Items where Author is "Kirk, Edwin P"

Article

Patrick, Ralph and Kirk, Edwin P and Moradi Marjaneh, Mahdi and Alankarage, Dimuthu and Humphreys, David T and Del Monte-Nieto, Gonzalo and Cornejo-Paramo, Paola and Janbandhu, Vaibhao and Doan, Tram B and Dunwoodie, Sally L and Wong, Emily S and Moran, Chris and Martin, Ian CA and Thomson, Peter C and Harvey, Richard P (2023) Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line. eLife, 12. ISSN 2050-084X

Alankarage, Dimuthu and Ip, Eddie and Szot, Justin O and Munro, Jacob and Blue, Gillian M and Harrison, Katrina and Cuny, Hartmut and Enriquez, Annabelle and Troup, Michael and Humphreys, David T and Wilson, Meredith and Harvey, Richard P and Sholler, Gary F and Graham, Robert M and Ho, Joshua W K and Kirk, Edwin P and Pachter, Nicholas and Chapman, Gavin and Winlaw, David S and Giannoulatou, Eleni and Dunwoodie, Sally L (2018) Identification of clinically actionable variants from genome sequencing of families with congenital heart disease. Genetics in Medicine, ePub. ISSN 1098-3600 (Not OA)

Blue, Gillian M and Ip, Eddie and Walker, Karen and Kirk, Edwin P and Loughran-Fowlds, Alison and Sholler, Gary F and Dunwoodie, Sally L and Harvey, Richard P and Giannoulatou, Eleni and Badawi, Nadia and Winlaw, David S (2018) Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease. American Heart Journal, 201. pp.33-39. ISSN 00028703 (Not OA)

Winlaw, David S and Dunwoodie, Sally L and Kirk, Edwin P (2017) Four-Generation Family With Ebstein Anomaly Highlights Future Challenges in Congenital Heart Disease Genetics. Circulation: Cardiovascular Genetics, 10 (6). pp. e001967. ISSN 1942-325X (OA)

Blue, Gillian M and Humphreys, David and Szot, Justin and Major, Joelene and Chapman, Gavin and Bosman, Alexis and Kirk, Edwin P and Sholler, Gary F and Harvey, Richard P and Dunwoodie, Sally L and Winlaw, David S (2017) The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease. International Journal of Cardiology, 230. pp.155-163. ISSN 1874-1754 (PP OA)

Blue, Gillian M and Kirk, Edwin P and Giannoulatou, Eleni and Sholler, Gary F and Dunwoodie, Sally L and Harvey, Richard P and Winlaw, David S (2017) Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide. Journal of the American College of Cardiology, 69 (7). pp.859-870. ISSN 1558-3597 (OA)

Blue, Gillian M and Kirk, Edwin P and Giannoulatou, Eleni and Dunwoodie, Sally L and Ho, Joshua W K and Hilton, Desiree C K and White, Susan M and Sholler, Gary F and Harvey, Richard P and Winlaw, David S (2014) Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease. Journal of the American College of Cardiology, 64 (23). pp.2498-506. ISSN 1558-3597 (OA)

Blue, Gillian M and Kirk, Edwin P and Sholler, Gary F and Harvey, Richard P and Winlaw, David S (2012) Congenital heart disease: current knowledge about causes and inheritance. The Medical journal of Australia, 197 (3). pp.155-9. ISSN 1326-5377 (OA)

Moradi Marjaneh, M and Martin, I C A and Kirk, Edwin P and Harvey, Richard P and Moran, C and Thomson, P C (2012) QTL mapping of complex binary traits in an advanced intercross line. Animal genetics, 43 Sup. pp.97-101. ISSN 1365-2052 (PP OA)

Granados-Riveron, Javier T and Pope, Mark and Bu'lock, Frances A and Thornborough, Christopher and Eason, Jacqueline and Setchfield, Kerry and Ketley, Ami and Kirk, Edwin P and Fatkin, Diane and Feneley, Michael P and Harvey, Richard P and Brook, J David (2012) Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations. Congenital heart disease, 7 (2). pp.151-9. ISSN 1747-0803 (PMC OA)