Gillian M. Blue - Concepedia

Author

Gillian M. Blue

Also Known As

Chris Barnett, G. Blue, Gavin Chapman, Gillian Blue, Gillian M Blue, Gillian M. Blue, Gillian M. Blue, Sally L. Dunwoodie, Samantha Lain

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Children's Hospital at Westmead The University of Sydney UNSW Sydney Victor Chang Cardiac Research Institute Sydney Children's Hospital

About

Gillian M. Blue is an author at Children's Hospital at Westmead specializing in medicine, genetics, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	583
2	Engineering	3	3	209
3	Public Health	1	1	37
4	Social Sciences	1	1	35
5	Biomedical Engineering	1	1	19

Gillian M. Blue

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease Rachel Soemedi, Ian Wilson, Jamie Bentham, The American Journal of Human Genetics	2012	335
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls Rachel Soemedi, Ana Töpf, Ian Wilson, Human Molecular Genetics	2011	162
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 Heather J. Cordell, Jamie Bentham, Ana Töpf, Nature Genetics Atrial Septal DefectGenome-wide Association StudyGenetic DisorderGeneticsGenetic Epidemiology	2013	156
A Universal and Robust Integrated Platform for the Scalable Production of Human Cardiomyocytes From Pluripotent Stem Cells Hananeh Fonoudi, Hassan Ansari, Saeed Abbasalizadeh, Stem Cells Translational Medicine	2015	128
Targeted Next-Generation Sequencing Identifies Pathogenic Variants in Familial Congenital Heart Disease Gillian M. Blue, Edwin P. Kirk, Eleni Giannoulatou, Journal of the American College of Cardiology SequencingEngineeringMedicineGeneticsNext-generation Sequencing	2014	106
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot Heather J. Cordell, Ana Töpf, Chrysovalanto Mamasoula, Human Molecular Genetics	2013	103
A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data Justin O. Szot, Hartmut Cuny, Gillian M. Blue, Circulation Genomic and Precision Medicine	2018	99
Identification of clinically actionable variants from genome sequencing of families with congenital heart disease Dimuthu Alankarage, Eddie Ip, Justin O. Szot, Genetics in Medicine EngineeringVariant InterpretationMedicineGeneticsActionable Variants	2018	84
<i>GATA4</i> Mutations in 357 Unrelated Patients with Congenital Heart Malformation Tanya L. Butler, Giorgia Esposito, Gillian M. Blue, Genetic Testing and Molecular Biomarkers Gata4 MutationsCardiomyopathyDevelopmental BiologyGenetic DisorderCongenital Heart Malformation	2010	58
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants Gavin Chapman, Julie Moreau, I P Eddie, Human Molecular Genetics GeneticsCardiac Progenitor CellsMolecular GeneticsDisease Gene IdentificationGenomics	2019	49

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