A. Stephenson

1.1k total citations
29 papers, 827 citations indexed

About

A. Stephenson is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Cell Biology. According to data from OpenAlex, A. Stephenson has authored 29 papers receiving a total of 827 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 6 papers in Cell Biology. Recurrent topics in A. Stephenson's work include Thyroid Disorders and Treatments (6 papers), Skin and Cellular Biology Research (5 papers) and Hair Growth and Disorders (4 papers). A. Stephenson is often cited by papers focused on Thyroid Disorders and Treatments (6 papers), Skin and Cellular Biology Research (5 papers) and Hair Growth and Disorders (4 papers). A. Stephenson collaborates with scholars based in United Kingdom, United States and France. A. Stephenson's co-authors include P. Kendall‐Taylor, Jonathan L. Rees, D. F. Roberts, C.S. Munro, Rumaisa Bashir, Colin S. Munro, A L Crombie, E. T. Young, Tom Strachan and Eugene Healy and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Human Molecular Genetics.

In The Last Decade

A. Stephenson

28 papers receiving 794 citations

Peers

A. Stephenson

GENET

EDM

PFM

Björn E. Wenzel Germany

Olov Ekwall Sweden

Fulvia Baldinotti Italy

Cynthia S. Cook United States

Natalia A. Veniaminova United States

H Fujii Japan

M A Berman United States

Chiara Di Bella Italy

Anne Polvi Finland

G Gheri Italy

Björn E. Wenzel Germany

A. Stephenson

158 ×0.5

117 ×0.5

GENET

181 ×0.9

EDM

126 ×0.7

55 ×0.5

PFM

Citations per year, relative to A. Stephenson A. Stephenson (= 1×) peers Björn E. Wenzel

Countries citing papers authored by A. Stephenson

Since Specialization

Citations

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

Fields of papers citing papers by A. Stephenson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Stephenson

This figure shows the co-authorship network connecting the top 25 collaborators of A. Stephenson. A scholar is included among the top collaborators of A. Stephenson 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 A. Stephenson. A. Stephenson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sykes, Jenna, et al.. (2024). 863 The changing transplant landscape in the era of elexacaftor/tezacaftor/ivacaftor: a word of caution. Journal of Cystic Fibrosis. 23. S500–S500. 1 indexed citations

Li, Weili, Lei Sun, Mary Corey, et al.. (2010). Understanding the population structure of North American patients with cystic fibrosis. Clinical Genetics. 79(2). 136–146. 18 indexed citations

Goldstein, E., et al.. (2001). A genetic analysis of the cytological region 46C-F containing the Drosophila melanogaster homolog of the jun proto-oncogene. Molecular Genetics and Genomics. 266(4). 695–700. 12 indexed citations

Korge, Bernhard, Akemi Ishida‐Yamamoto, P. J. Dopping-Hepenstal, et al.. (1997). Loricrin Mutation in Vohwinkel’s Keratoderma Is Unique to the Variant with Ichthyosis. Journal of Investigative Dermatology. 109(4). 604–610. 80 indexed citations

Birch‐Machin, Mark A., Eugene Healy, Richard Turner, et al.. (1997). Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity. British Journal of Dermatology. 137(3). 339–343. 16 indexed citations

Blackwood, Douglas, W.J. Muir, A. Stephenson, et al.. (1996). Reduced expression of HLA-B35 in schizophrenia. Psychiatric Genetics. 6(2). 51–60. 18 indexed citations

Healy, Eugene, et al.. (1995). A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13. Human Molecular Genetics. 4(12). 2399–2402. 44 indexed citations

Passos-Bueno, Maria-Rita, Eloísa S. Moreira, Mariz Vainzof, et al.. (1995). Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region. Genomics. 27(1). 192–195. 31 indexed citations

Lindsay, Susan, et al.. (1993). Isolation and Characterization of Three Microsatellite Markers in the Proximal Long Arm of the Human X Chromosome. Genomics. 17(1). 208–210. 4 indexed citations

10.

Inglehearn, Chris F., Simon Carter, Janet C. Lindsey, et al.. (1993). A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nature Genetics. 4(1). 51–53. 69 indexed citations

11.

Bashir, Rumaisa, et al.. (1993). Localisation of a gene for Darier's disease. Human Molecular Genetics. 2(11). 1937–1939. 54 indexed citations

12.

Stephenson, A., et al.. (1993). Linkage studies of hla and primary sjögren's syndrome in multicase families. Arthritis & Rheumatism. 36(4). 473–484. 18 indexed citations

13.

Bashir, R., C.F. Inglehearn, T J Keen, et al.. (1992). Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP. Genomics. 14(1). 191–193. 4 indexed citations

14.

Phillips, David, Sandra M. McLachlan, A. Stephenson, et al.. (1990). Autosomal Dominant Transmission of Autoantibodies to Thyroglobulin and Thyroid Peroxidase*. The Journal of Clinical Endocrinology & Metabolism. 70(3). 742–746. 54 indexed citations

15.

Kendall‐Taylor, P., et al.. (1988). Intravenous methylprednisolone in the treatment of Graves' ophthalmopathy.. BMJ. 297(6663). 1574–1578. 71 indexed citations

16.

Young, E. T., et al.. (1988). Prediction of remission after antithyroid drug treatment in Graves' disease.. PubMed. 66(250). 175–89. 46 indexed citations

17.

Kendall‐Taylor, P., et al.. (1988). DIFFERENTIATION OF AUTOIMMUNE OPHTHALMOPATHY FROM GRAVES’HYPERTHYROIDISM BY ANALYSIS OF GENETIC MARKERS. Clinical Endocrinology. 28(6). 601–610. 35 indexed citations

18.

Connell, John W., William J. Black, Thomas H. Kawula, et al.. (1988). Recombination among Protein II genes of Neisseria gonorrhoeae generates new coding sequences and increases structural variability in the Protein II family. Molecular Microbiology. 2(2). 227–236. 95 indexed citations

19.

Walker, David, John Burn, I D Griffiths, D. F. Roberts, & A. Stephenson. (1987). Linkage studies of hla and rheumatoid arthritis in multicase families. Arthritis & Rheumatism. 30(1). 31–35. 20 indexed citations

20.

Walker, David, A. Stephenson, I D Griffiths, D. F. Roberts, & D. C. Rao. (1987). Classification of rheumatoid arthritis: The importance of including data from the siblings. Genetic Epidemiology. 4(4). 249–253. 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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