Items where Author is "Dunwoodie, Sally L"

Patrick, Ralph and Kirk, Edwin P and Moradi Marjaneh, Mahdi and Alankarage, Dimuthu and Humphreys, David T and Del Monte-Nieto, Gonzalo and Cornejo-Paramo, Paola and Janbandhu, Vaibhao and Doan, Tram B and Dunwoodie, Sally L and Wong, Emily S and Moran, Chris and Martin, Ian CA and Thomson, Peter C and Harvey, Richard P (2023) Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line. eLife, 12. ISSN 2050-084X

Chapman, Gavin and Moreau, Julie L M and Ip, Eddie and Szot, Justin O and Iyer, Kavitha R and Shi, Hongjun and Yam, Michelle X and O’Reilly, Victoria C and Enriquez, Annabelle and Greasby, Joelene A and Alankarage, Dimuthu and Martin, Ella M M A and Hanna, Bernadette C and Edwards, Matthew and Monger, Steven and Blue, Gillian M and Winlaw, David and Ritchie, Helen E and Grieve, Stuart M and Giannoulatou, Eleni and Sparrow, Duncan B and Dunwoodie, Sally L (2020) Functional genomics and gene-environment interaction highlight the complexity of Congenital Heart Disease caused by Notch pathway variants. Human Molecular Genetics. ISSN 0964-6906

Alankarage, Dimuthu and Szot, Justin O and Pachter, Nick and Slavotinek, Anne and Selleri, Licia and Shieh, Joseph T and Winlaw, David and Giannoulatou, Eleni and Chapman, Gavin and Dunwoodie, Sally L (2020) Functional characterisation of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Human Molecular Genetics. ISSN 0964-6906

Martin, Ella M M A and Enriquez, Annabelle and Sparrow, Duncan B and Humphreys, David T and McInerney-Leo, Aideen M and Leo, Paul J and Duncan, Emma L and Iyer, Kavitha R and Greasby, Joelene A and Ip, Eddie and Giannoulatou, Eleni and Sheng, Delicia and Wohler, Elizabeth and Dimartino, Clémantine and Amiel, Jeanne and Capri, Yline and Lehalle, Daphné and Mory, Adi and Wilnai, Yael and Lebenthal, Yael and Gharavi, Ali G and Krzemień, Grażyna G and Miklaszewska, Monika and Steiner, Robert D and Raggio, Cathy and Blank, Robert and Baris Feldman, Hagit and Milo Rasouly, Hila and Sobreira, Nara L M and Jobling, Rebekah and Gordon, Christopher T and Giampietro, Philip F and Dunwoodie, Sally L and Chapman, Gavin (2020) Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Human Molecular Genetics, 29 (22). pp.3662-3678. ISSN 0964-6906

Boycott, Kym M and Hartley, Taila and Biesecker, Leslie G and Gibbs, Richard A and Innes, A. Micheil and Riess, Olaf and Belmont, John and Dunwoodie, Sally L and Jojic, Nebojsa and Lassmann, Timo and Mackay, Deborah and Temple, I. Karen and Visel, Axel and Baynam, Gareth (2019) A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next Frontiers. Cell, 177 (1). pp.32-37. ISSN 00928674 (Not OA)

Moreau, Julie L. M and Kesteven, Scott and Martin, Ella M M A and Lau, Kin S and Yam, Michelle X and O'Reilly, Victoria C and del Monte-Nieto, Gonzalo and Baldini, Antonio and Feneley, Michael P and Moon, Anne M and Harvey, Richard P and Sparrow, Duncan B and Chapman, Gavin and Dunwoodie, Sally L (2019) Gene-environment interaction impacts on heart development and embryo survival. Development, 146 (4). pp. dev172957. ISSN 0950-1991 (Not OA)

