The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants

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LD mapping of maternally and non-maternally derived alleles and atopy in FcεRI-β

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The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI

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Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

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Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy

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Alpha-synuclein degradation by serine protease neurosin: implication for pathogenesis of synucleinopathies

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Allele-specific silencing of a pathogenic mutant acetylcholine receptor subunit by RNA interference

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Phenotypic effects of heterozygosity for a BRCA2 mutation

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Mutation in a short-chain collagen gene, CTRP5 , results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

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A reporter for amyloid precursor protein γ-secretase activity in Drosophila

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A comprehensive haplotype analysis of CYP19 and breast cancer risk: the Multiethnic Cohort

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Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

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Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia

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Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres

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Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader–Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes

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