Author details

Full Name

Michael N Weedon

Affiliation

ORCID

Career Start Year

2002

Papers

240

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37888801	Diabetes Study of Children of Diverse Ethnicity and Race: Study design.	Diabetes Metab Res Rev	2024
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
36368478	Identifying type 1 and 2 diabetes in research datasets where classification biomarkers are unavailable: assessing the accuracy of published approaches.	Journal of Clinical Epidemiology	2023
36038257	A founder variant is a common cause of hereditary nephropathy in the British population.	Journal of Medical Genetics	2023
36355183	The relationship between islet autoantibody status and the genetic risk of type 1 diabetes in adult-onset type 1 diabetes.	Diabetologia	2023
35977816	Prevalence of Fabry disease-causing variants in the UK Biobank.	Journal of Medical Genetics	2023
37936660	Influence of family history on penetrance of hereditary cancers in a population setting.		2023
37733769	Identification and analysis of individuals who deviate from their genetically-predicted phenotype.	PLoS Genet	2023
37988592	Penetrance and expressivity of mitochondrial variants in a large clinically unselected population.		2023
37639628	The Role of ONECUT1 Variants in Monogenic and Type 2 Diabetes Mellitus.		2023
37784116	Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records.		2023
37957254	Correlations in sleeping patterns and circadian preference between spouses.	Commun Biol	2023
37316353	Corrigendum to 'Identifying type 1 and 2 diabetes in research datasets where classification biomarkers are unavailable: assessing the accuracy of published approaches' [Journal of Clinical Epidemiology (2023) 34-44].		2023
36798175	Identification and analysis of individuals who deviate from their genetically-predicted phenotype.	bioRxiv	2023
36536048	Response to: Genetic risk scores may compound rather than solve the issue of prostate cancer overdiagnosis (BJC-LT3342090).		2023
36726473	Genome-wide characterization of mitochondrial DNA methylation in human brain.	Front Endocrinol (Lausanne)	2023
37506364	Type 1 Diabetes Genetic Risk Score Differentiates Subgroups of Ketosis-Prone Diabetes.		2023
37492488	Associations between sleep health and grey matter volume in the UK Biobank cohort (<i>n</i> = 33 356).	Brain Commun	2023
35241534	A Comparative Safety Analysis of Medicines Based on the UK Pharmacovigilance and General Practice Prescribing Data in England.	In Vivo	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
35978138	Applying a genetic risk score for prostate cancer to men with lower urinary tract symptoms in primary care to predict prostate cancer diagnosis: a cohort study in the UK Biobank.	British Journal of Cancer	2022
34686905	Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics.	Diabetologia	2022
35312757	Utility of Diabetes Type-Specific Genetic Risk Scores for the Classification of Diabetes Type Among Multiethnic Youth.	Diabetes Care	2022
35294448	SavvyCNV: Genome-wide CNV calling from off-targetÂ reads.	PLoS Comput Biol	2022
34618178	Association of birthweight and penetrance of diabetes in individuals with HNF4A-MODY: a cohort study.	Diabetologia	2022
35235652	PLIN1 Haploinsufficiency Causes a Favorable Metabolic Profile.	Journal of Clinical Endocrinology and Metabolism	2022
35246685	Corrigendum to: A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio.	Human Molecular Genetics	2022
35165454	Author Correction: A combined risk score enhances prediction of type 1 diabetes among susceptible children.	Nat Med	2022
35108381	Evaluation of Evidence for Pathogenicity Demonstrates That BLK, KLF11, and PAX4 Should Not Be Included in Diagnostic Testing for MODY.	Diabetes	2022
34698873	Correction to: DR15-DQ6 remains dominantly protective against type 1 diabetes throughout the first five decades of life.	Diabetologia	2022
35349659	Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study.	Diabetes Care	2022
34750397	Estimating disease prevalence in large datasets using genetic risk scores.	Nature Communications	2021
33798434	Unreliability of genotyping arrays for detecting very rare variants in human genetic studies: Example from a recent study of MC4R.	Cell	2021
34112773	A meta-analysis of epigenome-wide association studies in Alzheimer's disease highlights novel differentially methylated loci across cortex.	Nat Commun	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
34272580	DR15-DQ6 remains dominantly protective against type 1 diabetes throughout the first five decades of life.	Diabetologia	2021
34099873	Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health.	Molecular Psychiatry	2021
33150399	Is disrupted sleep a risk factor for Alzheimer's disease? Evidence from a two-sample Mendelian randomization analysis.	Int J Epidemiol	2021
33420133	Sleep classification from wrist-worn accelerometer data using random forests.	Sci Rep	2021
34748000	Objective assessment of sleep regularity in 60 000 UK Biobank participants using an open-source package.	Sleep	2021
32497177	Clinical Features and Genetic Risk of Demyelination Following Anti-TNF Treatment.		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
31704690	Absence of Islet Autoantibodies and Modestly Raised Glucose Values at Diabetes Diagnosis Should Lead to Testing for MODY: Lessons From a 5-Year Pediatric Swedish National Cohort Study.	Diabetes Care	2020
31751445	Comparison of Genetic Liability for Sleep Traits Among Individuals With Bipolar Disorder I or II and Control Participants.	JAMA Psychiatry	2020
33102956	IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank.	Kidney International Reports	2020