Adlam, David and Kovacic, Jason C and Iismaa, Siiri E and Al-Hussaini, Abtehale and Wong, Claire Mei Yi and Giannoulatou, Eleni and Sweeting, Michael and Muller, David and Wood, Alice and McGrath-Cadell, Lucy and Fatkin, Diane and Dunwoodie, Sally L and Harvey, Richard and Holloway, Cameron and Empana, Jean-Philippe and Graham, Robert M and Motreff, Pascal and Meneveau, Nicolas and Gilard, Martine and Rioufol, Gilles and Range, Grégoire and Brunel, Philippe and Delarche, Nicolas and Filippi, Emmanuelle and Le Bivic, Louis and Harbaoui, Brahim and Benamer, Hakim and Cayla, Guillaume and Varenne, Olivier and Manzo-Silberman, Stephane Peggy and Silvain, Johanne and Spaulding, Christian and Caussin, Christophe and Gerbaud, Edouard and Valy, Yann and Koning, René and Lhermusier, Thibault and Champin, Stanislas and Salengro, Emmanuel and Fluttaz, Arnaud and Zabalawi, Amer and Cottin, Yves and Teiger, Emmanuel and Saint-Etienne, Christophe and Ducrocq, Grégory and Marliere, Stéphanie and Boiffard, Emmanuel and Aubry, Pierre and Georges, Jean Louis and Benamer, Hakim and Bresson, Didier and De Poli, Fabien and Karrillon, Gaëtan and Roule, Vincent and Bali, Laurent and Valla, Mathieu and Gerbay, Antoine and Houpe, David and Dubreuil, Olivier and Monnier, Arsène and Mayaud, Norbert and Manchuelle, Aurélie and Commeau, Philippe and Bedossa, Marc and Nikpay, Majid and Goel, Anuj and Won, Hong-Hee and Hall, Leanne M. and Willenborg, Christina and Kanoni, Stavroula and Saleheen, Danish and Kyriakou, Theodosios and Nelson, Christopher P. and Hopewell, Jemma C. and Webb, Thomas R. and Zeng, Lingyao and Dehghan, Abbas and Alver, Maris and Armasu, Sebastian M and Auro, Kirsi and Bjonnes, Andrew and Chasman, Daniel I. and Chen, Shufeng and Ford, Ian and Franceschini, Nora and Gieger, Christian and Grace, Christopher and Gustafsson, Stefan and Huang, Jie and Hwang, Shih-Jen and Kim, Yun Kyoung and Kleber, Marcus E. and Lau, King Wai and Lu, Xiangfeng and Lu, Yingchang and Lyytikäinen, Leo P. and Mihailov, Evelin and Morrison, Alanna and Pervjakova, Natalia and Qu, Liming and Rose, Lynda M. and Salfati, Elias and Saxena, Richa and Scholz, Markus and Smith, Albert V. and Tikkanen, Emmi and Uitterlinden, Andre and Yang, Xueli and Zhang, Weihua and Zhao, Wei and de Andrade, Mariza and de Vries, Paul S. and van Zuydam, Natalie R. and Anand, Sonia S. and Bertram, Lars and Beutner, Frank and Dedoussis, George and Frossard, Philippe and Gauguier, Dominique and Goodall, Alison H. and Gottesman, Omri and Haber, Marc and Han, Bok-Ghee and Huang, Jianfeng and Jalilzadeh, Shapour and Kessler, Thorsten and Thiery, Joachim and Zalloua, Pierre A. and O'Donnell, Christopher J. and Reilly, Muredach P. and Assimes, Themistocles L. and Thompson, John R. and Erdmann, Jeanette and Clarke, Robert and Watkins, Hugh and Kathiresan, Sekar and McPherson, Ruth and Deloukas, Panos and Schunkert, Heribert and Samani, Nilesh J. and Farrall, Martin (2019) Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection. Journal of the American College of Cardiology, 73 (1). pp.58-66. ISSN 1558-3597 (Not OA)

Verrall, Charlotte E and Blue, Gillian M and Loughran-Fowlds, Alison and Kasparian, Nadine and Gecz, Jozef and Walker, Karen and Dunwoodie, Sally L and Cordina, Rachael and Sholler, Gary and Badawi, Nadia and Winlaw, David (2019) ‘Big issues’ in neurodevelopment for children and adults with congenital heart disease. Open Heart, 6 (2). pp. e000998. ISSN 2053-3624

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)

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)

