Browsing publications by Dr John O'Sullivan

Newcastle AuthorsTitleYear
Professor Heather Cordell
Dr Ana Topf
Valentina Mamasoula
Dr Rebecca Darlay
Rachel Soemedi
et al.		Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot2013
Valentina Mamasoula
Dr Ana Topf
Dr Thahira Rahman
Dr John O'Sullivan
Dr Christopher Wren
et al.		Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis2012
Dr Annette Klinge
Dr Ding Chang Zheng
Professor Alan Murray
Dr John O'Sullivan
Dr John Allen
et al.		Feasibility of monitoring vascular ageing by multi-site photoplethysmography2012
Dr Ana Topf
Professor Judith Goodship
Professor Deborah Henderson
Dr John O'Sullivan
Professor Bernard Keavney
et al.		Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to congenital heart disease2012
Dr Elise Glen
Dr Ana Topf
Dr Darroch Hall
Dr John O'Sullivan
Linda Sneddon
et al.		Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation2012
Dr Daniel Raine
Dr John O'Sullivan
Dr John Bourke
Ablation of atrial tachyarrhythmias late after surgical repair of tetralogy of Fallot2011
Dr Elise Glen
Dr Ana Topf
Dr Darroch Hall
Dr John O'Sullivan
Linda Sneddon
et al.		Non-synonymous SMAD6 mutations impaired inhibition of BMP signalling in patients with congenital cardiovascular malformation2011
Dr Nicola Leech
Dr John O'Sullivan
Dr Peter Avery
Laura Pascoe
Professor Mark Walker
et al.		Increased maternal Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) associated with older age at diagnosis of Type 1 diabetes in offspring2010
Dr Ana Topf
Dr Elise Glen
Dr John O'Sullivan
Professor Sir John Burn
Professor Heather Cordell
et al.		Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants2010
Dr Helen Griffin
Dr Ana Topf
Dr Elise Glen
Dr John O'Sullivan
Professor Sir John Burn
et al.		Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants2010
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