Select Publications
Journal articles
2005, 'Assessing the role of Cited2 in human congenital heart disease (CHD)', MECHANISMS OF DEVELOPMENT, 122, pp. S54 - S54, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100198&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'Cited2 is essential for the establishment of the left-right axis', MECHANISMS OF DEVELOPMENT, 122, pp. S104 - S104, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100390&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'Cited2 is required for normal cardiovascular development', MECHANISMS OF DEVELOPMENT, 122, pp. S93 - S93, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100348&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'Mutation of the LUNATIC FRINGE gene causes spondylocostal dysostosis in humans', MECHANISMS OF DEVELOPMENT, 122, pp. S152 - S153, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100576&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'T-box transcription factor Tbx20 is an important transcriptional repressor in vivo and is essential for murine embryonic heart development', MECHANISMS OF DEVELOPMENT, 122, pp. S58 - S59, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100214&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'The expression profile of the germ layers and primitive streak in 7.5 dpc mouse embryos', MECHANISMS OF DEVELOPMENT, 122, pp. S147 - S147, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100555&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'Understanding the various roles that Cited2 plays during mouse development', MECHANISMS OF DEVELOPMENT, 122, pp. S67 - S68, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000207524100249&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2005, 'Cited1 Is a bifunctional transcriptional cofactor that regulates early nephronic patterning', Journal of the American Society of Nephrology, 16, pp. 1632 - 1644
,2005, 'Cited2 is required both for heart mophogenesis and establishment of the left-right axis in mouse development', Development (Cambridge), 132, pp. 1337 - 1348
,2005, 'Cited2 is required for heart morphogenesis and establishment of the left-right axis in mouse', Developmental Biology, 283, pp. 677 - 677
,2005, 'Evolution of distinct EGF domains with specific functions', Protein Science, 14, pp. 1091 - 1103
,2005, 'Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaption', Development (Cambridge), 132, pp. 2451 - 2462
,2004, 'Erratum: Edd, the murine ortholog of the hyperplastic discs (hyd) gene, is essential for yolk sac vascularization and chorioallantoic fusion (Molecular and Cellular Biology (2004) 24: 16 (7225-7234))', Molecular and Cellular Biology, 24, pp. 9262, http://dx.doi.org/10.1128/MCB.24.20.9262.2004
,2004, 'Dll3 pudgy mutation differentially disrupts dynamic expression of somite genes', Genesis (United States), 39, pp. 115 - 121, http://dx.doi.org/10.1002/gene.20034
,2004, '016.Role of cited genes in placental morphogenesis: studies in null mutant mice', Reproduction, Fertility and Development, 16, pp. 16 - 16, http://dx.doi.org/10.1071/srb04abs016
,2004, 'Breaking symmetry: a clinical overview of left-right patterning', Clinical Geriatrics, 65, pp. 441 - 457
,2004, 'Cited1 is required in trophoblasts for placental development and for embryo growth and survival', Molecular and Cellular Biology, 24, pp. 228 - 244, http://dx.doi.org/10.1128/MCB.24.1.228-244.2004
,2004, 'Developmental regulation of Notch signaling genes in the embryonicpituitary: Prop1 deficiency affects Notch2 expression', Developmental Biology, 265, pp. 329 - 340
,2004, 'DII3 pudgy mutation differentially disrupts dynamic expression ofsomite genes', Genesis, 39, pp. 115 - 121
,2004, 'Edd, the murine hyperplastic disc gene, is essential for yolk sac vascularization and chorioallantoic fusion', Molecular and Cellular Biology, 24, pp. 7225 - 7234, http://dx.doi.org/10.1128/MCB.24.16.7225-7234.2004
,2004, 'Evolution of distinct EGF domain sub-types with specific functions', Federation of American Societies for Experimantal Biology Journal, 18, pp. C151 - C151
,2004, 'Kousseff syndrome: A causally heterogeneous disorder', American Journal of Medical Genetics Part A, 124A, pp. 307 - 312
,2004, 'Mutated MESP2 causes spondylocostal dysostosis in humans', American Journal of Human Genetics, 74, pp. 1249 - 1254
,2003, 'Characterising Embryonic Gene Expression Patterns in the Mouse Using Non-Redundant Sequence-Based Selection.', Genome Research, pp. 2609 - 2620
,2003, 'Cited1 is required for embryonic survival and normal placental development.', Molecular and Cellular Biology, 24, pp. 228 - 244
,2003, 'Developmental regulation of Noteh signaling genes in the embryonic pituitary: Notch 2 is a target of Propl.', Mechanisms of Development, 2, pp. 329 - 340
,2003, 'Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis.', Journal of Medical Genetics, pp. 333 - 339
