A. Fenstermaker

发表

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

T. Ideker, J. Al-Aama, Matan Hofree, 2014, Science.

Exome Sequencing Can Improve Diagnosis and Alter Patient Management

Vineet Bafna, Nitin Udpa, Carrie Sougnez, 2012, Science Translational Medicine.

Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model

L. Notterpek, A. Fenstermaker, B. Fletcher, 2005, Journal of neurochemistry.

Phosphatidylinositol-3-Kinase–Atypical Protein Kinase C Signaling Is Required for Wnt Attraction and Anterior–Posterior Axon Guidance

A. Wolf, Y. Zou, A. Fenstermaker, 2008, The Journal of Neuroscience.

Off-Target Effect of doublecortin Family shRNA on Neuronal Migration Associated with Endogenous MicroRNA Dysregulation

Ji Eun Lee, Joseph G. Gleeson, J. Gleeson, 2014, Neuron.

AMPD2 Regulates GTP Synthesis and Is Mutated in a Potentially Treatable Neurodegenerative Brainstem Disorder

S. Gabriel, E. Nickerson, R. Naviaux, 2013, Cell.

Wnt/Planar Cell Polarity Signaling Controls the Anterior–Posterior Organization of Monoaminergic Axons in the Brainstem

Y. Zou, A. Goffinet, F. Tissir, 2010, The Journal of Neuroscience.

Oligodendrocyte-Specific Activation of PERK Signaling Protects Mice against Experimental Autoimmune Encephalomyelitis

D. Ron, H. Harding, A. Fenstermaker, 2013, The Journal of Neuroscience.

Mutations in CSPP1 lead to classical Joubert syndrome.

S. Gabriel, M. Gunel, M. Kabra, 2014, American journal of human genetics.

Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis

S. Gabriel, J. Gleeson, A. Fenstermaker, 2015, Clinical genetics.