| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/3123 |
| P698 | PubMed publication ID | 9806554 |
| P50 | author | Karine Clément | Q62104165 |
| P2093 | author name string | Froguel P | |
| Dubois S | |||
| Basdevant A | |||
| Dina C | |||
| Guy-Grand B | |||
| Hager J | |||
| Houari M | |||
| Vatin V | |||
| Vaillant E | |||
| Francke S | |||
| Lorentz N | |||
| P2860 | cites work | Evidence against either a premature stop codon or the absence of obese gene mRNA in human obesity | Q22241899 |
| Positional cloning of the mouse obese gene and its human homologue | Q22251285 | ||
| A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction | Q24322907 | ||
| Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans | Q24323379 | ||
| Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity | Q24336776 | ||
| A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2 | Q28118289 | ||
| A candidate gene for the mouse mutation tubby | Q28276460 | ||
| Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results | Q29547377 | ||
| Serum immunoreactive-leptin concentrations in normal-weight and obese humans | Q29617230 | ||
| Congenital leptin deficiency is associated with severe early-onset obesity in humans | Q29618702 | ||
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| The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance | Q34289777 | ||
| Evidence that the diabetes gene encodes the leptin receptor: identification of a mutation in the leptin receptor gene in db/db mice | Q34376178 | ||
| Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians | Q34384734 | ||
| Linkage between obesity and a marker near the tumor necrosis factor-alpha locus in Pima Indians | Q35750063 | ||
| Anthropometric reference data for international use: recommendations from a World Health Organization Expert Committee | Q36823478 | ||
| Genetic studies of the leptin receptor gene in morbidly obese French Caucasian families | Q38342315 | ||
| Absence of linkage of obesity and energy metabolism to markers flanking homologues of rodent obesity genes in Pima Indians | Q38353604 | ||
| Extreme obesity may be linked to markers flanking the human OB gene | Q38358626 | ||
| Indication for linkage of the human OB gene region with extreme obesity | Q38358630 | ||
| Segregation analysis of height-adjusted weight with generation- and age-dependent effects: the Nancy Family Study | Q41106577 | ||
| The human obesity gene map: the 1997 update | Q41732076 | ||
| Insulin resistance, adipose tissue and coronary heart disease | Q54281835 | ||
| Affected sib-pair tests for linkage: Type I errors with dependent sib-pairs | Q56893861 | ||
| The investigation of linkage between a quantitative trait and a marker locus | Q70059116 | ||
| P433 | issue | 3 | |
| P921 | main subject | obesity | Q12174 |
| P304 | page(s) | 304-308 | |
| P577 | publication date | 1998-11-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10 | |
| P478 | volume | 20 |
| Q93060218 | A Systematically Assembled Signature of Genes to be Deep-Sequenced for Their Associations with the Blood Pressure Response to Exercise |
| Q35764466 | A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program |
| Q50645302 | A genome-wide scan for body mass index among Nigerian families. |
| Q46453534 | A genome-wide scan for quantitative trait loci linked to obesity phenotypes among West Africans |
| Q35764160 | A genomewide linkage scan for quantitative-trait loci for obesity phenotypes |
| Q34044595 | A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q |
| Q30498786 | A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans |
| Q28361785 | A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans |
| Q37217251 | A major predisposition locus for severe obesity, at 4p15-p14 |
| Q28505277 | A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler mice |
| Q34698747 | A novel nuclear-encoded mitochondrial poly(A) polymerase PAPD1 is a potential candidate gene for the extreme obesity related phenotypes in mammals |
| Q30837785 | A novel procedure for efficient genotyping of single nucleotide polymorphisms |
| Q36106407 | A review and primer of molecular genetic studies of anorexia nervosa. |
| Q44391093 | A search for candidate genes for lipodystrophy, obesity and diabetes via gene expression analysis of A-ZIP/F-1 mice |
| Q37219579 | A whole-genome scan for obstructive sleep apnea and obesity |
| Q33450573 | Admixture mapping of 15,280 African Americans identifies obesity susceptibility loci on chromosomes 5 and X. |
| Q33835637 | Admixture mapping of obesity-related traits in African Americans: the Atherosclerosis Risk in Communities (ARIC) Study |
| Q33665882 | Advances in the molecular genetics of obesity |
| Q59150822 | An autosomal genomic scan for loci linked to plasma leptin concentration in Pima Indians |
| Q24794466 | Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population |
| Q31142214 | Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis |
| Q51741318 | Association between variants in the genes for leptin, leptin receptor, and proopiomelanocortin with chronic heart failure in the Czech population. |
| Q53541764 | Association of a polymorphism of ABCB1 with obesity in Japanese individuals. |
| Q48640183 | Association of genetic polymorphisms of glutamate decarboxylase 2 and the dopamine D2 receptor with obesity in Taiwanese subjects |
| Q33599343 | Association of obesity risk SNPs in PCSK1 with insulin sensitivity and proinsulin conversion |
