Alexis Robinson

Mutations in the planar cell polarity genes<i>CELSR1</i>and<i>SCRIB</i>are associated with the severe neural tube defect craniorachischisis

Alexis Robinson, Sarah Escuin, Kit Doudney et al. · Human Mutation · 2011 · 194 citations · Full text

Craniofacial Disorder, Genetics, Molecular Genetics +21

Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene

Stephen R.F. Twigg, Sarah L. Versnel, Gudrun Nürnberg et al. · The American Journal of Human Genetics · 2009 · 138 citations · Full text

Developmental Anomaly, Distinctive Presentation, Developmental Biology +6

Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

Ayumi Narisawa, Shoko Komatsuzaki, Atsuo Kikuchi et al. · Human Molecular Genetics · 2011 · 117 citations · Full text

Molecular Neuroscience, Developmental Biology, Molecular Physiology +14

Distinct Mechanisms of Pathogenic DJ-1 Mutations in Mitochondrial Quality Control

Daniela Strobbe, Alexis Robinson, Kirsten Harvey et al. · Frontiers in Molecular Neuroscience · 2018 · 31 citations · Full text

Is <i>LMNB1</i> a susceptibility gene for neural tube defects in humans?

Alexis Robinson, Darren Partridge, Ashraf N. Malhas et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2013 · 16 citations · Full text