Jamie E. Craig

24.2k total citations
311 papers, 8.7k citations indexed

About

Jamie E. Craig is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Molecular Biology. According to data from OpenAlex, Jamie E. Craig has authored 311 papers receiving a total of 8.7k indexed citations (citations by other indexed papers that have themselves been cited), including 209 papers in Ophthalmology, 112 papers in Radiology, Nuclear Medicine and Imaging and 92 papers in Molecular Biology. Recurrent topics in Jamie E. Craig's work include Glaucoma and retinal disorders (169 papers), Retinal Diseases and Treatments (124 papers) and Corneal surgery and disorders (53 papers). Jamie E. Craig is often cited by papers focused on Glaucoma and retinal disorders (169 papers), Retinal Diseases and Treatments (124 papers) and Corneal surgery and disorders (53 papers). Jamie E. Craig collaborates with scholars based in Australia, United Kingdom and United States. Jamie E. Craig's co-authors include David A. Mackey, Alex W. Hewitt, Kathryn P. Burdon, Shiwani Sharma, John Landers, Richard Mills, David P. Dimasi, Sotoodeh Abhary, Emmanuelle Souzeau and Tim Henderson and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Jamie E. Craig

305 papers receiving 8.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jamie E. Craig Australia 49 5.1k 3.2k 2.7k 1.0k 809 311 8.7k
Richard A. Lewis United States 62 4.9k 1.0× 7.1k 2.2× 2.4k 0.9× 3.9k 3.8× 760 0.9× 255 13.1k
Alexander J. Smith United Kingdom 58 2.0k 0.4× 7.6k 2.4× 1.0k 0.4× 2.0k 1.9× 293 0.4× 150 11.6k
Scott E. Brodie United States 37 2.7k 0.5× 2.0k 0.6× 1.0k 0.4× 241 0.2× 297 0.4× 145 5.8k
Carmen Ayuso Spain 50 1.9k 0.4× 5.7k 1.8× 707 0.3× 2.2k 2.1× 287 0.4× 351 9.0k
Stefan Seregard Sweden 47 4.9k 1.0× 2.5k 0.8× 2.1k 0.8× 217 0.2× 139 0.2× 151 7.2k
David L. Epstein United States 60 6.7k 1.3× 3.4k 1.1× 2.9k 1.1× 336 0.3× 903 1.1× 231 10.0k
Menno van Lookeren Campagne United States 45 1.2k 0.2× 2.6k 0.8× 1.7k 0.6× 296 0.3× 151 0.2× 84 7.4k
Toichiro Kuwabara United States 51 3.4k 0.7× 3.4k 1.1× 1.6k 0.6× 321 0.3× 541 0.7× 182 8.0k
Carel B. Hoyng Netherlands 65 9.5k 1.9× 8.3k 2.6× 4.7k 1.7× 1.4k 1.4× 151 0.2× 327 14.3k
Michael B. Gorin United States 40 2.5k 0.5× 3.0k 0.9× 1.4k 0.5× 781 0.8× 96 0.1× 147 5.5k

Countries citing papers authored by Jamie E. Craig

Since Specialization
Citations

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

Fields of papers citing papers by Jamie E. Craig

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jamie E. Craig. 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 Jamie E. Craig. The network helps show where Jamie E. Craig may publish in the future.

