A simplified method of generating transgenic Xenopus by Sparrow, D, Latinkic, B, Mohun, T

Environmental risk factors for congenital heart disease by Kalisch-Smith, J, Ved, N, Sparrow, D

MEF2 proteins, including MEF2A, are expressed in both muscle and non-muscle cells by Dodou, E, Sparrow, D, Mohun, T, Treisman, R

Tamoxifen administration in pregnant mice can be deleterious to both mother and embryo by Ved, N, Curran, A, Ashcroft, FM, Sparrow, D

The RSRF/MEF2 protein SL1 regulates cardiac muscle-specific transcription of a myosin light-chain gene in Xenopus embryos. by Chambers, A, Logan, M, Kotecha, S, Towers, N, Sparrow, D, Mohun, T

Cited1 is required in trophoblasts for placental development and for embryo growth and survival by Rodriguez, T, Sparrow, D, Scott, A, Withington, S, Preis, J, Michalicek, J, Clements, M, Tsang, T, Shioda, T, Beddington, R, Dunwoodie, S

Complex SUMO-1 regulation of cardiac transcription factor Nkx2-5 by Costa, M, Lee, S, Furtado, M, Xin, L, Sparrow, D, Martinez, C, Dunwoodie, S, Kurtenbach, E, Mohun, T, Rosenthal, N, Harvey, R

Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo by Geffers, I, Serth, K, Chapman, G, Jaekel, R, Schuster-Gossler, K, Cordes, R, Sparrow, D, Kremmer, E, Dunwoodie, S, Klein, T, Gossler, A

Gestational stress induces the unfolded protein response resulting in heart defects by Shi, H, O'Reilly, V, Moreau, J, Bewes, T, Yam, M, Chapman, B, Grieve, S, Stocker, R, Graham, R, Chapman, G, Sparrow, D, Dunwoodie, S

The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner by Palmer, S, Groves, N, Schindeler, A, Yeoh, T, Biben, C, Wang, C, Sparrow, D, Barnett, L, Jenkins, N, Copeland, N, Koentgen, F, Mohun, T, Harvey, R

Analysis of placental arteriovenous formation reveals new insights into embryos with congenital heart defects by Kalisch-Smith, J, Morris, E, Strevens, M, Redpath, A, Klaourakis, K, Szumska, D, Outhwaite, J, Sun, X, Vieira, J, Smart, N, De Val, S, Riley, P, Sparrow, D

A screening approach to identify clinically actionable variants causing congenital heart disease in exome data by Szot, J, Cuny, H, Blue, G, Humphreys, D, Ip, E, Harrison, K, Sholler, G, Giannoulatou, E, Leo, P, Duncan, E, Sparrow, D, Ho, J, Graham, R, Pachter, N, Chapman, G, Winlaw, D, Dunwoodie, S

Neutrophil-mediated IL-6 receptor trans-signaling and the risk of chronic obstructive pulmonary disease and asthma by Farahi, N, Paige, E, Balla, J, Prudence, E, Ferreira, RC, Southwood, M, Appleby, SL, Bakke, P, Gulsvik, A, Litonjua, A, Sparrow, D, Silverman, EK, Cho, MH, Danesh, J, Paul, DS, Freitag, DF, Chilvers, ER

Insights into the role of a cardiomyopathy-causing genetic variant in ACTN2 by Broadway-Stringer, S, Jiang, H, Wadmore, K, Hooper, C, Douglas, G, Steeples, V, Azad, A, Singer, E, Rayet, J, Galatik, F, Ehler, E, Bennett, P, Kalisch-Smith, J, Sparrow, D, Davies, B, Djinovic-Carugo, K, Gautel, M, Watkins, H, Gehmlich, K

Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants by Chapman, G, Moreau, J, Ip, E, Szot, J, Iyer, K, Shi, H, Yam, M, O'Reilly, V, Enriquez, A, Greasby, J, Alankarage, D, Martin, E, Hanna, B, Edwards, M, Monger, S, Blue, G, Winlaw, D, Ritchie, H, Grieve, S, Giannoulatou, E, Sparrow, D, Dunwoodie, S

