American journal of human genetics

A second-generation genomic screen for multiple sclerosis.

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.

Methods for high-density admixture mapping of disease genes.

Methods for high-density admixture mapping of disease genes.

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.

Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.

Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.

HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course.

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