|
| 36922513 | A rare human variant that disrupts GPR10 signalling causes weight gain in mice. | | 2023 |
| 34753797 | An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript. | Diabetes | 2022 |
| 36536256 | Human loss-of-function variants in the serotonin 2C receptor associated with obesity and maladaptive behavior. | | 2022 |
| 35048991 | Associations Between Glycemic Traits and Colorectal Cancer: A Mendelian Randomization Analysis. | J Natl Cancer Inst | 2022 |
| 35064169 | Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations. | Sci Rep | 2022 |
| 34875679 | Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution. | Journal of Clinical Endocrinology and Metabolism | 2022 |
| 34748544 | Predicting novel candidate human obesity genes and their site of action by systematic functional screening in Drosophila. | PLoS Biology | 2021 |
| 36082306 | Workshop proceedings: GWAS summary statistics standards and sharing. | Cell Genom | 2021 |
| 32989287 | Genome-wide association study identifies 48 common genetic variants associated with handedness. | Nat Hum Behav | 2021 |
| 33323478 | Processes Underlying Glycemic Deterioration in Type 2 Diabetes: An IMI DIRECT Study. | Diabetes Care | 2021 |
| 34595549 | The importance of increasing population diversity in genetic studies of type 2 diabetes and related glycaemic traits. | Diabetologia | 2021 |
| 32737300 | Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections. | Nat Commun | 2020 |
| 32493978 | Human BDNF/TrkB variants impair hippocampal synaptogenesis and associate with neurobehavioural abnormalities. | Sci Rep | 2020 |
| 32492392 | Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription. | Cell Metab | 2020 |
| 32150548 | The influence of rare variants in circulating metabolic biomarkers. | PLoS Genet | 2020 |
| 33045005 | Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits. | PLoS Genet | 2020 |
| 33188205 | Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study. | Sci Data | 2020 |
| 31439647 | Crucial Role of the SH2B1 PH Domain for the Control of Energy Balance. | | 2019 |
| 31675503 | Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. | Cell | 2019 |
| 30478441 | A linear mixed-model approach to study multivariate gene-environment interactions. | Nat Genet | 2019 |
| 31235872 | Genomics of disease risk in globally diverse populations. | Nature Reviews Genetics | 2019 |
| 31270439 | Author Correction: Genomics of disease risk in globally diverse populations. | Nature Reviews Genetics | 2019 |
| 31263163 | Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. | Sci Rep | 2019 |
| 30901536 | The Genetic Basis of Metabolic Disease. | Cell | 2019 |
| 31006513 | A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development. | Am J Hum Genet | 2019 |
| 31358974 | New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. | Nat Hum Behav | 2019 |
| 31049640 | Genome-wide association study of type 2 diabetes in Africa. | Diabetologia | 2019 |
| 29273807 | Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 30405126 | Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. | Nat Commun | 2018 |
| 30503519 | DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency. | Am J Hum Genet | 2018 |
| 30010810 | Genome-Wide Sequence Analysis of Kaposi Sarcoma-Associated Herpesvirus Shows Diversification Driven by Recombination. | Journal of Infectious Diseases | 2018 |
| 30100123 | Editorial overview: Molecular and genetic basis of [metabolic] disease: Genes, glucose, glycerol and girth: metabolism in our DNA. | Current Opinion in Genetics and Development | 2018 |
| 30568165 | Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. | Nat Commun | 2018 |
| 30325923 | ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls. | PLoS Genetics | 2018 |
| 29374254 | ADCY3, neuronal primary cilia and obesity. | Nature Genetics | 2018 |
| 29549330 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29549329 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29632382 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. | Nat Genet | 2018 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 27864399 | Novel genetic loci associated with long-term deterioration in blood lipid concentrations and coronary artery disease in European adults. | Int J Epidemiol | 2017 |
| 28552196 | Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. | Am J Hum Genet | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 28724990 | Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. | Nat Commun | 2017 |
| 28898252 | Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. | PLoS Med | 2017 |
| 28448500 | Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. | PLoS Genet | 2017 |
| 28414270 | Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression. | eLife | 2017 |
| 28977447 | Genetic aetiology of glycaemic traits: approaches and insights. | Human Molecular Genetics | 2017 |
| 28663568 | Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity. | Sci Rep | 2017 |
| 28832619 | Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. | PLoS Genet | 2017 |
| 28566443 | Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase. | Eur J Endocrinol | 2017 |