Author

Evan Jeffrey Giangrande

Broad InstituteORCID 0000-0002-8023-0062Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Anders J. KämpeiD· 1 shared Annamari Tuulio‐HenrikssoniD· 1 shared Benjamin M. NealeiD· 1 shared Calwing LiaoiD· 1 shared Eija Hämäläinen· 1 shared Emilia VartiaineniD· 1 shared Erkki Tapio IsometsäiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarno V. PalotieORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 1, 2026

Ultra-rare coding variants in schizophrenia risk genes are associated with longitudinal phenotypic differences across psychotic disorders

Anders J. Kämpe, Julia Sealock, Evan Jeffrey Giangrande…·Olli P. H. Pietiläinen

This study identifies ultra-rare damaging variants in schizophrenia risk genes and shows they are associated with earlier hospitalizations, greater childhood adversity, and poorer neuropsychological outcomes across psychotic disorders.

DOI 10.64898/2026.10.30.26366332

humanwhole-exome sequencing

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