Stephen Lynn

1.2k citations

24 papers · 692 indexed · h-index 17

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Sensory Systems top 10%

Papers in ⓘ

Molecular Biology 15
- Ion channel regulation and function 5
- Mitochondrial Function and Pathology 5
- Muscle Physiology and Disorders 3
Clinical Biochemistry 5
- Metabolism and Genetic Disorders 5

Co-authors: Douglass M. Turnbull (7 shared papers)Mark Walker (6 shared papers)James Gillespie (4 shared papers)Patrick F. Chinnery (4 shared papers)Volker Straub (4 shared papers)Kate Bushby (2 shared papers)Lynsey Cree (1 shared paper)Stephen J. Yeaman (1 shared paper)
Journals: Diabetes (5 papers)FEBS Letters (3 papers)Diabetologia (2 papers)Neuromuscular Disorders (2 papers)Orphanet Journal of Rare Diseases (1 paper)
Partner nations: United Kingdom United States France

In The Last Decade

Stephen Lynn

23 papers receiving 675 citations

Peers

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-authors

The 25 scholars most cited alongside Stephen Lynn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stephen Lynn Line = papers co-authored together Stephen Lynn links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Age-related decline in mitochondrial DNA copy number in isolated human pancreatic islets Diabetologia ·Lynsey Cree, Sheila K. Patel, Angela Pyle, Stephen Lynn, Douglass M. Turnbull, Patrick F. Chinnery, Mark Walker	2008	71
2	Variation in the Calpain-10 Gene Affects Blood Glucose Levels in the British Population Diabetes ·Stephen Lynn, Julie Evans, Chris White, Timothy M. Frayling, Andrew T. Hattersley, Douglass M. Turnbull, Yukio Horikawa, Nancy J. Cox, Graeme I. Bell, Mark Walker	2002	67
3	Decreased insulin responsiveness of glucose uptake in cultured human skeletal muscle cells from insulin-resistant nondiabetic relatives of type 2 diabetic families. Diabetes ·Sandra L. Jackson, Stephanie M. Bagstaff, Stephen Lynn, Stephen J. Yeaman, Douglass M. Turnbull, Mark Walker	2000	58
4	A comparison of functional, patient-based scores in subacromial impingement Journal of Shoulder and Elbow Surgery ·David Cloke, Stephen Lynn, Hannah Watson, I Nick Steen, Sarah Purdy, John R. Williams	2005	51
5	Familial myopathy: New insights into the T14709C mitochondrial tRNA mutation Annals of Neurology ·Robert McFarland, Andrew M. Schaefer, Julie L. Gardner, Stephen Lynn, Christine Hayes, Martin Barron, Mark Walker, Patrick F. Chinnery, Robert W. Taylor, Douglass M. Turnbull	2004	51
6	Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes. Diabetes ·Timothy M. Frayling, Mark Walker, Mark I. McCarthy, Julie Evans, Lisa I.S. Allen, Stephen Lynn, Susan Ayres, Barbara A. Millauer, Claire Turner, R. C. Turner, Mike Sampson, G. A. Hitman, Sian Ellard, Andrew T. Hattersley	1999	42
7	Heteroplasmic ratio of the A3243G mitochondrial DNA mutation in single pancreatic beta cells Diabetologia ·Stephen Lynn, Gillian M. Borthwick, Richard Charnley, Mark Walker, Douglass M. Turnbull	2003	39
8	Mitochondrial diabetes: investigation and identification of a novel mutation. Diabetes ·Stephen Lynn, Teressa M. Wardell, Mark Johnson, Patrick F. Chinnery, Mark Daly, Mark S. Walker, Douglass M. Turnbull	1998	36
9	A novel ryanodine sensitive calcium release mechanism in cultured human myometrial smooth‐muscle cells FEBS Letters ·Stephen Lynn, Joanna M. Morgan, James Gillespie, J. R. Greenwell	1993	33
10	Measuring clinical effectiveness of medicinal products for the treatment of Duchenne muscular dystrophy Neuromuscular Disorders ·Stephen Lynn, Annemieke Aartsma‐Rus, Kate Bushby, Pat Furlong, Nathalie Goemans, Annamaria De Luca, Anna Mayhew, Craig M. McDonald, Eugenio Mercuri, Francesco Muntoni, Marita Pohlschmidt, Jan J.G.M. Verschuuren, Thomas Voït, Elizabeth Vroom, Dominic J. Wells, Volker Straub	2014	31
