American journal of human genetics

Deep whole-genome sequencing of 100 southeast Asian Malays.

Copy-number disorders are a common cause of congenital kidney malformations.

Copy-number disorders are a common cause of congenital kidney malformations.

Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans.

Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans.

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.

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