Found: 117
Select item for more details and to access through your institution.
Medical semiology of patients with monogenic obesity: A systematic review.
- Published in:
- Obesity Reviews, 2024, v. 25, n. 10, p. 1, doi. 10.1111/obr.13797
- By:
- Publication type:
- Article
Allelic frequency differences of DAOA variants between Caucasians and Asians and their association with major mood disorders.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study.
- Published in:
- Scientific Reports, 2016, p. 18672, doi. 10.1038/srep18672
- By:
- Publication type:
- Article
Consequences of Paternal Nutrition on Offspring Health and Disease.
- Published in:
- Nutrients, 2021, v. 13, n. 8, p. 2818, doi. 10.3390/nu13082818
- By:
- Publication type:
- Article
From big data analysis to personalized medicine for all: challenges and opportunities.
- Published in:
- BMC Medical Genomics, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s12920-015-0108-y
- By:
- Publication type:
- Article
From big data analysis to personalized medicine for all: challenges and opportunities.
- Published in:
- BMC Medical Genomics, 2015, v. 8, n. 1, p. 33, doi. 10.1186/s12920-015-0108-y
- By:
- Publication type:
- Article
Polymorphisms in the amino acid transporter solute carrier family 6 (neurotransmitter transporter) member 14 gene contribute to polygenic obesity in French Caucasians.
- Published in:
- 2004
- By:
- Publication type:
- journal article
SREBF-1 gene polymorphisms are associated with obesity and type 2 diabetes in French obese and diabetic cohorts.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.
- Published in:
- 2004
- By:
- Publication type:
- journal article
A Genome-Wide Scan for Childhood Obesity-Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2.
- Published in:
- Diabetes, 2004, v. 53, n. 3, p. 803, doi. 10.2337/diabetes.53.3.803
- By:
- Publication type:
- Article
A genome-wide association study identifies novel risk loci for type 2 diabetes.
- Published in:
- Nature, 2007, v. 445, n. 7130, p. 881, doi. 10.1038/nature05616
- By:
- Publication type:
- Article
Adiponectin is associated with cardio-metabolic traits in Mexican children.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39801-2
- By:
- Publication type:
- Article
Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French population.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 4, p. 227, doi. 10.1038/jhg.2010.10
- By:
- Publication type:
- Article
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 16, p. 3727, doi. 10.1093/hmg/dds187
- By:
- Publication type:
- Article
Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 13, p. 1916, doi. 10.1093/hmg/ddn089
- By:
- Publication type:
- Article
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 12, p. 1803, doi. 10.1093/hmg/ddn072
- By:
- Publication type:
- Article
R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 12, p. 1798, doi. 10.1093/hmg/ddn070
- By:
- Publication type:
- Article
Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 15, p. 1837, doi. 10.1093/hmg/ddm132
- By:
- Publication type:
- Article
Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French children.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2020, v. 58, n. 11, p. 1819, doi. 10.1515/cclm-2019-0292
- By:
- Publication type:
- Article
A Candidate-Gene Approach Identifies Novel Associations Between Common Variants in/Near Syndromic Obesity Genes and BMI in Pediatric and Adult European Populations.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Give GWAS a Chance.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Genetic Dissection of Diabetes: Facing the Giant.
- Published in:
- 2013
- By:
- Publication type:
- Opinion
Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity.
- Published in:
- Diabetes, 2012, v. 61, n. 2, p. 383, doi. 10.2337/db11-0305
- By:
- Publication type:
- Article
Evaluation of A2BP1 as an Obesity Gene.
- Published in:
- Diabetes, 2010, v. 59, n. 11, p. 2837, doi. 10.2337/db09-1604
- By:
- Publication type:
- Article
Genetic and Functional Assessment of the Role of the rs13431652-A and rs573225-A Alleles in the G6PC2 Promoter That Are Strongly Associated With Elevated Fasting Glucose Levels.
- Published in:
- Diabetes, 2010, v. 59, n. 10, p. 2662, doi. 10.2337/db10-0389
- By:
- Publication type:
- Article
MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans.
- Published in:
- Diabetes, 2010, v. 59, n. 6, p. 1530, doi. 10.2337/db09-1757
- By:
- Publication type:
- Article
Prevalence of Loss of-Function FTO Mutations in Lean and Obese Individuals.
- Published in:
- Diabetes, 2010, v. 59, n. 1, p. 311, doi. 10.2337/db09-0703
- By:
- Publication type:
- Article
Common Variation in SIM1 Is Reproducibly Associated With BMI in Pima Indians.
