P. Vandehaar

发表

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

Lars G Fritsche, Joshua C Denny, Wei-Qi Wei, 2017, Nature Genetics.

Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb

Stephanie E. Moser, Sarah A. Gagliano, Robert B Peng, 2018, bioRxiv.

A powerful subset-based gene-set analysis method identifies novel associations and improves interpretation in UK Biobank

M. Boehnke, L. Scott, Seunggeun Lee, 2019, bioRxiv.

Whole genome comparison of a large collection of mycobacteriophages reveals a continuum of phage genetic diversity

John Vu, Eric Mayer, J. Paul Robinson, 2015, eLife.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2020, Nature Genetics.

Simulating evolution of protein complexes through gene duplication and co-option.

Serita M. Nelesen, James G. Lamine, L. Haarsma, 2016, Journal of theoretical biology.

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Ivana V. Yang, Zhaohui S. Qin, Andrew D. Johnson, 2018, Nature Communications.

Exploring Various Polygenic Risk Scores for Basal Cell Carcinoma, Cutaneous Squamous Cell Carcinoma and Melanoma in the Phenomes of the Michigan Genomics Initiative and the UK Biobank

Bhramar Mukherjee, Gonçalo R. Abecasis, Stephanie E. Moser, 2018 .

Exploring Various Polygenic Risk Scores for Skin Cancer in the Phenomes of the Michigan Genomics Initiative and the UK Biobank with a Visual Catalog: PRSWeb

Bhramar Mukherjee, Gonçalo R. Abecasis, Stephanie E. Moser, 2018, bioRxiv.

LocusZoom.js: interactive and embeddable visualization of genetic association study results

Andrew P. Boughton, G. Abecasis, M. Boehnke, 2021, bioRxiv.

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Ryan D. Hernandez, May E. Montasser, Min A. Jhun, 2018, Nature Communications.

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.

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.

Exploring and visualizing large-scale genetic associations by using PheWeb

Andrew P. Boughton, Ellen M. Schmidt, G. Abecasis, 2020, Nature Genetics.

Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with asthma.

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2019, Chest.

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.

Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks

Lars G Fritsche, Bhramar Mukherjee, Xiang Zhou, 2020, American journal of human genetics.

Cancer PRSweb – an Online Repository with Polygenic Risk Scores (PRS) for Major Cancer Traits and Their Phenome-wide Exploration in Two Independent Biobanks

Bhramar Mukherjee, Daniel Taliun, Peter VandeHaar, 2020, bioRxiv.

Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

Emily C. Hector, N. Freimer, M. Laakso, 2022, Nature Communications.

Genome-wide association study of 1,391 plasma metabolites in 6,136 Finnish men identifies 303 novel signals and provides biological insights into human diseases

Emily C. Hector, Ripatti, N. Freimer, 2021, medRxiv.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Ivana V. Yang, Sebastian M. Armasu, Andrew D. Johnson, 2020, Nature.

FIVEx: an interactive multi-tissue eQTL browser

Alan M. Kwong, Andrew P. Boughton, G. Abecasis, 2021, bioRxiv.

UK-Biobank Whole Exome Sequence Binary Phenome Analysis with Robust Region-based Rare Variant Test

Seunggeun Lee, Wei Zhou, Zhangchen Zhao, 2019, bioRxiv.

Exploring and visualizing large-scale genetic associations by using PheWeb

Andrew P. Boughton, Ellen M. Schmidt, G. Abecasis, 2020, Nature Genetics.

False discovery rates for genome-wide association tests in biobanks with thousands of phenotypes

G. Abecasis, M. Boehnke, M. Zawistowski, 2021 .

A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank.

M. Boehnke, L. Scott, Seunggeun Lee, 2021, American journal of human genetics.

Clonal haematopoiesis and risk of chronic liver disease

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

An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

Ivana V. Yang, Andrew D. Johnson, Ryan D. Hernandez, 2018, Circulation.

FIVEx: an interactive eQTL browser across public datasets

Gonçalo R. Abecasis, Michael Boehnke, Alan M. Kwong, 2021, Bioinform..

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.

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Andrew D. Johnson, May E. Montasser, Nicholette D. Palmer, 2020, Nature Genetics.

Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium

Andrew D. Johnson, Benjamin D. Heavner, May E. Montasser, 2020, Genome Medicine.