Stephanie Barton

2.9k total citations · 1 hit paper
26 papers, 1.9k citations indexed

About

Stephanie Barton is a scholar working on Molecular Biology, Genetics and Immunology and Allergy. According to data from OpenAlex, Stephanie Barton has authored 26 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Immunology and Allergy. Recurrent topics in Stephanie Barton's work include Retinal Development and Disorders (11 papers), Cell Adhesion Molecules Research (7 papers) and Retinal Diseases and Treatments (6 papers). Stephanie Barton is often cited by papers focused on Retinal Development and Disorders (11 papers), Cell Adhesion Molecules Research (7 papers) and Retinal Diseases and Treatments (6 papers). Stephanie Barton collaborates with scholars based in United Kingdom, United States and Finland. Stephanie Barton's co-authors include A. Paul Mould, Martin J. Humphries, Susan E. Craig, Janet A. Askari, Kent M. Samuelson, John F. Carlquist, Scott M. Stevens, Joseph B. Muhlestein, Jeffrey L. Anderson and Paul McEwan and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and Biochemical Journal.

In The Last Decade

Stephanie Barton

26 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Randomized Trial of Genotype-Guided Versus Standard Warfarin Dosing in Patients Initiating Oral Anticoagulation

2007 545 citations Jeffrey L. Anderson, Benjamin D. Horne et al. Circulation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephanie Barton United Kingdom	18	804	482	480	359	265	26	1.9k
Karl Welzenbach Switzerland	15	586 0.7×	353 0.7×	31 0.1×	44 0.1×	101 0.4×	18	1.7k
Jun Katada Japan	20	481 0.6×	67 0.1×	49 0.1×	81 0.2×	286 1.1×	36	1.3k
Clifford Stephan United States	21	949 1.2×	31 0.1×	23 0.0×	70 0.2×	206 0.8×	65	1.9k
Yoshino Matsuo Japan	24	735 0.9×	109 0.2×	34 0.1×	39 0.1×	550 2.1×	65	1.6k
Toshihiko Nagasawa Japan	23	439 0.5×	67 0.1×	23 0.0×	67 0.2×	55 0.2×	98	1.4k
Christophe Schmitt Switzerland	28	597 0.7×	27 0.1×	341 0.7×	105 0.3×	55 0.2×	73	3.8k
Cinzia Ciccacci Italy	25	492 0.6×	10 0.0×	215 0.4×	160 0.4×	111 0.4×	78	1.6k
Jianming Liu China	20	675 0.8×	39 0.1×	84 0.2×	61 0.2×	118 0.4×	81	1.4k
David Austin United Kingdom	19	774 1.0×	19 0.0×	28 0.1×	92 0.3×	162 0.6×	77	1.6k
Sonia Lamontagne Canada	19	525 0.7×	93 0.2×	25 0.1×	120 0.3×	64 0.2×	22	1.3k

Countries citing papers authored by Stephanie Barton

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie Barton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Barton

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Barton. A scholar is included among the top collaborators of Stephanie Barton 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 Stephanie Barton. Stephanie Barton 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

Stępień, Karolina M., Christopher Campbell, Stephanie Barton, et al.. (2023). Clinical, biochemical and molecular analysis in a cohort of individuals with gyrate atrophy. Orphanet Journal of Rare Diseases. 18(1). 265–265. 6 indexed citations

Sergouniotis, Panagiotis I., Stephanie Barton, Simon Ramsden, et al.. (2020). Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar. European Journal of Human Genetics. 28(9). 1274–1282. 15 indexed citations

Taylor, Rachel L., Eva Lenassi, Jill Smith, et al.. (2019). Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease. European Journal of Human Genetics. 28(5). 576–586. 20 indexed citations

Avela, Kristiina, et al.. (2019). The genetic aetiology of retinal degeneration in children in Finland – new founder mutations identified. Acta Ophthalmologica. 97(8). 805–814. 14 indexed citations

Banka, Siddharth, Catherine Breen, Stephanie Barton, et al.. (2019). Genotype–phenotype specificity in Menke–Hennekam syndrome caused by missense variants in exon 30 or 31 of CREBBP. American Journal of Medical Genetics Part A. 179(6). 1058–1062. 16 indexed citations

