Items where Author is "Winlaw, David"

Article

Lain, Samantha J. and Blue, Gillian and O’Malley, Bridget and Winlaw, David and Sholler, Gary and Dunwoodie, Sally and Nassar, Natasha and The Congenital Heart Disease Synergy Study group, x (2023) Using novel data linkage of biobank data with administrative health data to inform genomic analysis for future precision medicine treatment of congenital heart disease. International Journal of Population Data Science, 8 (1). ISSN 2399-4908

Chapman, Gavin and Moreau, Julie L M and Ip, Eddie and Szot, Justin O and Iyer, Kavitha R and Shi, Hongjun and Yam, Michelle X and O’Reilly, Victoria C and Enriquez, Annabelle and Greasby, Joelene A and Alankarage, Dimuthu and Martin, Ella M M A and Hanna, Bernadette C and Edwards, Matthew and Monger, Steven and Blue, Gillian M and Winlaw, David and Ritchie, Helen E and Grieve, Stuart M and Giannoulatou, Eleni and Sparrow, Duncan B and Dunwoodie, Sally L (2020) Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants. Human Molecular Genetics. ISSN 0964-6906

Alankarage, Dimuthu and Szot, Justin O and Pachter, Nick and Slavotinek, Anne and Selleri, Licia and Shieh, Joseph T and Winlaw, David and Giannoulatou, Eleni and Chapman, Gavin and Dunwoodie, Sally L (2020) Functional characterisation of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Human Molecular Genetics. ISSN 0964-6906

Verrall, Charlotte E and Blue, Gillian M and Loughran-Fowlds, Alison and Kasparian, Nadine and Gecz, Jozef and Walker, Karen and Dunwoodie, Sally L and Cordina, Rachael and Sholler, Gary and Badawi, Nadia and Winlaw, David (2019) ‘Big issues’ in neurodevelopment for children and adults with congenital heart disease. Open Heart, 6 (2). pp. e000998. ISSN 2053-3624

Ip, Eddie and Chapman, Gavin and Winlaw, David and Dunwoodie, Sally L. and Giannoulatou, Eleni (2019) VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated Variants. Genomics, Proteomics & Bioinformatics. ISSN 16720229