|
1
|
Evolution and functions of long noncoding RNAs.
|
Cell
|
2009
|
17.54
|
|
2
|
Mouse genomic variation and its effect on phenotypes and gene regulation.
|
Nature
|
2011
|
10.66
|
|
3
|
A functional genetic link between distinct developmental language disorders.
|
N Engl J Med
|
2008
|
4.99
|
|
4
|
The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.
|
Hum Mol Genet
|
2006
|
3.39
|
|
5
|
Genomic and transcriptional co-localization of protein-coding and long non-coding RNA pairs in the developing brain.
|
PLoS Genet
|
2009
|
3.38
|
|
6
|
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
|
Cell
|
2007
|
3.06
|
|
7
|
Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes.
|
Genome Biol
|
2010
|
2.20
|
|
8
|
A transcriptomic atlas of mouse neocortical layers.
|
Neuron
|
2011
|
2.08
|
|
9
|
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.
|
Proc Natl Acad Sci U S A
|
2009
|
1.66
|
|
10
|
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
|
PLoS Genet
|
2011
|
1.56
|
|
11
|
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
|
J Neurosci
|
2003
|
1.29
|
|
12
|
Sexual selection and the adaptive evolution of mammalian ejaculate proteins.
|
Mol Biol Evol
|
2007
|
1.28
|
|
13
|
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse.
|
Proc Natl Acad Sci U S A
|
2007
|
1.22
|
|
14
|
The long non-coding RNA Paupar regulates the expression of both local and distal genes.
|
EMBO J
|
2014
|
1.19
|
|
15
|
Brain, know thy transcriptome, know thyself.
|
Neuron
|
2012
|
1.08
|
|
16
|
Evaluating the links between schizophrenia and sleep and circadian rhythm disruption.
|
J Neural Transm (Vienna)
|
2012
|
1.05
|
|
17
|
SNARE proteins and schizophrenia: linking synaptic and neurodevelopmental hypotheses.
|
Acta Biochim Pol
|
2008
|
1.02
|
|
18
|
Behavioural characterization of neuregulin 1 type I overexpressing transgenic mice.
|
Neuroreport
|
2009
|
0.99
|
|
19
|
Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophy.
|
Hum Mol Genet
|
2013
|
0.93
|
|
20
|
Human-mouse quantitative trait locus concordance and the dissection of a human neuroticism locus.
|
Biol Psychiatry
|
2008
|
0.87
|
|
21
|
AF4 is a critical regulator of the IGF-1 signaling pathway during Purkinje cell development.
|
J Neurosci
|
2009
|
0.85
|
|
22
|
TBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features.
|
Neurology
|
2016
|
0.85
|
|
23
|
HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes.
|
J Neurochem
|
2011
|
0.81
|
|
24
|
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.
|
Mol Cell Neurosci
|
2002
|
0.80
|
|
25
|
Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit.
|
Neuromuscul Disord
|
2004
|
0.79
|
|
26
|
Identification and characterisation of a Maf1/Macoco protein complex that interacts with GABAA receptors in neurons.
|
Mol Cell Neurosci
|
2010
|
0.75
|
|
27
|
Corrigendum: Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7.
|
Nat Struct Mol Biol
|
2015
|
0.75
|