Author

Howard Andrews

Columbia UniversityORCID 0000-0002-7726-0551Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam M. BrickmaniD· 2 shared Giuseppe TostoiD· 2 shared Jennifer Jaie ManlyiD· 2 shared Alexa BeiseriD· 1 shared Antonio Spagnolo‐AllendeiD· 1 shared Badri Narayan VardarajaniD· 1 shared Bruce Alan WassermaniD· 1 shared Charles J. WolockiD· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adam M. BrickmanORCID

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2 papers

Recent·Most cited

Chromosome 10q24.32 Variants Associate with Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study

Minghua Liu, Farid Khasiyev, Sanjeev Sariya, Antonio Spagnolo‐Allende, Danurys L. Sanchez, Howard Andrews, Qiong Yang, Alexa Beiser, Ye Qiao, Emy A. Thomas, Jose Rafael Romero, Tatjana Rundek, Adam M. Brickman, Jennifer Jaie Manly, Mitchell S.V. Elkind, , José Gutierrez

This study identifies three novel genetic loci associated with brain arterial diameters through a genome-wide association analysis across diverse populations.

Journal of the American Heart Association · Dec 1, 2023Peer-reviewedGenetic & Genomic Medicine

Whole Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer Disease

Neha S. Raghavan, Adam M. Brickman, Howard Andrews, Jennifer Jaie Manly, Nicole Schupf, Rafael Lantigua, The Alzheimer’s Disease Sequencing Project, Charles J. Wolock, Sitharthan Kamalakaran, Slavé Petrovski, Giuseppe Tosto, Badri Narayan Vardarajan, David B. Goldstein, Richard P Mayeux

The paper uses whole exome sequencing in 20,197 individuals to identify rare variants associated with Alzheimer's disease, finding significant associations with SORL1 loss-of-function variants.

bioRxiv · Apr 23, 2018 · PreprintGenetics