| Q46820678 | Association of proopiomelanocortin gene polymorphisms with obesity in the IRAS family study |
| Q37374005 | Association of the -243 A-->G polymorphism of the glutamate decarboxylase 2 gene with obesity in girls with premature pubarche |
| Q37312495 | Association of variants in the PCSK1 gene with obesity in the EPIC-Norfolk study |
| Q27007024 | CART in the regulation of appetite and energy homeostasis |
| Q57249730 | Common nonsynonymous variants in PCSK1 confer risk of obesity |
| Q36509138 | Commonality of functional annotation: a method for prioritization of candidate genes from genome-wide linkage studies |
| Q28118375 | Determination of cDNA, gene structure and chromosomal localization of the novel human 17beta-hydroxysteroid dehydrogenase type 7(1) |
| Q44731099 | Dissection of multigenic obesity traits in congenic mouse strains |
| Q33630569 | Do allelic variants of SLC6A14 predispose to obesity? |
| Q33731374 | Eating disorders: the current status of molecular genetic research |
| Q24323036 | Effects of the new C1q/TNF-related protein (CTRP-3) "cartonectin" on the adipocytic secretion of adipokines |
| Q42148081 | Effects of variants in proopiomelanocortin and neuropeptide y genes on growth, carcass, and meat quality traits in rabbits |
| Q33198443 | Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses |
| Q33964719 | Energy balance and weight regulation: genetics versus environment |
| Q33909623 | Evidence of a novel quantitative-trait locus for obesity on chromosome 4p in Mexican Americans |
| Q46682026 | Familial resemblance for plasma leptin: sample homogeneity across adiposity and ethnic groups |
| Q34271555 | Finding the molecular basis of quantitative traits: successes and pitfalls. |
| Q34649752 | From obesity genetics to the future of personalized obesity therapy |
| Q24791984 | GAD2 on chromosome 10p12 is a candidate gene for human obesity |
| Q80088326 | Genetic effects on obesity assessed by bivariate genome scan: the Mexican-American coronary artery disease study |
| Q33892344 | Genetics of body-weight regulation |
| Q73141361 | Genetics of insulin resistance |
| Q79827591 | Genetics of obesity |
| Q34064050 | Genome partitioning and whole-genome analysis |
| Q34329091 | Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease |
| Q51741041 | Genome-wide scan of plasma cholecystokinin in baboons shows linkage to human chromosome 17. |
| Q57316423 | Genome-wide search for genes related to the fat-free body mass in the Québec family study |
| Q22337170 | Genomewide scans of complex human diseases: true linkage is hard to find |
| Q34144320 | Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24. |
| Q34143823 | How obesity develops: insights from the new biology |
| Q37230950 | Human QTL linkage mapping |
| Q34116512 | Human genomics and obesity: finding appropriate drug targets. |
| Q34984890 | Hypothalamic proopiomelanocortin processing and the regulation of energy balance |
| Q47182091 | Identification of a potential functional single nucleotide polymorphism for fatness and growth traits in the 3'-untranslated region of the PCSK1 gene in chickens. |
| Q33724465 | Identification of neuronal enhancers of the proopiomelanocortin gene by transgenic mouse analysis and phylogenetic footprinting |
| Q35176549 | Identification of the transcription factor ZEB1 as a central component of the adipogenic gene regulatory network |
| Q57249762 | Impact of a CART promoter genetic variation on plasma lipid profile in a general population |
| Q28587870 | Impaired insulin secretion and glucose tolerance in beta cell-selective Ca(v)1.2 Ca2+ channel null mice |
| Q33826673 | Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome |
| Q37205163 | Interacting genetic loci on chromosomes 20 and 10 influence extreme human obesity |
| Q34974732 | Interleukin-15, IL-15 Receptor-Alpha, and Obesity: Concordance of Laboratory Animal and Human Genetic Studies |
| Q36196340 | LIM-homeodomain genes in mammalian development and human disease. |
| Q43830332 | Lack of association of glutamate decarboxylase 2 gene polymorphisms with severe obesity in utah |
| Q24816535 | Lack of support for the association between GAD2 polymorphisms and severe human obesity |
| Q36990366 | Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates |
| Q44971626 | Linkage analysis of circulating levels of adiponectin in Hispanic children. |
| Q34943973 | Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia |
| Q57779137 | Linkage and association of the CA repeat polymorphism of the IL6 gene, obesity-related phenotypes, and bone mineral density (BMD) in two independent Caucasian populations |
| Q42637379 | Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene |
| Q74200439 | Linkage exclusion analysis of the chromosome 11 region containing UCP2 and UCP3 with obesity-related phenotypes in Mexican Americans |
| Q37079760 | Linkage mapping of CVD risk traits in the isolated Norfolk Island population. |
| Q24290696 | Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin |
| Q35126395 | Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity |
| Q56968892 | Meta-Analysis of Genome-wide Linkage Studies in BMI and Obesity* |
| Q37358544 | Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36). |
| Q56895448 | Molecular characterization of the porcine MTPAP gene associated with meat quality traits: chromosome localization, expression distribution, and transcriptional regulation |
| Q61695488 | Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations |
