Items where Author is "Bhattacharya, Shoumo"

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)

Bouveret, Romaric and Waardenberg, Ashley J and Schonrock, Nicole and Ramialison, Mirana and Doan, Tram and de Jong, Danielle and Bondue, Antoine and Kaur, Gurpreet and Mohamed, Stephanie and Fonoudi, Hananeh and Chen, Chiann-Mun and Wouters, Merridee A and Bhattacharya, Shoumo and Plachta, Nicolas and Dunwoodie, Sally L and Chapman, Gavin and Blanpain, Cédric and Harvey, Richard P (2015) NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets. eLife, 4. ISSN 2050-084X (OA)