Publications by authors named "David E Barton"

30Publications

Left main percutaneous coronary intervention versus coronary artery bypass surgery: A case of true equivalence in low and intermediate complexity anatomy or a question yet to be answered?

Authors:

David E Barton Michalis Hamilos Yiannis S Chatzizisis

Atherosclerosis 2020 09 30;308:45-47. Epub 2020 Jul 30.

Cardiovascular Division, University of Nebraska Medical Center, Omaha, NE, USA. Electronic address:

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September 2020

National Newborn Screening for cystic fibrosis in the Republic of Ireland: genetic data from the first 6.5 years.

Authors:

Erina Sasaki Marija Kostocenko Niamh Lang Tara Clark Melissa Rogers Rebecca Muldowney Olivia Walsh Loretta O'Grady Gillian Edge Alana Ward Barry Linnane Ingrid Borovickova David E Barton Sally Ann Lynch

Eur J Hum Genet 2020 12 1;28(12):1669-1674. Epub 2020 Jun 1.

Department of Clinical Genetics, Children's Health Ireland (CHI) at Crumlin, Dublin, Ireland.

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December 2020

Investigation of DNA variants specific to ROBO2 Isoform 'a' in Irish vesicoureteric reflux patients reveals marked CpG island variation.

Authors:

John M Darlow Mark G Dobson Andrew J Green Prem Puri David E Barton

Sci Rep 2020 02 10;10(1):2265. Epub 2020 Feb 10.

Department of Clinical Genetics, Dublin, Ireland.

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February 2020

Managing uncertainty in inherited cardiac pathologies-an international multidisciplinary survey.

Authors:

Terri Patricia McVeigh Luke J Kelly Elizabeth Whitmore Tara Clark Brendan Mullaney David E Barton Alana Ward Sally Ann Lynch

Eur J Hum Genet 2019 08 12;27(8):1178-1185. Epub 2019 Apr 12.

Our Lady's Children's Hospital Crumlin, Dublin 12, Dublin, Ireland.

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August 2019

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Authors:

Miguel Verbitsky Rik Westland Alejandra Perez Krzysztof Kiryluk Qingxue Liu Priya Krithivasan Adele Mitrotti David A Fasel Ekaterina Batourina Matthew G Sampson Monica Bodria Max Werth Charlly Kao Jeremiah Martino Valentina P Capone Asaf Vivante Shirlee Shril Byum Hee Kil Maddalena Marasa Jun Y Zhang Young-Ji Na Tze Y Lim Dina Ahram Patricia L Weng Erin L Heinzen Alba Carrea Giorgio Piaggio Loreto Gesualdo Valeria Manca Giuseppe Masnata Maddalena Gigante Daniele Cusi Claudia Izzi Francesco Scolari Joanna A E van Wijk Marijan Saraga Domenico Santoro Giovanni Conti Pasquale Zamboli Hope White Dorota Drozdz Katarzyna Zachwieja Monika Miklaszewska Marcin Tkaczyk Daria Tomczyk Anna Krakowska Przemyslaw Sikora Tomasz Jarmoliński Maria K Borszewska-Kornacka Robert Pawluch Maria Szczepanska Piotr Adamczyk Malgorzata Mizerska-Wasiak Grazyna Krzemien Agnieszka Szmigielska Marcin Zaniew Mark G Dobson John M Darlow Prem Puri David E Barton Susan L Furth Bradley A Warady Zoran Gucev Vladimir J Lozanovski Velibor Tasic Isabella Pisani Landino Allegri Lida M Rodas Josep M Campistol Cécile Jeanpierre Shumyle Alam Pasquale Casale Craig S Wong Fangming Lin Débora M Miranda Eduardo A Oliveira Ana Cristina Simoes-E-Silva Jonathan M Barasch Brynn Levy Nan Wu Friedhelm Hildebrandt Gian Marco Ghiggeri Anna Latos-Bielenska Anna Materna-Kiryluk Feng Zhang Hakon Hakonarson Virginia E Papaioannou Cathy L Mendelsohn Ali G Gharavi Simone Sanna-Cherchi

Nat Genet 2019 04;51(4):764

Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.

