Steven Lubbe

11.1k total citations
44 papers, 1.1k citations indexed

About

Steven Lubbe is a scholar working on Molecular Biology, Neurology and Pathology and Forensic Medicine. According to data from OpenAlex, Steven Lubbe has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Neurology and 13 papers in Pathology and Forensic Medicine. Recurrent topics in Steven Lubbe's work include Parkinson's Disease Mechanisms and Treatments (15 papers), Genetic factors in colorectal cancer (13 papers) and RNA regulation and disease (7 papers). Steven Lubbe is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (15 papers), Genetic factors in colorectal cancer (13 papers) and RNA regulation and disease (7 papers). Steven Lubbe collaborates with scholars based in United States, United Kingdom and Germany. Steven Lubbe's co-authors include Richard S. Houlston, Ian Chandler, Huw R. Morris, Maria Chiara Di Bernardo, Peter Broderick, Andrew Singleton, Bernabé I. Bustos, Nigel Williams, Isabelle Chandler and Valentina Escott‐Price and has published in prestigious journals such as Science, Journal of Biological Chemistry and Neuron.

In The Last Decade

Steven Lubbe

43 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven Lubbe United States 21 503 332 311 202 198 44 1.1k
Stephen Sikkink United Kingdom 15 407 0.8× 204 0.6× 96 0.3× 88 0.4× 172 0.9× 20 892
Robin L. Avila United States 16 534 1.1× 95 0.3× 155 0.5× 77 0.4× 87 0.4× 37 1.2k
Yah‐Huei Wu Chou Taiwan 12 558 1.1× 271 0.8× 130 0.4× 227 1.1× 218 1.1× 17 1.3k
Juliana Karrim United States 8 401 0.8× 232 0.7× 104 0.3× 119 0.6× 116 0.6× 8 731
Maria Rosário Almeida Portugal 15 362 0.7× 199 0.6× 70 0.2× 99 0.5× 171 0.9× 47 896
Ana Sofia Correia Portugal 14 575 1.1× 137 0.4× 110 0.4× 40 0.2× 149 0.8× 29 989
Bitao Bu China 15 318 0.6× 146 0.4× 144 0.5× 48 0.2× 118 0.6× 42 898
Xingxing Xu China 15 595 1.2× 56 0.2× 101 0.3× 116 0.6× 74 0.4× 33 934
Graeme R. Clark United Kingdom 12 367 0.7× 233 0.7× 47 0.2× 181 0.9× 72 0.4× 19 815
Silvia Pozzi Italy 16 644 1.3× 324 1.0× 31 0.1× 94 0.5× 127 0.6× 28 1.0k

Countries citing papers authored by Steven Lubbe

Since Specialization
Citations

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

Fields of papers citing papers by Steven Lubbe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Lubbe

