Sally L. Dunwoodie

Mouse <i>Dll3</i>: a novel divergent <i>Delta</i> gene which may complement the function of other <i>Delta</i> homologues during early pattern formation in the mouse embryo

Sally L. Dunwoodie, Domingos Henrique, Stephen Harrison et al. · Development · 1997 · 376 citations

SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation

Marnie E. Blewitt, Anne-Valérie Gendrel, Zhenyi Pang et al. · Nature Genetics · 2008 · 354 citations

Chromatin, Genome Instability, X Inactivation +13

<i>TBX6</i> Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis

Nan Wu, Ming Xuan, Jianqiu Xiao et al. · New England Journal of Medicine · 2015 · 310 citations · Full text

Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype

Duncan B. Sparrow, Gavin Chapman, Merridee A. Wouters et al. · The American Journal of Human Genetics · 2005 · 243 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

NAD Deficiency, Congenital Malformations, and Niacin Supplementation

Hongjun Shi, Annabelle Enriquez, Melissa Rapadas et al. · New England Journal of Medicine · 2017 · 235 citations · Full text