Cargando…

Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

Detalles Bibliográficos
Autores principales:	Gilly, Arthur, Suveges, Daniel, Kuchenbaecker, Karoline, Pollard, Martin, Southam, Lorraine, Hatzikotoulas, Konstantinos, Farmaki, Aliki-Eleni, Bjornland, Thea, Waples, Ryan, Appel, Emil V. R., Casalone, Elisabetta, Melloni, Giorgio, Kilian, Britt, Rayner, Nigel W., Ntalla, Ioanna, Kundu, Kousik, Walter, Klaudia, Danesh, John, Butterworth, Adam, Barroso, Inês, Tsafantakis, Emmanouil, Dedoussis, George, Moltke, Ida, Zeggini, Eleftheria
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2018
Materias:	Author Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300593/ https://www.ncbi.nlm.nih.gov/pubmed/30568165 http://dx.doi.org/10.1038/s41467-018-07730-9

Ejemplares similares

Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
por: Gilly, Arthur, et al.
Publicado: (2018)

Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations
por: Kuchenbaecker, Karoline, et al.
Publicado: (2022)

Very low-depth whole-genome sequencing in complex trait association studies
por: Gilly, Arthur, et al.
Publicado: (2019)

Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation
por: Gilly, Arthur, et al.
Publicado: (2016)

Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits
por: Southam, Lorraine, et al.
Publicado: (2017)

Population‐wide copy number variation calling using variant call format files from 6,898 individuals
por: Png, Grace, et al.
Publicado: (2019)

Whole-genome sequencing analysis of the cardiometabolic proteome
por: Gilly, Arthur, et al.
Publicado: (2020)

Genome-wide meta-analysis of 92 cardiometabolic protein serum levels
por: Gilly, Arthur, et al.
Publicado: (2023)

Replication of Established Common Genetic Variants for Adult BMI and Childhood Obesity in Greek Adolescents: The TEENAGE Study
por: Ntalla, Ioanna, et al.
Publicado: (2013)

Using population isolates in genetic association studies
por: Hatzikotoulas, Konstantinos, et al.
Publicado: (2014)

Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants
por: Panoutsopoulou, Kalliope, et al.
Publicado: (2014)

A novel variant in GLIS3 is associated with osteoarthritis
por: Casalone, Elisabetta, et al.
Publicado: (2018)

A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates
por: Tachmazidou, Ioanna, et al.
Publicado: (2013)

A Dietary Pattern with High Sugar Content Is Associated with Cardiometabolic Risk Factors in the Pomak Population
por: Farmaki, Aliki-Eleni, et al.
Publicado: (2019)

The transferability of lipid loci across African, Asian and European cohorts
por: Kuchenbaecker, Karoline, et al.
Publicado: (2019)

Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations
por: Gilly, Arthur, et al.
Publicado: (2022)

Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing
por: Png, Grace, et al.
Publicado: (2022)

Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study
por: Mamakou, Vasiliki, et al.
Publicado: (2018)

Mapping the serum proteome to neurological diseases using whole genome sequencing
por: Png, Grace, et al.
Publicado: (2021)

Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups
por: Gebresilase, Tewodros, et al.
Publicado: (2021)

Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes
por: Grarup, Niels, et al.
Publicado: (2018)

An epigenome-wide view of osteoarthritis in primary tissues
por: Kreitmaier, Peter, et al.
Publicado: (2022)

Trans-ethnic study design approaches for fine-mapping
por: Asimit, Jennifer L, et al.
Publicado: (2016)

The influence of rare variants in circulating metabolic biomarkers
por: Riveros-Mckay, Fernando, et al.
Publicado: (2020)

Widespread epigenomic, transcriptomic and proteomic differences between hip osteophytic and articular chondrocytes in osteoarthritis
por: Steinberg, Julia, et al.
Publicado: (2018)

Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis
por: Zengini, Eleni, et al.
Publicado: (2018)

Pathways to understanding the genomic aetiology of osteoarthritis
por: Cibrián Uhalte, Elena, et al.
Publicado: (2017)

Allele frequency‐free inference of close familial relationships from genotypes or low‐depth sequencing data
por: Waples, Ryan K., et al.
Publicado: (2019)

Using multivariable Mendelian randomization to estimate the causal effect of bone mineral density on osteoarthritis risk, independently of body mass index
por: Hartley, April, et al.
Publicado: (2021)

Type 2 diabetes risks and determinants in second-generation migrants and mixed ethnicity people of South Asian and African Caribbean descent in the UK
por: Farmaki, Aliki-Eleni, et al.
Publicado: (2021)

Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank
por: Tachmazidou, Ioanna, et al.
Publicado: (2019)

Bridging the diversity gap: Analytical and study design considerations for improving the accuracy of trans-ancestry genetic prediction
por: Bocher, Ozvan, et al.
Publicado: (2023)

Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases
por: Carland, Corinne, et al.
Publicado: (2023)

Using genetically isolated populations to understand the genomic basis of disease
por: Zeggini, Eleftheria
Publicado: (2014)

Editorial: Genetics of Complex Traits and Diseases From Under-Represented Populations
por: Fatumo, Segun, et al.
Publicado: (2022)

Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations
por: Prins, Bram P., et al.
Publicado: (2017)

A molecular map of long non-coding RNA expression, isoform switching and alternative splicing in osteoarthritis
por: Katsoula, Georgia, et al.
Publicado: (2022)

Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations
por: Xue, Yali, et al.
Publicado: (2017)

Evaluating the glucose raising effect of established loci via a genetic risk score
por: Marouli, Eirini, et al.
Publicado: (2017)

Testing for rare variant associations in complex diseases
por: Asimit, Jennifer, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_u7isnnsaue4te5k1f5npujbtsc