PubRank

Robert W Burgess

Author PubWeight™ 47.67‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model. Neuron 2006 2.86
2 DSCAM and DSCAML1 function in self-avoidance in multiple cell types in the developing mouse retina. Neuron 2009 2.73
3 Neurite arborization and mosaic spacing in the mouse retina require DSCAM. Nature 2008 2.65
4 Imaging axonal transport of mitochondria in vivo. Nat Methods 2007 2.60
5 Genetic evidence that relative synaptic efficacy biases the outcome of synaptic competition. Nature 2003 2.51
6 Roles of neurotransmitter in synapse formation: development of neuromuscular junctions lacking choline acetyltransferase. Neuron 2002 2.16
7 Rab3 dynamically controls protein composition at active zones. Neuron 2009 2.07
8 A novel null allele of mouse DSCAM survives to adulthood on an inbred C3H background with reduced phenotypic variability. Genesis 2010 1.68
9 Two-photon NADH imaging exposes boundaries of oxygen diffusion in cortical vascular supply regions. J Cereb Blood Flow Metab 2010 1.64
10 Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. Am J Pathol 2007 1.43
11 Disruption and recovery of patterned retinal activity in the absence of acetylcholine. J Neurosci 2005 1.36
12 Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels. PLoS Genet 2011 1.25
13 An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Dis Model Mech 2009 1.22
14 A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations. Hum Mol Genet 2011 1.10
15 An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations. Mol Cell Neurosci 2010 1.08
16 Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability. Proc Natl Acad Sci U S A 2002 1.06
17 Defects in eye development in transgenic mice overexpressing the heparan sulfate proteoglycan agrin. Dev Biol 2006 1.02
18 Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease. Dis Model Mech 2013 1.02
19 Age, experience and genetic background influence treadmill walking in mice. Physiol Behav 2008 1.01
20 The Down syndrome critical region regulates retinogeniculate refinement. J Neurosci 2011 1.00
21 A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination. J Cell Sci 2008 0.99
22 Cell autonomy of DSCAM function in retinal development. Dev Biol 2011 0.98
23 Adhesion molecules in establishing retinal circuitry. Curr Opin Neurobiol 2009 0.96
24 Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D mice. Hum Mol Genet 2013 0.92
25 Neuronal clustering and fasciculation phenotype in Dscam- and Bax-deficient mouse retinas. J Comp Neurol 2012 0.91
26 Changes in brain β-amyloid deposition and aquaporin 4 levels in response to altered agrin expression in mice. J Neuropathol Exp Neurol 2011 0.90
27 A valid mouse model of AGRIN-associated congenital myasthenic syndrome. Hum Mol Genet 2011 0.90
28 A novel mouse Dscam mutation inhibits localization and shedding of DSCAM. PLoS One 2012 0.88
29 DSCAMs: restoring balance to developmental forces. Front Mol Neurosci 2012 0.87
30 Cell adhesion to agrin presented as a nanopatterned substrate is consistent with an interaction with the extracellular matrix and not transmembrane adhesion molecules. BMC Cell Biol 2008 0.84
31 Candidate molecular mechanisms for establishing cell identity in the developing retina. Dev Neurobiol 2011 0.82
32 A MusD retrotransposon insertion in the mouse Slc6a5 gene causes alterations in neuromuscular junction maturation and behavioral phenotypes. PLoS One 2012 0.79
33 A spontaneous mutation in contactin 1 in the mouse. PLoS One 2011 0.79
34 Lack of neuropathy-related phenotypes in hint1 knockout mice. J Neuropathol Exp Neurol 2014 0.78
35 Introduction to mechanisms of neural circuit formation. Front Mol Neurosci 2013 0.78
36 A mouse model of heritable cerebrovascular disease. PLoS One 2010 0.76
37 Corrigendum: CMT2D neuropathy is linked to the neomorphic binding activity of glycyl-tRNA synthetase. Nature 2016 0.75
38 Corrigendum: Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases. Nat Commun 2016 0.75