Found: 67
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Variation in the eNOS gene modifies the association between total energy expenditure and glucose intolerance.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Mendelian randomization study of B-type natriuretic peptide and type 2 diabetes: evidence of causal association from population studies.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-021-04436-9
- By:
- Publication type:
- Article
Partial lipodystrophy and insulin resistant diabetes in a patient with a homozygous nonsense mutation in CIDEC.
- Published in:
- EMBO Molecular Medicine, 2009, v. 1, n. 5, p. 280, doi. 10.1002/emmm.200900037
- By:
- Publication type:
- Article
Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 4, p. 1065, doi. 10.1210/clinem/dgab877
- By:
- Publication type:
- Article
Controlled Release of Epigenetically-Enhanced Extracellular Vesicles from a GelMA/Nanoclay Composite Hydrogel to Promote Bone Repair.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 2, p. 832, doi. 10.3390/ijms23020832
- By:
- Publication type:
- Article
The influence of rare variants in circulating metabolic biomarkers.
- Published in:
- PLoS Genetics, 2020, v. 16, n. 3, p. 1, doi. 10.1371/journal.pgen.1008605
- By:
- Publication type:
- Article
Genetic architecture of human thinness compared to severe obesity.
- Published in:
- PLoS Genetics, 2019, v. 15, n. 1, p. 1, doi. 10.1371/journal.pgen.1007603
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- Publication type:
- Article
ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 10, p. 1, doi. 10.1371/journal.pgen.1007591
- By:
- Publication type:
- Article
Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance.
- Published in:
- Journal of Clinical Investigation, 2014, v. 124, n. 9, p. 4028, doi. 10.1172/JCI73264
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- Publication type:
- Article
Human SH2B1 mutations are associated with maladaptive behaviors and obesity.
- Published in:
- Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4732, doi. 10.1172/JCI62696
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- Publication type:
- Article
Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.23813.001
- By:
- Publication type:
- Article
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
- Published in:
- Nature Genetics, 2015, v. 47, n. 11, p. 1282, doi. 10.1038/ng.3405
- By:
- Publication type:
- Article
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
- Published in:
- Nature Genetics, 2013, v. 45, n. 5, p. 513, doi. 10.1038/ng.2607
- By:
- Publication type:
- Article
Meta-analysis and imputation refines the association of 15q25 with smoking quantity.
- Published in:
- Nature Genetics, 2010, v. 42, n. 5, p. 436, doi. 10.1038/ng.572
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- Publication type:
- Article
Genome-wide association study identifies five loci associated with lung function.
- Published in:
- Nature Genetics, 2010, v. 42, n. 1, p. 36, doi. 10.1038/ng.501
- By:
- Publication type:
- Article
Digenic inheritance of severe insulin resistance in a human pedigree.
- Published in:
- Nature Genetics, 2002, v. 31, n. 4, p. 379, doi. 10.1038/ng926
- By:
- Publication type:
- Article
Whole genome–amplified DNA: insights and imputation.
- Published in:
- 2008
- By:
- Publication type:
- Letter
HbA<sub>1c</sub> screening for the diagnosis of diabetes. Reply to Brož J, Brabec M, Krollová P et al [letter].
- Published in:
- 2023
- By:
- Publication type:
- Letter
Correction to: The impact of population-level HbA<sub>1c</sub> screening on reducing diabetes diagnostic delay in middle-aged adults: a UK Biobank analysis.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
The impact of population-level HbA<sub>1c</sub> screening on reducing diabetes diagnostic delay in middle-aged adults: a UK Biobank analysis.
- Published in:
- Diabetologia, 2023, v. 66, n. 2, p. 300, doi. 10.1007/s00125-022-05824-0
- By:
- Publication type:
- Article
The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits.
- Published in:
- Diabetologia, 2021, v. 64, n. 12, p. 2653, doi. 10.1007/s00125-021-05575-4
- By:
- Publication type:
- Article
Genome-wide association study of type 2 diabetes in Africa.
- Published in:
- Diabetologia, 2019, v. 62, n. 7, p. 1204, doi. 10.1007/s00125-019-4880-7
- By:
- Publication type:
- Article
Innate biology versus lifestyle behaviour in the aetiology of obesity and type 2 diabetes: the GLACIER Study.
- Published in:
- Diabetologia, 2016, v. 59, n. 3, p. 462, doi. 10.1007/s00125-015-3818-y
- By:
- Publication type:
- Article
Leveraging information between multiple population groups and traits improves fine-mapping resolution.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43159-5
- By:
- Publication type:
- Article
Genome-wide association studies and type 2 diabetes.
- Published in:
- Briefings in Functional Genomics, 2011, v. 10, n. 2, p. 52, doi. 10.1093/bfgp/elr008
- By:
- Publication type:
- Article
Loss of <i>FTO</i> Antagonises Wnt Signaling and Leads to Developmental Defects Associated with Ciliopathies.
