Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in European, Asian and Mexican populations. To determine whether common PCSK1 variants contribute to obesity in American population, we conducted association analyses in 8,359 subjects using two multi-ethnic American studies: the Coronary Artery Risk Development in Young Adults (CARDIA) study and the Multi-Ethnic Study of Atherosclerosis (MESA). By evaluating the contribution of rs6232 and rs6235 in each ethnic group, we found that in European-American subjects from CARDIA, only rs6232 was associated with BMI (P = 0.006) and obesity (P = 0.018) but also increased the obesity incidence during the 20 years of follow-up (HR = 1.53 [1.07–2.19], P = 0...
Recently, it was reported that heterozygous PCSK1 variants, causing partial PC1/3 deficiency, result...
<p>Controls: participants followed 20 years and remaining non-obese (BMI<30 kg/m<sup>2</sup>) over t...
Obesity is a major public health problem with a significant genetic component. Multiple DNA polymorp...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
<div><p>Common <i>PCSK1</i> variants (notably rs6232 and rs6235) have been shown to be associated wi...
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body...
Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity ...
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which enco...
Background: Common variants rs6232 and rs6235 in the PCSK1 gene have been associated with obesity in...
Common variants in PCSK1 have been reported to be associated with obesity in populations of European...
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...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
IntroductionOver 35% of all adults in the world are currently obese and risk of obesity in racial or...
Genome-wide association studies (GWAS) have successfully identified common obesity-associated varian...
Recently, it was reported that heterozygous PCSK1 variants, causing partial PC1/3 deficiency, result...
<p>Controls: participants followed 20 years and remaining non-obese (BMI<30 kg/m<sup>2</sup>) over t...
Obesity is a major public health problem with a significant genetic component. Multiple DNA polymorp...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
<div><p>Common <i>PCSK1</i> variants (notably rs6232 and rs6235) have been shown to be associated wi...
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body...
Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity ...
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which enco...
Background: Common variants rs6232 and rs6235 in the PCSK1 gene have been associated with obesity in...
Common variants in PCSK1 have been reported to be associated with obesity in populations of European...
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...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
IntroductionOver 35% of all adults in the world are currently obese and risk of obesity in racial or...
Genome-wide association studies (GWAS) have successfully identified common obesity-associated varian...
Recently, it was reported that heterozygous PCSK1 variants, causing partial PC1/3 deficiency, result...
<p>Controls: participants followed 20 years and remaining non-obese (BMI<30 kg/m<sup>2</sup>) over t...
Obesity is a major public health problem with a significant genetic component. Multiple DNA polymorp...