Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
J Clin Invest
2008
118
6
2260-8
A multimetric approach to analysis of genome-wide association by single markers and composite likelihood.
Proc Natl Acad Sci U S A
2008
105
7
2592-7
Polyneuropathy, scoliosis, tall stature, and oligodontia represent novel features of the interstitial 6p deletion phenotype.
Am J Med Genet A
2008
146A
22
2960-5
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.
PLoS Genet
2008
4
11
e1000282
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.
Eur J Hum Genet
2008
16
9
1126-34
Common variants near MC4R are associated with fat mass, weight and risk of obesity.
Nat Genet
2008
40
6
768-75
Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populations.
Stroke
2008
39
4
1109-14
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes.
Cerebrovasc Dis
2008
26
2
113-9
Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans.
Stroke
2008
39
5
1593-6
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy.
Epilepsia
2008
49
6
1108-9