| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1010256482 |
| P356 | DOI | 10.1186/1471-2350-7-83 |
| P932 | PMC publication ID | 1698479 |
| P698 | PubMed publication ID | 17137505 |
| P5875 | ResearchGate publication ID | 6660423 |
| P50 | author | Bernard Keavney | Q64858562 |
| P2093 | author name string | Thahira Rahman | |
| Peter J Avery | |||
| Darroch H Hall | |||
| P2860 | cites work | Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease | Q22337234 |
| Merlin--rapid analysis of dense genetic maps using sparse gene flow trees | Q27860829 | ||
| Obesity: preventing and managing the global epidemic. Report of a WHO consultation | Q29547404 | ||
| PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data | Q30991765 | ||
| A general test of association for quantitative traits in nuclear families | Q34146162 | ||
| CYP11B2-CYP11B1 haplotypes associated with decreased 11 beta-hydroxylase activity | Q45126720 | ||
| Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion. | Q45136957 | ||
| Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study. | Q46620692 | ||
| A common genetic variant is associated with adult and childhood obesity | Q46726890 | ||
| Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study | Q46820678 | ||
| Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis. | Q50753618 | ||
| Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein | Q57200477 | ||
| Measured Haplotype Analysis of the Angiotensin-I Converting Enzyme Gene | Q57377961 | ||
| Effects of gender and age on the heritability of body mass index | Q67782648 | ||
| Incidence and precursors of hypertension in young adults: the Framingham Offspring Study | Q69038435 | ||
| The heritability of body mass index among an international sample of monozygotic twins reared apart | Q71472808 | ||
| Obesity as an independent risk factor for cardiovascular disease: a 26-year follow-up of participants in the Framingham Heart Study | Q72779135 | ||
| P921 | main subject | obesity | Q12174 |
| P304 | page(s) | 83 | |
| P577 | publication date | 2006-11-30 | |
| P1433 | published in | BMC Medical Genetics | Q15759918 |
| P1476 | title | INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families | |
| P478 | volume | 7 |
| Q33520369 | A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans |
| Q46131433 | Absence of association between the INSIG2 gene polymorphism (rs7566605) and obesity in the European Youth Heart Study (EYHS). |
| Q33505812 | Association analyses of the INSIG2 polymorphism in the obesity and cholesterol levels of Korean populations |
| Q44477430 | Association between intramuscular fat in the arm following arm training and INSIG2. |
| Q33311602 | Association between the -455T>C promoter polymorphism of the APOC3 gene and the metabolic syndrome in a multi-ethnic sample |
| Q34995179 | Association of INSIG2 polymorphism with overweight and LDL in children |
| Q45229545 | Association of the common genetic variant upstream of INSIG2 gene with obesity related phenotypes in Chinese children and adolescents |
| Q33766402 | Common Genetic Variant of insig2 Gene rs7566605 Polymorphism Is Associated with Severe Obesity in North India |
| Q33925838 | Common INSIG2 polymorphisms are associated with age-related changes in body size and high-density lipoprotein cholesterol from young adulthood to middle age. |
| Q35687593 | Gender-Specific Effect of -102G>A Polymorphism in Insulin Induced Gene 2 on Obesity in Chinese Children |
| Q30368157 | Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. |
| Q81109431 | Genome-wide linkage scan for the metabolic syndrome: the GENNID study |
| Q34046787 | INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study |
| Q33395532 | INSIG2 gene polymorphism is associated with increased subcutaneous fat in women and poor response to resistance training in men. |
| Q36848982 | INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese. |
| Q39828005 | INSIG2 is Associated with Lower Gain in Weight-for-Length Between Birth and Age 6 Months |
| Q47255631 | INSIG2 polymorphism and weight gain, dyslipidemia and serum adiponectin in Finnish patients with schizophrenia treated with clozapine |
| Q46779321 | INSIG2 polymorphism is neither associated with BMI nor with phenotypes of lipoprotein metabolism |
| Q36790115 | INSIG2 variants, dietary patterns and metabolic risk in Samoa |
| Q51837210 | Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors. |
| Q33420094 | Mutations in genes involved in nonsense mediated decay ameliorate the phenotype of sel-12 mutants with amber stop mutations in Caenorhabditis elegans |
| Q33410654 | Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry |
| Q33358134 | Non-replication of genome-wide based associations between common variants in INSIG2 and PFKP and obesity in studies of 18,014 Danes |
| Q36719042 | On the replication of genetic associations: timing can be everything! |
| Q46815775 | Plasma potassium level is associated with common genetic variation in the beta-subunit of the epithelial sodium channel |
| Q35167237 | Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level |
| Q43936330 | Possible role for ENPP1 polymorphism in obesity but not for INSIG2 and PLIN variants. |
| Q47247238 | Potential association of INSIG2 rs7566605 polymorphism with body weight in a Chinese subpopulation |
| Q29614919 | Replicating genotype-phenotype associations |
| Q33509634 | Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study |
| Q33412882 | Studies of CTNNBL1 and FDFT1 variants and measures of obesity: analyses of quantitative traits and case-control studies in 18,014 Danes |
| Q33467104 | The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts |
| Q30990502 | The INSIG2 rs7566605 polymorphism is not associated with body mass index and breast cancer risk |
| Q21563458 | The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts |
| Q36772383 | The challenges for molecular nutrition research 1: linking genotype to healthy nutrition |
| Q30411895 | The gene-gene interaction of INSIG-SCAP-SREBP pathway on the risk of obesity in Chinese children |
| Q46526269 | The single nucleotide polymorphism upstream of insulin-induced gene 2 ( INSIG2) is associated with the prevalence of hypercholesterolaemia, but not with obesity, in Japanese American women |
| Q38953433 | Tumour biology of obesity-related cancers: understanding the molecular concept for better diagnosis and treatment. |
Search more.