Author

Brandon E. Avila

Broad InstituteORCID 0000-0002-8617-7186Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Brandon E. Avila1 paper

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Research Focus:fine-mapping· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Adam P. LevineiD· 1 shared Alain BittoniD· 1 shared Aleksejs SazonovsiD· 1 shared Alexandra CarliD· 1 shared Allan Daly· 1 shared Amanda SievertsiD· 1 shared Anastasia ZhivotoviD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarno V. PalotieORCID

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Author profile →

2 papers

Recent·Most cited

Demographic Composition of Participants in Sex Chromosome Aneuploidy Studies across the Globe: a 20-year Systematic Review

Karli S. Swenson, Samantha Bothwell, Anastasia Zhivotov, Amanda Sieverts, Shalika Devireddy, Kira Shuff, Kayla Nocon, Alexandra Carl, Kayla Molison, Lidia Grzybacz, Brisa Avila, Chijioke Ikomi, Lilian Liou Cohen, Ellie Svoboda, Shanlee Davis

This paper reviews 20 years of sex chromosome aneuploidy studies, finding geographic concentration and underrepresentation of diverse racial, ethnic, and socioeconomic groups in participant demographics.

American Journal of Medical Genetics Part A · Nov 5, 2025Peer-reviewedGenetic & Genomic Medicine

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

Aleksejs Sazonovs, Christine R. Stevens, Guhan Ram Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu, Tariq Ahmad, Matthieu Allez, Ashwin N. Ananthakrishnan, Gil Atzmon, Aris Baras, Jeffrey C. Barrett, Nir Barzilai, Laurent Beaugerie, Ashley Harris Beecham, , Rasha Shawky

The paper identifies ten new genes with coding variants linked to Crohn's disease risk using sequencing data from over 30,000 patients and 80,000 controls.

Nature Genetics · Aug 29, 2022Peer-reviewedGenetic & Genomic Medicine