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Identification of Liver Cancer Progenitors Whose Malignant Progression Depends on Autocrine IL-6 Signaling

Cell, 2013-10, Vol.155 (2), p.384-396

2013

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Transcriptome sequencing reveals potential mechanism of cryptic 3' splice site selection in SF3B1-mutated cancers

PLoS computational biology, 2015-03, Vol.11 (3), p.e1004105-e1004105

2015

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Human genetic variation and its contribution to complex traits

Nature reviews. Genetics, 2009-04, Vol.10 (4), p.241-251

2009

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Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants

Nature communications, 2020-02, Vol.11 (1), p.955-955, Article 955

2020

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Evaluation of next generation sequencing platforms for population targeted sequencing studies

Genome biology, 2009-01, Vol.10 (3), p.R32-R32

2009

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ADAR1 Activation Drives Leukemia Stem Cell Self-Renewal by Impairing Let-7 Biogenesis

Cell stem cell, 2016-08, Vol.19 (2), p.177-191

2016

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Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression

Nature communications, 2019-03, Vol.10 (1), p.1054-1054, Article 1054

2019

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PI3Kγ is a molecular switch that controls immune suppression

Nature (London), 2016-11, Vol.539 (7629), p.437-442

2016

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Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells

Cell stem cell, 2017-04, Vol.20 (4), p.533-546.e7

2017

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Common vs. rare allele hypotheses for complex diseases

Current opinion in genetics & development, 2009-06, Vol.19 (3), p.212-219

2009

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Decoding the human genome

Genome research, 2012-09, Vol.22 (9), p.1599-1601

Frazer, Kelly A

2012

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Enhancer release and retargeting activates disease-susceptibility genes

Nature (London), 2021-07, Vol.595 (7869), p.735-740

2021

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miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1

Blood, 2014-07, Vol.124 (1), p.84-95

2014

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PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3

Nature communications, 2017-05, Vol.8 (1), p.15223-15223, Article 15223

2017

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Effective filtering strategies to improve data quality from population-based whole exome sequencing studies

BMC bioinformatics, 2014-05, Vol.15 (1), p.125-125, Article 125

2014

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VISTA: computational tools for comparative genomics

Nucleic acids research, 2004-07, Vol.32 (Web Server issue), p.W273-W279

2004

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Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk

Nature communications, 2019-05, Vol.10 (1), p.2078-2078, Article 2078

2019

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Kataegis Expression Signature in Breast Cancer Is Associated with Late Onset, Better Prognosis, and Higher HER2 Levels

Cell reports (Cambridge), 2016-07, Vol.16 (3), p.672-683

2016

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High resolution long-read telomere sequencing reveals dynamic mechanisms in aging and cancer

Nature communications, 2024-06, Vol.15 (1), p.5149-11

2024

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In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms

PLoS computational biology, 2022-02, Vol.18 (2), p.e1009918-e1009918

2022

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Whole-Genome Sequencing Uncovers the Genetic Basis of Chronic Mountain Sickness in Andean Highlanders

American journal of human genetics, 2013-09, Vol.93 (3), p.452-462

2013

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Systematic analysis of binding of transcription factors to noncoding variants

Nature (London), 2021-03, Vol.591 (7848), p.147-151

2021

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9p21 DNA variants associated with coronary artery disease impair interferon―γ signalling response

Nature (London), 2011-02, Vol.470 (7333), p.264-268

2011

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Whole-Genome Patterns of Common DNA Variation in Three Human Populations

Science (American Association for the Advancement of Science), 2005-02, Vol.307 (5712), p.1072-1079

2005

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High-Resolution Whole-Genome Association Study of Parkinson Disease

American journal of human genetics, 2005-11, Vol.77 (5), p.685-693

2005

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Identification of Liver Cancer Progenitors Whose Malignant Progression Depends on Autocrine IL-6 Signaling

Transcriptome sequencing reveals potential mechanism of cryptic 3' splice site selection in SF3B1-mutated cancers

Human genetic variation and its contribution to complex traits

Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants

Evaluation of next generation sequencing platforms for population targeted sequencing studies

ADAR1 Activation Drives Leukemia Stem Cell Self-Renewal by Impairing Let-7 Biogenesis

Subtle changes in chromatin loop contact propensity are associated with differential gene regulation and expression

PI3Kγ is a molecular switch that controls immune suppression

Large-Scale Profiling Reveals the Influence of Genetic Variation on Gene Expression in Human Induced Pluripotent Stem Cells

Common vs. rare allele hypotheses for complex diseases

Decoding the human genome

Enhancer release and retargeting activates disease-susceptibility genes

miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1

PTEN regulates glioblastoma oncogenesis through chromatin-associated complexes of DAXX and histone H3.3

Effective filtering strategies to improve data quality from population-based whole exome sequencing studies

VISTA: computational tools for comparative genomics

Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk

Kataegis Expression Signature in Breast Cancer Is Associated with Late Onset, Better Prognosis, and Higher HER2 Levels

High resolution long-read telomere sequencing reveals dynamic mechanisms in aging and cancer

In heart failure reactivation of RNA-binding proteins is associated with the expression of 1,523 fetal-specific isoforms

Whole-Genome Sequencing Uncovers the Genetic Basis of Chronic Mountain Sickness in Andean Highlanders

Systematic analysis of binding of transcription factors to noncoding variants

9p21 DNA variants associated with coronary artery disease impair interferon―γ signalling response

Whole-Genome Patterns of Common DNA Variation in Three Human Populations

High-Resolution Whole-Genome Association Study of Parkinson Disease

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