- Published in:
- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0087662
- By:
- Publication type:
- Article
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07730-9
- By:
- Publication type:
- Article
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07070-8
- By:
- Publication type:
- Article
Complex disease: Pleiotropic gene effects in obesity and type 2 diabetes.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1243, doi. 10.1038/sj.ejhg.5201514
- By:
- Publication type:
- Article
Photocurable antimicrobial silk‐based hydrogels for corneal repair.
- Published in:
- Journal of Biomedical Materials Research, Part A, 2022, v. 110, n. 7, p. 1401, doi. 10.1002/jbm.a.37381
- By:
- Publication type:
- Article
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase.
- Published in:
- European Journal of Endocrinology, 2017, v. 177, n. 2, p. 175, doi. 10.1530/EJE-17-0132
- By:
- Publication type:
- Article
Habitual Energy Expenditure Modifies the Association Between NOS3 Gene Polymorphisms and Blood Pressure.
- Published in:
- American Journal of Hypertension, 2008, v. 21, n. 3, p. 297, doi. 10.1038/ajh.2007.69
- By:
- Publication type:
- Article
Human BDNF/TrkB variants impair hippocampal synaptogenesis and associate with neurobehavioural abnormalities.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65531-x
- By:
- Publication type:
- Article
Predicting novel candidate human obesity genes and their site of action by systematic functional screening in Drosophila.
- Published in:
- PLoS Biology, 2021, v. 19, n. 11, p. 1, doi. 10.1371/journal.pbio.3001255
- By:
- Publication type:
- Article
Photocurable GelMA Adhesives for Corneal Perforations.
- Published in:
- Bioengineering (Basel), 2022, v. 9, n. 2, p. 53, doi. 10.3390/bioengineering9020053
- By:
- Publication type:
- Article
Genetic aetiology of glycaemic traits: approaches and insights.
- Published in:
- Human Molecular Genetics, 2017, v. 26, p. R172, doi. 10.1093/hmg/ddx293
- By:
- Publication type:
- Article
Homozygous loss-of-function variants in European cosmopolitan and isolate populations.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 19, p. 5464, doi. 10.1093/hmg/ddv272
- By:
- Publication type:
- Article
Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations.
- Published in:
- American Journal of Epidemiology, 2009, v. 170, n. 5, p. 537, doi. 10.1093/aje/kwp145
- By:
- Publication type:
- Article
Population-Specific Risk of Type 2 Diabetes Conferred by HNF4A P2 Promoter Variants.
- Published in:
- Diabetes, 2008, v. 57, n. 11, p. 3161, doi. 10.2337/db08-0719
- By:
- Publication type:
- Article
Evaluating the Role of LPIN1 Variation in Insulin Resistance, Body Weight, and Human Lipodystrophy in U.K. Populations.
- Published in:
- Diabetes, 2008, v. 57, n. 9, p. 2527, doi. 10.2337/db08-0422
- By:
- Publication type:
- Article
TCF7L2 polymorphisms modulate proinsulin levels and beta-cell function in a British Europid population.
- Published in:
- 2007
- By:
- Publication type:
- journal article
TCF7L2 Polymorphisms Modulate Proinsulin Levels and β-Cell Function in a British Europid Population.
- Published in:
- Diabetes, 2007, v. 56, n. 7, p. 1943, doi. 10.2337/db07-0055
- By:
- Publication type:
- Article
Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Analysis of genetic variation in Akt2/PKB-beta in severe insulin resistance, lipodystrophy, type 2 diabetes, and related metabolic phenotypes.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Lamin A/C Polymorphisms, Type 2 Diabetes, and the Metabolic Syndrome.
- Published in:
- Diabetes, 2007, v. 56, n. 3, p. 884, doi. 10.2337/db06-1055
- By:
- Publication type:
- Article
Analysis of Genetic Variation in Akt2/PKB-β in Severe Insulin Resistance, Lipodystrophy, Type 2 Diabetes, and Related Metabolic Phenotypes.
- Published in:
- Diabetes, 2007, v. 56, n. 3, p. 714, doi. 10.2337/db06-0921
- By:
- Publication type:
- Article
Genetic variants in human sterol regulatory element binding protein-1c in syndromes of severe insulin resistance and type 2 diabetes.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Correction: Candidate Gene Association Study in Type 2 Diabetes Indicates a Role for Genes Involved in β-Cell Function as Well as Insulin Action.
- Published in:
- 2003
- By:
- Publication type:
- Correction Notice
Candidate Gene Association Study in Type 2 Diabetes Indicates a Role for Genes Involved in β-Cell Function as Well as Insulin Action.
- Published in:
- PLoS Biology, 2003, v. 1, n. 10, p. 1, doi. 10.1371/journal.pbio.0000020
- By:
- Publication type:
- Article