Blue, Gillian M and Ip, Eddie and Walker, Karen and Kirk, Edwin P and Loughran-Fowlds, Alison and Sholler, Gary F and Dunwoodie, Sally L and Harvey, Richard P and Giannoulatou, Eleni and Badawi, Nadia and Winlaw, David S (2018) Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease. American Heart Journal, 201. pp.33-39. ISSN 00028703 (Not OA)

Szot, Justin O and Cuny, Hartmut and Blue, Gillian M and Humphreys, David T and Ip, Eddie and Harrison, Katrina and Sholler, Gary F and Giannoulatou, Eleni and Leo, Paul J and Duncan, Emma L and Sparrow, Duncan B and Ho, Joshua W K and Graham, Robert M and Pachter, Nicholas S and Chapman, Gavin and Winlaw, David S and Dunwoodie, Sally L (2018) A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. Circulation: Genomic and Precision Medicine, 11 (3). pp. e001978. ISSN (Not OA)

Giampietro, Philip F and Pourquie, Olivier and Raggio, Cathy and Ikegawa, Shiro and Turnpenny, Peter D and Gray, Ryan and Dunwoodie, Sally L and Gurnett, Christina A and Alman, Benjamin and Cheung, Kenneth and Kusumi, Kenro and Hadley-Miller, Nancy and Wise, Carol A (2018) Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16-18, 2017, Dallas, Texas. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 176 (1). pp.253-256. ISSN 1552-4833 (Not OA)

Winlaw, David S and Dunwoodie, Sally L and Kirk, Edwin P (2017) Four-Generation Family With Ebstein Anomaly Highlights Future Challenges in Congenital Heart Disease Genetics. Circulation: Cardiovascular Genetics, 10 (6). pp. e001967. ISSN 1942-325X (OA)

Slavotinek, Anne and Risolino, Maurizio and Losa, Marta and Cho, Megan T and Monaghan, Kristin G. and Schneidman-Duhovny, Dina and Parisotto, Sarah and Herkert, Johanna C and Stegmann, Alexander P.A. and Miller, Kathryn and Shur, Natasha and Chui, Jacqueline and Muller, Eric and DeBrosse, Suzanne and Szot, Justin O and Chapman, Gavin and Pachter, Nicholas S and Winlaw, David S and Mendelsohn, Bryce A. and Dalton, Joline and Sarafoglou, Kyriakie and Karachunski, Peter I. and Lewis, Jane M and Pedro, Helio and Dunwoodie, Sally L and Selleri, Licia and Shieh, Joseph (2017) De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. Human Molecular Genetics, 26 (24). pp.4849-4860. ISSN 0964-6906 (Not OA)

Shi, Hongjun and Enriquez, Annabelle and Rapadas, Melissa and Martin, Ella M M A and Wang, Roni and Moreau, Julie and Lim, Chai K and Szot, Justin O and Ip, Eddie and Hughes, James N and Sugimoto, Kotaro and Humphreys, David T and McInerney-Leo, Aideen M and Leo, Paul J and Maghzal, Ghassan J and Halliday, Jake and Smith, Janine and Colley, Alison and Mark, Paul R and Collins, Felicity and Sillence, David O and Winlaw, David S and Ho, Joshua W K and Guillemin, Gilles J and Brown, Matthew A and Kikuchi, Kazu and Thomas, Paul Q and Stocker, Roland and Giannoulatou, Eleni and Chapman, Gavin and Duncan, Emma L and Sparrow, Duncan B and Dunwoodie, Sally L (2017) NAD Deficiency, Congenital Malformations, and Niacin Supplementation. The New England Journal of Medicine, 377 (6). pp.544-552. ISSN 1533-4406 (OA)

Munro, Jacob E and Dunwoodie, Sally L and Giannoulatou, Eleni (2017) SVPV: a structural variant prediction viewer for paired-end sequencing datasets. Bioinformatics, 33 (13). pp.2032-2033. ISSN 1367-4811 (OA)

