Elizabeth C. Engle

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

Structural Grading of Foveal Hypoplasia Using Spectral-Domain Optical Coherence Tomography

Mervyn G. Thomas, Anil Kumar, Sarim Mohammad et al. · Ophthalmology · 2011 · 428 citations

Health Professions, Ophthalmology, Vision Science +12

Mutations in a Human <i>ROBO</i> Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis

Joanna C. Jen, Wai‐Man Chan, Thomas M. Bosley et al. · Science · 2004 · 384 citations · Full text

Life Sciences, Genetics, Neuroscience +16

Duane Radial Ray Syndrome (Okihiro Syndrome) Maps to 20q13 and Results from Mutations in SALL4, a New Member of the SAL Family

Raidah Albaradie, Koki Yamada, Cynthia St. Hilaire et al. · The American Journal of Human Genetics · 2002 · 319 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Deletions of <i>NRXN1</i> (neurexin‐1) predispose to a wide spectrum of developmental disorders

Michael S. Ching, Yiping Shen, Wen‐Hann Tan et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2010 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14