By Professor Sally Dunwoodie

Conference Papers

Tarr I; Hesselson S; Iismaa S; Troup M; Young P; Mishra K; Wong C; Junday K; Humphreys D; Dunwoodie S; Fatkin D; Muller D; Graham RM; Giannoulatou E, 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

Blue GM; Ip E; Sholler GF; Harvey RP; Giannoulatou E; Dunwoodie SL; Winlaw DS, 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

Page DJ; Miossec MJ; Williams SG; Monaghan RM; Fotiou E; Cordell HJ; Sutcliffe L; Topf A; Bourgey M; Bourque G; Eveleigh R; Dunwoodie SL; Winlaw DS; Bhattacharya S; Breckpot J; Devriendt K; Gewillig M; Brook D; Setchfield K; Bu'Lock FA; O'Sullivan J; Stuart G; Bezzina C; Mulder BJM; Postma AV; Bentham JR; Baron M; Bhaskar SS; Black GC; Newman WG; Hentges KE; Lathrop M; Santibanez-Koref M; Keavney BD, 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

Blue GM; Ip E; Walker K; Kirk EP; Loughran-Fowlds A; Sholler GF; Dunwoodie SL; Harvey RP; Giannoulatou E; Badawi N; Winlaw DS, 2017, 'Genetic Variants Explaining Neurodevelopmental Disorders in Patients With Congenital Heart Disease - Are We Ready for the Clinic?', in CIRCULATION, LIPPINCOTT WILLIAMS & WILKINS, CA, Anaheim, presented at Scientific Sessions of the American-Heart-Association / Resuscitation Science Symposium, CA, Anaheim, 11 November 2017 - 15 November 2017, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000437035905488&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Fisher RE; Chapman G; Dunwoodie SL; Kusumi K, 2016, 'The Application of Iodine-Enhanced Micro-CT Scanning Protocols to Analyze Multiple Tissue Types and Organ Systems in Mouse Embryos with Short-term Gestational Hypoxia', in FASEB JOURNAL, FEDERATION AMER SOC EXP BIOL, CA, San Diego, presented at Experimental Biology Meeting, CA, San Diego, 02 April 2016 - 06 April 2016

Fisher RE; Chapman G; Dunwoodie SL; Kusumi K, 2016, 'The Application of Iodine-Enhanced Micro-CT Scanning Protocols to Analyze Multiple Tissue Types and Organ Systems in Mouse Embryos with Short-term Gestational Hypoxia', in FASEB JOURNAL, FEDERATION AMER SOC EXP BIOL, San Diego, CA, presented at Experimental Biology Meeting, San Diego, CA, 02 April 2016 - 06 April 2016, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000406444004137&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Fisher RE; Chapman G; Dunwoodie SL; Kusumi K, 2016, 'The Application of Iodine-Enhanced Micro-CT Scanning Protocols to Analyze Multiple Tissue Types and Organ Systems in Mouse Embryos with Short-term Gestational Hypoxia', in FASEB JOURNAL, FEDERATION AMER SOC EXP BIOL, San Diego, CA, presented at Experimental Biology Meeting, San Diego, CA, 02 April 2016 - 06 April 2016, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000406444004645&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Fisher RE; Chapman G; Dunwoodie SL; Kusumi K, 2016, 'The Application of Iodine-Enhanced Micro-CT Scanning Protocols to Analyze Multiple Tissue Types and Organ Systems in Mouse Embryos with Short-term Gestational Hypoxia', in FASEB JOURNAL, FEDERATION AMER SOC EXP BIOL, San Diego, CA, presented at Experimental Biology Meeting, San Diego, CA, 02 April 2016 - 06 April 2016, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000406444001286&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Du J; Chen Y; Li Q; Wang Z; Dunwoodie S; Bunting KD; Yang Y-C, 2011, 'Cited2 Regulates Hematopoietic Stem Cell Quiescence Through HIF-1 alpha Dependent and Independent Pathways', in BLOOD, AMER SOC HEMATOLOGY, CA, San Diego, pp. 416 - 417, presented at 53rd Annual Meeting and Exposition of the American-Society-of-Hematology (ASH)/Symposium on the Basic Science of Hemostasis and Thrombosis, CA, San Diego, 10 December 2011 - 13 December 2011

Cantley J; Davenport A; Dunwoodie SL; Biden TJ, 2011, 'Deletion of the Cited2 gene in beta cells causes impaired insulin secretion and glucose intolerance in mice', in DIABETOLOGIA, SPRINGER, PORTUGAL, Lisbon, pp. S21 - S21, presented at 47th Annual Meeting of the European-Association-for-the-Study-of-Diabetes (EASD), PORTUGAL, Lisbon, 12 September 2011 - 16 September 2011, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000307671300035&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Artap S; Lopes Floro K; Saga Y; Hamada H; Sparrow DB; Dunwoodie SL, 2009, 'Cited2 transactivates Nodal expression in the left lateral plate mesoderm through interaction with FoxH1', in Mechanisms of Development, Elsevier Science BV, Amsterdam, Netherlands, pp. S188 - S188, presented at 16th International Society of Developmental Biologists Congress, Edinburgh, http://dx.doi.org/10.1016/j.mod.2009.06.453

Stevens S; Gonzalez D; Pratt S; Dunwoodie SL; Loomes K; Kusumi K, 2008, 'Notch pathway mutants display craniofacial birth defects and disrupt expression of the pharyngeal arch gene Barx1', in Developmental Biology, Academic Press Inc Elsevier Science, San Diego, Ca, USA, pp. 585 - 586, presented at Society for Developmental Biology 67th Annual Meeting Program, http://dx.doi.org/10.1016/j.ydbio.2008.05.421

Kusumi K; Stevens SA; Mimoto MS; Dunwoodie SL; Loomes KM, 2003, 'Dll3-Notch1 double mutant mice are a model for congenital scoliosis and craniofacial disorders.', in AMERICAN JOURNAL OF HUMAN GENETICS, UNIV CHICAGO PRESS, CALIFORNIA, LOS ANGELES, pp. 172 - 172, presented at Annual Meeting of the American-Society-of-Human-Genetics, CALIFORNIA, LOS ANGELES, 04 November 2003 - 08 November 2003, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000185599700052&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Sparrow DB; Withington SL; Scott AN; Preis J; Rodriguez T; Beddington RSP; Dunwoodie SL, 2003, 'Cited1 is required for normal placental development in mouse.', in DEVELOPMENTAL BIOLOGY, ACADEMIC PRESS INC ELSEVIER SCIENCE, MASSACHUSETTS, BOSTON, pp. 558 - 558, presented at 62nd Annual Meeting of the Society-for-Development-Biology, MASSACHUSETTS, BOSTON, 30 July 2003 - 02 August 2003, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000184373300465&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Capra V; De Marco P; Moroni A; Merello E; Raso A; Dunwoodie S; Carna A, 2002, 'CITED2 is not a major determinant of human NTDs.', in AMERICAN JOURNAL OF HUMAN GENETICS, UNIV CHICAGO PRESS, MARYLAND, BALTIMORE, pp. 468 - 468, presented at 52nd Annual Meeting of the American-Society-of-Human-Genetics, MARYLAND, BALTIMORE, 15 October 2002 - 19 October 2002, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000178025801743&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

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