Browsing by Author Blue, Gillian

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Showing results 1 to 13 of 13
Issue DateTitleAuthor(s)Citation
2017Advances in the Genetics of Congenital Heart Disease: A Clinician's GuideBlue, Gillian; Sholler, Gary; Winlaw, David; Dunwoodie, Sally L; Giannoulatou, Eleni; Harvey, Richard P; Kirk, Edwin P.; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthAdvances in the Genetics of Congenital Heart Disease: A Clinician's Guide, Journal of the American College of Cardiology, vol.69, 7, 2017,pp 859-870
2015Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart DiseaseBlue, Gillian; Edel, Michael; Winlaw, David; Bosman, Alexis; Dilley, Rodney J; Harvey, Richard P; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthBioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease, Journal of Clinical Medicine, vol.4, 4, 2015,pp 768-781
2012Congenital heart disease: current knowledge about causes and inheritanceSholler, Gary; Winlaw, David; Blue, Gillian; Harvey, Richard P; Kirk, Edwin; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child HealthCongenital heart disease: current knowledge about causes and inheritance, Medical Journal of Australia, vol.197, 3, 2012,pp 155-159
2010GATA4 Mutations in 357 Unrelated Patients with Congenital Heart MalformationButler, Tanya; Sholler, Gary; Winlaw, David; Blue, Gillian; Cole, Andrew; Costa, Mauro; Esposito, Giorgia; Feneley, Michael; Harvey, Richard P; Kirk, E. P. E.; Waddell, Leigh; Walizada, Gina; Children's Hospital Westmead: Paediatrics & Child Health; Medical Radiation Sciences; Children's Hospital Westmead: Paediatrics & Child HealthGATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation, Genetic Testing and Molecular Biomarkers, vol.14, 6,pp 1-6
2018Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart diseaseBadawi, Nadia; Blue, Gillian; Loughran-Fowlds, Alison; Sholler, Gary; Walker, Karen Sheelagh; Winlaw, David; Dunwoodie, Sally L; Giannoulatou, Eleni; Harvey, Richard; Ip, Eddie; Kirk, Edwin P.; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthGenetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease, American Heart Journal, vol.201, N/A, 2018,pp 33-39
2015Genetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioningBlue, Gillian; Sholler, Gary; Winlaw, David; Kasparian, Nadine A; Kirk, Edwin; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthGenetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioning, International Journal of Cardiology, vol.178, N/A, 2015,pp 124-130
2013Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotWinlaw, David; Ayers, Kristin L; Bentham, Jamie; Blue, Gillian; Cordell, Heather J; Cosgrove, Catherine; Darlay, Rebecca; et al, Various; Granados-Riveron, Javier; Heath, Simon; Mamasoula, Chrysovalanto; Postma, Alex V; Rahman, Thahira; Soemedi, Rachel; Topf, Ana; Wilson, Ian J; Zelenika, Diana; Children's Hospital Westmead: Paediatrics & Child HealthGenome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot, Human Molecular Genetics, vol.22, 7, 2013,pp 1473-1481
2016Large-scale production of cardiomyocytes from human pluripotent stem cells using a highly reproducible small molecule-based differentiation protocolBlue, Gillian; Winlaw, David; Abbasalizadeh, Saeed; Aghdami, Nasser; Ansari, Hassan; Baharvand, Hossein; Bosman, Alexis; Fonoudi, Hananeh; Harvey, Richard; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthLarge-scale production of cardiomyocytes from human pluripotent stem cells using a highly reproducible small molecule-based differentiation protocol, Journal of Visualized Experiments: JOVE, vol.2016, 113, 2016,pp 1-10
2007The negative impact of Alagille syndrome on survival of infants with pulmonary atresiaChard, Richard; Cole, Andrew; Sherwood, Megan; Sholler, Gary; Winlaw, David; Blue, Gillian; Hawker, Richard E.; Lal, Vanita; Mah, Jean M; Wilson, Meredith J; Medicine; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child HealthThe negative impact of Alagille syndrome on survival of infants with pulmonary atresia, Journal of Thoracic and Cardiovascular Surgery, vol.133,(N/A),2007,pp 1094-1096
2016The promises and challenges of exome sequencing in familial, non-syndromic congenital heart diseaseBlue, Gillian; Sholler, Gary; Winlaw, David; Bosman, Alexis Gina; Chapman, Gavin; Dunwoodie, Sally; Harvey, Richard; Humphreys, David; Kirk, Edwin P.; Major, Joelene; Szot, Justin O.; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthThe promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease, International Journal of Cardiology, vol.230, N/A, 2016,pp 155-163
2011Somatic Mutations in NKX2-5, GATA4, and HAND1 Are Not a Common Cause of Tetralogy of Fallot or Hypoplastic Left HeartBlue, Gillian; Butler, Tanya; Sholler, Gary; Winlaw, David; Cole, Andrew; Esposito, Giorgia; Grossfeld, Paul; Harvey, Richard P; Kirk, E. P. E.; Perryman, Benjamin; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Medicine; Children's Hospital Westmead: Paediatrics & Child HealthSomatic Mutations in NKX2-5, GATA4, and HAND1 Are Not a Common Cause of Tetralogy of Fallot or Hypoplastic Left Heart, American Journal of Medical Genetics. Part A, vol.155, 10, 2011,pp 2416-2421
2014Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart diseaseBlue, Gillian; Sholler, Gary; Winlaw, David; Dunwoodie, Sally; Giannoulatou, Eleni; Harvey, Richard P; Hilton, Desiree C.K; Ho, Joshua W.K.; Kirk, Edwin; White, Susan M.; Childrens Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Medicine; Childrens Hospital Westmead: Paediatrics & Child HealthTargeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease, Journal of the American College of Cardiology, vol.64, 23, 2014,pp 2498-2506
2015A universal and robust integrated platform for the scalable production of human cardiomyocytes from pluripotent stem cellsBlue, Gillian; Winlaw, David; Abbasalizadeh, Saeed; Aghdami, Nasser; Ansari, Hassan; Baharvand, Hossein; Bosman, Alexis Gina; Fonoudi, Hananeh; Harvey, Richard; Hashemizadeh, Shiva; Kiani, Sahar; Larijani, Mehran Rezaei; Mayorchak, Y; Orr, Yishay; Pahlavan, Sara; Perry, Matthew; Talkhabi, Mahmood; Vandenberg, Jamie I; Zarchi, Ali Sharifi; Childrens Hospital Westmead: Paediatrics & Child Health; Childrens Hospital Westmead: Paediatrics & Child HealthA universal and robust integrated platform for the scalable production of human cardiomyocytes from pluripotent stem cells, Stem Cells Translational Medicine, vol.4, 12, 2015,pp 1-13