|
| 37349538 | Penetrance of pathogenic genetic variants associated with premature ovarian insufficiency. | Nat Med | 2023 |
| 36109160 | Recurrent 17q12 microduplications contribute to renal disease but not diabetes. | Journal of Medical Genetics | 2023 |
| 36048866 | Genetically proxied therapeutic prolyl-hydroxylase inhibition and cardiovascular risk. | Hum Mol Genet | 2023 |
| 35977816 | Prevalence of Fabry disease-causing variants in the UK Biobank. | Journal of Medical Genetics | 2023 |
| 37733769 | Identification and analysis of individuals who deviate from their genetically-predicted phenotype. | PLoS Genet | 2023 |
| 37280435 | Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. | Diabetologia | 2023 |
| 36693378 | Loci for insulin processing and secretion provide insight into type 2 diabetes risk. | Am J Hum Genet | 2023 |
| 36798216 | Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion. | medRxiv | 2023 |
| 36798175 | Identification and analysis of individuals who deviate from their genetically-predicted phenotype. | bioRxiv | 2023 |
| 37544968 | Does physical activity moderate the association between shorter leukocyte telomere length and incident coronary heart disease? Data from 54,180 UK Biobank participants. | | 2023 |
| 35349659 | Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study. | Diabetes Care | 2022 |
| 35388897 | Simulated distributions from negative experiments highlight the importance of the body mass index distribution in explaining depression-body mass index genetic risk score interactions. | International Journal of Epidemiology | 2022 |
| 35700724 | Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population. | Am J Hum Genet | 2022 |
| 35687092 | Detection and characterization of male sex chromosome abnormalities in the UK Biobank study. | Genet Med | 2022 |
| 36137075 | The impact of Mendelian sleep and circadian genetic variants in a population setting. | PLoS Genet | 2022 |
| 36257325 | Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts. | Am J Hum Genet | 2022 |
| 36055212 | Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies. | Am J Hum Genet | 2022 |
| 34108397 | Understanding Factors That Cause Tinnitus: A Mendelian Randomization Study in the UK Biobank. | Ear and Hearing | 2022 |
| 34897462 | Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight. | Hum Mol Genet | 2022 |
| 35061033 | Babies of South Asian and European Ancestry Show Similar Associations With Genetic Risk Score for Birth Weight Despite the Smaller Size of South Asian Newborns. | | 2022 |
| 34542646 | Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile. | Diabetologia | 2021 |
| 34111113 | A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor. | PLoS Genetics | 2021 |
| 34270736 | Higher adiposity and mental health: causal inference using Mendelian randomization. | Human Molecular Genetics | 2021 |
| 34099873 | Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health. | Molecular Psychiatry | 2021 |
| 33563987 | Genetic predictors of participation in optional components of UK Biobank. | Nat Commun | 2021 |
| 33980691 | Genetic Evidence for Different Adiposity Phenotypes and Their Opposing Influences on Ectopic Fat and Risk of Cardiometabolic Disease. | | 2021 |
| 33501652 | Genetically defined favourable adiposity is not associated with a clinically meaningful difference in clinical course in people with type 2 diabetes but does associate with a favourable metabolic profile. | Diabetic Medicine | 2021 |
| 33150399 | Is disrupted sleep a risk factor for Alzheimer's disease? Evidence from a two-sample Mendelian randomization analysis. | Int J Epidemiol | 2021 |
| 33199855 | Sleep characteristics across the lifespan in 1.1â¿¿million people from the Netherlands, United Kingdom and United States: a systematic review and meta-analysis. | Nat Hum Behav | 2021 |
| 33197388 | Telomere length and risk of idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease: a mendelian randomisation study. | Lancet Respiratory Medicine,The | 2021 |
| 32944759 | Genome-Wide Association Analysis of Pancreatic Beta-Cell Glucose Sensitivity. | Journal of Clinical Endocrinology and Metabolism | 2021 |
| 34561431 | Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome. | Nat Commun | 2021 |
| 33107437 | RETRACTION: Mendelian randomization supports a causative effect of TSH on thyroid carcinoma. | | 2020 |
| 31800047 | Effects of body mass index on relationship status, social contact and socio-economic position: Mendelian randomization and within-sibling study in UK Biobank. | Int J Epidemiol | 2020 |
| 32191790 | Mitochondrial genetic variation is enriched in G-quadruplex regions that stall DNA synthesis in vitro. | Hum Mol Genet | 2020 |
| 32170055 | Quantification of the overall contribution of gene-environment interaction for obesity-related traits. | Nat Commun | 2020 |
| 32392279 | Does Obesity Cause Thyroid Cancer? A Mendelian Randomization Study. | Journal of Clinical Endocrinology and Metabolism | 2020 |
| 31665112 | Methods for quick, accurate and cost-effective determination of the type 1 diabetes genetic risk score (T1D-GRS). | Clinical Chemistry and Laboratory Medicine | 2020 |
| 31757795 | Assessment of <i>MTNR1B</i> Type 2 Diabetes Genetic Risk Modification by Shift Work and Morningness-Eveningness Preference in the UK Biobank. | Diabetes | 2020 |
| 32588049 | Genetic evidence that higher central adiposity causes gastro-oesophageal reflux disease: a Mendelian randomization study. | International Journal of Epidemiology | 2020 |
| 32698144 | Mendelian randomization supports a causative effect of TSH on thyroid carcinoma. | | 2020 |
| 32574563 | Large Copy-Number Variants in UK Biobank Caused by Clonal Hematopoiesis May Confound Penetrance Estimates. | Am J Hum Genet | 2020 |
| 33284794 | Common maternal and fetal genetic variants show expected polygenic effects on risk of small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies. | PLoS Genetics | 2020 |
| 32790217 | A single nucleotide polymorphism genetic risk score to aid diagnosis of coeliac disease: a pilot study in clinical care. | Alimentary Pharmacology and Therapeutics | 2020 |
| 32497177 | Clinical Features and Genetic Risk of Demyelination Following Anti-TNF Treatment. | | 2020 |
| 31409809 | Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes. | Nat Commun | 2019 |
| 31630189 | A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio. | Human Molecular Genetics | 2019 |
| 30352878 | Genome-Wide and Abdominal MRI Data Provide Evidence That a Genetically Determined Favorable Adiposity Phenotype Is Characterized by Lower Ectopic Liver Fat and Lower Risk of Type 2 Diabetes, Heart Disease, and Hypertension. | | 2019 |
| 30583798 | GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology. | Am J Hum Genet | 2019 |
| 30573795 | Response to Prakash et al. | Genetics in Medicine | 2019 |