Alex V. Levin

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

Max A. Tischfield, Hagit Baris, Chen Wu et al. · Cell · 2010 · 589 citations · Full text

Axon Guidance, Protein Function, Molecular Biology +8

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L. Collins et al. · Nature Genetics · 2016 · 346 citations · Full text

Human Congenital Anomalies, Developmental Anomaly, Developmental Biology +8

Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene

Andrea L. Vincent, Gail Billingsley, Yvonne M. Buys et al. · The American Journal of Human Genetics · 2002 · 307 citations · Full text

Ophthalmology, Genetic Disorder, Genetics +5

Prevalence, risk factors, and outcome of uveitis in juvenile idiopathic arthritis: A long‐term followup study

Rotraud K. Saurenmann, Alex V. Levin, Brian M. Feldman et al. · Arthritis & Rheumatism · 2007 · 282 citations

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 · 260 citations

Extraocular Muscles, Congenital Fibrosis, Fibrosis +9