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April 2019

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Authors:

Miguel Verbitsky Rik Westland Alejandra Perez Krzysztof Kiryluk Qingxue Liu Priya Krithivasan Adele Mitrotti David A Fasel Ekaterina Batourina Matthew G Sampson Monica Bodria Max Werth Charlly Kao Jeremiah Martino Valentina P Capone Asaf Vivante Shirlee Shril Byum Hee Kil Maddalena Marasà Jun Y Zhang Young-Ji Na Tze Y Lim Dina Ahram Patricia L Weng Erin L Heinzen Alba Carrea Giorgio Piaggio Loreto Gesualdo Valeria Manca Giuseppe Masnata Maddalena Gigante Daniele Cusi Claudia Izzi Francesco Scolari Joanna A E van Wijk Marijan Saraga Domenico Santoro Giovanni Conti Pasquale Zamboli Hope White Dorota Drozdz Katarzyna Zachwieja Monika Miklaszewska Marcin Tkaczyk Daria Tomczyk Anna Krakowska Przemyslaw Sikora Tomasz Jarmoliński Maria K Borszewska-Kornacka Robert Pawluch Maria Szczepanska Piotr Adamczyk Malgorzata Mizerska-Wasiak Grazyna Krzemien Agnieszka Szmigielska Marcin Zaniew Mark G Dobson John M Darlow Prem Puri David E Barton Susan L Furth Bradley A Warady Zoran Gucev Vladimir J Lozanovski Velibor Tasic Isabella Pisani Landino Allegri Lida M Rodas Josep M Campistol Cécile Jeanpierre Shumyle Alam Pasquale Casale Craig S Wong Fangming Lin Débora M Miranda Eduardo A Oliveira Ana Cristina Simões-E-Silva Jonathan M Barasch Brynn Levy Nan Wu Friedhelm Hildebrandt Gian Marco Ghiggeri Anna Latos-Bielenska Anna Materna-Kiryluk Feng Zhang Hakon Hakonarson Virginia E Papaioannou Cathy L Mendelsohn Ali G Gharavi Simone Sanna-Cherchi

Nat Genet 2019 01 21;51(1):117-127. Epub 2018 Dec 21.

Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.

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January 2019

Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.

Authors:

John M Darlow Rebecca Darlay Mark G Dobson Aisling Stewart Pimphen Charoen Jennifer Southgate Simon C Baker Yaobo Xu Manuela Hunziker Heather J Lambert Andrew J Green Mauro Santibanez-Koref John A Sayer Timothy H J Goodship Prem Puri Adrian S Woolf Rajko B Kenda David E Barton Heather J Cordell

Sci Rep 2018 01 8;8(1):459. Epub 2018 Jan 8.

Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK.

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January 2018

Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.

Authors:

John M Darlow Rebecca Darlay Mark G Dobson Aisling Stewart Pimphen Charoen Jennifer Southgate Simon C Baker Yaobo Xu Manuela Hunziker Heather J Lambert Andrew J Green Mauro Santibanez-Koref John A Sayer Timothy H J Goodship Prem Puri Adrian S Woolf Rajko B Kenda David E Barton Heather J Cordell

Sci Rep 2017 11 6;7(1):14595. Epub 2017 Nov 6.

Institute of Genetic Medicine, Newcastle University, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK.

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November 2017

Incidence of Fragile X syndrome in Ireland.

Authors:

James J O'Byrne Michael Sweeney Deirdre E Donnelly Deborah M Lambert Eleanor D Beattie Celine M Gervin David E Barton Sally A Lynch

Am J Med Genet A 2017 Mar 3;173(3):678-683. Epub 2017 Feb 3.

National Rare Diseases Office, Mater Misericordiae Hospital, Dublin, Ireland.

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March 2017

Reply to Sajantila and Budowle.

Authors:

David E Barton Mireille Claustres Viktor Kozich Els Dequeker Brian Fowler Jayne Y Hehir-Kwa Konstantin Miller Cor Oosterwijk Borut Peterlin Conny van Ravenswaaij-Arts Uwe Zimmermann Orsetta Zuffardi Rosalind J Hastings

Eur J Hum Genet 2016 Mar 14;24(3):330. Epub 2015 Jan 14.

