Cargando…

Increased COVID-19 mortality rate in rare disease patients: a retrospective cohort study in participants of the Genomics England 100,000 Genomes project

BACKGROUND: Several common conditions have been widely recognised as risk factors for COVID-19 related death, but risks borne by people with rare diseases are largely unknown. Therefore, we aim to estimate the difference of risk for people with rare diseases comparing to the unaffected. METHOD: To e...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Huayu, Thygesen, Johan H., Shi, Ting, Gkoutos, Georgios V., Hemingway, Harry, Guthrie, Bruce, Wu, Honghan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9003178/ https://www.ncbi.nlm.nih.gov/pubmed/35414031 http://dx.doi.org/10.1186/s13023-022-02312-x

Ejemplares similares

The $1,000 genome, the $100,000 analysis?
por: Mardis, Elaine R
Publicado: (2010)

The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer
por: Trotman, Jamie, et al.
Publicado: (2022)

The UK’s 100,000 Genomes Project: manifesting policymakers’ expectations
por: Samuel, Gabrielle Natalie, et al.
Publicado: (2017)

Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
por: Peter, Michelle, et al.
Publicado: (2022)

Opportunities and Challenges for Molecular Understanding of Ciliopathies–The 100,000 Genomes Project
por: Wheway, Gabrielle, et al.
Publicado: (2019)

Sarcoma and the 100,000 Genomes Project: our experience and changes to practice
por: Prendergast, Sophie C, et al.
Publicado: (2020)

$100,000 Premium
Publicado: (1883)

The $100,000 Pyramid
por: Moore, Justin B., et al.
Publicado: (2022)

Public trust and ‘ethics review’ as a commodity: the case of Genomics England Limited and the UK’s 100,000 genomes project
por: Samuel, Gabrielle Natalie, et al.
Publicado: (2017)

AACR Project GENIE: 100,000 Cases and Beyond
por: Pugh, Trevor J., et al.
Publicado: (2022)

Corrigendum: Opportunities and Challenges for Molecular Understanding of Ciliopathies–The 100,000 Genomes Project
por: Wheway, Gabrielle, et al.
Publicado: (2019)

How the £100,000 Is to Be Distributed
Publicado: (1919)

Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project
por: Best, Sunayna, et al.
Publicado: (2022)

Knowledge, attitudes and decision regret: a longitudinal survey study of participants offered genome sequencing in the 100,000 Genomes Project
por: Peter, Michelle, et al.
Publicado: (2023)

Celebrating 100'000 followers on Youtube
por: Hertzog, Samuel Joseph
Publicado: (2020)

Diccionario academia enciclopédico 100,000
por: Campillo Cuautli, Héctor
Publicado: (1997)

A Premium of 100,000 Dollars
Publicado: (1883)

Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project
por: Bourinaris, Thomas, et al.
Publicado: (2020)

A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project
por: Blakes, Alexander J. M., et al.
Publicado: (2022)

Increased COVID-19 related mortality rate for patients with rare diseases: a retrospective cohort study with data from Genomics England
por: Zhang, Huayu, et al.
Publicado: (2021)

Coronaviridae: 100,000 Years of Emergence and Reemergence
por: Kasmi, Yassine, et al.
Publicado: (2020)

100,000-spin coherent Ising machine
por: Honjo, Toshimori, et al.
Publicado: (2021)

Genomics England’s implementation of its public engagement strategy: Blurred boundaries between engagement for the United Kingdom’s 100,000 Genomes project and the need for public support
por: Samuel, Gabrielle Natalie, et al.
Publicado: (2017)

BlastFrost: fast querying of 100,000s of bacterial genomes in Bifrost graphs
por: Luhmann, Nina, et al.
Publicado: (2021)

Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting results
por: Magiorkinis, Gkikas, et al.
Publicado: (2019)

A gene pathogenicity tool ‘GenePy’ identifies missed biallelic diagnoses in the 100,000 Genomes Project
por: Seaby, Eleanor G., et al.
Publicado: (2023)

A 100,000 Scale Factor Radar Range
por: Blanche, Pierre-Alexandre, et al.
Publicado: (2017)

GrapeTree: visualization of core genomic relationships among 100,000 bacterial pathogens
por: Zhou, Zhemin, et al.
Publicado: (2018)

Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden
por: Chalmers, Zachary R., et al.
Publicado: (2017)

Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project
por: Robbe, Pauline, et al.
Publicado: (2018)

A million random digits with 100,000 normal deviates.
Publicado: (1966)

100.000 computer per l'Internet del futuro
Publicado: (2008)

CERN exhibition attracts over 100,000 visitors in Belgrade
por: Antonella Del Rosso
Publicado: (2012)

Language Did Not Spring Forth 100,000 Years Ago
por: Lieberman, Philip
Publicado: (2015)

Using data from the 100,000 Genomes Project to resolve conflicting interpretations of a recurrent TUBB2A mutation
por: Ragoussis, Vassilis, et al.
Publicado: (2022)

Unlocking the potential of the UK 100,000 Genomes Project—lessons learned from analysis of the “Congenital Malformations caused by Ciliopathies” cohort
por: Best, Sunayna, et al.
Publicado: (2022)

Targeting de novo loss-of-function variants in constrained disease genes improves diagnostic rates in the 100,000 Genomes Project
por: Seaby, Eleanor G., et al.
Publicado: (2022)

Evaluation of the anaesthetic properties and tolerance of 1:100,000 articaine versus 1:100,000 lidocaine. A comparative study in surgery of the lower third molar
por: Martínez-Rodríguez, Natalia, et al.
Publicado: (2012)

Whole genome sequencing in the 100,000 Genomes project identifies a RYR2 variant associating with dilated cardiomyopathy and sudden unexpected death in the young
por: Ben-Haim, Y, et al.
Publicado: (2023)

Indicators of retention in remote digital health studies: a cross-study evaluation of 100,000 participants
por: Pratap, Abhishek, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_6cgrf2cdjs0j97hkqlrsgrpt8e