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Publications by Andrew J. Sharp
Determining Multiallelic Complex Copy Number and Sequence Variation From High Coverage Exome Sequencing Data
BMC Genomics
Biotechnology
Genetics
Identification of the Translocation Breakpoints in the Ts65Dn and Ts1Cje Mouse Lines: Relevance for Modeling Down Syndrome
Mammalian Genome
Genetics
Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms Within Duplicated Regions of the Human Genome
American Journal of Human Genetics
Genetics
Detection of Genomic Variation by Selection of a 9 Mb DNA Region and High Throughput Sequencing
PLoS ONE
Multidisciplinary
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Sequencing Studies in Human Genetics: Design and Interpretation
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Evolution of Genetic and Genomic Features Unique to the Human Lineage
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Recent Human Adaptation: Genomic Approaches, Interpretation and Insights
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ChIP–seq and Beyond: New and Improved Methodologies to Detect and Characterize Protein–DNA Interactions
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Sex and the Singular DM Domain: Insights Into Sexual Regulation, Evolution and Plasticity
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Putting Gene Essentiality Into Context
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Promoter-Proximal Pausing of RNA Polymerase II: Emerging Roles in Metazoans
Nature Reviews Genetics
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Stress and the Epigenetic Landscape: A Link to the Pathobiology of Human Diseases?
Nature Reviews Genetics
Genetics
Molecular Biology
Autoimmune Diseases — Connecting Risk Alleles With Molecular Traits of the Immune System
Nature Reviews Genetics
Genetics
Molecular Biology
Bayesian Molecular Clock Dating of Species Divergences in the Genomics Era
Nature Reviews Genetics
Genetics
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