel, & John P. Quinn. (2009). A regulatory domain spanning the repeat sequence RE1 from herpes simplex virus type 1 has cell specific differential functions in trigeminal neurons and fibroblasts. FEBS Letters. 583(20). 3335–3338. 6 indexed citations
16.
Ali, Fahad, K. Haddley, Ursula M. Paredes, et al.. (2009). Combinatorial interaction between two human serotonin transporter gene variable number tandem repeats and their regulation by CTCF. Journal of Neurochemistry. 112(1). 296–306. 59 indexed citations
20.
White, Susan M., Vivien J. Bubb, & Andrew H. Wyllie. (1996). Germline APC mutation (Gln1317) in a cancer-prone family that does not result in familial adenomatous polyposis. Genes Chromosomes and Cancer. 15(2). 122–128. 32 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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