Jenn Watt

发表

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2022, Nature Genetics.

Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

Jennifer F. Hughes, T. Graves, R. Wilson, 2014, Nature.

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Andrew D. Johnson, Benjamin D. Heavner, Michael E. Hall, 2022, Nature Communications.

Genome sequencing unveils a regulatory landscape of platelet reactivity

Benjamin D. Heavner, May E. Montasser, Nicholette D. Palmer, 2019, Nature Communications.

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Andrew D. Johnson, Benjamin D. Heavner, Ryan D. Hernandez, 2022, Nature Genetics.

Clonal haematopoiesis and risk of chronic liver disease

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2023, Nature.

Corrigendum: Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

Jennifer F. Hughes, T. Graves, R. Wilson, 2014, Nature.

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2023, EBioMedicine.

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2021, Nature Communications.

A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

Benjamin D. Heavner, May E. Montasser, Nicholette D. Palmer, 2021, bioRxiv.