Items where Author is "Winlaw, David S"

Article

Page, Donna J and Miossec, Matthieu J and Williams, Simon G and Monaghan, Richard M and Fotiou, Elisavet and Cordell, Heather and Sutcliffe, Louise and Topf, Ana and Bourgey, Mathieu and Bourque, Guillaume and Eveleigh, Robert and Dunwoodie, Sally L and Winlaw, David S and Bhattacharya, Shoumo and Breckpot, Jeroen and Devriendt, Koenraad and Gewillig, Marc and Brook, J David and Setchfield, Kerry Jane and Bu'Lock, Frances and O'sullivan, John J and Stuart, Graham and Bezzina, Connie R and Mulder, Barbara Jm and Postma, Alex V and Bentham, James R and Baron, Martin and Bhaskar, Sanjeev S and Black, Graeme C and Newman, William G and Hentges, Kathryn E and Lathrop, G Mark and Santibanez Koref, Mauro and Keavney, Bernard (2018) Whole Exome Sequencing Reveals the Major Genetic Contributors to Non-Syndromic Tetralogy of Fallot. Circulation Research, ePub. ISSN 1524-4571 (Not OA)

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)

Winlaw, David S and Sholler, Gary F and Barach, Paul (2018) Regional consolidation of pediatric cardiac surgery in New York State – Are we there yet? A destination reached or a step in the right direction? Progress in Pediatric Cardiology, 50. pp.1-3. ISSN 10589813 (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)

Szot, Justin O and Cuny, Hartmut and Blue, Gillian M and Humphreys, David T and Ip, Eddie and Harrison, Katrina and Sholler, Gary F and Giannoulatou, Eleni and Leo, Paul J and Duncan, Emma L and Sparrow, Duncan B and Ho, Joshua W K and Graham, Robert M and Pachter, Nicholas S and Chapman, Gavin and Winlaw, David S and Dunwoodie, Sally L (2018) A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. Circulation: Genomic and Precision Medicine, 11 (3). pp. e001978. ISSN (Not OA)

Winlaw, David S (2018) Hypoplastic left heart: the next chapter in our unsolved problem. Heart, epub. ISSN 1355-6037 (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)

Slavotinek, Anne and Risolino, Maurizio and Losa, Marta and Cho, Megan T and Monaghan, Kristin G. and Schneidman-Duhovny, Dina and Parisotto, Sarah and Herkert, Johanna C and Stegmann, Alexander P.A. and Miller, Kathryn and Shur, Natasha and Chui, Jacqueline and Muller, Eric and DeBrosse, Suzanne and Szot, Justin O and Chapman, Gavin and Pachter, Nicholas S and Winlaw, David S and Mendelsohn, Bryce A. and Dalton, Joline and Sarafoglou, Kyriakie and Karachunski, Peter I. and Lewis, Jane M and Pedro, Helio and Dunwoodie, Sally L and Selleri, Licia and Shieh, Joseph (2017) De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. Human Molecular Genetics, 26 (24). pp.4849-4860. ISSN 0964-6906 (Not OA)

Shi, Hongjun and Enriquez, Annabelle and Rapadas, Melissa and Martin, Ella M M A and Wang, Roni and Moreau, Julie and Lim, Chai K and Szot, Justin O and Ip, Eddie and Hughes, James N and Sugimoto, Kotaro and Humphreys, David T and McInerney-Leo, Aideen M and Leo, Paul J and Maghzal, Ghassan J and Halliday, Jake and Smith, Janine and Colley, Alison and Mark, Paul R and Collins, Felicity and Sillence, David O and Winlaw, David S and Ho, Joshua W K and Guillemin, Gilles J and Brown, Matthew A and Kikuchi, Kazu and Thomas, Paul Q and Stocker, Roland and Giannoulatou, Eleni and Chapman, Gavin and Duncan, Emma L and Sparrow, Duncan B and Dunwoodie, Sally L (2017) NAD Deficiency, Congenital Malformations, and Niacin Supplementation. The New England Journal of Medicine, 377 (6). pp.544-552. ISSN 1533-4406 (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)

Fonoudi, Hananeh and Ansari, Hassan and Abbasalizadeh, Saeed and Blue, Gillian M and Aghdami, Nasser and Winlaw, David S and Harvey, Richard P and Bosman, Alexis and Baharvand, Hossein (2016) Large-Scale Production of Cardiomyocytes from Human Pluripotent Stem Cells Using a Highly Reproducible Small Molecule-Based Differentiation Protocol. Jove-Journal of Visualized Experiments (113). pp.1-10. ISSN 1940-087X (Not OA)

Fonoudi, Hananeh and Ansari, Hassan and Abbasalizadeh, Saeed and Larijani, Mehran Rezaei and Kiani, Sahar and Hashemizadeh, Shiva and Zarchi, Ali Sharifi and Bosman, Alexis and Blue, Gillian M and Pahlavan, Sara and Perry, Matthew D and Orr, Yishay and Mayorchak, Yaroslav and Vandenberg, Jamie I and Talkhabi, Mahmood and Winlaw, David S and Harvey, Richard P and Aghdami, Nasser and Baharvand, Hossein (2015) A Universal and Robust Integrated Platform for the Scalable Production of Human Cardiomyocytes From Pluripotent Stem Cells. Stem Cells Translational Medicine, 4 (12). pp.1482-94. ISSN 2157-6564 (PP OA)

Bosman, Alexis and Edel, Michael J and Blue, Gillian M and Dilley, Rodney J and Harvey, Richard P and Winlaw, David S (2015) Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease. Journal of Clinical Medicine, 4 (4). pp.768-81. ISSN 2077-0383 (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)