| Q33864624 | Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci |
| Q34142135 | Multipoint linkage analysis of the pseudoautosomal regions, using affected sibling pairs |
| Q61181314 | Multivariate linkage analysis of blood pressure and body mass index |
| Q44435384 | Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians |
| Q37569283 | Neuropeptide transmission in brain circuits |
| Q57285626 | No evidence for involvement of the calpain-10 gene `high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity |
| Q35181584 | Novel family-based approaches to genetic risk in thrombosis |
| Q35555011 | Obesity – is it a genetic disorder? |
| Q59672916 | Obesity: on the eve of a major conceptual revolution |
| Q34390826 | Osteoarthritis-susceptibility locus on chromosome 11q, detected by linkage. |
| Q62511339 | POMC: The Physiological Power of Hormone Processing |
| Q80312477 | Pharmacogenetics of antipsychotic-induced weight gain |
| Q43750703 | Polymorphisms in stearoyl coa desaturase and sterol regulatory element binding protein interact with N-3 polyunsaturated fatty acid intake to modify associations with anthropometric variables and metabolic phenotypes in Yup'ik people. |
| Q33938638 | Possible genomic imprinting of three human obesity-related genetic loci |
| Q33894087 | Principal component and linkage analysis of cardiovascular risk traits in the Norfolk isolate |
| Q79088021 | Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals |
| Q52053232 | Proopiomelanocortin gene variants are associated with serum leptin and body fat in a normal female population. |
| Q45145892 | Quantitative genetic analysis of glucose transporter 4 mRNA levels in baboon adipose |
| Q33796965 | Quantitative trait linkage mapping in anthropology |
| Q53880259 | Quantitative trait loci for abdominal fat and BMI in Hispanic-Americans and African-Americans: the IRAS Family study. |
| Q35846048 | Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome. |
| Q24633105 | Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study |
| Q34020356 | Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups |
| Q35855592 | Recent advances in obesity: genetics and beyond |
| Q33951541 | Recent advances in the genetics of severe childhood obesity |
| Q28512438 | Regulation and function of collagenous repeat containing sequence of 26-kDa protein gene product "cartonectin" |
| Q36387434 | Schizophrenia, antipsychotics and diabetes: Genetic aspects. |
| Q34586797 | Searching for the mountains of the moon: genome scans for atherosclerosis |
| Q44729119 | Serum leptin concentration is linked to chromosomes 2 and 6 in the OLETF rat, an animal model of type 2 diabetes with mild obesity |
| Q25256864 | Sex and age specific effects of chromosomal regions linked to body mass index in the Framingham Study. |
| Q46689747 | Sex-specific findings from a genome-wide linkage analysis of human fatness in non-Hispanic whites and African Americans: the HyperGEN study. |
| Q34529746 | Significant linkage on chromosome 10p in families with bulimia nervosa |
| Q48499962 | The Eating Inventory and body adiposity from leanness to massive obesity: a study of 2509 adults |
| Q34146763 | The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. |
| Q57316399 | The Human Obesity Gene Map: The 2004 Update |
| Q48182272 | The Na+/Cl--Coupled, Broad-Specific, Amino Acid Transporter SLC6A14 (ATB0,+): Emerging Roles in Multiple Diseases and Therapeutic Potential for Treatment and Diagnosis |
| Q39004698 | The Relevance of Genomic Signatures at Adhesion GPCR Loci in Humans |
| Q24654114 | The SLC6A14 gene shows evidence of association with obesity |
| Q33521230 | The ZEB1 transcription factor is a novel repressor of adiposity in female mice |
| Q24339493 | The arrestin domain-containing 3 protein regulates body mass and energy expenditure |
| Q33801241 | The association of insertions/deletions (INDELs) and variable number tandem repeats (VNTRs) with obesity and its related traits and complications |
| Q73599728 | The beta 3-adrenergic receptor gene and obesity in a population sample of African Americans |
| Q28740403 | The effect of PCSK1 variants on waist, waist-hip ratio and glucose metabolism is modified by sex and glucose tolerance status |
| Q36036700 | The genetics of human obesity |
| Q30336529 | The genetics of obesity. |
| Q33839687 | The human obesity gene map: the 1999 update. |
| Q34227908 | The human obesity gene map: the 2000 update |
| Q34557274 | The human obesity gene map: the 2001 update |
| Q35084465 | The human obesity gene map: the 2002 update |
| Q35715184 | The human obesity gene map: the 2003 update |
| Q34567973 | The human obesity gene map: the 2005 update |
| Q34020848 | The power to detect linkage disequilibrium with quantitative traits in selected samples |
| Q34635467 | The role of melanocortins in body weight regulation: opportunities for the treatment of obesity |
| Q74604281 | The role of melanocortins in body weight regulation: opportunities for the treatment of obesity |
| Q34750310 | Using mouse models to dissect the genetics of obesity |
| Q41126480 | Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes |
| Q37072395 | Voluntary exercise prevents the obese and diabetic metabolic syndrome of the melanocortin-4 receptor knockout mouse |
| Q80260756 | [Genomics of body weight regulation: unraveling the molecular mechanisms predisposing to obesity] |
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