|
1
|
Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease.
|
J Mol Med (Berl)
|
2010
|
1.13
|
|
2
|
Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF.
|
Neuromuscul Disord
|
2009
|
1.01
|
|
3
|
Complex genetic predisposition in adult and juvenile rheumatoid arthritis.
|
BMC Genet
|
2004
|
1.01
|
|
4
|
Are there specific genetic risk factors for the different forms of ANCA-associated vasculitis?
|
Ann Rheum Dis
|
2010
|
0.86
|
|
5
|
The canine Recoverin (RCV1) gene: a candidate gene for generalized progressive retinal atrophy.
|
Mol Vis
|
2002
|
0.81
|
|
6
|
Is the retina affected in Huntington disease?
|
Acta Neuropathol
|
2005
|
0.80
|
|
7
|
Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy.
|
BMC Genet
|
2002
|
0.78
|
|
8
|
The canine Phosducin gene: characterization of the exon-intron structure and exclusion as a candidate gene for generalized progressive retinal atrophy in 11 dog breeds.
|
Mol Vis
|
2002
|
0.78
|
|
9
|
Evaluation of the canine RPE65 gene in affected dogs with generalized progressive retinal atrophy.
|
Mol Vis
|
2003
|
0.77
|
|
10
|
AZFc region of the Y chromosome shows singular structural organization.
|
Chromosome Res
|
2010
|
0.76
|
|
11
|
Truly hypervariable DNA fingerprints due to exceptionally high mutation rates.
|
Electrophoresis
|
2002
|
0.75
|
|
12
|
Gene symbol: GJB1. Disease: Hereditary motor and sensory neuropathy type X?
|
Hum Genet
|
2008
|
0.75
|
|
13
|
Gene symbol: GJB1. Disease: Hereditary motor and sensory neuropathy type X.
|
Hum Genet
|
2008
|
0.75
|