Blue, Gillian M and Humphreys, David and Szot, Justin and Major, Joelene and Chapman, Gavin and Bosman, Alexis and Kirk, Edwin P and Sholler, Gary F and Harvey, Richard P and Dunwoodie, Sally L and Winlaw, David S (2017) The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease. International Journal of Cardiology, 230. pp.155-163. ISSN 1874-1754 (PP OA)

Blue, Gillian M and Kirk, Edwin P and Giannoulatou, Eleni and Sholler, Gary F and Dunwoodie, Sally L and Harvey, Richard P and Winlaw, David S (2017) Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide. Journal of the American College of Cardiology, 69 (7). pp.859-870. ISSN 1558-3597 (OA)

Wang, Xuanchun and Lockhart, Samuel M and Rathjen, Thomas and Albadawi, Hassan and Sørensen, Ditte and O'Neill, Brian T and Dwivedi, Nishant and Preil, Simone R and Beck, Hans Christian and Dunwoodie, Sally L and Watkins, Michael T and Rasmussen, Lars Melholt and Rask-Madsen, Christian (2016) Insulin Downregulates the Transcriptional Coregulator CITED2, an Inhibitor of Proangiogenic Function in Endothelial Cells. Diabetes, 65 (12). pp.3680-3690. ISSN 1939-327X (OA)

Shi, Hongjun and O'Reilly, Victoria C and Moreau, Julie L M and Bewes, Therese R and Yam, Michelle X and Chapman, Bogdan E and Grieve, Stuart M and Stocker, Roland and Graham, Robert M and Chapman, Gavin and Sparrow, Duncan B and Dunwoodie, Sally L (2016) Gestational stress induces the unfolded protein response, resulting in heart defects. Development, 143 (14). pp.2561-72. ISSN 1477-9129 (OA)

Fame, Ryann M and MacDonald, Jessica L and Dunwoodie, Sally L and Takahashi, Emi and Macklis, Jeffrey D (2016) Cited2 Regulates Neocortical Layer II/III Generation and Somatosensory Callosal Projection Neuron Development and Connectivity. The Journal of Neuroscience, 36 (24). pp.6403-19. ISSN 1529-2401 (OA)

Chapman, Gavin and Major, J A and Iyer, K Swaminathan and James, Alexander C and Pursglove, S E and Moreau, J L M and Dunwoodie, Sally L (2016) Notch1 endocytosis is induced by ligand and is required for signal transduction. Biochimica et Biophysica Acta, 1863 (1). pp.166-77. ISSN 0006-3002 (OA)

Monger, Steven and Troup, Michael and Ip, Eddie and Dunwoodie, Sally L and Giannoulatou, Eleni and Birol, Inanc (2016) Spliceogen: an integrative, scalable tool for the discovery of splice-altering variants. Bioinformatics. ISSN 1367-4803

Yoo, Jung-Yoon and Kim, Tae Hoon and Lee, Jae Hee and Dunwoodie, Sally L and Ku, Bon Jeong and Jeong, Jae-Wook (2015) Mig-6 regulates endometrial genes involved in cell cycle and progesterone signaling. Biochemical and Biophysical Research Communications, 462 (4). pp.409-14. ISSN 1090-2104 (PMC 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)

Wilkinson, Lorine J and Neal, Cailda S and Singh, Reetu R and Sparrow, Duncan B and Kurniawan, Nyoman D and Ju, Adler and Grieve, Stuart M and Dunwoodie, Sally L and Moritz, Karen M and Little, Melissa H (2015) Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signaling. Kidney International, 87 (5). pp.975-83. ISSN 1523-1755 (PP OA)

McInerney-Leo, Aideen M and Sparrow, Duncan B and Harris, Jessica E and Gardiner, Brooke B and Marshall, Mhairi S and O'Reilly, Victoria C and Shi, Hongjun and Brown, Matthew A and Leo, Paul J and Zankl, Andreas and Dunwoodie, Sally L and Duncan, Emma L (2015) Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects. Human Molecular Genetics, 24 (5). pp.1234-42. ISSN 1460-2083 (PP OA)

