|
1
|
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.
|
Lancet Neurol
|
2010
|
3.61
|
|
2
|
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.
|
Nat Genet
|
2010
|
2.56
|
|
3
|
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.
|
Lancet Neurol
|
2008
|
2.54
|
|
4
|
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
|
Proc Natl Acad Sci U S A
|
2009
|
2.03
|
|
5
|
Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients.
|
BMC Genomics
|
2009
|
1.72
|
|
6
|
Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
|
Hum Mol Genet
|
2012
|
1.62
|
|
7
|
Gene-network analysis identifies susceptibility genes related to glycobiology in autism.
|
PLoS One
|
2009
|
1.23
|
|
8
|
Analysis of genome-wide copy number variation in Irish and Dutch ALS populations.
|
Hum Mol Genet
|
2008
|
1.12
|
|
9
|
FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.
|
Arch Neurol
|
2010
|
1.08
|
|
10
|
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder.
|
Am J Med Genet B Neuropsychiatr Genet
|
2010
|
1.06
|
|
11
|
Alzheimer's disease beyond APOE.
|
Nat Genet
|
2009
|
1.02
|
|
12
|
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
|
Neurobiol Aging
|
2012
|
1.02
|
|
13
|
Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene.
|
Hum Reprod
|
2009
|
1.01
|
|
14
|
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
|
Hum Mol Genet
|
2013
|
0.98
|
|
15
|
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
|
PLoS One
|
2012
|
0.95
|
|
16
|
UNC13A is a modifier of survival in amyotrophic lateral sclerosis.
|
Neurobiol Aging
|
2011
|
0.95
|
|
17
|
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
|
Hum Mol Genet
|
2010
|
0.92
|
|
18
|
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient.
|
Neurobiol Aging
|
2012
|
0.91
|
|
19
|
Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients.
|
Neurobiol Aging
|
2011
|
0.90
|
|
20
|
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.
|
Neurobiol Aging
|
2012
|
0.87
|
|
21
|
Genetic overlap between apparently sporadic motor neuron diseases.
|
PLoS One
|
2012
|
0.84
|
|
22
|
Amyotrophic lateral sclerosis is not linked to multiple sclerosis in a population based study.
|
J Neurol Neurosurg Psychiatry
|
2013
|
0.83
|
|
23
|
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.
|
Ann Neurol
|
2014
|
0.83
|
|
24
|
Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.
|
Neurobiol Aging
|
2012
|
0.82
|
|
25
|
Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle.
|
Amyotroph Lateral Scler Frontotemporal Degener
|
2013
|
0.77
|
|
26
|
Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
|
Neurobiol Aging
|
2012
|
0.76
|
|
27
|
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis.
|
Neurobiol Aging
|
2010
|
0.76
|
|
28
|
Mutational analysis of TARDBP in Parkinson's disease.
|
Neurobiol Aging
|
2012
|
0.75
|