This figure shows the co-authorship network connecting the top 25 collaborators of Steven Lubbe. A scholar is included among the top collaborators of Steven Lubbe 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 Steven Lubbe. Steven Lubbe 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.
Hanson, Barbara A., Xin Dang, Pouya Jamshidi, et al.. (2025). Human pegivirus alters brain and blood immune and transcriptomic profiles of patients with Parkinson’s disease. JCI Insight. 10(13). 2 indexed citations
2.
Goh, Lay Hoon, et al.. (2025). Factors affecting antibiotic appropriateness in uncomplicated urinary tract infections in primary care. Scientific Reports. 15(1). 15055–15055.
3.
Bustos, Bernabé I., Sara Bandrés‐Ciga, Thiago Peixoto Leal, et al.. (2024). Genome-wide epistasis analysis reveals significant epistatic signals associated with Parkinson’s disease risk. Brain. 148(6). 2060–2074. 1 indexed citations
4.
Smela, Merrick Pierson, et al.. (2024). SeqVerify: An accessible analysis tool for cell line genomic integrity, contamination, and gene editing outcomes. Stem Cell Reports. 19(10). 1505–1515. 1 indexed citations
5.
Bustos, Bernabé I., Kimberley J. Billingsley, Cornelis Blauwendraat, et al.. (2022). Genome-wide contribution of common short-tandem repeats to Parkinson’s disease genetic risk. Brain. 146(1). 65–74. 20 indexed citations
6.
Simkin, Dina, Bernabé I. Bustos, Christina M. Ambrosi, et al.. (2022). Homozygous might be hemizygous: CRISPR/Cas9 editing in iPSCs results in detrimental on-target defects that escape standard quality controls. Stem Cell Reports. 17(4). 993–1008. 36 indexed citations
7.
Simkin, Dina, Carlos G. Vanoye, Reshma R. Desai, et al.. (2021). Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy. eLife. 10. 26 indexed citations
8.
Bustos, Bernabé I., Sara Bandrés‐Ciga, J. Raphael Gibbs, et al.. (2020). Replication assessment of NUS1 variants in Parkinson's disease. Neurobiology of Aging. 101. 300.e1–300.e3. 7 indexed citations
9.
Lamb, Ruth, Jonathan D. Rohrer, Raquel Real, et al.. (2019). A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders. Molecular Case Studies. 5(3). a003913–a003913. 22 indexed citations
10.
Jansen, Iris E., J. Raphael Gibbs, T. Ryan Price, et al.. (2017). Establishing the role of rare coding variants in known Parkinson's disease risk loci. Neurobiology of Aging. 59. 220.e11–220.e18. 11 indexed citations
11.
Escott‐Price, Valentina, Mike A. Nalls, Huw R. Morris, et al.. (2015). Polygenic risk of Parkinson disease is correlated with disease age at onset. Annals of Neurology. 77(4). 582–591. 93 indexed citations
12.
Nichols, Noah, José Brás, Dena G. Hernandez, et al.. (2015). EIF4G1 mutations do not cause Parkinson's disease. Neurobiology of Aging. 36(8). 2444.e1–2444.e4. 15 indexed citations
13.
Kiely, Aoife P., Helen Ling, Yasmine T. Asi, et al.. (2015). Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation. Molecular Neurodegeneration. 10(1). 41–41. 90 indexed citations
14.
Whiffin, Nicola, Peter Broderick, Steven Lubbe, et al.. (2011). MLH1-93G > A is a risk factor for MSI colorectal cancer. Carcinogenesis. 32(8). 1157–1161. 34 indexed citations
15.
Lubbe, Steven, Nicola Whiffin, Ian Chandler, Peter Broderick, & Richard S. Houlston. (2011). Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients. Carcinogenesis. 33(1). 108–112. 21 indexed citations
16.
Lubbe, Steven, Alan Pittman, Philip Twiss, et al.. (2010). Evaluation of germline BMP4 mutation as a cause of colorectal cancer. Human Mutation. 32(1). E1928–E1938. 27 indexed citations
17.
Lubbe, Steven, Maria Chiara Di Bernardo, Ian Chandler, & Richard S. Houlston. (2009). Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation. Journal of Clinical Oncology. 27(24). 3975–3980. 146 indexed citations
18.
Ramsay, Michèle, Zané Lombard, Robyn Labrum, et al.. (2009). Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals. Journal of Dermatological Science. 54(3). 198–204. 8 indexed citations
19.
Pittman, Alan, Philip Twiss, Peter Broderick, et al.. (2009). The CDH1‐160C>A polymorphism is a risk factor for colorectal cancer. International Journal of Cancer. 125(7). 1622–1625. 18 indexed citations
20.
Lubbe, Steven, Mohammed Tikly, Lize van der Merwe, Bridget Hodkinson, & Michèle Ramsay. (2008). Interleukin-1 receptor antagonist gene polymorphisms are associated with disease severity in Black South Africans with rheumatoid arthritis. Joint Bone Spine. 75(4). 422–425. 11 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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