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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

PLoS genetics, 2009-06, Vol.5 (6), p.e1000529-e1000529

2009

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A new multipoint method for genome-wide association studies by imputation of genotypes

Nature genetics, 2007-07, Vol.39 (7), p.906-913

2007

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Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Nature genetics, 2012-08, Vol.44 (8), p.955-959

2012

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Landscape of immunogenic tumor antigens in successful immunotherapy of virally induced epithelial cancer

Science (American Association for the Advancement of Science), 2017-04, Vol.356 (6334), p.200-205

2017

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1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

European journal of human genetics : EJHG, 2012-07, Vol.20 (7), p.801-805

2012

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Detection of Minimal Residual Disease in B Lymphoblastic Leukemia by High-Throughput Sequencing of IGH

Clinical cancer research, 2014-09, Vol.20 (17), p.4540-4548

2014

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Analytical evaluation of the clonoSEQ Assay for establishing measurable (minimal) residual disease in acute lymphoblastic leukemia, chronic lymphocytic leukemia, and multiple myeloma

BMC cancer, 2020-06, Vol.20 (1), p.612-15, Article 612

2020

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Genotype imputation for genome-wide association studies

Nature reviews. Genetics, 2010-07, Vol.11 (7), p.499-511

2010

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The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes

Genome research, 2013-05, Vol.23 (5), p.749-761

2013

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Genotype imputation with thousands of genomes

G3 : genes - genomes - genetics, 2011-11, Vol.1 (6), p.457-470

2011

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Efficient selection of tagging single-nucleotide polymorphisms in multiple populations

Human genetics, 2006-08, Vol.120 (1), p.58-68

2006

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Life's onslaught

Nature (London), 2010-09, Vol.467 (7314), p.1-1

Howie, Bryan

2010

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Comparing Algorithms for Genotype Imputation

American journal of human genetics, 2008-10, Vol.83 (4), p.535-539

2008

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Faux scientist?

Nature (London), 2010-06, Vol.465 (7299), p.831-831

Howie, Bryan

2010

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Savouring the moment

Nature (London), 2010-06, Vol.465 (7299), p.1-1

Howie, Bryan

2010

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High-throughput pairing of T cell receptor α and β sequences

Science translational medicine, 2015-08, Vol.7 (301), p.301ra131

2015

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High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Nature genetics, 2012-12, Vol.44 (12), p.1336-1340

2012

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Tumor- and Neoantigen-Reactive T-cell Receptors Can Be Identified Based on Their Frequency in Fresh Tumor

Cancer immunology research, 2016-09, Vol.4 (9), p.734-743

2016

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Identification of loci associated with schizophrenia by genome-wide association and follow-up

Nature genetics, 2008-09, Vol.40 (9), p.1053-1055

2008

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A statin-dependent QTL for GATM expression is associated with statin-induced myopathy

Nature (London), 2013-10, Vol.502 (7471), p.377-380

2013

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Nature, 2007-06, Vol.447 (7145), p.661-678

2007

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Reduction Of Immune Repertoire Diversity Through DNA Sequence Constraints At VDJ Junctions

Blood, 2013-11, Vol.122 (21), p.4944-4944

2013

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Assessment of Immunoglobulin Heavy Chain Variable Region (IGHV) Mutation Status with a Next-Generation Sequencing (NGS) Immunosequencing Assay for Measurable Residual Disease (MRD)

Blood, 2021-11, Vol.138 (Supplement 1), p.4676-4676

2021

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Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

Nature communications, 2019-04, Vol.10 (1), p.1718-14, Article 1718

2019

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Estimating the Ages of Selection Signals from Different Epochs in Human History

Molecular biology and evolution, 2016-03, Vol.33 (3), p.657-669

2016

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

A new multipoint method for genome-wide association studies by imputation of genotypes

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Landscape of immunogenic tumor antigens in successful immunotherapy of virally induced epithelial cancer

1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

Detection of Minimal Residual Disease in B Lymphoblastic Leukemia by High-Throughput Sequencing of IGH

Analytical evaluation of the clonoSEQ Assay for establishing measurable (minimal) residual disease in acute lymphoblastic leukemia, chronic lymphocytic leukemia, and multiple myeloma

Genotype imputation for genome-wide association studies

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes

Genotype imputation with thousands of genomes

Efficient selection of tagging single-nucleotide polymorphisms in multiple populations

Life's onslaught

Comparing Algorithms for Genotype Imputation

Faux scientist?

Savouring the moment

High-throughput pairing of T cell receptor α and β sequences

High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

Tumor- and Neoantigen-Reactive T-cell Receptors Can Be Identified Based on Their Frequency in Fresh Tumor

Identification of loci associated with schizophrenia by genome-wide association and follow-up

A statin-dependent QTL for GATM expression is associated with statin-induced myopathy

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Reduction Of Immune Repertoire Diversity Through DNA Sequence Constraints At VDJ Junctions

Assessment of Immunoglobulin Heavy Chain Variable Region (IGHV) Mutation Status with a Next-Generation Sequencing (NGS) Immunosequencing Assay for Measurable Residual Disease (MRD)

Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

Estimating the Ages of Selection Signals from Different Epochs in Human History

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