American journal of human genetics

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

The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research.

The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research.

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.

Medical sequencing at the extremes of human body mass.

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