,2002, 'Diverse requirements for Notch signalling in mammals', International Journal of Developmental Biology, 46, pp. 365 - 374
,2002, 'The expression of the imprinted gene Ipl is restricted to extra-embryonic tissues and embryonic lateral mesoderm during early mouse development', International Journal of Developmental Biology, 46, pp. 459 - 466
,2002, 'Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm', Development, 129, pp. 1795 - 1806
,2002, 'Folic acid prevents exencephaly in Cited2 deficient mice', Human Molecular Genetics, 11, pp. 283 - 293
,2002, 'Cloning of mouse cited4, a member of the CITED family p300/CBP-binding transcriptional coactivators: Induced expression in mammary epithelial cells', Genomics, 80, pp. 601 - 613, http://dx.doi.org/10.1006/geno.2002.7005
,2002, 'Diverse requirements for Notch signalling in mammals', INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 46, pp. 365 - 374, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000176824700007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2002, 'Remembering Rosa Beddington--a tribute from her friends and colleagues.', Developmental dynamics : an official publication of the American Association of Anatomists, 223, pp. 3 - 11, http://dx.doi.org/10.1002/dvdy.10053
,2002, 'The expression of the imprinted gene Ipl is restricted to extra-embryonic tissues and embryonic lateral mesoderm during early mouse development', INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY, 46, pp. 459 - 466, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000176824700017&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2001, 'Erratum: A radiation hybrid transcript map of the mouse genome (Nature Genetics (2001) 29 (194-200))', Nature Genetics, 29, pp. 352, http://dx.doi.org/10.1038/ng1101-352a
,2001, 'A radiation hybrid transcript map of the mouse genome', Nature Genetics, 29, pp. 194 - 200, http://dx.doi.org/10.1038/ng1001-194
,2001, 'Delta3 mutational analysis in mouse defines the developmental origins of skeletal dysplasia in spondylocostal dysostosis.', DEVELOPMENTAL BIOLOGY, 235, pp. 293 - 293, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000169701100504&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2001, 'Dynamic expression patterns of the pudgy/spondylocostal dysostosis gene Dll3 in the developing nervous system', Mechanisms of Development, 100, pp. 141 - 144, http://dx.doi.org/10.1016/S0925-4773(00)00514-1
,2000, 'Sp5, a new member of the Sp1 family, is dynamically expressed during development and genetically interacts with Brachyury', Developmental Biology, 227, pp. 358 - 372, http://dx.doi.org/10.1006/dbio.2000.9878
,1998, 'Transcriptional activating activity of Smad4: Roles of SMAD hetero-oligomerization and enhancement by an associating transactivator', Proceedings of the National Academy of Sciences of the United States of America, 95, pp. 9785 - 9790, http://dx.doi.org/10.1073/pnas.95.17.9785
,1998, 'Msg1 and mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis', Mechanisms of Development, 72, pp. 27 - 40, http://dx.doi.org/10.1016/S0925-4773(98)00011-2
,1997, 'Mouse Dll3: A novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo', Development, 124, pp. 3065 - 3076
,1997, 'Unrestricted lineage differentiation of parthenogenetic ES cells', Development Genes and Evolution, 206, pp. 377 - 388, http://dx.doi.org/10.1007/s004270050067
,1995, 'Isolation of novel tissue-specific genes from cDNA libraries representing the individual tissue constituents of the gastrulating mouse embryo', Development, 121, pp. 2479 - 2489
,1994, 'Multiple regions of the human cardiac actin gene are necessary for maturation-based expression in striated muscle', Journal of Biological Chemistry, 269, pp. 12212 - 12219
,1991, 'Coordination of skeletal muscle gene expression occurs late in mammalian development', Developmental Biology, 146, pp. 167 - 178, http://dx.doi.org/10.1016/0012-1606(91)90457-E
,Conference Papers
2021, 'Disease-Specific and Comorbidity-Related Polygenic Risk in Spontaneous Coronary Artery Dissection', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000752020004372&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2019, 'Whole Genome Sequencing Provides Insight Into the Genetic Composition Underlying CHD Severity', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, PA, Philadelphia, presented at Scientific Sessions of the American-Heart-Association, PA, Philadelphia, 16 November 2019 - 18 November 2019, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000529998004425&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
,2019, 'IDENTIFICATION OF THE MAJOR GENETIC CONTRIBUTORS TO TETRALOGY OF FALLOT', in HEART, BMJ PUBLISHING GROUP, ENGLAND, Manchester, pp. A182 - A183, presented at Annual Conference of the British-Cardiovascular-Society (BCS) - Digital Health Revolution, ENGLAND, Manchester, 03 June 2019 - 05 June 2019, http://dx.doi.org/10.1136/heartjnl-2019-BCS.226
,