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List of works by Gillian M Blue

"Why and how did this happen?": development and evaluation of an information resource for parents of children with CHD

scientific article published on 10 January 2020

'Big issues' in neurodevelopment for children and adults with congenital heart disease

scientific article published on 03 July 2019

A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data

scientific article published on 01 March 2018

A Universal and Robust Integrated Platform for the Scalable Production of Human Cardiomyocytes From Pluripotent Stem Cells

scientific article

Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide.

scientific article published on February 2017

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

scientific article published on 10 December 2021

Congenital heart disease: current knowledge about causes and inheritance ⬇️

scientific article published on August 6, 2012

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

scientific article

Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants

scientific article published on 01 March 2020

Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease

scientific article published on 05 April 2018

Genetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioning

scientific article

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

scientific journal article

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

scientific article published on 26 May 2013

Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

scientific article published on 08 October 2018

Large-Scale Production of Cardiomyocytes from Human Pluripotent Stem Cells Using a Highly Reproducible Small Molecule-Based Differentiation Protocol

scientific article published on 25 July 2016

Management of People With a Fontan Circulation: a Cardiac Society of Australia and New Zealand Position statement

scientific article published on 14 November 2019

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

scientific article

Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease

scientific article published on December 2014

The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease

scientific article published on 13 December 2016

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