Genome-wide patterns and properties of de novo mutations in humans. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Identification of cis-suppression of human disease mutations by comparative genomics. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
APOBEC-Induced Cancer Mutations Are Uniquely Enriched in Early-Replicating, Gene-Dense, and Active Chromatin Regions. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Genes with monoallelic expression contribute disproportionately to genetic diversity in humans. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation Society. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
Excess of Deleterious Mutations around HLA Genes Reveals Evolutionary Cost of Balancing Selection. All Authors: Author Profiles: Publish Date: Journal: , Read Publication
