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Autism has a strong, complex genetic component, most likely involving several genes. Multiple genomic screens have… Expand Type 1 diabetes is a common, multifactorial disease with strong familial clustering (genetic risk ratio [lambda(S)] approximately… Expand Autism has a strong and complex genetic component, involving several genes. Genomic screens, including our own, have shown… Expand BackgroundAnnotations of completely sequenced genomes reveal that nearly half of the genes identified are of unknown function… Expand Familial primary pulmonary hypertension (PPH) is a rare autosomal dominant disease characterized by distinctive changes in… Expand Primary pulmonary hypertension (PPH), an often fatal disorder, is characterized by sustained elevation of pulmonary artery… Expand Graves' disease (GD) is an autoimmune thyroid disorder that is inherited as a complex trait. We have genotyped 77 affected sib… Expand This review summarizes reports of recurrent DNA sequence copy number amplifications in human neoplasms detected by comparative… Expand Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disease. To date, mutations in four members of the… Expand Previous genome-wide mapping studies have provided suggestive linkage evidence for several novel susceptibility loci responsible… Expand