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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

PUBLICATIONS

Showing 1-10 out of 165
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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...
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...
POSTER
Incidence of fragile X syndrome in Ireland - an all Ireland study
6 Jun 2015European Human Genetics Conference
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