Benjamin M. Nash

450 total citations
17 papers, 200 citations indexed

About

Benjamin M. Nash is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Benjamin M. Nash has authored 17 papers receiving a total of 200 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Ophthalmology and 5 papers in Genetics. Recurrent topics in Benjamin M. Nash's work include Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (7 papers) and CRISPR and Genetic Engineering (3 papers). Benjamin M. Nash is often cited by papers focused on Retinal Development and Disorders (12 papers), Retinal Diseases and Treatments (7 papers) and CRISPR and Genetic Engineering (3 papers). Benjamin M. Nash collaborates with scholars based in Australia, Indonesia and New Zealand. Benjamin M. Nash's co-authors include Dale Wright, Robyn V. Jamieson, John Grigg, Bruce Bennetts, Louise Carey, Marcel E. Dinger, Richard J. Symes, Kristi Jones, Kathryn N. North and Susan Brammah and has published in prestigious journals such as International Journal of Molecular Sciences, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Benjamin M. Nash

17 papers receiving 196 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benjamin M. Nash Australia 7 152 59 39 38 26 17 200
Katherine R. Chao United States 8 120 0.8× 17 0.3× 43 1.1× 45 1.2× 16 0.6× 16 177
Asma Ali Khan Pakistan 9 201 1.3× 23 0.4× 10 0.3× 82 2.2× 6 0.2× 20 275
Phillip Gonzalez Brazil 4 316 2.1× 85 1.4× 11 0.3× 84 2.2× 43 1.7× 8 352
Lucas Fares‐Taie France 8 177 1.2× 32 0.5× 4 0.1× 86 2.3× 16 0.6× 15 238
Orla Galvin United Kingdom 7 147 1.0× 101 1.7× 6 0.2× 31 0.8× 21 0.8× 10 224
Xiao Guo China 10 112 0.7× 101 1.7× 10 0.3× 10 0.3× 22 0.8× 25 273
Lorida Llaci United States 8 95 0.6× 17 0.3× 2 0.1× 25 0.7× 13 0.5× 12 170
James J. O’Byrne Ireland 8 95 0.6× 28 0.5× 2 0.1× 81 2.1× 7 0.3× 24 174
Parimal Rana United States 5 233 1.5× 103 1.7× 9 0.2× 80 2.1× 52 2.0× 18 303
Cristina Skrypnyk Bahrain 8 95 0.6× 7 0.1× 7 0.2× 28 0.7× 6 0.2× 17 155

Countries citing papers authored by Benjamin M. Nash

Since Specialization
Citations

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

Fields of papers citing papers by Benjamin M. Nash

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benjamin M. Nash. 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 Benjamin M. Nash. The network helps show where Benjamin M. Nash may publish in the future.

Co-authorship network of co-authors of Benjamin M. Nash

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

All Works

17 of 17 papers shown
1.
Ma, Alan, et al.. (2025). A Practical Guide to Genetic Eye Conditions for Paediatricians. Journal of Paediatrics and Child Health. 61(10). 1538–1548. 1 indexed citations
2.
Cornish, Elisa E., Vannessa Leung, M. Ali Raza, et al.. (2025). Understanding the phenotype of genetically associated electronegative ERG retinopathies: comparing the full-field ERG b:a ratio. Graefe s Archive for Clinical and Experimental Ophthalmology. 263(8). 2247–2255. 1 indexed citations
3.
Cornish, Elisa E., M. Ali Raza, Lívia S. Carvalho, et al.. (2024). Natural history and biomarkers of KCNV2‐associated retinopathy. Clinical and Experimental Ophthalmology. 52(5). 528–544. 1 indexed citations
4.
Bennetts, Bruce, Artur Darmanian, Luke Jones, et al.. (2023). SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory. Pathology. 55(6). 818–826. 1 indexed citations
5.
Cornish, Elisa E., Clare L. Fraser, Benjamin M. Nash, et al.. (2023). Early recognition of CLN3 disease facilitated by visual electrophysiology and multimodal imaging. Documenta Ophthalmologica. 146(3). 241–256. 4 indexed citations
6.
Jamieson, Robyn V., Elizabeth H Barnes, Benjamin M. Nash, et al.. (2023). A natural history study of autosomal dominant GUCY2D-associated cone–rod dystrophy. Documenta Ophthalmologica. 147(3). 189–201. 2 indexed citations
7.
Cornish, Elisa E., et al.. (2023). IMPDH1 -associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search. Ophthalmic Genetics. 44(5). 437–455. 1 indexed citations
8.
Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations
9.
Ma, Alan, Benjamin M. Nash, John Grigg, et al.. (2022). Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic RPGR Variant Assessment for Therapy Suitability. Journal of Personalized Medicine. 12(3). 502–502. 14 indexed citations
10.
Nash, Benjamin M., Milan Fernando, James P. Robinson, et al.. (2021). Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells. Stem Cells International. 2021. 1–12. 4 indexed citations
11.
Nash, Benjamin M., Edward Hughes, Bruce Bennetts, et al.. (2021). Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachment. European Journal of Human Genetics. 29(5). 881–886. 8 indexed citations
12.
Cornish, Elisa E., Sulekha Rajagopalan, Lisa Ewans, et al.. (2021). MERTK retinopathy: biomarkers assessing vision loss. Ophthalmic Genetics. 42(6). 706–716. 5 indexed citations
13.
Nash, Benjamin M., Richard J. Symes, Himanshu Goel, et al.. (2017). NMNAT1 variants cause cone and cone-rod dystrophy. European Journal of Human Genetics. 26(3). 428–433. 16 indexed citations
14.
Sandaradura, Sarah A., Adam Bournazos, Amali Mallawaarachchi, et al.. (2017). Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant. Human Mutation. 39(3). 383–388. 46 indexed citations
15.
Wright, Dale, et al.. (2016). Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities. Genetic Testing and Molecular Biomarkers. 20(12). 791–798. 2 indexed citations
16.
Nash, Benjamin M., Dale Wright, John Grigg, Bruce Bennetts, & Robyn V. Jamieson. (2015). Retinal dystrophies, genomic applications in diagnosis and prospects for therapy.. PubMed. 4(2). 139–63. 69 indexed citations
17.
Carey, Louise, Benjamin M. Nash, & Dale Wright. (2015). Molecular genetic studies of complete hydatidiform moles.. PubMed. 4(2). 181–8. 18 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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2026