Cargando…

Rare-variant collapsing analyses of arterial hypertension in the UK biobank

Detalles Bibliográficos
Autores principales:	Zöller, Bengt, Manderstedt, Eric, Lind-Halldén, Christina, Halldén, Christer
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2023
Materias:	Letter
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632123/ https://www.ncbi.nlm.nih.gov/pubmed/37059828 http://dx.doi.org/10.1038/s41371-023-00829-7

Ejemplares similares

Bioinformatic and rare‐variant collapsing analyses for type 1 and type 2 diabetes in the UK Biobank reveal novel pleiotropic susceptibility loci
por: Zöller, Bengt, et al.
Publicado: (2023)

Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank
por: Zöller, Bengt, et al.
Publicado: (2023)

Contribution of rare and common coding variants to haematological malignancies in the UK biobank
por: Zöller, Bengt, et al.
Publicado: (2023)

Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients
por: Manderstedt, Eric, et al.
Publicado: (2020)

Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study
por: Manderstedt, Eric, et al.
Publicado: (2022)

Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
por: Manderstedt, Eric, et al.
Publicado: (2018)

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients
por: Manderstedt, Eric, et al.
Publicado: (2018)

Targeted re-sequencing of F8, F9 and VWF: Characterization of Ion Torrent data and clinical implications for mutation screening
por: Manderstedt, Eric, et al.
Publicado: (2019)

Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR
por: Manderstedt, Eric, et al.
Publicado: (2020)

Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle‐aged and older adults: A population‐based cohort study
por: Manderstedt, Eric, et al.
Publicado: (2022)

Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study
por: Manderstedt, Eric, et al.
Publicado: (2022)

Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population
por: Henmyr, V., et al.
Publicado: (2017)

Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2
por: Henmyr, Viktor, et al.
Publicado: (2016)

Copy Number Variants in the Kallikrein Gene Cluster
por: Lindahl, Pernilla, et al.
Publicado: (2013)

Rare variant associations with plasma protein levels in the UK Biobank
por: Dhindsa, Ryan S., et al.
Publicado: (2023)

Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
por: Barton, Alison R., et al.
Publicado: (2021)

Comprehensive evaluation of genetic variation in S100A7 suggests an association with the occurrence of allergic rhinitis
por: Bryborn, Malin, et al.
Publicado: (2008)

Oncolytic adenovirus-mediated therapy for prostate cancer
por: Sweeney, Katrina, et al.
Publicado: (2016)

Rare variant contribution to human disease in 281,104 UK Biobank exomes
por: Wang, Quanli, et al.
Publicado: (2021)

Characterizing the hypertensive cardiovascular phenotype in the UK Biobank
por: Elghazaly, Hussein, et al.
Publicado: (2023)

Prevalence of Hypertrophic Cardiomyopathy in the UK Biobank Population
por: Lopes, Luis R., et al.
Publicado: (2021)

Targeting Triple Negative Breast Cancer With Oncolytic Adenoviruses
por: Green-Tripp, Gabriela, et al.
Publicado: (2022)

Obesity and risk of COVID-19: analysis of UK biobank
por: Yates, Thomas, et al.
Publicado: (2020)

Rare-variant collapsing analyses identified risk genes for neonatal acute respiratory distress syndrome
por: Chen, Huiyao, et al.
Publicado: (2022)

Analysing electrocardiographic traits and predicting cardiac risk in UK biobank
por: Ramírez, Julia, et al.
Publicado: (2021)

Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank
por: Hofmeister, Robin J., et al.
Publicado: (2023)

Prevalence of Fabry disease-causing variants in the UK Biobank
por: Gilchrist, Mark, et al.
Publicado: (2023)

The relationship between isolated hypertension with brain volumes in UK Biobank
por: Newby, Danielle, et al.
Publicado: (2022)

The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees
por: Guo, Wei, et al.
Publicado: (2014)

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
por: Henne, Sabrina Katrin, et al.
Publicado: (2023)

Neurological diseases and COVID-19: prospective analyses using the UK Biobank
por: Veronese, Nicola, et al.
Publicado: (2021)

Participation bias in the UK Biobank distorts genetic associations and downstream analyses
por: Schoeler, Tabea, et al.
Publicado: (2023)

The E1B19K-deleted oncolytic adenovirus mutant AdΔ19K sensitizes pancreatic cancer cells to drug-induced DNA-damage by down-regulating Claspin and Mre11
por: Pantelidou, Constantia, et al.
Publicado: (2016)

Comparison of collapsing methods for the statistical analysis of rare variants
por: Dering, Carmen, et al.
Publicado: (2011)

Identification of novel genetic variants, including PIM1 and LINC01491, with ICD-10 based diagnosis of pulmonary arterial hypertension in the UK Biobank cohort
por: Pu, Alex, et al.
Publicado: (2023)

Response to ‘Multimorbidity and SARS-CoV-2 infection in UK biobank’
por: Sur Roy, Abhipsha, et al.
Publicado: (2020)

Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants
por: He, Karen Y., et al.
Publicado: (2023)

Primary hypertension, anti-hypertensive medications and the risk of severe COVID-19 in UK Biobank
por: Pavey, Holly, et al.
Publicado: (2022)

A Systematic Study of Gene Mutations in Urothelial Carcinoma; Inactivating Mutations in TSC2 and PIK3R1
por: Sjödahl, Gottfrid, et al.
Publicado: (2011)

Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study
por: Nilsson, Daniel, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_e099pe7aqcnhpoqns2m46m4hsk