Adrian Dockery

744 total citations
19 papers, 302 citations indexed

About

Adrian Dockery is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Adrian Dockery has authored 19 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Ophthalmology. Recurrent topics in Adrian Dockery's work include Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (7 papers) and Genomics and Rare Diseases (6 papers). Adrian Dockery is often cited by papers focused on Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (7 papers) and Genomics and Rare Diseases (6 papers). Adrian Dockery collaborates with scholars based in Ireland, United Kingdom and Netherlands. Adrian Dockery's co-authors include G. Jane Farrar, Paul F. Kenna, Laura Whelan, Pete Humphries, Matthew Carrigan, Kirk Stephenson, David Keegan, James J. O’Byrne, Sophia Millington‐Ward and Giuliana Silvestri and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Adrian Dockery

17 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Adrian Dockery Ireland	9	248	115	101	37	18	19	302
Inmaculada Martín-Mérida Spain	10	225 0.9×	77 0.7×	95 0.9×	22 0.6×	24 1.3×	15	251
Zachry T. Soens United States	9	249 1.0×	161 1.4×	111 1.1×	21 0.6×	31 1.7×	12	325
Zixi Sun China	11	224 0.9×	67 0.6×	110 1.1×	36 1.0×	32 1.8×	37	304
Aaron Black United States	5	209 0.8×	83 0.7×	107 1.1×	37 1.0×	22 1.2×	10	264
Raquel Pérez-Carro Spain	10	278 1.1×	72 0.6×	139 1.4×	25 0.7×	38 2.1×	12	299
Lizhu Yang China	13	322 1.3×	111 1.0×	184 1.8×	59 1.6×	53 2.9×	30	377
Olga Zurita Spain	9	251 1.0×	63 0.5×	128 1.3×	25 0.7×	30 1.7×	14	285
Marta de Castro‐Miró Spain	9	277 1.1×	95 0.8×	114 1.1×	26 0.7×	33 1.8×	12	304
Fadi Nasser Germany	10	235 0.9×	81 0.7×	155 1.5×	51 1.4×	18 1.0×	20	292
Luísa Coutinho Santos Portugal	7	219 0.9×	161 1.4×	141 1.4×	66 1.8×	36 2.0×	11	372

Countries citing papers authored by Adrian Dockery

Since Specialization

Citations

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

Fields of papers citing papers by Adrian Dockery

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adrian Dockery

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

All Works

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19 of 19 papers shown

Matthews, Emma, Adrian Dockery, Laura Whelan, et al.. (2024). Novel Splice-Altering Variants in the CHM and CACNA1F Genes Causative of X-Linked Choroideremia and Cone Dystrophy. Genes. 16(1). 25–25.

Stephenson, Kirk, Julia Zhu, Adrian Dockery, et al.. (2024). The Role of the Ophthalmic Genetics Multidisciplinary Team in the Management of Inherited Retinal Degenerations—A Case-Based Review. Life. 14(1). 107–107.

Dockery, Adrian, et al.. (2024). Variant reclassification and clinical implications. Journal of Medical Genetics. 61(3). 207–211. 24 indexed citations

Stephenson, Kirk, Laura Whelan, Julia Zhu, et al.. (2023). Usher Syndrome on the Island of Ireland: A Genotype-Phenotype Review. Investigative Ophthalmology & Visual Science. 64(10). 23–23. 7 indexed citations

Whelan, Laura, Adrian Dockery, Kirk Stephenson, et al.. (2023). Detailed analysis of an enriched deep intronic ABCA4 variant in Irish Stargardt disease patients. Scientific Reports. 13(1). 9380–9380. 3 indexed citations

Zhu, Julia, Kirk Stephenson, Adrian Dockery, et al.. (2022). Electrophysiology-Guided Genetic Characterisation Maximises Molecular Diagnosis in an Irish Paediatric Inherited Retinal Degeneration Population. Genes. 13(4). 615–615. 5 indexed citations

Stephenson, Kirk, Julia Zhu, Adrian Dockery, et al.. (2022). Clinical and Genetic Re-Evaluation of Inherited Retinal Degeneration Pedigrees following Initial Negative Findings on Panel-Based Next Generation Sequencing. International Journal of Molecular Sciences. 23(2). 995–995. 11 indexed citations

O’Connell, Ann A., Julia Zhu, Kirk Stephenson, et al.. (2022). <i>MFRP</i>-Associated Retinopathy and Nanophthalmos in Two Irish Probands: A Case Report. Case Reports in Ophthalmology. 13(3). 1015–1023. 5 indexed citations

Whelan, Laura, Tamar Ben‐Yosef, Adrian Dockery, et al.. (2021). Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases. npj Genomic Medicine. 6(1). 97–97. 34 indexed citations

10.

Dockery, Adrian, G. Jane Farrar, Monika Ołdak, et al.. (2021). Molecular Inversion Probe-Based Sequencing of USH2A Exons and Splice Sites as a Cost-Effective Screening Tool in USH2 and arRP Cases. International Journal of Molecular Sciences. 22(12). 6419–6419. 5 indexed citations

11.

Dockery, Adrian, Laura Whelan, Pete Humphries, & G. Jane Farrar. (2021). Next-Generation Sequencing Applications for Inherited Retinal Diseases. International Journal of Molecular Sciences. 22(11). 5684–5684. 32 indexed citations

12.

Whelan, Laura, Adrian Dockery, L. Ingeborgh van den Born, et al.. (2021). BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa. Journal of Medical Genetics. 59(5). 438–444. 17 indexed citations

13.

Whelan, Laura, Adrian Dockery, Julia Zhu, et al.. (2020). Findings from a Genotyping Study of over 1000 People with Inherited Retinal Disorders in Ireland. Genes. 11(1). 105–105. 34 indexed citations

14.

Stephenson, Kirk, Adrian Dockery, Michael O’Keefe, et al.. (2019). A FBN1 variant manifesting as non-syndromic ectopia lentis with retinal detachment: clinical and genetic characteristics. Eye. 34(4). 690–694. 10 indexed citations

15.

Dockery, Adrian, Matthew Carrigan, Kirk Stephenson, et al.. (2019). A Novel FLVCR1 Variant Implicated in Retinitis Pigmentosa. Advances in experimental medicine and biology. 1185. 203–207. 7 indexed citations

16.

Stephenson, Kirk, Adrian Dockery, Matthew Carrigan, et al.. (2018). Multimodal imaging in a pedigree of X-linked Retinoschisis with a novel RS1 variant. BMC Medical Genetics. 19(1). 195–195. 4 indexed citations

17.

Carrigan, Matthew, et al.. (2017). Intrafamilial Phenotype Variation Associated with BBS1 Met390Arg. Investigative Ophthalmology & Visual Science. 58(8). 3257–3257. 1 indexed citations

18.

Dockery, Adrian, Kirk Stephenson, David Keegan, et al.. (2017). Target 5000: Target Capture Sequencing for Inherited Retinal Degenerations. Genes. 8(11). 304–304. 36 indexed citations

19.

Farrar, G. Jane, Matthew Carrigan, Adrian Dockery, et al.. (2017). Toward an elucidation of the molecular genetics of inherited retinal degenerations. Human Molecular Genetics. 26(R1). R2–R11. 67 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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