Author

Matthew Bookman

Verily Life Sciences LLC (United States)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Ada J. S. Chan· 1 shared Afiqah YusufiD· 1 shared Alana Iaboni· 1 shared Alastair John NoyceiD· 1 shared Alireza Torkamani· 1 shared Andrew SingletoniD· 1 shared Annabel Rutherford· 1 shared Anthony R. SoltisiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ada J. S. Chan

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2 papers

Recent·Most cited

Genomic architecture of autism spectrum disorder from comprehensive whole-genome sequence annotation

Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe, Livia Oliveira Loureiro, Miriam S. Reuter, Delnaz Roshandel, Joe Whitney, Mehdi Zarrei, Matthew Bookman, Cherith Somerville, Rulan Shaath, Mona Abdi, , Evdokia A. Anagnostou

This study identifies 135 ASD-associated protein-coding genes using whole-genome sequencing data from 11,312 individuals and exome sequencing from over 18,000 trios, with a false discovery rate of 80%.

medRxiv · May 5, 2022 · PreprintGenetic & Genomic Medicine

Large-scale pathway-specific polygenic risk, transcriptomic community networks and functional inferences in Parkinson disease

Sara Bandrés‐Ciga, Sara Sáez-Atiénzar, Jeff Kim, Mary B. Makarious, Faraz Faghri, Mónica Díez-Fairén, Hirotaka Iwaki, Hampton L. Leonard, Juan Antonio Botía, Mina Ryten, Dena G. Hernandez, Jesse Raphael Gibbs, Jinhui Ding, Ziv Gan‐Or, Alastair John Noyce, , Andrew Singleton

The paper identifies pathway-specific polygenic risk factors and transcriptomic networks associated with Parkinson disease using large-scale genetic and expression data.

Acta Neuropathologica · Jun 29, 2020Peer-reviewedGenetics