Cargando…

Phenome‐Wide Association Study of Severe COVID‐19 Genetic Risk Variants

Detalles Bibliográficos
Autores principales:	Regan, Jessica A., Abdulrahim, Jawan W., Bihlmeyer, Nathan A., Haynes, Carol, Kwee, Lydia Coulter, Patel, Manesh R., Shah, Svati H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Research Letter
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075057/ https://www.ncbi.nlm.nih.gov/pubmed/35179038 http://dx.doi.org/10.1161/JAHA.121.024004

Ejemplares similares

Novel plasma biomarkers improve discrimination of metabolic health independent of weight
por: Ellison, Stephen, et al.
Publicado: (2020)

Epigenome‐Wide Association Study for All‐Cause Mortality in a Cardiovascular Cohort Identifies Differential Methylation in Castor Zinc Finger 1 (CASZ1)
por: Abdulrahim, Jawan W., et al.
Publicado: (2019)

Risk Factor Burden and Long‐Term Prognosis of Patients With Premature Coronary Artery Disease
por: Zeitouni, Michel, et al.
Publicado: (2020)

Metabolomic profiling identifies complex lipid species and amino acid analogues associated with response to weight loss interventions
por: Bihlmeyer, Nathan A., et al.
Publicado: (2021)

Metabolites and diabetes remission after weight loss
por: Kwee, Lydia Coulter, et al.
Publicado: (2021)

Microbiome-associated human genetic variants impact phenome-wide disease risk
por: Markowitz, Robert H. George, et al.
Publicado: (2022)

The association of accelerated epigenetic age with all-cause mortality in cardiac catheterization patients as mediated by vascular and cardiometabolic outcomes
por: Jiang, Rong, et al.
Publicado: (2022)

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
por: Schmidt, Amand F., et al.
Publicado: (2019)

Rare variants in drug target genes contributing to complex diseases, phenome-wide
por: Verma, Shefali Setia, et al.
Publicado: (2018)

Phenome-wide examination of comorbidity burden and multiple sclerosis disease severity
por: Zhang, Tingting, et al.
Publicado: (2020)

A phenome-wide scan reveals convergence of common and rare variant associations
por: Zhou, Dan, et al.
Publicado: (2023)

Phenome-wide analysis of genome-wide polygenic scores
por: Krapohl, E, et al.
Publicado: (2016)

Mouse Phenome Database
por: Grubb, Stephen C., et al.
Publicado: (2014)

Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness
por: Abdellaoui, Abdel, et al.
Publicado: (2019)

A phenome-wide association study of genetically mimicked statins
por: Li, Shun, et al.
Publicado: (2021)

Phenome-wide association study on miRNA-related sequence variants: the UK Biobank
por: Mustafa, Rima, et al.
Publicado: (2023)

Mouse Phenome Database
por: Grubb, Stephen C., et al.
Publicado: (2009)

Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide
por: Verma, Shefali Setia, et al.
Publicado: (2018)

Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature
por: Zekavat, Seyedeh Maryam, et al.
Publicado: (2021)

Phenome-wide heritability analysis of the UK Biobank
por: Ge, Tian, et al.
Publicado: (2017)

Phenome-wide and genome-wide analyses of quality of life in schizophrenia
por: Pazoki, Raha, et al.
Publicado: (2020)

PHENOME-WIDE GENETIC CORRELATION AND CAUSALITY OF COVID-19 SEVERITY HIGHLIGHTS OVERLAP WITH SUBSTANCE-USE TRAITS
por: Pathak, Gita, et al.
Publicado: (2021)

A phenome-wide examination of neural and cognitive function
por: Poldrack, R.A., et al.
Publicado: (2016)

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index
por: Cronin, Robert M., et al.
Publicado: (2014)

Mouse Phenome Database (MPD)
por: Bogue, Molly A., et al.
Publicado: (2007)

Mouse Phenome Database (MPD)
por: Maddatu, Terry P., et al.
Publicado: (2012)

Joy of Ping-Pong: Genome-Wide and Phenome-Wide Association Studies
por: Park, Heung-Woo
Publicado: (2020)

Phenome-wide and genome-wide analyses of quality of life in schizophrenia – ERRATUM
por: Pazoki, Raha, et al.
Publicado: (2021)

The challenges, advantages and future of phenome-wide association studies
por: Hebbring, Scott J
Publicado: (2014)

Correction: Phenome-wide heritability analysis of the UK Biobank
por: Ge, Tian, et al.
Publicado: (2018)

Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry
por: Dumitrescu, Logan, et al.
Publicado: (2015)

Phenome-wide genetic-correlation analysis and genetically informed causal inference of amyotrophic lateral sclerosis
por: D’Antona, Salvatore, et al.
Publicado: (2023)

Enhanced rare disease mapping for phenome-wide genetic association in the UK Biobank
por: Patrick, Matthew T., et al.
Publicado: (2022)

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants
por: Verma, Anurag, et al.
Publicado: (2016)

An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank
por: James, Glen, et al.
Publicado: (2019)

Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols
por: Moore, Carrie B., et al.
Publicado: (2014)

EHR-based phenome wide association study in pancreatic cancer
por: Adamusiak, Tomasz, et al.
Publicado: (2014)

A phenome-wide association study of ABO blood groups
por: Li, Shun, et al.
Publicado: (2020)

Genome–phenome wide association study of broadly defined headache
por: Hsu, Wan-Ting, et al.
Publicado: (2023)

Multivariate genome-wide analysis of education, socioeconomic status, and brain phenome
por: Wendt, Frank R., et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_56osjvnh50st3bm011k3cu3d3d