Wu, N and Ming, X and Xiao, J and Wu, Z and Chen, X and Shinawi, M and Shen, Y and Yu, G and Liu, J and Xie, H and Gucev, Z S and Liu, S and Yang, N and Al-Kateb, H and Chen, J and Zhang, J and Hauser, N and Zhang, T and Tasic, V and Liu, P and Su, X and Pan, X and Liu, C and Wang, L and Shen, J and Shen, J and Chen, Y and Zhang, T and Zhang, J and Choy, K W and Wang, J and Wang, Q and Li, S and Zhou, W and Guo, J and Wang, Y and Zhang, C and Zhao, Hong and An, Yu and Zhao, Yu and Wang, J and Liu, Z and Zuo, Y and Tian, Y and Weng, X and Sutton, V R and Wang, H and Ming, Y and Kulkarni, S and Zhong, T P and Giampietro, P F and Dunwoodie, Sally L and Cheung, S W and Zhang, X and Jin, L and Lupski, J R and Qiu, G and Zhang, F (2015) TBX6 null variants and a common hypomorphic allele in congenital scoliosis. The New England Journal of Medicine, 372 (4). pp.341-50. ISSN 1533-4406 (OA)

Blue, Gillian M and Kirk, Edwin P and Giannoulatou, Eleni and Dunwoodie, Sally L and Ho, Joshua W K and Hilton, Desiree C K and White, Susan M and Sholler, Gary F and Harvey, Richard P and Winlaw, David S (2014) Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease. Journal of the American College of Cardiology, 64 (23). pp.2498-506. ISSN 1558-3597 (OA)

Moreau, Julie L M and Artap, Stanley T and Shi, Hongjun and Chapman, Gavin and Leone, Gustavo and Sparrow, Duncan B and Dunwoodie, Sally L (2014) Cited2 is required in trophoblasts for correct placental capillary patterning. Developmental Biology, 392 (1). pp.62-79. ISSN 1095-564X (OA)

O'Reilly, Victoria C and Lopes Floro, Kylie and Shi, Hongjun and Chapman, Bogdan E and Preis, Jost I and James, Alexander C and Chapman, Gavin and Harvey, Richard P and Johnson, Randall S and Grieve, Stuart M and Sparrow, Duncan B and Dunwoodie, Sally L (2014) Gene-environment interaction demonstrates the vulnerability of the embryonic heart. Developmental Biology, 391 (1). pp.99-110. ISSN 1095-564X (OA)

James, Alexander C and Szot, Justin and Iyer, K Swaminathan and Major, Joelene A and Pursglove, Sharon and Chapman, Gavin and Dunwoodie, Sally L (2014) Notch4 reveals a novel mechanism regulating Notch signal transduction. Biochimica et Biophysica Acta, 1843 (7). pp.1272-84. ISSN 0006-3002 (OA)

Londono, Douglas and Kou, Ikuyo and Johnson, Todd A and Sharma, Swarkar and Ogura, Yoji and Tsunoda, Tatsuhiko and Takahashi, Atsushi and Matsumoto, Morio and Herring, John A and Lam, Tsz-Ping and Wang, Xingyan and Tam, Elisa M S and Song, You-Qiang and Fan, Yan-Hui and Chan, Danny and Cheah, Kathryn S E and Qiu, Xusheng and Jiang, Hua and Huang, Dongsheng and TSRHC IS Clinical Group, International Consortium for Scoliosis Genetics and Su, Peiqiang and Sham, Pak and Cheung, Kenneth M C and Luk, Keith D K and Gordon, Derek and Qiu, Yong and Cheng, Jack and Tang, Nelson and Ikegawa, Shiro and Wise, Carol A and Dunwoodie, Sally L (2014) A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups. Journal of Medical Genetics, 51 (6). pp.401-6. ISSN 1468-6244 (Not OA)

Du, Jinwei and Li, Qiang and Tang, Fangqiang and Puchowitz, Michelle A and Fujioka, Hisashi and Dunwoodie, Sally L and Danielpour, David and Yang, Yu-Chung (2014) Cited2 is required for the maintenance of glycolytic metabolism in adult hematopoietic stem cells. Stem Cells and Development, 23 (2). pp.83-94. ISSN 1557-8534 (PMC OA)

