Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity in a meta-analysis comprising more than 13 000 individuals of European ancestry. Each additional minor allele of rs6232 or rs6235 was associated with a 1.34- or 1.22-fold increase in the risk of obesity, respectively. So far, only one relatively small study has aimed to replicate these findings, but could not confirm the association of the rs6235 SNP and did not study the rs6232 variant. In the present study, we examined the associations of the rs6232 and rs6235 SNPs with obesity in a population-based cohort consisting of 20 249 individuals of European descent from Norfolk, UK. Logistic regression and generalized linear models were used to te...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
<p>Controls: participants followed 20 years and remaining non-obese (BMI<30 kg/m<sup>2</sup>) over t...
Background:A significant proportion of severe familial forms of obesity remain genetically elusive. ...
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body...
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which enco...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
Common variants in PCSK1 have been reported to be associated with obesity in populations of European...
<div><p>Common <i>PCSK1</i> variants (notably rs6232 and rs6235) have been shown to be associated wi...
Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recently been assoc...
[[abstract]]Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recentl...
Recently, it was reported that heterozygous PCSK1 variants, causing partial PC1/3 deficiency, result...
Proprotein convertase subtilisin/kexin-type 1 (PCSK1) activates precursors pro-opiomelanocortin (POM...
BackgroundMeta-analysis of case–control genome-wide association studies (GWAS) for early onset and m...
Background: Common variants rs6232 and rs6235 in the PCSK1 gene have been associated with obesity in...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
<p>Controls: participants followed 20 years and remaining non-obese (BMI<30 kg/m<sup>2</sup>) over t...
Background:A significant proportion of severe familial forms of obesity remain genetically elusive. ...
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body...
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which enco...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
Common variants in PCSK1 have been reported to be associated with obesity in populations of European...
<div><p>Common <i>PCSK1</i> variants (notably rs6232 and rs6235) have been shown to be associated wi...
Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recently been assoc...
[[abstract]]Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recentl...
Recently, it was reported that heterozygous PCSK1 variants, causing partial PC1/3 deficiency, result...
Proprotein convertase subtilisin/kexin-type 1 (PCSK1) activates precursors pro-opiomelanocortin (POM...
BackgroundMeta-analysis of case–control genome-wide association studies (GWAS) for early onset and m...
Background: Common variants rs6232 and rs6235 in the PCSK1 gene have been associated with obesity in...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
<p>Controls: participants followed 20 years and remaining non-obese (BMI<30 kg/m<sup>2</sup>) over t...
Background:A significant proportion of severe familial forms of obesity remain genetically elusive. ...