Author details

Full Name

Brooke Rhead

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35410379	Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects.	Nat Genet	2022
36223959	COVID-19 susceptibility and severity risks in a cross-sectional survey of over 500 000 US adults.	BMJ Open	2022
34873174	Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome.	Nat Commun	2021
32109229	Author Correction: A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus.	Nature Communications	2020
32231389	Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs.	PLoS ONE	2020
31366909	Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology.	Nature Communications	2019
30653506	Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry.	PLoS Genet	2019
31467281	A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus.	Nature Communications	2019
31211169	miRNA contributions to pediatric-onset multiple sclerosis inferred from GWAS.	Ann Clin Transl Neurol	2019
29287311	Hypomethylation of CYP2E1 and DUSP22 Promoters Associated With Disease Activity and Erosive Disease Among Rheumatoid Arthritis Patients.	Arthritis and Rheumatology	2018
28980494	Genetic risk factors for pediatric-onset multiple sclerosis.	Mult Scler	2018
30379917	Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients.	PLoS ONE	2018
27723282	Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes.	Arthritis Rheumatol	2017
28356466	Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS.	Neurology	2017
28073764	Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility.	Am J Epidemiol	2017
27652346	Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk.	Neurology: Genetics	2016
26740527	UCSC Data Integrator and Variant Annotation Integrator.	Bioinformatics	2016
24270787	The UCSC Genome Browser database: 2014 update.	Nucleic Acids Res	2014
23155063	The UCSC Genome Browser database: extensions and updates 2013.	Nucleic Acids Res	2013
22075998	ENCODE whole-genome data in the UCSC Genome Browser: update 2012.	Nucleic Acids Res	2012
22086951	The UCSC Genome Browser database: extensions and updates 2011.	Nucleic Acids Res	2012
20959295	The UCSC Genome Browser database: update 2011.	Nucleic Acids Res	2011
21037257	ENCODE whole-genome data in the UCSC genome browser (2011 update).	Nucleic Acids Res	2011
19906737	The UCSC Genome Browser database: update 2010.	Nucleic Acids Res	2010
19920125	ENCODE whole-genome data in the UCSC Genome Browser.	Nucleic Acids Res	2010
18996895	The UCSC Genome Browser Database: update 2009.	Nucleic Acids Res	2009
18086701	The UCSC Genome Browser Database: 2008 update.	Nucleic Acids Res	2008
17142222	The UCSC genome browser database: update 2007.	Nucleic Acids Res	2007
17151077	Variation resources at UC Santa Cruz.	Nucleic Acids Res	2007
17166863	The ENCODE Project at UC Santa Cruz.	Nucleic Acids Res	2007
15616286	Identification of novel inhibitors of bacterial translation elongation factors.	Antimicrobial Agents and Chemotherapy	2005