Stephen Mullin

1.9k total citations
35 papers, 1.0k citations indexed

About

Stephen Mullin is a scholar working on Neurology, Physiology and Cell Biology. According to data from OpenAlex, Stephen Mullin has authored 35 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Neurology, 12 papers in Physiology and 10 papers in Cell Biology. Recurrent topics in Stephen Mullin's work include Parkinson's Disease Mechanisms and Treatments (14 papers), Lysosomal Storage Disorders Research (11 papers) and Cellular transport and secretion (10 papers). Stephen Mullin is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (14 papers), Lysosomal Storage Disorders Research (11 papers) and Cellular transport and secretion (10 papers). Stephen Mullin collaborates with scholars based in United Kingdom, United States and Italy. Stephen Mullin's co-authors include Anthony H.V. Schapira, Jacob Day, Derralynn Hughes, Atul Mehta, Laura Smith, Fabio Blandini, Jane Simpson, Christos Proukakis, Marco Toffoli and José L. Lanciego and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Stephen Mullin

33 papers receiving 1.0k citations

Peers

Stephen Mullin
Derek Burke United Kingdom
Martha L. Escobar Galvis United States
Patricia García‐Sanz Spain
Saori Odagiri Japan
Eng-King Tan Singapore
Jonathan Janssens Belgium
Alida Spalloni Italy
Sara Bandrés‐Ciga United States
Emilia Gatto Argentina
Matthew J. Benskey United States
Derek Burke United Kingdom
Stephen Mullin
Citations per year, relative to Stephen Mullin Stephen Mullin (= 1×) peers Derek Burke

Countries citing papers authored by Stephen Mullin

Since Specialization
Citations

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

Fields of papers citing papers by Stephen Mullin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephen Mullin

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen Mullin. A scholar is included among the top collaborators of Stephen Mullin 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 Stephen Mullin. Stephen Mullin 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.
Allen, Michael, et al.. (2025). Machine learning to predict stroke risk from routine hospital data: A systematic review. International Journal of Medical Informatics. 196. 105811–105811. 1 indexed citations
2.
Grant, Stephen G., Tom W. Andrew, Stephen Mullin, et al.. (2024). 408 Enhanced melanoma risk stratification by machine learning based on clinicopathologic features. Journal of Investigative Dermatology. 144(12). S298–S298. 1 indexed citations
3.
Toffoli, Marco, Elisa Menozzi, Stephen Mullin, et al.. (2024). Consensus Guidance for Genetic Counseling in GBA1 Variants: A Focus on Parkinson's Disease. Movement Disorders. 39(12). 2144–2154. 3 indexed citations
4.
5.
Toffoli, Marco, Xiaohong Chen, Fritz J. Sedlazeck, et al.. (2022). Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson’s disease-associated GBA gene. Communications Biology. 5(1). 670–670. 17 indexed citations
6.
Toffoli, Marco, et al.. (2021). The Remote Assessment of Parkinsonism Supporting the Ongoing Development of Interventions in Gaucher Disease. Neurodegenerative Disease Management. 11(6). 451–458. 6 indexed citations
7.
8.
Mullin, Stephen, Morten Gersel Stokholm, Derralynn Hughes, et al.. (2020). Brain Microglial Activation Increased in Glucocerebrosidase (GBA) Mutation Carriers without Parkinson's disease. Movement Disorders. 36(3). 774–779. 53 indexed citations
9.
Mullin, Stephen, et al.. (2019). 137 Usability testing of a non-motor symptom app in PD. Journal of Neurology Neurosurgery & Psychiatry. 90(12). e38.3–e38. 1 indexed citations
10.
Avenali, Micol, Marco Toffoli, Stephen Mullin, et al.. (2019). Evolution of prodromal parkinsonian features in a cohort ofGBAmutation-positive individuals: a 6-year longitudinal study. Journal of Neurology Neurosurgery & Psychiatry. 90(10). 1091–1097. 46 indexed citations
11.
Mullin, Stephen, Michelle Beavan, Jonathan P. Bestwick, et al.. (2019). Evolution and clustering of prodromal parkinsonian features in GBA1 carriers. Movement Disorders. 34(9). 1365–1373. 37 indexed citations
12.
Sedlazeck, Fritz J., Marco Toffoli, Stephen Mullin, et al.. (2019). Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinION. Molecular Genetics & Genomic Medicine. 7(3). e564–e564. 51 indexed citations
13.
Smith, Laura, Stephen Mullin, & Anthony H.V. Schapira. (2017). Insights into the structural biology of Gaucher disease. Experimental Neurology. 298(Pt B). 180–190. 60 indexed citations
14.
Arkadir, David, Tama Dinur, Stephen Mullin, et al.. (2016). Trio approach reveals higher risk of PD in carriers of severe vs. mild GBA mutations. Blood Cells Molecules and Diseases. 68. 115–116. 16 indexed citations
15.
Mullin, Stephen & Anthony H.V. Schapira. (2015). The genetics of Parkinson's disease. British Medical Bulletin. 114(1). 39–52. 56 indexed citations
16.
Porcari, Riccardo, Christos Proukakis, Christopher A. Waudby, et al.. (2014). The H50Q Mutation Induces a 10-fold Decrease in the Solubility of α-Synuclein. Journal of Biological Chemistry. 290(4). 2395–2404. 63 indexed citations
17.
Mullin, Stephen, et al.. (2014). Are metacognitive processes associated with posttraumatic stress symptom severity following acquired brain injury?. Disability and Rehabilitation. 37(8). 692–700. 8 indexed citations
18.
19.
Mullin, Stephen & Anthony H.V. Schapira. (2013). α-Synuclein and Mitochondrial Dysfunction in Parkinson’s Disease. Molecular Neurobiology. 47(2). 587–597. 114 indexed citations
20.
Mullin, Stephen, et al.. (2011). High prevalence of distal sensory polyneuropathy in antiretroviral‐treated and untreated people with HIV in Tanzania. Tropical Medicine & International Health. 16(10). 1291–1296. 21 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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