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Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.The New England Journal of Medicine|September 12, 2008
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypesHeather C Mefford, Andrew J Sharp, Carl Baker, et al.Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.Molecular Psychiatry|September 21, 2022
Rare copy number variation in posttraumatic stress disorderAdam X Maihofer, Worrawat Engchuan, Guillaume Huguet, et al.Nature Genetics|November 22, 2016
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjectsChristian R Marshall, Daniel P Howrigan, Daniele Merico, et al.Biological Psychiatry|December 6, 2021
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure InformationAdam X Maihofer, Karmel W Choi, Jonathan R I Coleman, et al.Medrxiv : the Preprint Server for Health Sciences|August 12, 2025
A cross-disorder analysis of CNVs finds novel loci and dose-dependent relationships of genes to psychiatric traitsOmar Shanta, Marieke Klein, Molly Sacks, et al.Medrxiv : the Preprint Server for Health Sciences|August 12, 2025
Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effectsWorrawat Engchuan, Omar Shanta, Kuldeep Kumar, et al.Nature|April 9, 2022
Mapping genomic loci implicates genes and synaptic biology in schizophreniaVassily Trubetskoy, Antonio F Pardiñas, Ting Qi, et al.Pageof 12