Co-authorship network of co-authors of Jamie E. Craig

This figure shows the co-authorship network connecting the top 25 collaborators of Jamie E. Craig. A scholar is included among the top collaborators of Jamie E. Craig 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 Jamie E. Craig. Jamie E. Craig 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.
Hassall, Mark, et al.. (2025). Development and evaluation of patient-centred polygenic risk score reports for glaucoma screening. BMC Medical Genomics. 18(1). 21–21.
2.
Souzeau, Emmanuelle, et al.. (2025). Progress in Translating Glaucoma Genetics Into the Clinic: A Review. Clinical and Experimental Ophthalmology. 53(3). 246–259. 1 indexed citations
3.
FitzGerald, Liesel M., Bennet J. McComish, Georgia Kaidonis, et al.. (2025). Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic Maculopathy. Investigative Ophthalmology & Visual Science. 66(3). 55–55.
4.
5.
Gharahkhani, Puya, Yeda Wu, Nathan Ingold, et al.. (2023). Study profile: the Genetics of Glaucoma Study. BMJ Open. 13(8). e068811–e068811. 2 indexed citations
6.
Thorp, Jackson G., Sahba Seddighi, Sean Mullany, et al.. (2023). Disentangling the genetic overlap and causal relationships between primary open-angle glaucoma, brain morphology and four major neurodegenerative disorders. EBioMedicine. 92. 104615–104615. 12 indexed citations
7.
White, Sam, Ajay Taranath, Deepa Taranath, et al.. (2023). Neuroimaging Findings in Axenfeld-Rieger Syndrome: A Case Series. American Journal of Neuroradiology. 44(10). 1231–1235. 1 indexed citations
8.
Hassall, Mark, Shari Javadiyan, Sonja Klebe, et al.. (2023). Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse. Scientific Reports. 13(1). 11017–11017. 2 indexed citations
9.
Burdon, Kathryn P., John D. Hulleman, Francesca Pasutto, et al.. (2022). Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel. Human Mutation. 43(12). 2170–2186. 11 indexed citations
10.
Ridge, Bronwyn, et al.. (2022). The Caregiver Experience in Childhood Glaucoma. Ophthalmology Glaucoma. 5(5). 531–543. 5 indexed citations
11.
Siggs, Owen M., Mona S. Awadalla, Emmanuelle Souzeau, et al.. (2020). The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohort. Clinical Genetics. 97(5). 764–769. 19 indexed citations
12.
Han, Xikun, Ayub Qassim, Jiyuan An, et al.. (2019). Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology. Human Molecular Genetics. 28(21). 3680–3690. 16 indexed citations
13.
Kuot, Abraham, Alex W. Hewitt, Grant R. Snibson, et al.. (2017). TGC repeat expansion in the TCF4 gene increases the risk of Fuchs’ endothelial corneal dystrophy in Australian cases. PLoS ONE. 12(8). e0183719–e0183719. 29 indexed citations
14.
Craig, Jamie E., Alex W. Hewitt, Shiwani Sharma, et al.. (2011). Genome Wide Association Study For Open Angle Glaucoma Blindness Identifies Novel Replicated Susceptibility Loci. Investigative Ophthalmology & Visual Science. 52(14). 5317–5317. 1 indexed citations
15.
Green, Catherine, et al.. (2007). How significant is a family history of glaucoma? Experience from the Glaucoma Inheritance Study in Tasmania. Clinical and Experimental Ophthalmology. 35(9). 793–799. 55 indexed citations
16.
Mackey, David A., et al.. (2005). Are Glaucomatous Disc Changes Evident Prior to Diagnosis of Glaucoma in Myocilin Pedigrees. Investigative Ophthalmology & Visual Science. 46(13). 33–33. 1 indexed citations
17.
Charlesworth, Jac, et al.. (2005). Confirmation of the Adult-Onset Primary Open Angle Glaucoma Locus GLC1B at 2cen-q13 in an Australian Family. Ophthalmologica. 220(1). 23–30. 5 indexed citations
18.
Toomes, Carmel, H.M. Bottomley, Richard M. Jackson, et al.. (2004). Mutations in LRP5 or FZD4 underlie the common FEVR locus on chromosome 11q13. Investigative Ophthalmology & Visual Science. 45(13). 1021–1021. 3 indexed citations
19.
Craig, Jamie E., et al.. (2002). Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease. Journal of Medical Genetics. 39. 47–48. 4 indexed citations
20.
Craig, Jamie E., Susan J. Kelly, Rebecca A. Barnetson, & Swee Lay Thein. (1992). Molecular characterization of a novel 10.3 kb deletion causing β‐thalassaemia with unusually high Hb A2. British Journal of Haematology. 82(4). 735–744. 39 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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