Author details

Full Name

Nigel W Rayner

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37066341	Systematic visualisation of molecular QTLs reveals variant mechanisms at GWAS loci.	bioRxiv	2023
36349687	Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing.	Hum Mol Genet	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36896826	Longitudinal Reading Measures and Genome Imputation in the National Child Development Study: Prospects for Future Reading Research.		2023
36536132	Aberrant expression of agouti signaling protein (ASIP) as a cause of monogenic severe childhood obesity.		2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
33303764	Whole-genome sequencing analysis of the cardiometabolic proteome.	Nature Communications	2020
31118516	Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.	Nature	2019
31847144	A Dietary Pattern with High Sugar Content Is Associated with Cardiometabolic Risk Factors in the Pomak Population.	Nutrients	2019
30239591	Gimpute: an efficient genetic data imputation pipeline.	Bioinformatics	2019
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
30405126	Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.	Nat Commun	2018
30071838	Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study.	BMC Psychiatry	2018
29930110	Analysis of shared heritability in common disorders of the brain.	Science	2018
30297969	Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.	Nat Genet	2018
30568165	Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits.	Nat Commun	2018
29703844	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	Diabetes	2018
29436472	A novel variant in is associated with osteoarthritis.	Annals of the Rheumatic Diseases	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
27974301	Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis.	Annals of the Rheumatic Diseases	2017
28552196	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Am J Hum Genet	2017
28989980	Bone mineral density and risk of type 2 diabetes and coronary heart disease: A Mendelian randomization study.	Wellcome Open Research	2017
28548082	Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.	Nat Commun	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
28566273	An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.	Diabetes	2017
29030403	New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475â¿¿000 Individuals.	Circ Cardiovasc Genet	2017
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
27647854	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	J Am Soc Nephrol	2017
27989266	The mountainous Cretan dietary patterns and their relationship with cardiovascular risk factors: the Hellenic Isolated Cohorts MANOLIS study.	Public Health Nutr	2017
27618452	The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.	Nat Genet	2016
27355579	Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2016
27466198	Analysis with the exome array identifies multiple new independent variants in lipid loci.	Hum Mol Genet	2016
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
27618447	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Nat Genet	2016
27876822	A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.	Nat Commun	2016
26426971	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2015
25673413	Genetic studies of body mass index yield new insights for obesity biology.	Nature	2015
25673412	New genetic loci link adipose and insulin biology to body fat distribution.	Nature	2015
25631608	Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.	Nat Commun	2015
25625282	Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.	PLoS Genet	2015
26551672	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.	Nat Genet	2015
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
25373335	Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.	Nat Commun	2014
25282103	Defining the role of common variation in the genomic and biological architecture of adult human height.	Nat Genet	2014
24498077	BMI-associated alleles do not constitute risk alleles for polycystic ovary syndrome independently of BMI: a case-control study.	PLoS One	2014
24514567	A genome-wide association study of anorexia nervosa.	Mol Psychiatry	2014