Maree Flaherty

1.5k citations

30 papers · 566 indexed · h-index 14

Impact in

Ophthalmology top 5%
- Intraocular Surgery and Lenses
- Glaucoma and retinal disorders
Genetics top 10%
- Ocular Disorders and Treatments
- Congenital Ear and Nasal Anomalies

Papers in ⓘ

Ophthalmology 13
- Intraocular Surgery and Lenses 7
- Ophthalmology and Visual Health Research 3
Genetics 13
- Ocular Disorders and Treatments 10
- Craniofacial Disorders and Treatments 6
- Congenital Ear and Nasal Anomalies 3

Co-authors: Robyn V. Jamieson (11 shared papers)John Grigg (9 shared papers)James E. Smith (3 shared papers)Ivan Prokudin (4 shared papers)Padraic J. Grattan‐Smith (4 shared papers)Frank Martin (3 shared papers)John W. Nelson (2 shared papers)Bruce Bennetts (2 shared papers)
Journals: Ophthalmic Genetics (3 papers)European Journal of Human Genetics (2 papers)Journal of Pediatric Ophthalmology & Strabismus (2 papers)Clinical Genetics (2 papers)Asia-Pacific Journal of Ophthalmology (1 paper)
Partner nations: Australia United States United Kingdom

In The Last Decade

Maree Flaherty

30 papers receiving 558 citations

Peers

Countries citing papers authored by Maree Flaherty

Since Specialization

Citations

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

Fields of papers citing papers by Maree Flaherty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Maree Flaherty, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Maree Flaherty Line = papers co-authored together Maree Flaherty links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing Human Mutation ·Alan Ma, John Grigg, Gladys Ho, Ivan Prokudin, Elizabeth Farnsworth, Katherine Holman, Anson Cheng, Frank A. Billson, Frank Martin, Clare L. Fraser, David Mowat, James E. Smith, John Christodoulou, Maree Flaherty, Bruce Bennetts, Robyn V. Jamieson	2015	103
2	An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation Human Molecular Genetics ·G. Cederquist, Anna Łuchniak, Max A. Tischfield, Maya Peeva, 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	2012	95
3	Microphthalmia, Anophthalmia, and Coloboma and Associated Ocular and Systemic Features JAMA Ophthalmology ·Simon E. Skalicky, Andrew White, John Grigg, Frank Martin, Jeremy B. Smith, Michael Jones, Craig Donaldson, James E. Smith, Maree Flaherty, Robyn V. Jamieson	2013	53
4	Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1 European Journal of Human Genetics ·Ivan Prokudin, Cas Simons, John Grigg, Rebecca Storen, Vikrant Kumar, Zai Yang Phua, James E. Smith, Maree Flaherty, Sonia Dávila, Robyn V. Jamieson	2013	52
5	Neurofibromatosis Type 1: Review and Update on Emerging Therapies Asia-Pacific Journal of Ophthalmology ·Tanya Karaconji, Eline Whist, Robyn V. Jamieson, Maree Flaherty, John Grigg	2018	35
6	Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome Clinical Genetics ·Isabelle Schrauwen, Manou Sommen, Charlotte Claes, Jason Pinner, Maree Flaherty, Felicity Collins, Guy Van Camp	2013	33
7	Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia Ophthalmology ·Maree Flaherty, Padraic J. Grattan‐Smith, Adam C. Steinberg, Robyn V. Jamieson, Elizabeth C Engle	2001	22
8	Eye–hand co-ordination skills in very preterm infants <29 weeks gestation at 3 years: effects of preterm birth and retinopathy of prematurity Early Human Development ·T-A Goyen, David A Todd, M. Veddovi, AKA Wright, Maree Flaherty, John F. Kennedy	2006	21
9	Novel SOX2 partner-factor domain mutation in a four-generation family European Journal of Human Genetics ·Marija Mihelec, Peter Abraham, Kate Gibson, Renata Krowka, Rachel Susman, Rebecca Storen, Yongjuan Chen, Jennifer A. Donald, Patrick Tam, John Grigg, Maree Flaherty, Glen A. Gole, Robyn V. Jamieson	2009	19
