2q31-q33

OBJECTIVE Autism has a strong, complex genetic component, most likely involving several genes. Multiple genomic screens have… (More)

Type 1 diabetes is a common, multifactorial disease with strong familial clustering (genetic risk ratio [lambda(S)] approximately… (More)

Autism has a strong and complex genetic component, involving several genes. Genomic screens, including our own, have shown… (More)

Annotations of completely sequenced genomes reveal that nearly half of the genes identified are of unknown function, and that… (More)

Familial primary pulmonary hypertension (PPH) is a rare autosomal dominant disease characterized by distinctive changes in… (More)

Primary pulmonary hypertension (PPH), an often fatal disorder, is characterized by sustained elevation of pulmonary artery… (More)

Graves' disease (GD) is an autoimmune thyroid disorder that is inherited as a complex trait. We have genotyped 77 affected sib… (More)

Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disease. To date, mutations in four members of the… (More)

Previous genome-wide mapping studies have provided suggestive linkage evidence for several novel susceptibility loci responsible… (More)

We have performed intrafamilial and case-control association studies to examine the previously reported linkage disequilibrium… (More)