Robyn V. Jamieson

4.1k total citations
88 papers, 2.1k citations indexed

About

Robyn V. Jamieson is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Robyn V. Jamieson has authored 88 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 33 papers in Ophthalmology and 31 papers in Genetics. Recurrent topics in Robyn V. Jamieson's work include Retinal Development and Disorders (28 papers), Retinal Diseases and Treatments (19 papers) and Ocular Disorders and Treatments (14 papers). Robyn V. Jamieson is often cited by papers focused on Retinal Development and Disorders (28 papers), Retinal Diseases and Treatments (19 papers) and Ocular Disorders and Treatments (14 papers). Robyn V. Jamieson collaborates with scholars based in Australia, United States and United Kingdom. Robyn V. Jamieson's co-authors include John Grigg, Patrick Tam, Maree Flaherty, James E. Smith, Bruce Bennetts, John Pearn, Frank Martin, Benjamin M. Nash, Jozef Gécz and Stephen Hing and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Development.

In The Last Decade

Robyn V. Jamieson

85 papers receiving 2.1k citations

Peers

Countries citing papers authored by Robyn V. Jamieson

Since Specialization

Citations

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

Fields of papers citing papers by Robyn V. Jamieson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robyn V. Jamieson. 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 Robyn V. Jamieson. The network helps show where Robyn V. Jamieson may publish in the future.

Co-authorship network of co-authors of Robyn V. Jamieson

This figure shows the co-authorship network connecting the top 25 collaborators of Robyn V. Jamieson. A scholar is included among the top collaborators of Robyn V. Jamieson 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 Robyn V. Jamieson. Robyn V. Jamieson 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

#	Work	Indexed citations
1	Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measures 2025 ·Eye ·(unknown), Elisa E. Cornish, Jonathan V. Nguyen, Elizabeth H Barnes, (unknown), (unknown), Robyn V. Jamieson, John Grigg	1
2	Managing the apparently blind child presenting in the first year of life: A review 2024 ·Clinical and Experimental Ophthalmology ·(unknown), (unknown), Robyn V. Jamieson, John Grigg	0
3	A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome 2024 ·Clinical Genetics ·Lama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula, (unknown), Firdous Abdulwahab, Arif O. Khan, Lisa G. Riley, Amal Alhashem, Nicolas Chassaing, Robyn V. Jamieson, Fowzan S. Alkuraya	0
4	Spectrum of ocular disease in children aged between 0 and 3 years at an Australian paediatric tertiary hospital 2023 ·Clinical and Experimental Ophthalmology ·(unknown), Stephanie Crofts, (unknown), Robyn V. Jamieson, John Grigg	2
5	Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in Australia 2022 ·Gene Therapy ·Heather G. Mack, Alexis Ceecee Britten‐Jones, Myra B. McGuinness, Fred K. Chen, John Grigg, Robyn V. Jamieson, Thomas L. Edwards, John N. De Roach, Fleur O’Hare, Keith R. Martin, Lauren N. Ayton	8
6	Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies 2022 ·International Journal of Molecular Sciences ·Benjamin M. Nash, Alan Ma, Gladys Ho, Elizabeth Farnsworth, André E. Minoche, Mark J. Cowley, Christopher Barnett, Janine Smith, (unknown), Karen Wong, Luke St Heaps, Dale Wright, Marcel E. Dinger, Bruce Bennetts, John Grigg, Robyn V. Jamieson	7
7	Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey 2021 ·BMJ Open ·Heather G. Mack, Fred K. Chen, John Grigg, Robyn V. Jamieson, John N. De Roach, Fleur O’Hare, Alexis Ceecee Britten‐Jones, Myra B. McGuinness, (unknown), Lauren N. Ayton	9
8	Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells 2021 ·Stem Cells International ·Benjamin M. Nash, (unknown), Milan Fernando, (unknown), James P. Robinson, (unknown), Steven S. Eamegdool, Elizabeth Farnsworth, Bruce Bennetts, John Grigg, Seo‐Kyung Chung, Anai Gonzalez-Cordero, Robyn V. Jamieson	4
9	Surgical Management for Glaucoma in Sturge-Weber Syndrome: Experience from a Tertiary Referral Paediatric Hospital 2020 ·Investigative Ophthalmology & Visual Science ·(unknown), (unknown), Sophia Zagora, (unknown), Robyn V. Jamieson, John Grigg	1
10	NMNAT1 variants cause cone and cone-rod dystrophy 2017 ·European Journal of Human Genetics ·Benjamin M. Nash, Richard J. Symes, Himanshu Goel, Marcel E. Dinger, Bruce Bennetts, John Grigg, Robyn V. Jamieson	16
11	Primary Congenital Glaucoma Outcomes: Lessons From 23 Years of Follow-up 2015 ·American Journal of Ophthalmology ·Sophia Zagora, C L Funnell, Frank Martin, James E. Smith, Stephen Hing, Francis A. Billson, (unknown), Robyn V. Jamieson, John Grigg	75
12	An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation 2012 ·Human Molecular Genetics ·G. Cederquist, Anna Łuchniak, Max A. Tischfield, (unknown), Yuyu Song, Manoj P. Menezes, Wai‐Man Chan, Caroline Andrews, Sheena Chew, Robyn V. Jamieson, Lavier Gomes, Maree Flaherty, P. Ellen Grant, Mohan L. Gupta, Elizabeth C. Engle	95
13	A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family 2012 ·Clinical Genetics ·Wy Ching Ng, Francesca Pasutto, (unknown), (unknown), Geoffrey Watson, Adele Schneider, (unknown), John Grigg, Martin Zenker, Robyn V. Jamieson	13
14	Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring 2011 ·European Journal of Human Genetics ·Zornitza Stark, (unknown), Bruce Bennetts, Ravi Savarirayan, Robyn V. Jamieson	27
15	A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding 2003 ·Human Molecular Genetics ·(unknown), Robyn V. Jamieson, Rahat Perveen, P. H. Glenister, Roland R. Griffiths, Yvonne Boyd, L H Glimcher, Jack Favor, (unknown), Graeme C. Black	45
16	Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family 2003 ·British Journal of Ophthalmology ·Robyn V. Jamieson	37
17	Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma 2002 ·Human Molecular Genetics ·Robyn V. Jamieson	201
18	The allocation and differentiation of mouse primordial germ cells. 2001 ·SPIRE - Sciences Po Institutional REpository ·Tom C. Tsang, Poh‐Lynn Khoo, Robyn V. Jamieson, Sheng Zhou, S L Ang, Richard R. Behringer, Patrick Tam	20
19	Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda 1999 ·Nature Genetics ·Ági K. Gedeon, Alison Colley, Robyn V. Jamieson, Elizabeth M. Thompson, John Rogers, David Sillence, George E. Tiller, John C. Mulley, Jozef Gécz	145
20	X-chromosome activity: impact of imprinting and chromatin structure 1996 ·The International Journal of Developmental Biology ·Robyn V. Jamieson, (unknown), Margaret Gardiner‐Garden	29

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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