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Nature|October 19, 2007
A second generation human haplotype map of over 3.1 million SNPs, Kelly A Frazer, Dennis G Ballinger, 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.Nature Genetics|May 3, 2019
Genome-wide association study identifies 30 loci associated with bipolar disorderEli A Stahl, Gerome Breen, Andreas J Forstner, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.Nature Genetics|August 13, 2013
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs, S Hong Lee, Stephan Ripke, 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 33