Avril Kennan

816 total citations
16 papers, 612 citations indexed

About

Avril Kennan is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Avril Kennan has authored 16 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Ophthalmology and 4 papers in Cell Biology. Recurrent topics in Avril Kennan's work include Retinal Development and Disorders (7 papers), CRISPR and Genetic Engineering (3 papers) and Skin and Cellular Biology Research (2 papers). Avril Kennan is often cited by papers focused on Retinal Development and Disorders (7 papers), CRISPR and Genetic Engineering (3 papers) and Skin and Cellular Biology Research (2 papers). Avril Kennan collaborates with scholars based in Ireland, United States and United Kingdom. Avril Kennan's co-authors include Pete Humphries, Aileen Aherne, Paul F. Kenna, Peter Humphries, G. Jane Farrar, Anna‐Sophia Kiang, Sophia Millington‐Ward, Fiona C. Mansergh, Marius Ader and Arpad Palfi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Avril Kennan

15 papers receiving 603 citations

Peers

Countries citing papers authored by Avril Kennan

Since Specialization

Citations

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

Fields of papers citing papers by Avril Kennan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avril Kennan

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Prioritising Key Concepts for informed health choices in cancer: An evidence-based online educational programme 2024 ·SHILAP Revista de lepidopterología ·(unknown), Declan Devane, (unknown), Maura Dowling, Austin G. Duffy, (unknown), (unknown), Avril Kennan, (unknown), Allen Nsangi, Andrew D Oxman, Derek Stewart, Elaine Toomey, Marie Tierney	0
2	A design-led framework for engaged research: Using a design approach to understand and place the public at the core of health and social care 2021 ·SHILAP Revista de lepidopterología ·Mary Galvin, Avril Kennan, Éidín Ní Shé	1
3	Direct Costs of Epidermolysis Bullosa by Disease Severity 2020 ·Acta Dermato Venereologica ·Darragh Flannery, Claire Doyle, (unknown), (unknown), Avril Kennan	11
4	Adopting a Sustainable Community of Practice Model when Developing a Service to Support Patients with Epidermolysis Bullosa (EB): A Stakeholder-Centered Approach 2014 ·Patient ·Rosemary Joan Gowran, Avril Kennan, (unknown), (unknown), (unknown), (unknown), (unknown)	17
5	Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10) 2008 ·Human Molecular Genetics ·Lawrence C. S. Tam, Anna‐Sophia Kiang, Avril Kennan, Paul F. Kenna, Naomi Chadderton, Marius Ader, Arpad Palfi, Aileen Aherne, Carmen Ayuso, Matthew Campbell, Alison Reynolds, (unknown), Marian M. Humphries, G. Jane Farrar, Pete Humphries	45
6	Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by IMPDH1 Mutations 2007 ·Advances in experimental medicine and biology ·Aileen Aherne, Avril Kennan, Paul F. Kenna, (unknown), G. Jane Farrar, Pete Humphries	2
7	Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal recessive Retinitis pigmentosa: The Rho(−/−) mouse 2006 ·Experimental Eye Research ·Matthew Campbell, Marian M. Humphries, Avril Kennan, (unknown), Peter Humphries, Brenda Brankin	29
8	Toward a Gene Therapy for Dominant Disease: Validation of an RNA Interference-Based Mutation-Independent Approach 2005 ·Molecular Therapy ·Anna‐Sophia Kiang, Arpad Palfi, Marius Ader, Paul F. Kenna, Sophia Millington‐Ward, (unknown), Avril Kennan, Mary O’Reilly, (unknown), Aileen Aherne, (unknown), Pete Humphries, G. Jane Farrar	73
9	Light in retinitis pigmentosa 2004 ·Trends in Genetics ·Avril Kennan, Aileen Aherne, Pete Humphries	111
10	Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP 2003 ·Advances in experimental medicine and biology ·Stephen P. Daiger, Lori S. Sullivan, Sara J. Bowne, Avril Kennan, Peter Humphries, David G. Birch, John R. Heckenlively	5
11	On the Role of IMPDH1 in Retinal Degeneration 2003 ·Advances in experimental medicine and biology ·Avril Kennan, Aileen Aherne, Sara J. Bowne, Stephen P. Daiger, G. Jane Farrar, Paul F. Kenna, Pete Humphries	12
12	Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene. 2003 ·PubMed ·(unknown), (unknown), (unknown), (unknown), Avril Kennan, Pete Humphries, Dianna K. Hughbanks-Wheaton, David G. Birch, Yongsheng Liu, Eric A. Pierce, Jianping Zuo, Qian Huang, (unknown), (unknown)	36
13	Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice 2002 ·Human Molecular Genetics ·Avril Kennan	141
14	Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q. 2000 ·PubMed ·Sara J. Bowne, Lori S. Sullivan, (unknown), Elie Traer, Stephen M. Prescott, David G. Birch, Avril Kennan, Peter Humphries, Stephen P. Daiger	4
15	Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene 1999 ·The American Journal of Human Genetics ·Fiona C. Mansergh, Sophia Millington‐Ward, Avril Kennan, Anna‐Sophia Kiang, (unknown), G. Jane Farrar, Peter Humphries, Paul F. Kenna	82
16	A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucoma. 1998 ·Journal of Medical Genetics ·Avril Kennan, Fiona C. Mansergh, John H. Fingert, Tyson A. Clark, Carmen Ayuso, Paul F. Kenna, Peter Humphries, G. Jane Farrar	43

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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