Christina Pieh

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

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 · 381 citations · Full text

Axon Guidance, Molecular Neuroscience, Developmental Biology +15

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Patrick Tarpey, Shery Thomas, Nagini Sarvananthan et al. · Nature Genetics · 2006 · 211 citations · Full text

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +6

VEGF-A, VEGFR-1, VEGFR-2 and Tie2 levels in plasma of premature infants: relationship to retinopathy of prematurity

Christina Pieh, Hansjürgen Agostini, C Buschbeck et al. · British Journal of Ophthalmology · 2008 · 69 citations

Brainstem hypoplasia in familial horizontal gaze palsy and scoliosis

Christina Pieh, Dora Lengyel, Anton W. Neff et al. · Neurology · 2002 · 59 citations

Ocular Disease, Seesaw Nystagmus, Ophthalmology +15