Mary Jane Gray

Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss

Michael A. Simpson, Melita Irving, Esra Asilmaz et al. · Nature Genetics · 2011 · 306 citations

Progressive Bone Loss, Craniofacial Disorder, Genetic Disorder +4

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Silvia Cappello, Mary Jane Gray, Caroline Badouel et al. · Nature Genetics · 2013 · 276 citations

Molecular Neuroscience, Developmental Biology, Signaling Pathway +7

Mutations in PYCR1 cause cutis laxa with progeroid features

Bruno Reversade, Nathalie Escande‐Beillard, Aikaterini Dimopoulou et al. · Nature Genetics · 2009 · 252 citations

Biology, Plant Biology, Genetics +5

Hematoporphyrin derivative for detection and management of cancer

Richard L. Lipson, Edward J. Baldes, Mary Jane Gray · Cancer · 1967 · 235 citations · Full text

Radiology, Cancer Detection, Malignant Disease +13

Craniosynostosis and Multiple Skeletal Anomalies in Humans and Zebrafish Result from a Defect in the Localized Degradation of Retinoic Acid

Kathrin Laue, Hans‐Martin Pogoda, Philip B. Daniel et al. · The American Journal of Human Genetics · 2011 · 184 citations · Full text

Developmental Biology, Ophthalmology, Retinoic Acid +5