Items where Author is "Munro, Jacob"

Article

Kalisch-Smith, Jacinta I. and Ved, Nikita and Szumska, Dorota and Munro, Jacob and Troup, Michael and Harris, Shelley E. and Rodriguez-Caro, Helena and Jacquemot, Aimée and Miller, Jack J. and Stuart, Eleanor M. and Wolna, Magda and Hardman, Emily and Prin, Fabrice and Lana-Elola, Eva and Aoidi, Rifdat and Fisher, Elizabeth M. C. and Tybulewicz, Victor L. J. and Mohun, Timothy J. and Lakhal-Littleton, Samira and De Val, Sarah and Giannoulatou, Eleni and Sparrow, Duncan B. (2021) Maternal iron deficiency perturbs embryonic cardiovascular development in mice. Nature Communications, 12 (1). ISSN 2041-1723

Horvat, Claire and Johnson, Renee and Lam, Lien and Munro, Jacob and Mazzarotto, Francesco and Roberts, Angharad M and Herman, Daniel S and Parfenov, Michael and Haghighi, Alireza and McDonough, Barbara and DePalma, Steven R and Keogh, Anne M and Macdonald, Peter S and Hayward, Christopher S and Roberts, Amy and Barton, Paul J R and Felkin, Leanne E and Giannoulatou, Eleni and Cook, Stuart A and Seidman, Jonathan G and Seidman, Christine E and Fatkin, Diane (2019) A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy. Genetics in Medicine, 21 (1). pp.133-143. ISSN 1098-3600 (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)