Cargando…

Genome‐wide and Phenome‐wide Approaches to Understand Variable Drug Actions in Electronic Health Records

Detalles Bibliográficos
Autores principales:	Robinson, Jamie R., Denny, Joshua C., Roden, Dan M., Van Driest, Sara L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2017
Materias:	Reviews
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866959/ https://www.ncbi.nlm.nih.gov/pubmed/29148204 http://dx.doi.org/10.1111/cts.12522

Ejemplares similares

Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record
por: Wei, Wei-Qi, et al.
Publicado: (2017)

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations
por: Denny, Joshua C., et al.
Publicado: (2010)

Phenome-Wide Association Study of Polygenic Risk Score for Alzheimer’s Disease in Electronic Health Records
por: Fu, Mingzhou, et al.
Publicado: (2022)

Applying semantic web technologies for phenome-wide scan using an electronic health record linked Biobank
por: Pathak, Jyotishman, et al.
Publicado: (2012)

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

Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
por: Joo, Yoonjung Yoonie, et al.
Publicado: (2023)

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

Enabling Genomic-Phenomic Association Discovery without Sacrificing Anonymity
por: Heatherly, Raymond D., et al.
Publicado: (2013)

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)

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

Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing Anonymity
por: Heatherly, Raymond D., et al.
Publicado: (2013)

Phenome-wide association study identifies marked increased in burden of comorbidities in African Americans with systemic lupus erythematosus
por: Barnado, April, et al.
Publicado: (2018)

Genetically predicted sex hormone levels and health outcomes: phenome-wide Mendelian randomization investigation
por: Yuan, Shuai, et al.
Publicado: (2022)

A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR
por: Safarova, Maya S., et al.
Publicado: (2019)

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)

A phenome-wide association study (PheWAS) of COVID-19 outcomes by race using the electronic health records data in Michigan Medicine
por: Salvatore, Maxwell, et al.
Publicado: (2021)

A Phenome-Wide Association Study (PheWAS) of COVID-19 Outcomes by Race Using the Electronic Health Records Data in Michigan Medicine
por: Salvatore, Maxwell, et al.
Publicado: (2021)

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

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

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

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

Phenome-wide association studies across large population cohorts support drug target validation
por: Diogo, Dorothée, et al.
Publicado: (2018)

Joint mouse–human phenome-wide association to test gene function and disease risk
por: Wang, Xusheng, et al.
Publicado: (2016)

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases
por: Zheng, Jie, et al.
Publicado: (2020)

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

Genome-wide study of resistant hypertension identified from electronic health records
por: Dumitrescu, Logan, et al.
Publicado: (2017)

Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
por: Huang, Rose D. L., et al.
Publicado: (2022)

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)

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

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

A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data
por: Niarchou, Maria, et al.
Publicado: (2022)

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

PheMIME: An Interactive Web App and Knowledge Base for Phenome-Wide, Multi-Institutional Multimorbidity Analysis
por: Zhang, Siwei, et al.
Publicado: (2023)

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

A Case-Crossover Phenome-wide association study (PheWAS) for understanding Post-COVID-19 diagnosis patterns
por: Haupert, Spencer R., et al.
Publicado: (2022)

A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort
por: Schlauch, Karen A., et al.
Publicado: (2019)

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

Cannot write session to /tmp/vufind_sessions/sess_num9fs8u7p8h0irahsk4ebj2o8