John N. De Roach

935 total citations
53 papers, 527 citations indexed

About

John N. De Roach is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, John N. De Roach has authored 53 papers receiving a total of 527 indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 30 papers in Ophthalmology and 7 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in John N. De Roach's work include Retinal Development and Disorders (48 papers), Retinal Diseases and Treatments (27 papers) and CRISPR and Genetic Engineering (13 papers). John N. De Roach is often cited by papers focused on Retinal Development and Disorders (48 papers), Retinal Diseases and Treatments (27 papers) and CRISPR and Genetic Engineering (13 papers). John N. De Roach collaborates with scholars based in Australia, Singapore and Thailand. John N. De Roach's co-authors include Terri L. McLaren, Tina M. Lamey, Jennifer A. Thompson, Fred K. Chen, David A. Mackey, Samuel McLenachan, Dan Zhang, H. C. Montgomery, Rachael C. Heath Jeffery and Jason Charng and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

John N. De Roach

53 papers receiving 521 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
John N. De Roach Australia	13	451	330	102	76	73	53	527
Terri L. McLaren Australia	13	451 1.0×	324 1.0×	103 1.0×	76 1.0×	77 1.1×	59	526
Tina M. Lamey Australia	13	474 1.1×	324 1.0×	102 1.0×	80 1.1×	77 1.1×	63	557
Janneke J.C. van Lith-Verhoeven Netherlands	9	383 0.8×	289 0.9×	86 0.8×	53 0.7×	86 1.2×	12	483
Marijke N. Zonneveld-Vrieling Netherlands	9	354 0.8×	259 0.8×	62 0.6×	53 0.7×	89 1.2×	9	432
Ilaria Passerini Italy	15	452 1.0×	318 1.0×	118 1.2×	67 0.9×	31 0.4×	49	574
Patrícia José Spain	12	358 0.8×	232 0.7×	75 0.7×	78 1.0×	40 0.5×	25	433
Vittoria Murro Italy	14	350 0.8×	356 1.1×	154 1.5×	97 1.3×	58 0.8×	72	538
Frederick T. Collison United States	13	456 1.0×	373 1.1×	119 1.2×	39 0.5×	65 0.9×	25	550
Rola Ba‐Abbad United Kingdom	11	292 0.6×	234 0.7×	154 1.5×	68 0.9×	39 0.5×	29	431
Xunlun Sheng China	14	386 0.9×	249 0.8×	121 1.2×	118 1.6×	61 0.8×	48	598

Countries citing papers authored by John N. De Roach

Since Specialization

Citations

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

Fields of papers citing papers by John N. De Roach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John N. De Roach. 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 John N. De Roach. The network helps show where John N. De Roach may publish in the future.

Co-authorship network of co-authors of John N. De Roach

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

All Works

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20 of 20 papers shown

Britten‐Jones, Alexis Ceecee, Chi D. Luu, Jasleen K. Jolly, et al.. (2024). Longitudinal Assessment of Structural and Functional Changes in Rod-cone Dystrophy: A 10-year Follow-up Study. SHILAP Revista de lepidopterología. 5(2). 100649–100649. 1 indexed citations

Jeffery, Rachael C. Heath, Johnny Lo, Jennifer A. Thompson, et al.. (2023). Analysis of the Outer Retinal Bands in ABCA4 and PRPH2-Associated Retinopathy using OCT. Ophthalmology Retina. 8(2). 174–183. 9 indexed citations

Mack, Heather G., Alexis Ceecee Britten‐Jones, Myra B. McGuinness, et al.. (2022). Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in Australia. Gene Therapy. 30(3-4). 336–346. 8 indexed citations

Zhang, Xiao, Dan Zhang, Jennifer A. Thompson, et al.. (2021). Gene correction of the CLN3 c.175G>A variant in patient‐derived induced pluripotent stem cells prevents pathological changes in retinal organoids. Molecular Genetics & Genomic Medicine. 9(3). e1601–e1601. 17 indexed citations

Mack, Heather G., Fred K. Chen, John Grigg, et al.. (2021). Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey. BMJ Open. 11(6). e048361–e048361. 9 indexed citations

Jeffery, Rachael C. Heath, Jennifer A. Thompson, Johnny Lo, et al.. (2021). Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus Autofluorescence. Australasian Journal of Paramedicine. 1(1). 100005–100005. 12 indexed citations

McLenachan, Samuel, Dan Zhang, Xiao Zhang, et al.. (2021). Determinants of Disease Penetrance in PRPF31-Associated Retinopathy. Genes. 12(10). 1542–1542. 15 indexed citations

Jeffery, Rachael C. Heath, Jennifer A. Thompson, Ian J. Constable, et al.. (2021). A novel phenotype in a family with autosomal dominant retinal dystrophy due to c.1430A > G in retinoid isomerohydrolase (RPE65) and c.37C > T in bestrophin 1 (BEST1). Documenta Ophthalmologica. 143(1). 61–73. 2 indexed citations

Zhang, Dan, Samuel McLenachan, Xiao Zhang, et al.. (2021). Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200. Stem Cell Research. 51. 102154–102154. 2 indexed citations

10.

Zhang, Dan, Tina M. Lamey, Jennifer A. Thompson, et al.. (2021). Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1. Stem Cell Research. 54. 102403–102403. 5 indexed citations

11.

Thompson, Jennifer A., Jason Charng, Samuel McLenachan, et al.. (2020). Phenotype–genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion–insertion variant causing a splicing defect. Molecular Genetics & Genomic Medicine. 8(7). e1259–e1259. 11 indexed citations

12.

McLaren, Terri L., John N. De Roach, Jennifer A. Thompson, et al.. (2020). Expanding the genetic spectrum of choroideremia in an Australian cohort: report of five novel CHM variants. Human Genome Variation. 7(1). 35–35. 4 indexed citations

13.

Zhang, Dan, Tina M. Lamey, Jennifer A. Thompson, et al.. (2020). Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4. Stem Cell Research. 48. 101947–101947. 3 indexed citations

14.

Wong, Elaine Y.M., Xiao Zhang, Dan Zhang, et al.. (2020). Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene. Stem Cell Research. 50. 102129–102129. 4 indexed citations

15.

McLenachan, Samuel, Elaine Y.M. Wong, Xiao Zhang, et al.. (2019). Generation of two induced pluripotent stem cell lines from a patient with compound heterozygous mutations in the USH2A gene. Stem Cell Research. 36. 101420–101420. 5 indexed citations

16.

Chen, Fred K., Xiao Zhang, Dan Zhang, et al.. (2018). Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3). Documenta Ophthalmologica. 138(1). 55–70. 17 indexed citations

17.

Roach, John N. De, et al.. (2016). A computer-assisted method for pathogenicity assessment and genetic reporting of variants stored in the Australian Inherited Retinal Disease Register. Australasian Physical & Engineering Sciences in Medicine. 39(1). 239–245. 2 indexed citations

18.

Lamey, Tina M., et al.. (2015). Progress and prospects of next-generation sequencing testing for inherited retinal dystrophy. Expert Review of Molecular Diagnostics. 15(10). 1269–1275. 52 indexed citations

19.

Crowley, Claire, et al.. (2014). Autosomal recessive bestrophinopathy associated with angle-closure glaucoma. Documenta Ophthalmologica. 129(1). 57–63. 27 indexed citations

20.

Lamey, Tina M., et al.. (2009). Genotypic Analysis of X-linked Retinoschisis in Western Australia. Advances in experimental medicine and biology. 664. 283–291. 2 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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