A. Kennan

发表

Light in retinitis pigmentosa.

A. Kennan, A. Aherne, Peter Humphries, 2005, Trends in genetics : TIG.

A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucoma.

A. Kennan, F. Mansergh, P. Humphries, 1998, Journal of medical genetics.

Strategems in vitro for gene therapies directed to dominant mutations.

A. Kennan, F. Mansergh, P. Humphries, 1997, Human molecular genetics.

On the role of IMPDH1 in retinal degeneration.

A. Kennan, A. Aherne, S. Daiger, 2003, Advances in experimental medicine and biology.

Adopting a Sustainable Community of Practice Model when Developing a Service to Support Patients with Epidermolysis Bullosa (EB): A Stakeholder-Centered Approach

Rosemary Joan Gowran, Sarah Beasley, A. Kennan, 2015, The Patient - Patient-Centered Outcomes Research.

Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.

A. Kennan, F. Mansergh, P. Humphries, 1999, American journal of human genetics.

Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach.

A. Kennan, A. Aherne, M. O'Reilly, 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10).

Alison L. Reynolds, A. Kennan, A. Aherne, 2008, Human molecular genetics.

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.

A. Kennan, A. Aherne, Alan W. Stitt, 2002, Human molecular genetics.

Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.

Jian Zuo, A. Kennan, S. Daiger, 2003, Molecular vision.

On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa.

I. Alberts, A. Kennan, A. Aherne, 2004, Human molecular genetics.

Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal recessive Retinitis pigmentosa: The Rho(−/−) mouse

A. Kennan, P. Humphries, P. Kenna, 2006 .

Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP.

A. Kennan, S. Daiger, S. Bowne, 2003, Advances in experimental medicine and biology.

Molecular mechanisms of photoreceptor degeneration in RP caused by IMPDH1 mutations.

A. Kennan, A. Aherne, P. Humphries, 2006, Advances in experimental medicine and biology.

Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q.

A. Kennan, S. Daiger, S. Bowne, 2000, Molecular vision.

Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in Ireland

S. Ennis, T. Kroll, A. Kennan, 2020, HRB open research.

8th Meeting of the Irish Society of Human Genetics, Monday 19th September 2005

M. Gill, S. Ennis, N. Miller, 2006, Ulster medical journal.

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

A. Kennan, É. N. Shé, M. Galvin, 2021, Administration.