Author

Zhouzhi Wang

Hospital for Sick Children

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· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

Bhooma ThiruvahindrapuramiD· 3 shared Daniele MericoiD· 3 shared Ingrid AgartziD· 3 shared Aniket ShettyiD· 2 shared Dalila PintoiD· 2 shared Dominique CampioniD· 2 shared Elizabeth Bevilacqua· 2 shared Guiqing Cai· 2 shared

Activity by Year

2016-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Bhooma ThiruvahindrapuramORCID

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3 papers

Recent·Most cited

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects

Worrawat Engchuan, Omar Shanta, Kuldeep Kumar, Jeffrey R. MacDonald, Bhooma Thiruvahindrapuram, Omar Hamdan, Marieke Klein, Adam X. Maihofer, James Guevara, Oanh Hong, Guillaume Huguet, Molly Sacks, Mohammad Mehdi Ahangari, Rayssa M.M.W. Feitosa, Kara Han, , Michael Foster Green

The paper identifies shared and divergent genetic mechanisms across psychiatric disorders using gene-set burden analysis of copy number variants.

medRxiv · Jul 11, 2025 · PreprintGenetic & Genomic Medicine

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris, Prashanth Rajarajan, Erin K. Flaherty, Schahram Akbarian, Andrew J. Chess, Steven A. McCarroll, Po‐Ru Loh, Jennifer E. Phillips‐Cremins, Kristen Brennand, Evan Z. Macosko, , Brandon K. Wormley

This study identifies somatic copy number variants (sCNVs) in schizophrenia cases, revealing their contribution to risk and specific NRXN1 disruptions.

Cell Genomics · Jul 6, 2023Peer-reviewedGenetic & Genomic Medicine

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

Christian Marshall, Daniel Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas Greer, Daniel Antaki, Aniket Shetty, Peter Holmans, Dalila Pinto, Madhusudan Gujral, William Brandler, Dheeraj Malholtra, Zhouzhi Wang, Karin Fuentes Fajarado, , Rita Ca

This study identifies eight genome-wide significant CNV loci associated with schizophrenia using a large cohort of 41,321 subjects.

Nature Genetics · Nov 21, 2016Peer-reviewedGenetics