Li, Qiang and Hakimi, Parvin and Liu, Xia and Yu, Wen-Mei and Ye, Fang and Fujioka, Hisashi and Raza, Syed and Shankar, Eswar and Tang, Fangqiang and Dunwoodie, Sally L and Danielpour, David and Hoppel, Charles L and Ramírez-Bergeron, Diana L and Qu, Cheng-Kui and Hanson, Richard W and Yang, Yu-Chung (2014) Cited2, a transcriptional modulator protein, regulates metabolism in murine embryonic stem cells. The Journal of biological chemistry, 289 (1). pp.251-63. ISSN 1083-351X (PMC OA)

Sparrow, Duncan B and Faqeih, Eissa Ali and Sallout, Bahauddin and Alswaid, Abdulrahman and Ababneh, Faroug and Al-Sayed, Moeenaldeen and Rukban, Hadeel and Eyaid, Wafaa M and Kageyama, Ryoichiro and Ellard, Sian and Turnpenny, Peter D and Dunwoodie, Sally L (2013) Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 161A (9). pp.2244-9. ISSN 1552-4833 (Not OA)

Dunwoodie, Sally L and Hamada, Hiroshi (2013) Ways, means and consequences of shaping morphogen gradients. Current opinion in genetics & development, 23 (4). pp.361-2. ISSN 1879-0380 (PP OA)

Sparrow, Duncan B and McInerney-Leo, Aideen and Gucev, Zoran S and Gardiner, Brooke and Marshall, Mhairi and Leo, Paul J and Chapman, Deborah L and Tasic, Velibor and Shishko, Abduhadi and Brown, Matthew A and Duncan, Emma L and Dunwoodie, Sally L (2013) Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. Human Molecular Genetics, 22 (8). pp.1625-31. ISSN 1460-2083 (OA)

Méniel, Valérie and Song, Fei and Phesse, Toby and Young, Madeleine and Poetz, Oliver and Parry, Lee and Jenkins, John R and Williams, Geraint T and Dunwoodie, Sally L and Watson, Alasdair J and Clarke, Alan R (2013) Cited1 deficiency suppresses intestinal tumorigenesis. PLoS Genetics, 9 (8). pp. e1003638. ISSN 1553-7404 (Gold OA)

Li, Qiang and Ramírez-Bergeron, Diana L and Dunwoodie, Sally L and Yang, Yu-Chung (2012) Cited2 gene controls pluripotency and cardiomyocyte differentiation of murine embryonic stem cells through Oct4 gene. The Journal of biological chemistry, 287 (34). pp.29088-100. ISSN 1083-351X (PMC OA)

Sparrow, Duncan B and Chapman, Gavin and Smith, Allanceson J and Mattar, Muhammad Z and Major, Joelene A and O'Reilly, Victoria C and Saga, Yumiko and Zackai, Elaine H and Dormans, John P and Alman, Benjamin A and McGregor, Lesley and Kageyama, Ryoichiro and Kusumi, Kenro and Dunwoodie, Sally L (2012) A mechanism for gene-environment interaction in the etiology of congenital scoliosis. Cell, 149 (2). pp.295-306. ISSN 1097-4172 (OA)

Du, Jinwei and Chen, Yu and Li, Qiang and Han, Xiangzi and Cheng, Cindy and Wang, Zhengqi and Danielpour, David and Dunwoodie, Sally L and Bunting, Kevin D and Yang, Yu-Chung (2012) HIF-1α deletion partially rescues defects of hematopoietic stem cell quiescence caused by Cited2 deficiency. Blood, 119 (12). pp.2789-98. ISSN 1528-0020 (PMC OA)

Huang, Tai-Qin and Wang, Yiwei and Ebrahem, Quteba and Chen, Yu and Cheng, Cindy and Doughman, Yong Qiu and Watanabe, Michiko and Dunwoodie, Sally L and Yang, Yu-Chung (2012) Deletion of HIF-1α partially rescues the abnormal hyaloid vascular system in Cited2 conditional knockout mouse eyes. Molecular vision, 18. pp.1260-70. ISSN 1090-0535 (PMC OA)