Author

Ana Maria Olivares

Broad InstituteORCID 0000-0002-7325-9211Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:whole-exome sequencing· 3 Research Focus:GWAS / association mapping· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Assay:GWAS summary statistics· 1 Research Focus:synaptic & neural circuits· 1

Frequent Co-Authors

Carlos N. PatoiD· 3 shared Daniel P. HowriganiD· 3 shared Hailiang HuangiD· 3 shared Michele T. PatoiD· 3 shared Nelson B. FreimeriD· 3 shared Sinéad B. ChapmaniD· 3 shared Aarno V. PalotieiD· 2 shared Aiden Peter CorviniD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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Focal author (center)Selected co-authorORCID co-authorUnlinked name

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3 shared papersGenetic & Genomic Medicine

Carlos N. PatoORCID

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Author profile →

3 papers

Recent·Most cited

Rare coding variation implicates thirteen genes in bipolar disorder across 232,536 individuals from global populations

Calwing Liao, Robert Ye, Julia Sealock, Toni A. Boltz, Franjo Ivankovic, Hilary K. Finucane, Daniel P. Howrigan, Yijia Christiana Liu, F. Kyle Satterstrom, Arsalan Hassan, Melkam Alemayehu Kebede, Stella Gichuru, Rehema M. Mwende, Charles R. J. C. Newton, Nastassja Koen, , Benjamin M. Neale

medRxiv · Oct 5, 2026 · PreprintGenetic & Genomic Medicine

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner

Toni A. Boltz, Benjamin B. Chu, Calwing Liao, Julia Sealock, Robert Ye, Lerato Majara, Jack M. Fu, Susan K. Service, Lingyu Zhan, Sarah Elizabeth Medland, Sinéad B. Chapman, Simone Rubinacci, Matthew T. DeFelice, Jonna Grimsby, Tamrat Abebe, , Alicia R. Martin

The paper introduces BGE, a sequencing method that combines low-pass whole genome and deep whole exome data, showing high accuracy and cost-effectiveness for genetic variant discovery.

bioRxiv · Sep 6, 2024 · PreprintGenomics

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam M. AlEissa, Jack D. Barchas, Nicholas James Bass, Tim B. Bigdeli, Gerome D. Breen, Evelyn J. Bromet, P.F. Buckley, William E. Bunney, Jonas Bybjerg‐Grauholm, William Byerley, Sinéad B. Chapman, , David St Clair

Exomes of 24,248 schizophrenia cases and 97,322 controls implicate ultra-rare damaging variants in 10 genes, including GRIN2A and GRIA3, with odds ratios of 3 to 50.

Nature · Apr 8, 2022Peer-reviewedGenetic & Genomic Medicine✦ In-depth digest