| The role of hypoxia in development of the Mammalian embryo SL Dunwoodie Developmental cell 17 (6), 755-773, 2009 | 750 | 2009 |
| Mouse Dll3: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo SL Dunwoodie, D Henrique, SM Harrison, RSP Beddington Development 124 (16), 3065-3076, 1997 | 477 | 1997 |
| SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation ME Blewitt, AV Gendrel, Z Pang, DB Sparrow, N Whitelaw, JM Craig, ... Nature genetics 40 (5), 663-669, 2008 | 404 | 2008 |
| TBX6 null variants and a common hypomorphic allele in congenital scoliosis N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, ... New England Journal of Medicine 372 (4), 341-350, 2015 | 298 | 2015 |
| Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation FA Stennard, MW Costa, D Lai, C Biben, MB Furtado, MJ Solloway, ... Oxford University Press for The Company of Biologists Limited 132 (10), 2451 …, 2005 | 277 | 2005 |
| Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype DB Sparrow, G Chapman, MA Wouters, NV Whittock, S Ellard, D Fatkin, ... The American Journal of Human Genetics 78 (1), 28-37, 2006 | 271 | 2006 |
| Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the … SL Dunwoodie, M Clements, DB Sparrow, X Sa, RA Conlon, ... Oxford University Press for The Company of Biologists Limited 129 (7), 1795-1806, 2002 | 266 | 2002 |
| NAD deficiency, congenital malformations, and niacin supplementation H Shi, A Enriquez, M Rapadas, EMMA Martin, R Wang, J Moreau, CK Lim, ... New England Journal of Medicine 377 (6), 544-552, 2017 | 248 | 2017 |
| A mechanism for gene-environment interaction in the etiology of congenital scoliosis DB Sparrow, G Chapman, AJ Smith, MZ Mattar, JA Major, VC O'Reilly, ... Cell 149 (2), 295-306, 2012 | 240 | 2012 |
| Notch inhibition by the ligand DELTA-LIKE 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis G Chapman, DB Sparrow, E Kremmer, SL Dunwoodie Human molecular genetics 20 (5), 905-916, 2011 | 239 | 2011 |
| Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo I Geffers, K Serth, G Chapman, R Jaekel, K Schuster-Gossler, R Cordes, ... The Journal of cell biology 178 (3), 465-476, 2007 | 215 | 2007 |
| Msg1 and Mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis SL Dunwoodie, TA Rodriguez, RSP Beddington Mechanisms of development 72 (1-2), 27-40, 1998 | 203 | 1998 |
| Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ... Journal of the American College of Cardiology 73 (1), 58-66, 2019 | 198 | 2019 |
| Mutated MESP2 causes spondylocostal dysostosis in humans NV Whittock, DB Sparrow, MA Wouters, D Sillence, S Ellard, ... The American Journal of Human Genetics 74 (6), 1249-1254, 2004 | 194 | 2004 |
| Abnormal vertebral segmentation and the notch signaling pathway in man PD Turnpenny, B Alman, AS Cornier, PF Giampietro, A Offiah, O Tassy, ... Developmental dynamics: an official publication of the American Association …, 2007 | 191 | 2007 |
| Evolution of distinct EGF domains with specific functions MA Wouters, I Rigoutsos, CK Chu, LL Feng, DB Sparrow, SL Dunwoodie Protein Science 14 (4), 1091-1103, 2005 | 183 | 2005 |
| Folic acid prevents exencephaly in Cited2 deficient mice JPM Barbera, TA Rodriguez, NDE Greene, WJ Weninger, A Simeone, ... Human molecular genetics 11 (3), 283-293, 2002 | 178 | 2002 |
| Transcriptional activating activity of Smad4: roles of SMAD hetero-oligomerization and enhancement by an associating transactivator T Shioda, RJ Lechleider, SL Dunwoodie, H Li, T Yahata, ... Proceedings of the National Academy of Sciences 95 (17), 9785-9790, 1998 | 176 | 1998 |
| Whole exome sequencing reveals the major genetic contributors to nonsyndromic tetralogy of Fallot DJ Page, MJ Miossec, SG Williams, RM Monaghan, E Fotiou, HJ Cordell, ... Circulation research 124 (4), 553-563, 2019 | 175 | 2019 |
| Developmental regulation of Notch signaling genes in the embryonic pituitary: Prop1 deficiency affects Notch2 expression LT Raetzman, SA Ross, S Cook, SL Dunwoodie, SA Camper, PQ Thomas Developmental biology 265 (2), 329-340, 2004 | 169 | 2004 |
Gavin ChapmanVictor Chang Cardiac Research InstituteAdresse e-mail validée de victorchang.edu.au