Moss, Joanna, Morad Ansari, Stephanie Barton, et al.. (2017). Genotype–phenotype correlations in Cornelia de Lange syndrome: Behavioral characteristics and changes with age. American Journal of Medical Genetics Part A. 173(6). 1566–1574. 18 indexed citations

Taylor, Rachel L., Neil R. A. Parry, Stephanie Barton, et al.. (2017). Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal Disease. Ophthalmology. 124(7). 985–991. 46 indexed citations

Ellingford, Jamie M., Christopher Campbell, Stephanie Barton, et al.. (2017). Validation of copy number variation analysis for next-generation sequencing diagnostics. European Journal of Human Genetics. 25(6). 719–724. 64 indexed citations

Avela, Kristiina, Eeva‐Marja Sankila, Sanna Seitsonen, et al.. (2017). A founder mutation in CERKL is a major cause of retinal dystrophy in Finland. Acta Ophthalmologica. 96(2). 183–191. 23 indexed citations

10.

Ellingford, Jamie M., Stephanie Barton, Sanjeev S. Bhaskar, et al.. (2016). Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. Ophthalmology. 123(5). 1143–1150. 93 indexed citations

11.

Rose, Anna M., Panagiotis I. Sergouniotis, Giovanna Alfano, et al.. (2015). Diverse clinical phenotypes associated with a nonsense mutation in FAM161A. Eye. 29(9). 1226–1232. 9 indexed citations

12.

Ramsden, Simon, Anna O’Grady, Tracy Fletcher, et al.. (2013). A clinical molecular genetic service for United Kingdom families with choroideraemia. European Journal of Medical Genetics. 56(8). 432–438. 16 indexed citations

13.

Anderson, Jeffrey L., Benjamin D. Horne, Scott M. Stevens, et al.. (2007). Randomized Trial of Genotype-Guided Versus Standard Warfarin Dosing in Patients Initiating Oral Anticoagulation. Circulation. 116(22). 2563–2570. 545 indexed citations breakdown →

14.

Tompson, Stuart W., Víctor L. Ruiz‐Pérez, Helen J. Blair, et al.. (2006). Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients. Human Genetics. 120(5). 663–670. 83 indexed citations

15.

Mould, A. Paul, Mark A. Travis, Stephanie Barton, et al.. (2004). Evidence That Monoclonal Antibodies Directed against the Integrin β Subunit Plexin/Semaphorin/Integrin Domain Stimulate Function by Inducing Receptor Extension. Journal of Biological Chemistry. 280(6). 4238–4246. 46 indexed citations

16.

Mould, A. Paul, Stephanie Barton, Janet A. Askari, et al.. (2003). Conformational Changes in the Integrin औA Domain Provide a Mechanism for Signal Transduction via Hybrid Domain Movement. Journal of Biological Chemistry. 278(19). 17028–17035. 104 indexed citations

17.

Mould, A. Paul, Stephanie Barton, Janet A. Askari, Susan E. Craig, & Martin J. Humphries. (2003). Role of ADMIDAS Cation-binding Site in Ligand Recognition by Integrin α5β1. Journal of Biological Chemistry. 278(51). 51622–51629. 72 indexed citations

18.

Mould, A. Paul, Patrick A. Buckley, J. Günter Grossmann, et al.. (2003). Structure of an Integrin-Ligand Complex Deduced from Solution X-ray Scattering and Site-directed Mutagenesis. Journal of Biological Chemistry. 278(41). 39993–39999. 90 indexed citations

19.

Humphries, Martin J., Paul McEwan, Stephanie Barton, et al.. (2003). Integrin structure: heady advances in ligand binding, but activation still makes the knees wobble. Trends in Biochemical Sciences. 28(6). 313–320. 104 indexed citations

20.

Mould, A. Paul, Janet A. Askari, Stephanie Barton, et al.. (2002). Integrin Activation Involves a Conformational Change in the α1 Helix of the β Subunit A-domain. Journal of Biological Chemistry. 277(22). 19800–19805. 113 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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