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Professor David Barton

Professor

David Barton

Adjunct Professor
School of Medicine
(01) 4096749
University College Dublin, School of Medicine, Our Lady's Hospital Crumlin Dublin 12

Outputs

Showing 1-25 out of 229
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JOURNAL ARTICLE
Investigation of DNA variants specific to ROBO2 Isoform 'a' in Irish vesicoureteric reflux patients reveals marked CpG island variation
10 Feb 2020Scientific reports10(1):2265
Darlow JM, Dobson MG, Green AJ, Puri P, Barton DE
JOURNAL ARTICLE
Managing uncertainty in inherited cardiac pathologies—an international multidisciplinary survey
1 Aug 2019European Journal of Human Genetics27(8):1178-1185
McVeigh TP, Kelly LJ, Whitmore E, Clark T, Mullaney B...
JOURNAL ARTICLE
Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract (Nature Genetics, (2019), 51, 1, (117-127), 10.1038/s41588-018-0281-y)
1 Apr 2019Nature Genetics51(4):764
Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q...
JOURNAL ARTICLE
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
1 Jan 2019Nature Genetics51(1):117-127
Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q...
JOURNAL ARTICLE
Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosis
1 Dec 2018European Journal of Human Genetics26(12):1832-1839
Farrell P, Férec C, Macek M, Frischer T, Renner S...
JOURNAL ARTICLE
Erratum: Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux (Scientific reports (2017) 7 1 (14595))
8 Jan 2018Scientific reports8(1):459
Darlow JM, Darlay R, Dobson MG, Stewart A, Charoen P...
JOURNAL ARTICLE
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
1 Dec 2017Scientific Reports7(1)
Darlow JM, Darlay R, Dobson MG, Stewart A, Charoen P...
CONFERENCE PAPER
Improvement in Diagnostic Laboratory Performance by Participation in External Quality Assessment for Molecular Pathology: Lessons Learned and the Need for Continued Quality Improvement
1 Nov 2017Annual Meeting of the Association-for-Molecular-Pathology (AMP)JOURNAL OF MOLECULAR DIAGNOSTICS19(6):1008 (1 page)
Cheetham MH, Barton DE, Wolstenholme NL, Patton SJ
JOURNAL ARTICLE
Incidence of Fragile X syndrome in Ireland
1 Mar 2017American Journal of Medical Genetics, Part A173(3):678-683
O'Byrne JJ, Sweeney M, Donnelly DE, Lambert DM, Beattie ED...
JOURNAL ARTICLE
Genetic drivers of kidney defects in the digeorge syndrome
23 Feb 2017New England Journal of Medicine376(8):742-754
Lopez-Rivera E, Liu YP, Verbitsky M, Anderson BR, Capone VP...
JOURNAL ARTICLE
Reply to Sajantila and Budowle
1 Mar 2016European Journal of Human Genetics24(3):330
Barton DE, Claustres M, Kozich V, Dequeker E, Fowler B...
CONFERENCE PAPER
External Quality Assessment of BRCA1 and BRCA2 Gene Sequencing: Challenges for Quality in a Changing Diagnostic Environment
1 Sep 20158th Joint Meeting of the British-Division of the International-Academy-of-Pathology and the Pathological-Society-of-Great-Britain-and-IrelandJOURNAL OF PATHOLOGY237:S20 (1 page)
Patton SJ, Ellison G, Kristoffersson U, Wallace A, Houdayer C...
POSTER
Incidence of fragile X syndrome in Ireland - an all Ireland study
6 Jun 2015European Human Genetics Conference
POSTER
Ten years of SCA external quality assessment (EQA) schemes organised by EMQN
6 Jun 2015European Human Genetics Conference
CONFERENCE CONTRIBUTION
New European IVD regulations - Update and analysis
13 Apr 2015Advanced Molecular Diagnostics
JOURNAL ARTICLE
Urinary tract effects of HPSE2 mutations
1 Apr 2015Journal of the American Society of Nephrology26(4):797-804
Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB...
JOURNAL ARTICLE
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)
1 Feb 2014European Journal of Human Genetics22(2):160-170
Claustres M, Kožich V, Dequeker E, Fowler B, Hehir-Kwa JY...
JOURNAL ARTICLE
A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development
1 Jan 2014Molecular Genetics and Genomic Medicine2(1):7-29
Darlow JM, Dobson MG, Darlay R, Molony CM, Hunziker M...
CONFERENCE PAPER
New developments in the regulation of diagnostic devices
1 Jun 2013CHROMOSOME RESEARCH21:S20 (1 page)
Barton D
JOURNAL ARTICLE
EMQN/CMGS best practice guidelines for the molecular genetic testing of huntington disease
1 May 2013European Journal of Human Genetics21(5):480-486
Losekoot M, Van Belzen MJ, Seneca S, Bauer P, Stenhouse SAR...
JOURNAL ARTICLE
Erratum: Preparation and validation of the first WHO international genetic reference panel for Fragile X syndrome (European Journal of Human Genetics (2013) 21 (478))
1 Apr 2013European Journal of Human Genetics21(4):478
Hawkins M, Boyle J, Wright KE, Elles R, Ramsden SC...
JOURNAL ARTICLE
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
1 Jan 2013PLoS Genetics9(3)
Couch FJ, Wang X, McGuffog L, Lee A, Olswold C...
JOURNAL ARTICLE
Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux
1 Jan 2013Kidney International84(2):327-337
Dobson MG, Darlow JM, Hunziker M, Green AJ, Barton DE...
JOURNAL ARTICLE
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
1 Jan 2013PLoS Genetics9(3)
Gaudet MM, Kuchenbaecker KB, Vijai J, Klein RJ, Kirchhoff T...
CONFERENCE PAPER
Gene mutations in the Irish epidermolysis bullosa population
1 Dec 2012Spring Meeting of the Irish-Association-of-DermatologistsBRITISH JOURNAL OF DERMATOLOGY167(6):E32 (1 page)
O'Donnell CF, McAleer MA, Kennan A, Barton DE, Irvine AD...
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