Stephen Lynn

1.2k total citations
24 papers, 692 citations indexed

About

Stephen Lynn is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Stephen Lynn has authored 24 papers receiving a total of 692 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Surgery. Recurrent topics in Stephen Lynn's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Ion channel regulation and function (5 papers). Stephen Lynn is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Ion channel regulation and function (5 papers). Stephen Lynn collaborates with scholars based in United Kingdom, United States and France. Stephen Lynn's co-authors include Douglass M. Turnbull, Mark Walker, James Gillespie, Patrick F. Chinnery, Volker Straub, Kate Bushby, Timothy M. Frayling, Julie Evans, Sandra L. Jackson and Stephen J. Yeaman and has published in prestigious journals such as The Lancet, Diabetes and Annals of Neurology.

In The Last Decade

Stephen Lynn

23 papers receiving 675 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen Lynn United Kingdom 17 462 132 123 119 94 24 692
Morad Khayat Israel 16 422 0.9× 115 0.9× 37 0.3× 38 0.3× 162 1.7× 50 664
Hamad Alzaidan Saudi Arabia 14 283 0.6× 132 1.0× 67 0.5× 55 0.5× 173 1.8× 39 578
Jiddeke M. van de Kamp Netherlands 15 222 0.5× 126 1.0× 148 1.2× 182 1.5× 196 2.1× 24 786
Nouriya Al‐Sannaa Saudi Arabia 13 290 0.6× 96 0.7× 67 0.5× 154 1.3× 150 1.6× 27 611
Argirios Dinopoulos Greece 14 410 0.9× 142 1.1× 101 0.8× 349 2.9× 111 1.2× 43 998
Moeenaldeen AlSayed Saudi Arabia 15 254 0.5× 86 0.7× 40 0.3× 333 2.8× 183 1.9× 49 737
Marcello Niceta Italy 18 489 1.1× 36 0.3× 60 0.5× 46 0.4× 304 3.2× 53 810
Hui Xiong China 17 652 1.4× 130 1.0× 121 1.0× 75 0.6× 97 1.0× 116 1.0k
Almundher Al‐Maawali Oman 14 312 0.7× 57 0.4× 29 0.2× 41 0.3× 142 1.5× 55 605
Junko Kanno Japan 12 264 0.6× 99 0.8× 39 0.3× 36 0.3× 188 2.0× 33 850

Countries citing papers authored by Stephen Lynn

Since Specialization
Citations

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

Fields of papers citing papers by Stephen Lynn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephen Lynn

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen Lynn. A scholar is included among the top collaborators of Stephen Lynn 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 Lynn. Stephen Lynn 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.
Lynn, Stephen, et al.. (2017). How the EUCERD Joint Action supported initiatives on Rare Diseases. European Journal of Medical Genetics. 60(3). 185–189. 7 indexed citations
2.
Evangelista, Teresinha, António Atalaia, Matt Johnson, et al.. (2016). The context for the thematic grouping of rare diseases to facilitate the establishment of European Reference Networks. Orphanet Journal of Rare Diseases. 11(1). 17–17. 25 indexed citations
3.
Aartsma‐Rus, Annemieke, Janbernd Kirschner, Anna Kole, et al.. (2015). TREAT-NMD (translational research in Europe, assessment and treatment for neuromuscular disorders). Neuromuscular Disorders. 25. S271–S271.
4.
Lynn, Stephen, Annemieke Aartsma‐Rus, Kate Bushby, et al.. (2014). Measuring clinical effectiveness of medicinal products for the treatment of Duchenne muscular dystrophy. Neuromuscular Disorders. 25(1). 96–105. 31 indexed citations
5.
Bushby, Kate, Hanns Lochmüller, Stephen Lynn, & Volker Straub. (2009). Interventions for muscular dystrophy: molecular medicines entering the clinic. The Lancet. 374(9704). 1849–1856. 29 indexed citations
6.
Cree, Lynsey, Sheila K. Patel, Angela Pyle, et al.. (2008). Age-related decline in mitochondrial DNA copy number in isolated human pancreatic islets. Diabetologia. 51(8). 1440–1443. 71 indexed citations
7.
Cloke, David, et al.. (2005). A comparison of functional, patient-based scores in subacromial impingement. Journal of Shoulder and Elbow Surgery. 14(4). 380–384. 51 indexed citations
8.
Lynn, Stephen, Eric J. Huang, Sailaja Elchuri, et al.. (2005). Selective neuronal vulnerability and inadequate stress response in superoxide dismutase mutant mice. Free Radical Biology and Medicine. 38(6). 817–828. 26 indexed citations
9.
McFarland, Robert, Andrew M. Schaefer, Stephen Lynn, et al.. (2004). Familial myopathy: New insights into the T14709C mitochondrial tRNA mutation. Annals of Neurology. 55(4). 478–484. 51 indexed citations
10.
Lynn, Stephen, Gillian M. Borthwick, Richard Charnley, Mark Walker, & Douglass M. Turnbull. (2003). Heteroplasmic ratio of the A3243G mitochondrial DNA mutation in single pancreatic beta cells. Diabetologia. 46(2). 296–299. 39 indexed citations
11.
Lynn, Stephen, Julie Evans, Chris White, et al.. (2002). Variation in the Calpain-10 Gene Affects Blood Glucose Levels in the British Population. Diabetes. 51(1). 247–250. 67 indexed citations
12.
Frayling, Timothy M., Mark Walker, Mark I. McCarthy, et al.. (1999). Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.. Diabetes. 48(12). 2475–2479. 42 indexed citations
13.
14.
15.
Lynn, Stephen, et al.. (1993). A novel ryanodine sensitive calcium release mechanism in cultured human myometrial smooth‐muscle cells. FEBS Letters. 330(2). 227–230. 33 indexed citations
16.
Goodacre, John, et al.. (1993). Human cartilage aggrecan CS1 region contains cryptic T-cell recognition sites.. PubMed. 78(4). 586–91. 14 indexed citations
17.
Morgan, JM, et al.. (1993). Measurements of intracellular Ca2+ in cultured human myometrial smooth muscle cells bathed in low Na+ solutions. Experimental Physiology. 78(5). 711–714. 5 indexed citations
18.
Lynn, Stephen, et al.. (1993). The induction of intracellular calcium acitivity in cultured human myometrial smooth muscle cells. Biochimica et Biophysica Acta (BBA) - General Subjects. 1158(1). 98–102. 8 indexed citations
19.
Pearson, Jeffrey P., Adrian Blackburn, Stephen Lynn, Adrian Allen, & Norman B. Roberts. (1992). HUMAN PEPSIN 1, A COMPLEX OF PROTEOGLYCAN AND PROTEIN. Biochemical Society Transactions. 20(4). 356S–356S. 1 indexed citations
20.
Goodacre, John, et al.. (1991). Comparative analysis of murine T lymphocyte responses to cartilage proteoglycans. Journal of Autoimmunity. 4(5). 743–753. 1 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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