- Published in:
- Diabetes, 2009, v. 58, n. 7, p. 1682, doi. 10.2337/db09-0028
- By:
- Publication type:
- Article
Prevalence of Melanocortin-4 Receptor Deficiency in Europeans and Their Age-Dependent Penetrance in Multigenerational Pedigrees.
- Published in:
- Diabetes, 2008, v. 57, n. 9, p. 2511, doi. 10.2337/db08-0153
- By:
- Publication type:
- Article
Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children.
- Published in:
- Diabetes, 2008, v. 57, n. 2, p. 494, doi. 10.2337/db07-1273
- By:
- Publication type:
- Article
Impact of Common Type 2 Diabetes Risk Polymorphisms in the DESIR Prospective Study.
- Published in:
- Diabetes, 2008, v. 57, n. 1, p. 244, doi. 10.2337/db07-0615
- By:
- Publication type:
- Article
Large-Scale Analysis of 11 Candidate Genes for Insulin Resistance in 5602 Samples from the UK and France: the BAIR Human Genetics Validation Study.
- Published in:
- Diabetes, 2007, v. 56, p. A306
- By:
- Publication type:
- Article
Prediction of Type 2 Diabetes Risk by Common Polymorphisms in a General Population: The D.E.S.I.R. Prospective Study.
- Published in:
- Diabetes, 2007, v. 56, p. A302
- By:
- Publication type:
- Article
A High Density Genome-Wide Association Study Identifies Novel Susceptibility Genes for Type 2 Diabetes Mellitus and Reveals New Mechanisms for Glucose Intolerance.
- Published in:
- Diabetes, 2007, v. 56, p. A94
- By:
- Publication type:
- Article
TCF7L2 Variation Predicts Hyperglycemia Incidence in a French General Population.
- Published in:
- Diabetes, 2006, v. 55, n. 11, p. 3189, doi. 10.2337/db06-0692
- By:
- Publication type:
- Article
Transcription Factor TCF7L2 Genetic Study in the French Population.
- Published in:
- Diabetes, 2006, v. 55, n. 10, p. 2903, doi. 10.2337/db06-0474
- By:
- Publication type:
- Article
Bardet-Biedl Syndrome Gene Variants Are Associated With Both Childhood and Adult Common Obesity in French Caucasians.
- Published in:
- Diabetes, 2006, v. 55, n. 10, p. 2876, doi. 10.2337/db06-0337
- By:
- Publication type:
- Article
ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity.
- Published in:
- Diabetes, 2006, v. 55, n. 2, p. 545, doi. 10.2337/diabetes.55.02.06.db05-0971
- By:
- Publication type:
- Article
Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Association of total and pancreatic serum amylase enzymatic activity with insulin resistance and the glucose and insulin responses to oral starch test in Mexican children.
- Published in:
- Pediatric Obesity, 2022, v. 17, n. 12, p. 1, doi. 10.1111/ijpo.12965
- By:
- Publication type:
- Article
Association of gut microbiome with fasting triglycerides, fasting insulin and obesity status in Mexican children.
- Published in:
- Pediatric Obesity, 2021, v. 16, n. 5, p. 1, doi. 10.1111/ijpo.12748
- By:
- Publication type:
- Article
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1126, doi. 10.1038/ejhg.2008.64
- By:
- Publication type:
- Article
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 3, p. 320, doi. 10.1038/sj.ejhg.5201754
- By:
- Publication type:
- Article
Structured diet and exercise guidance in pregnancy to improve health in women and their offspring: study protocol for the Be Healthy in Pregnancy (BHIP) randomized controlled trial.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.
- Published in:
- Nature Genetics, 2009, v. 41, n. 2, p. 157, doi. 10.1038/ng.301
- By:
- Publication type:
- Article
Variation in FTO contributes to childhood obesity and severe adult obesity.
- Published in:
- Nature Genetics, 2007, v. 39, n. 6, p. 724, doi. 10.1038/ng2048
- By:
- Publication type:
- Article
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes.
- Published in:
- Nature Genetics, 2005, v. 37, n. 8, p. 863, doi. 10.1038/ng1604
- By:
- Publication type:
- Article
A genetic link between prepregnancy body mass index, postpartum weight retention, and offspring weight in early childhood.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Assessing the effects of 35 European-derived BMI-associated SNPs in Mexican children.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Identification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delay.
- Published in:
- Obesity (19307381), 2014, v. 22, n. 12, p. 2621, doi. 10.1002/oby.20886
- By:
- Publication type:
- Article