Alison J. Hardcastle
Researcher · Biochemistry, Genetics and Molecular Biology
Source-listed associations: UK Biobank; University College London
United Kingdom
Alison J. Hardcastle has indexed research in Biochemistry, Genetics and Molecular Biology. Research topics in the source record include Retinal Development and Disorders, Corneal surgery and disorders, Retinal Diseases and Treatments.
Read biography ↓Biography, research & contributions
Alison J. Hardcastle has indexed research in Biochemistry, Genetics and Molecular Biology. Research topics in the source record include Retinal Development and Disorders, Corneal surgery and disorders, Retinal Diseases and Treatments.
Research and publications
The selected publications below appear in both the public ORCID record and the OpenAlex author record. The list is a subset of the researcher’s work.
Institutional record
OpenAlex lists UK Biobank; University College London among its last-known institutional associations. These records do not confirm a current appointment.
Identity and source coverage
The public ORCID name and at least one education or employment institution were matched with the OpenAlex record on 2026-10-03. Publication identifiers were also compared between the two sources. Positions, education, honors and portrait are included only when separately documented.
At a glance
- Full name
- Alison J. Hardcastle
- Alternative names
- A HARDCASTLE A J Hardcastle A. Hardcastle A. J Hardcastle A. J. HARDCASTLE A. J. Hardcastle A.J. Hardcastle ALISON J. HARDCASTLE Alison Hardcastle Alison J Hardcastle
- Fields
- Biochemistry, Genetics and Molecular Biology
- ORCID
- 0000-0002-0038-6770
- OpenAlex ID
- A5068050684
Research interests
- Retinal Development and Disorders
- Corneal surgery and disorders
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
- Corneal Surgery and Treatments
Research topics
Education
Not yet documented in this profile.
Selected research & further reading
A curated reading list, not a ranking by citation count. References use DOI metadata, matching public scholarly records or authoritative lecture sources.
- The pathogenesis of keratoconus ↗2013 · EyeDOI: 10.1038/eye.2013.278
- The cone dysfunction syndromes: Table 1 ↗2015 · British Journal of OphthalmologyDOI: 10.1136/bjophthalmol-2014-306505
- Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups ↗2016 · Cell stem cellDOI: 10.1016/j.stem.2016.03.021
- The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein ↗2000 · Nature GeneticsDOI: 10.1038/81627
- Progressive Cone and Cone-Rod Dystrophies: Phenotypes and Underlying Molecular Genetic Basis ↗2006 · Survey of OphthalmologyDOI: 10.1016/j.survophthal.2006.02.007
Citation & publication trends
Annual source counts; separate scales. OpenAlex coverage may be incomplete for historical researchers.
View exact annual counts
| Year | Publications | Citations |
|---|---|---|
| 1988 | 1 | 1 |
| 1990 | 1 | 10 |
| 1993 | 1 | 76 |
| 1994 | 3 | 49 |
| 1995 | 4 | 31 |
| 1996 | 2 | 32 |
| 1997 | 3 | 19 |
| 1999 | 9 | 234 |
| 2000 | 7 | 377 |
| 2001 | 7 | 133 |
| 2002 | 7 | 328 |
| 2003 | 10 | 314 |
| 2004 | 7 | 139 |
| 2005 | 15 | 300 |
| 2006 | 7 | 271 |
| 2007 | 5 | 275 |
| 2008 | 6 | 9 |
| 2009 | 4 | 168 |
| 2010 | 4 | 291 |
| 2011 | 4 | 45 |
| 2012 | 9 | 455 |
| 2013 | 8 | 654 |
| 2014 | 12 | 302 |
| 2015 | 9 | 589 |
| 2016 | 17 | 635 |
| 2017 | 13 | 416 |
| 2018 | 10 | 234 |
| 2019 | 19 | 618 |
| 2020 | 8 | 476 |
| 2021 | 11 | 774 |
| 2022 | 10 | 238 |
| 2023 | 9 | 1204 |
| 2024 | 12 | 80 |
| 2025 | 9 | 107 |
| 2026 | 6 | 18 |
Source: OpenAlex · Retrieved 2026-10-03T06:38:09+00:00. Metrics are database-specific and are not a scientific ranking.
Most-cited linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- The pathogenesis of keratoconus ↗2013-12-20 · Eye374OpenAlex citations
- The cone dysfunction syndromes: Table 1 ↗2015-03-13 · British Journal of Ophthalmology320OpenAlex citations
- 311OpenAlex citations
- 265OpenAlex citations
- Progressive Cone and Cone-Rod Dystrophies: Phenotypes and Underlying Molecular Genetic Basis ↗2006-05-01 · Survey of Ophthalmology233OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus ↗2021-03-01 · Communications Biology
- Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa ↗2020-10-05 · The American Journal of Human Genetics
- Modeling and Rescue of RP2 Retinitis Pigmentosa Using iPSC-Derived Retinal Organoids ↗2020-06-11 · Stem Cell Reports
- Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity ↗2018-03-08 · The American Journal of Human Genetics
Journals published in
- British Journal of Ophthalmology
- Cell Stem Cell
- Communications Biology
- Genomics
- Human Gene Therapy
- Human Molecular Genetics
- Investigative Ophthalmology & Visual Science
- Journal of Medical Genetics
- Nature Genetics
- Stem Cell Reports
- Survey of Ophthalmology
Related publishers
Institutions
Current verified institution
No verified record links added yet.
Previous institutions
No verified record links added yet.
Awards & honors
Not yet documented in this profile.
Career timeline
Not yet documented in this profile.
Co-authors
No verified record links added yet.
Education & career institution links
No verified record links added yet.
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Sign in to claim this profileSources & data information
Editorial review: Pending review · Last data update: 2026-10-03T08:16:47+00:00
Automated identity and publication-source comparison: 2026-10-03T07:04:40+00:00. This is separate from manual editorial review and profile ownership.
Unknown values are left blank. Linked publications may be a subset of total works. Identity verification, data retrieval and profile ownership are separate checks.