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Author Details
Full Name
Ali G Fenstermaker
Affiliation
Howard Hughes Medical Institute, University of California
ORCID
Career Start Year
2005
Papers
10
H Index
9
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
25496456
Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.
Clin Genet
2015
24482476
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.
Science
2014
24945770
Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous microRNA dysregulation.
Neuron
2014
24360807
Mutations in CSPP1 lead to classical Joubert syndrome.
Am J Hum Genet
2014
23554479
Oligodendrocyte-specific activation of PERK signaling protects mice against experimental autoimmune encephalomyelitis.
J Neurosci
2013
23911318
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder.
Cell
2013
22700954
Exome sequencing can improve diagnosis and alter patient management.
Sci Transl Med
2012
21106844
Wnt/planar cell polarity signaling controls the anterior-posterior organization of monoaminergic axons in the brainstem.
J Neurosci
2010
18367611
Phosphatidylinositol-3-kinase-atypical protein kinase C signaling is required for Wnt attraction and anterior-posterior axon guidance.
J Neurosci
2008
15748170
Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model.
J Neurochem
2005
1 - 10 of 10
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