Mike Shires

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

Manir Ali, Martin McKibbin, Adam Booth et al. · The American Journal of Human Genetics · 2009 · 325 citations · Full text

Medicine, Genetics, Ophthalmology +12

Toward Routine Use of 3D Histopathology as a Research Tool

Nicholas Roberts, Derek Magee, Yi Song et al. · American Journal Of Pathology · 2012 · 157 citations · Full text

Computing, Pathology, Visualization +17

Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

Clare V. Logan, Barbara Lucke, Caroline Pottinger et al. · Nature Genetics · 2011 · 113 citations

Life Sciences, Genetics, Molecular Genetics +13

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

Kamron N. Khan, Adam K Rudkin, David Parry et al. · The American Journal of Human Genetics · 2011 · 81 citations · Full text

Medicine, Genetics, Ophthalmology +17

Identification and validation of DOCK4 as a potential biomarker for risk of bone metastasis development in patients with early breast cancer

Jules A. Westbrook, Steven L. Wood, David A. Cairns et al. · The Journal of Pathology · 2018 · 48 citations · Full text

Medicine, Cell Biology, Oncology +17