CEQAS, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.

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March 2016

Urinary tract effects of HPSE2 mutations.

J Am Soc Nephrol 2015 Apr 21;26(4):797-804. Epub 2014 Aug 21.

Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Science Centre and the Royal Manchester Children's and St Mary's Hospitals, Manchester, United Kingdom;

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April 2015

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).

Authors:

Mireille Claustres Viktor Kožich Els Dequeker Brain Fowler Jayne Y Hehir-Kwa Konstantin Miller Cor Oosterwijk Borut Peterlin Conny van Ravenswaaij-Arts Uwe Zimmermann Orsetta Zuffardi Ros J Hastings David E Barton

Eur J Hum Genet 2014 Feb 14;22(2):160-70. Epub 2013 Aug 14.

National Centre for Medical Genetics, School of Medicine & Medical Sciences, University College Dublin, Our Lady's Children's Hospital, Dublin, Ireland.

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February 2014

Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux.

Authors:

Mark G Dobson John M Darlow Manuela Hunziker Andrew J Green David E Barton Prem Puri

Kidney Int 2013 Aug 27;84(2):327-37. Epub 2013 Mar 27.

National Centre for Medical Genetics, Crumlin, Dublin, Ireland.

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August 2013

EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington disease.

Authors:

Monique Losekoot Martine J van Belzen Sara Seneca Peter Bauer Susan A R Stenhouse David E Barton

Eur J Hum Genet 2013 May 19;21(5):480-6. Epub 2012 Sep 19.

Department of Clinical Genetics, Laboratory for Diagnostic Genome Analysis, Leiden University Medical Centre, Leiden, The Netherlands.

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May 2013

Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.

Fam Cancer 2012 Sep;11(3):509-18

Department of Cancer Genetics, Mater Private Hospital, Dublin 7, Ireland.

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September 2012

Quality assurance practices in Europe: a survey of molecular genetic testing laboratories.

Authors:

Sarah Berwouts Katrina Fanning Michael A Morris David E Barton Elisabeth Dequeker

Eur J Hum Genet 2012 Nov 27;20(11):1118-26. Epub 2012 Jun 27.

Department of Public Health, Biomedical Quality Assurance Research Unit, KU Leuven, Leuven, Belgium.

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November 2012

Genetics of vesicoureteral reflux.

Authors:

Prem Puri Jan-Hendrik Gosemann John Darlow David E Barton

Nat Rev Urol 2011 Aug 23;8(10):539-52. Epub 2011 Aug 23.

National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin 12, Ireland.

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August 2011

In search of an uncultured human-associated TM7 bacterium in the environment.

Authors:

Jorge M Dinis David E Barton Jamsheed Ghadiri Deepa Surendar Kavitha Reddy Fernando Velasquez Carol L Chaffee Mei-Chong Wendy Lee Helen Gavrilova Hazel Ozuna Samuel A Smits Cleber C Ouverney

PLoS One 2011 20;6(6):e21280. Epub 2011 Jun 20.

Department of Biological Sciences, San Jose State University, San Jose, California, United States of America.

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October 2011

Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes.

Authors:

Jennifer Boyle Malcolm Hawkins David E Barton Karen Meaney Miriam Guitart Anna O'Grady Simon Tobi Simon C Ramsden Rob Elles Elaine Gray Paul Metcalfe J Ross Hawkins

Eur J Hum Genet 2011 Aug 18;19(8):857-64. Epub 2011 May 18.

National Institute for Biological Standards and Control, Blanche Lane, South Mimms, Herts, UK.

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August 2011

Multiallelic synthetic quality control material: lessons learned from the cystic fibrosis external quality assessment scheme.

Authors:

Sarah Berwouts Todd M Christensen Jill Brandon Bassem A Bejjani David E Barton Elisabeth Dequeker

Genet Test Mol Biomarkers 2011 Sep 10;15(9):579-86. Epub 2011 Apr 10.

Biomedical Quality Assurance Research Unit, Department of Human Genetics, University of Leuven, Leuven, Belgium.

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September 2011