Adriano Magli

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

Max A. Tischfield, Hagit Baris, Chen Wu et al. · Cell · 2010 · 602 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +14

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

Koki Yamada, Caroline Andrews, Wai‐Man Chan et al. · Nature Genetics · 2003 · 262 citations

Medicine, Genetics, Molecular Genetics +14

Epithelium-Off Corneal Collagen Cross-linking Versus Transepithelial Cross-linking for Pediatric Keratoconus

Adriano Magli, Raimondo Forte, Achille Tortori et al. · Cornea · 2012 · 156 citations

Medicine, Ophthalmology, Pediatrics +17

Paralog Studies Augment Gene Discovery: DDX and DHX Genes

Ingrid S. Paine, Jennifer E. Posey, Christopher M. Grochowski et al. · The American Journal of Human Genetics · 2019 · 116 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Identification of<i>KIF21A</i>Mutations as a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 (CFEOM3)

Koki Yamada, Wai‐Man Chan, Caroline Andrews et al. · Investigative Ophthalmology & Visual Science · 2004 · 96 citations · Full text

Medicine, Genetics, Ophthalmology +13