10	Assessment and diagnosis of suspected glaucoma in patients with mucopolysaccharidosis Acta Ophthalmologica ·Jane Ashworth, Maree Flaherty, Susanne Pitz, Azura Ramlee	2015	18
11	Gillespie syndrome: a report of two further cases. PubMed ·John W. Nelson, Maree Flaherty, Padraic J. Grattan‐Smith	1997	17
12	Gillespie syndrome: A report of two further cases American Journal of Medical Genetics ·John W. Nelson, Maree Flaherty, Padraic J. Grattan‐Smith	1997	15
13	Chromosomal Rearrangements and Novel Genes in Disorders of Eye Development, Cataract and Glaucoma Twin Research and Human Genetics ·Marija Mihelec, Luke St Heaps, Maree Flaherty, Frank A. Billson, Christina Rudduck, Patrick Tam, John Grigg, Greg B. Peters, Robyn V. Jamieson	2008	13
14	New mutations in GJA8 expand the phenotype to include total sclerocornea Clinical Genetics ·Aiju Ma, John Grigg, Ivan Prokudin, Maree Flaherty, Bruce Bennetts, Robyn V. Jamieson	2017	13
15	Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of NovelTULP1Mutation in Leber Congenital Amaurosis Ophthalmic Genetics ·Yiran Guo, Ivan Prokudin, Cong Yu, Jinlong Liang, Yi Xie, Maree Flaherty, Lifeng Tian, Stephanie Crofts, Fengxiang Wang, James W. Snyder, Craig Donaldson, Nada Abdelmagid, Lyam Vazquez, Brendan J. Keating, Håkon Håkonarson, Jun Wang, Robyn V. Jamieson	2014	12
16	Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentials Journal of Clinical Neuroscience ·V. Jayanetti, Alexander Klistorner, Stuart L. Graham, Mark Dexter, Maree Flaherty, K. Jones, F. A. Billson, Meredith Wilson, Kathryn N. North, John Grigg, Clare L. Fraser	2018	6
17	Ocular and electrophysiological findings in a patient with Sly syndrome Ophthalmic Genetics ·Maree Flaherty, Katie Geering, Stephanie Crofts, John Grigg	2016	6
18	A variant microcephalic osteodysplastic slender-bone disorder with growth hormone deficiency and a pigmentary retinopathy Clinical Dysmorphology ·Kenneth N. Maclean, Geoffrey Ambler, Maree Flaherty, K. Kozlowski, L.C. Ad s	2002	5
19	Reporting on Australian childhood visual impairment: the first 10 years Eye ·Sue Silveira, Frank Martin, Maree Flaherty, Heather Russell	2021	4
20	Disc drusen: a headache for child and clinician Australian and New Zealand Journal of Ophthalmology ·Andrew C. Chang, Maree Flaherty	1996	4

About Maree Flaherty

Maree Flaherty is a scholar working on Ophthalmology, Genetics, Neurology, Genetics and Otorhinolaryngology, having authored 30 papers that have together received 566 indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (10 papers), Intraocular Surgery and Lenses (7 papers), Craniofacial Disorders and Treatments (6 papers), Connexins and lens biology (4 papers), Ophthalmology and Visual Impairment Studies (3 papers), Ophthalmology and Visual Health Research (3 papers), Congenital Ear and Nasal Anomalies (3 papers) and Moyamoya disease diagnosis and treatment (2 papers). The work is most often cited by research in Ophthalmology (153 citations), Genetics (257 citations), Genetics (62 citations), Cell Biology (83 citations) and Molecular Biology (286 citations). Maree Flaherty has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Robyn V. Jamieson, John Grigg, James E. Smith, Ivan Prokudin, Padraic J. Grattan‐Smith, Frank Martin, John W. Nelson, Bruce Bennetts, Frank A. Billson and Clare L. Fraser. Their work appears in journals such as Ophthalmic Genetics, European Journal of Human Genetics, Journal of Pediatric Ophthalmology & Strabismus, Clinical Genetics and Asia-Pacific Journal of Ophthalmology.

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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