Pages that link to "Q46726890"
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The following pages link to A common genetic variant is associated with adult and childhood obesity (Q46726890):
Displaying 50 items.
- Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study (Q21093317) (← links)
- Genome-wide association with select biomarker traits in the Framingham Heart Study (Q21261433) (← links)
- Learning genetic epistasis using Bayesian network scoring criteria (Q21284331) (← links)
- The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts (Q21563458) (← links)
- The genetic contribution to non-syndromic human obesity (Q22251027) (← links)
- Prevalence in the United States of selected candidate gene variants. Third National Health and Nutrition Examination Survey, 1991- 1994 (Q23917519) (← links)
- Fine mapping versus replication in whole-genome association studies (Q24289225) (← links)
- Characterization of the human insulin-induced gene 2 (INSIG2) promoter: the role of Ets-binding motifs (Q24598294) (← links)
- Analyses of shared genetic factors between asthma and obesity in children (Q24607084) (← links)
- A genome-wide study reveals copy number variants exclusive to childhood obesity cases (Q24607677) (← links)
- Beyond the fourth wave of genome-wide obesity association studies (Q24627723) (← links)
- The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI (Q24631490) (← links)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (Q24646434) (← links)
- A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity (Q24650037) (← links)
- Model of genetic variation in human social networks (Q24651850) (← links)
- A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis (Q24669981) (← links)
- Genetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in Sweden (Q24671765) (← links)
- Obesity: interactions of genome and nutrients intake (Q26853442) (← links)
- Genome-wide association studies of late-onset cardiovascular disease (Q27012711) (← links)
- Genetic & epigenetic approach to human obesity (Q28084624) (← links)
- Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease (Q28235756) (← links)
- A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk (Q28259831) (← links)
- Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects? (Q28264722) (← links)
- Polymorphisms of the FTO gene are associated with variation in energy intake, but not energy expenditure (Q28283768) (← links)
- Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study (Q28390241) (← links)
- Mapping the genetic architecture of gene expression in human liver (Q28472693) (← links)
- Genetic association study with metabolic syndrome and metabolic-related traits in a cross-sectional sample and a 10-year longitudinal sample of chinese elderly population (Q28539956) (← links)
- GENESTAT: an information portal for design and analysis of genetic association studies (Q28748267) (← links)
- The HapMap and genome-wide association studies in diagnosis and therapy (Q28752130) (← links)
- Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study (Q28943280) (← links)
- Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations (Q28943421) (← links)
- Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians (Q28943474) (← links)
- Replicating genotype-phenotype associations (Q29614919) (← links)
- Genetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass (Q30155618) (← links)
- Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. (Q30368157) (← links)
- The gene-gene interaction of INSIG-SCAP-SREBP pathway on the risk of obesity in Chinese children (Q30411895) (← links)
- Toward objective monitoring of ingestive behavior in free-living population. (Q30494359) (← links)
- Assessing gene-treatment interactions at the FTO and INSIG2 loci on obesity-related traits in the Diabetes Prevention Program (Q30496787) (← links)
- Gene by sex interaction for measures of obesity in the framingham heart study (Q30497912) (← links)
- Obesity susceptibility loci and dietary intake in the Look AHEAD Trial (Q30514020) (← links)
- Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study (Q30539203) (← links)
- FTO predicts weight regain in the Look AHEAD clinical trial (Q30543330) (← links)
- Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity (Q30669834) (← links)
- The oxytocin receptor (OXTR) contributes to prosocial fund allocations in the dictator game and the social value orientations task (Q30863831) (← links)
- Evaluation of a two-stage framework for prediction using big genomic data (Q30912379) (← links)
- The INSIG2 rs7566605 polymorphism is not associated with body mass index and breast cancer risk (Q30990502) (← links)
- Overcoming the winner's curse: estimating penetrance parameters from case-control data (Q31105516) (← links)
- Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis (Q31142214) (← links)
- Cis-regulatory variations: a study of SNPs around genes showing cis-linkage in segregating mouse populations (Q33257734) (← links)
- INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families (Q33265115) (← links)