11	Interventions for muscular dystrophy: molecular medicines entering the clinic The Lancet ·Kate Bushby, Hanns Lochmüller, Stephen Lynn, Volker Straub	2009	29
12	Isolation and partial cloning of ryanodine‐sensitive Ca²⁺ release channel protein isoforms from human myometrial smooth muscle FEBS Letters ·Stephen Lynn, Joanna M. Morgan, Heather K. Lamb, Gerhard Meissner, James Gillespie	1995	28
13	Defining the Importance of Mitochondrial Gene Defects in Maternally Inherited Diabetes by Sequencing the Entire Mitochondrial Genome Diabetes ·Alan T.W. Choo-Kang, Stephen Lynn, Geoffrey A. Taylor, Mark Daly, Sarbpreet S. Sihota, Teressa M. Wardell, Patrick F. Chinnery, Douglass M. Turnbull, Mark S. Walker	2002	28
14	Selective neuronal vulnerability and inadequate stress response in superoxide dismutase mutant mice Free Radical Biology and Medicine ·Stephen Lynn, Eric J. Huang, Sailaja Elchuri, Mohammed Naeemuddin, Yumiko Nishinaka, Junji Yodoi, Donna M. Ferriero, Charles J. Epstein, Ting‐Ting Huang	2005	26
15	The context for the thematic grouping of rare diseases to facilitate the establishment of European Reference Networks Orphanet Journal of Rare Diseases ·Teresinha Evangelista, Victoria Hedley, António Atalaia, Matt Johnson, Stephen Lynn, Yann Le Cam, Kate Bushby	2016	25
16	Collaborating to bring new therapies to the patient--the TREAT-NMD model. PubMed ·Kate Bushby, Stephen Lynn, Volker Straub	2009	23
17	Basic properties of a novel ryanodine‐sensitive, caffeine‐insensitive calcium‐induced calcium release mechanism in permeabilised human vascular smooth muscle cells FEBS Letters ·Stephen Lynn, James Gillespie	1995	18
18	Human cartilage aggrecan CS1 region contains cryptic T-cell recognition sites. PubMed ·John Goodacre, Shirley Middleton, Stephen Lynn, David A. Ross, J. R. A. Pearson	1993	14
19	The induction of intracellular calcium acitivity in cultured human myometrial smooth muscle cells Biochimica et Biophysica Acta (BBA) - General Subjects ·Joanna M. Morgan, Stephen Lynn, James Gillespie, J. R. Greenwell	1993	8
20	How the EUCERD Joint Action supported initiatives on Rare Diseases European Journal of Medical Genetics ·Stephen Lynn, Victoria Hedley, António Atalaia, Teresinha Evangelista, Kate Bushby	2017	7

About Stephen Lynn

Stephen Lynn is a scholar working on Molecular Biology, Clinical Biochemistry, Surgery, Cardiology and Cardiovascular Medicine and Physiology, having authored 24 papers that have together received 692 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (5 papers), Ion channel regulation and function (5 papers), Mitochondrial Function and Pathology (5 papers), Adipose Tissue and Metabolism (3 papers), Ion Channels and Receptors (3 papers), Muscle Physiology and Disorders (3 papers), Pancreatic function and diabetes (2 papers) and Cell Adhesion Molecules Research (2 papers). The work is most often cited by research in Clinical Biochemistry (132 citations), Sensory Systems (44 citations), Physiology (32 citations), Molecular Biology (462 citations) and Cell Biology (93 citations). Stephen Lynn has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Douglass M. Turnbull, Mark Walker, James Gillespie, Patrick F. Chinnery, Volker Straub, Kate Bushby, Lynsey Cree, Stephen J. Yeaman, Timothy M. Frayling and Sandra L. Jackson. Their work appears in journals such as Diabetes, FEBS Letters, Diabetologia, Neuromuscular Disorders and Orphanet Journal of Rare Diseases.

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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