Author

Alex J. Kopelowicz

University of California, Los AngelesORCID 0000-0002-1728-4105Unclaimed ORCID profile · follow to get notified of new preprints

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Genetics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Assay:electronic health records· 1 Research Focus:GWAS / association mapping· 1 Organism:human· 1 Assay:snRNA-seq· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A. M. McIntoshiD· 1 shared Aarno V. PalotieiD· 1 shared Adeniran OkewoleiD· 1 shared Aiden Peter CorviniD· 1 shared Akena Dickens· 1 shared Akira SawaiD· 1 shared Ana M. Díaz‐ZuluagaiD· 1 shared Ana M. Ramirez-DiaziD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

A. M. McIntoshORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintSep 21, 2026

✦ In-depth digest

Analysis of Rare Coding Variation Identifies New Genetic Contributors to Schizophrenia

Julia Sealock, Connor Dowd, Calwing Liao…·Akena Dickens

Ultra-rare damaging coding variants in 87,959 schizophrenia cases and 150,587 controls implicate 40 genes (16 exome-wide, 24 at 5% FDR), half overlapping autism, developmental delay or bipolar genes.

1 citation

humanwhole-exome sequencing

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