Stephanie Halford

4.7k total citations · 1 hit paper
75 papers, 3.3k citations indexed

About

Stephanie Halford is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Stephanie Halford has authored 75 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 16 papers in Ophthalmology and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in Stephanie Halford's work include Retinal Development and Disorders (29 papers), Retinal Diseases and Treatments (16 papers) and Circadian rhythm and melatonin (11 papers). Stephanie Halford is often cited by papers focused on Retinal Development and Disorders (29 papers), Retinal Diseases and Treatments (16 papers) and Circadian rhythm and melatonin (11 papers). Stephanie Halford collaborates with scholars based in United Kingdom, United States and Spain. Stephanie Halford's co-authors include F. Foster, Stuart N. Peirson, Peter Scambler, Mark I. McCarthy, Timothy M. Frayling, Katharine R. Owen, G. A. Hitman, Andrew T. Hattersley, Suzanne Broadgate and J Lévy and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Stephanie Halford

72 papers receiving 3.2k citations

Hit Papers

Large-Scale Association Studies of Variants in Genes Enco... 2003 2026 2010 2018 2003 100 200 300 400 500
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.

  1. Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) Confirm That the KCNJ11 E23K Variant Is Associated With Type 2 Diabetes
    2003 538 citations Stephanie Halford, Mark I. McCarthy et al. profile →

Peers

Stephanie Halford
J. Paul Chapple United Kingdom
Christian Becker Germany
Flora de Pablo Spain
Robert J. McEvilly United States
Anne Gansmüller France
Anna B. Auerbach United States
Juan Pedro Martı́nez-Barberá United Kingdom
Jesús M. Grondona Spain
Gerald M. Kidder Canada
Bernd Wollnik Germany
J. Paul Chapple United Kingdom
Stephanie Halford
Citations per year, relative to Stephanie Halford Stephanie Halford (= 1×) peers J. Paul Chapple

Countries citing papers authored by Stephanie Halford

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie Halford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Halford

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Halford. A scholar is included among the top collaborators of Stephanie Halford 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 Halford. Stephanie Halford 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.
2.
Pearce, Elizabeth, Sobha Sivaprasad, Suzanne Broadgate, et al.. (2023). Intraretinal Microvascular Abnormalities and Venous Beading Have Different Genetic Profiles in Caucasian Patients with Non-Proliferative Diabetic Retinopathy. Vision. 7(1). 18–18. 1 indexed citations
3.
Shah, Mital, Suzanne Broadgate, Morag Shanks, et al.. (2022). Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes. Genes. 13(8). 1423–1423. 5 indexed citations
4.
Broadgate, Suzanne, et al.. (2021). Whole genome sequencing in a Knobloch syndrome family confirms the molecular diagnosis. Ophthalmic Genetics. 43(2). 201–209.
5.
Broadgate, Suzanne, et al.. (2021). An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story. Genes. 12(8). 1241–1241. 38 indexed citations
6.
Hudspith, K, Suzanne Broadgate, Morag Shanks, et al.. (2021). Targeted next generation sequencing and family survey enable correct genetic diagnosis in CRX associated macular dystrophy – a case report. BMC Ophthalmology. 21(1). 168–168. 3 indexed citations
7.
Downes, Susan M., Vicky Tai, Suzanne Broadgate, et al.. (2020). Genetic and Clinical Findings in an Ethnically Diverse Cohort with Retinitis Pigmentosa Associated with Pathogenic Variants in CERKL. Genes. 11(12). 1497–1497. 6 indexed citations
8.
Broadgate, Suzanne, Stephanie Halford, Jasleen K. Jolly, et al.. (2020). Novel Pathogenic Sequence Variants in NR2E3 and Clinical Findings in Three Patients. Genes. 11(11). 1288–1288. 7 indexed citations
9.
Broadgate, Suzanne, Stephanie Halford, Robert E. MacLaren, et al.. (2020). “Genetic and clinical findings in an ethnically diverse retinitis pigmentosa cohort associated with pathogenic variants in EYS”. Eye. 35(5). 1440–1449. 7 indexed citations
10.
11.
Broadgate, Suzanne, Christine A. Kiire, Stephanie Halford, & Victor Chong. (2018). Diabetic macular oedema: under‐represented in the genetic analysis of diabetic retinopathy. Acta Ophthalmologica. 96(A111). 1–51. 10 indexed citations
12.
Kiire, Christine A., Suzanne Broadgate, Stephanie Halford, & Victor Chong. (2014). Diabetic macular edema with foveal eversion shows a distinct cytokine profile to other forms of diabetic macular edema in patients with type 2 diabetes. Investigative Ophthalmology & Visual Science. 55(13). 4408–4408. 5 indexed citations
13.
Parkinson, James R.C., Céline Charon, Barbara S. Baker, et al.. (2004). Variation at the IRF2 Gene and Susceptibility to Psoriasis in Chromosome 4q-Linked Families. Journal of Investigative Dermatology. 122(3). 640–643. 6 indexed citations
14.
Halford, Stephanie, James Bellingham, Louise Ocaka, et al.. (2001). Assignment<footref rid="foot01"><sup>1</sup></footref> of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybrids. Cytogenetic and Genome Research. 95(3-4). 234–235. 9 indexed citations
15.
Halford, Stephanie, et al.. (2001). Molecular basis of cone dystrophy associated with protanopia.. Investigative Ophthalmology & Visual Science. 42. 1 indexed citations
16.
Winton, Helen L., et al.. (2000). Genetically engineered human retinal pigment epithelial cells for intraocular transplantation therapy.. Bristol Research (University of Bristol). 2 indexed citations
17.
Halford, Stephanie, et al.. (2000). Characterization of the Human NMO-1 gene at 1q43 and genomic organisation of the region. NMO-1.. The American Journal of Human Genetics. 67. 187–187. 1 indexed citations
18.
Halford, Stephanie, et al.. (1993). Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11. Human Molecular Genetics. 2(2). 191–196. 66 indexed citations
19.
Lindsay, Elizabeth A., Stephanie Halford, Roy Wadey, Peter Scambler, & Antonio Baldini. (1993). Molecular Cytogenetic Characterization of the DiGeorge Syndrome Region Using Fluorescence in Situ Hybridization. Genomics. 17(2). 403–407. 71 indexed citations
20.
Scambler, Peter, Stephanie Halford, R Wadey, et al.. (1991). MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES. UCL Discovery (University College London). 4 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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