Functional analysis of a gene-edited mouse to gain insights into the disease mechanisms of a titin missense variant by Jiang, H, Hooper, C, Kelly, M, Steeples, V, Simon, J, Beglova, J, Azad, AJ, Leinhos, L, Bennett, P, Ehler, E, Kalisch-Smith, J, Sparrow, D, Fischer, R, Heilig, R, Isackson, H, Ehsan, M, Patone, G, Huebner, N, Davies, B, Watkins, H, Gehmlich, K

NAD deficiency, congenital malformations and niacin supplementation by Shi, H, Enriquez, A, Rapadas, M, Martin, E, Wang, R, Moreau, J, Lim, C, Szot, J, Ip, E, Hughes, J, Sugimoto, K, Humphreys, D, McInerney-Leo, A, Leo, P, Maghzal, G, Halliday, J, Smith, J, Colley, A, Mark, P, Collins, F, Sillence, D, Winlaw, D, Ho, J, Guillemin, G, Brown, M, Kikuchi, K, Thomas, P, Stocker, R, Giannoulatou, E, Chapman, G, Duncan, E, Sparrow, D, Dunwoodie, S

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice by Martin, E, Enriquez, A, Sparrow, D, Humphreys, D, McInerney-Leo, A, Leo, P, Duncan, E, Iyer, K, Greasby, J, Ip, E, Giannoulatou, E, Sheng, D, Wohler, E, Dimartino, C, Amiel, J, Capri, Y, Lehall, D, Mory, A, Wilnai, Y, Lebenthal, Y, Gharavi, A, Krzemień, G, Miklaszewska, M, Steiner, R, Raggio, C, Blank, R, Feldman, H, Rasouly, H, Sobreira, N, Jobling, R, Gordon, C, Giampietro, P, Dunwoodie, S, Chapman, G

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets by Wain, L, Shrine, N, Artigas, M, Erzurumluoglu, A, Noyvert, B, Bossini-Castillo, L, Obeidat, M, Henry, A, Portelli, M, Hall, R, Billington, C, Rimington, T, Fenech, A, John, C, Blake, T, Jackson, V, Allen, R, Prins, B, Understanding Society Scientific Group, Campbell, A, Porteous, D, Jarvelin, M, Wielscher, M, James, A, Hui, J, Wareham, N, Zhao, J, Wilson, J, Joshi, P, Stubbe, B, Rawal, R, Schulz, H, Imboden, M, Probst-Hensch, N, Karrasch, S, Gieger, C, Deary, I, Harris, S, Marten, J, Rudan, I, Enroth, S, Gyllensten, U, Kerr, S, Polasek, O, Kähönen, M, Surakka, I, Vitart, V, Hayward, C, Lehtimäki, T, Raitakari, O, Evans, D, Henderson, A, Pennell, C, Wang, C, Sly, P, Wan, E, Busch, R, Hobbs, B, Litonjua, A, Sparrow, D, Gulsvik, A, Bakke, P, Crapo, J, Beaty, T, Hansel, N, Mathias, R, Ruczinski, I, Barnes, K, Bossé, Y, Joubert, P, van den Berge, M, Brandsma, C, Paré, P, Sin, D, Nickle, D, Hao, K, Gottesman, O, Dewey, F, Bruse, S, Carey, D, Kirchner, H, Geisinger-Regeneron DiscovEHR Collaboration, Jonsson, S, Thorleifsson, G, Jonsdottir, I, Gislason, T, Stefansson, K, Schurmann, C, Nadkarni, G, Bottinger, E, Loos, R, Walters, R, Chen, Z, Millwood, I, Vaucher, J, Kurmi, O, Li, L, Hansell, A, Brightling, C, Zeggini, E, Cho, M, Silverman, E, Sayers, I, Trynka, G, Morris, A, Strachan, D, Hall, I, Tobin, M