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A Fast and Flexible Statistical Model for Large-Scale Population Genotype Data: Applications to Inferring Missing Genotypes and Haplotypic Phase

American journal of human genetics, 2006-04, Vol.78 (4), p.629-644

2006

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Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-Data Imputation

American journal of human genetics, 2005-03, Vol.76 (3), p.449-462

2005

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Single-Cell Transcriptomics of Pancreatic Cancer Precursors Demonstrates Epithelial and Microenvironmental Heterogeneity as an Early Event in Neoplastic Progression

Clinical cancer research, 2019-04, Vol.25 (7), p.2194-2205

2019

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Genotype imputation using the Positional Burrows Wheeler Transform

PLoS genetics, 2020-11, Vol.16 (11), p.e1009049-e1009049

2020

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Clonal evolution in breast cancer revealed by single nucleus genome sequencing

Nature (London), 2014-08, Vol.512 (7513), p.155-160

2014

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Genetic epidemiology, 2010-12, Vol.34 (8), p.816-834

2010

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The Transcriptomic Landscape of Mismatch Repair-Deficient Intestinal Stem Cells

Cancer research (Chicago, Ill.), 2021-05, Vol.81 (10), p.2760-2773

2021

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Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence data

Breast cancer research and treatment, 2014-07, Vol.146 (1), p.211-220

2014

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Defining the Comprehensive Genomic Landscapes of Pancreatic Ductal Adenocarcinoma Using Real-World Endoscopic Aspiration Samples

Clinical cancer research, 2021-02, Vol.27 (4), p.1082-1093

2021

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Early Events in the Molecular Pathogenesis of Lung Cancer

Cancer prevention research (Philadelphia, Pa.), 2016-07, Vol.9 (7), p.518-527

2016

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Attention-Deficit/Hyperactivity Disorder Polygenic Risk Scores Predict Attention Problems in a Population-Based Sample of Children

Journal of the American Academy of Child and Adolescent Psychiatry, 2014-10, Vol.53 (10), p.1123-1129.e6

2014

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Immune evolution from preneoplasia to invasive lung adenocarcinomas and underlying molecular features

Nature communications, 2021-05, Vol.12 (1), p.2722-2722, Article 2722

2021

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Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke

PLoS genetics, 2014-03, Vol.10 (3), p.e1004214-e1004214

2014

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Genomic Landscape of Atypical Adenomatous Hyperplasia Reveals Divergent Modes to Lung Adenocarcinoma

Cancer research (Chicago, Ill.), 2017-11, Vol.77 (22), p.6119-6130

2017

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RAD21 promotes oncogenesis and lethal progression of prostate cancer

Proceedings of the National Academy of Sciences - PNAS, 2024-09, Vol.121 (36), p.e2405543121

2024

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Evolution of DNA methylome from precancerous lesions to invasive lung adenocarcinomas

Nature communications, 2021-01, Vol.12 (1), p.687-13, Article 687

2021

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Novel Susceptibility Variants at 10p12.31-12.2 for Childhood Acute Lymphoblastic Leukemia in Ethnically Diverse Populations

JNCI : Journal of the National Cancer Institute, 2013-05, Vol.105 (10), p.733-742

2013

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Nature genetics, 2008-02, Vol.40 (2), p.161-169

2008

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Augmented Lipocalin-2 Is Associated with Chronic Obstructive Pulmonary Disease and Counteracts Lung Adenocarcinoma Development

American journal of respiratory and critical care medicine, 2021-01, Vol.203 (1), p.90-101

2021

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Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition

Genome research, 2012-01, Vol.22 (1), p.1-8

2012

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Mutational Heterogeneity in APC and KRAS Arises at the Crypt Level and Leads to Polyclonality in Early Colorectal Tumorigenesis

Clinical cancer research, 2017-10, Vol.23 (19), p.5936-5947

2017

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ARID5B Genetic Polymorphisms Contribute to Racial Disparities in the Incidence and Treatment Outcome of Childhood Acute Lymphoblastic Leukemia

Journal of clinical oncology, 2012-03, Vol.30 (7), p.751-757

2012

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Causes of Clonal Hematopoiesis: a Review

Current oncology reports, 2023-03, Vol.25 (3), p.211-220

2023

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A Fast and Flexible Statistical Model for Large-Scale Population Genotype Data: Applications to Inferring Missing Genotypes and Haplotypic Phase

Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-Data Imputation

Single-Cell Transcriptomics of Pancreatic Cancer Precursors Demonstrates Epithelial and Microenvironmental Heterogeneity as an Early Event in Neoplastic Progression

Genotype imputation using the Positional Burrows Wheeler Transform

Clonal evolution in breast cancer revealed by single nucleus genome sequencing

Tumor Microbiome Diversity and Composition Influence Pancreatic Cancer Outcomes

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

The Transcriptomic Landscape of Mismatch Repair-Deficient Intestinal Stem Cells

Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence data

Defining the Comprehensive Genomic Landscapes of Pancreatic Ductal Adenocarcinoma Using Real-World Endoscopic Aspiration Samples

Early Events in the Molecular Pathogenesis of Lung Cancer

Attention-Deficit/Hyperactivity Disorder Polygenic Risk Scores Predict Attention Problems in a Population-Based Sample of Children

Immune evolution from preneoplasia to invasive lung adenocarcinomas and underlying molecular features

Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke

Genomic Landscape of Atypical Adenomatous Hyperplasia Reveals Divergent Modes to Lung Adenocarcinoma

RAD21 promotes oncogenesis and lethal progression of prostate cancer

Evolution of DNA methylome from precancerous lesions to invasive lung adenocarcinomas

Novel Susceptibility Variants at 10p12.31-12.2 for Childhood Acute Lymphoblastic Leukemia in Ethnically Diverse Populations

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Augmented Lipocalin-2 Is Associated with Chronic Obstructive Pulmonary Disease and Counteracts Lung Adenocarcinoma Development

Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition

Mutational Heterogeneity in APC and KRAS Arises at the Crypt Level and Leads to Polyclonality in Early Colorectal Tumorigenesis

STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement

ARID5B Genetic Polymorphisms Contribute to Racial Disparities in the Incidence and Treatment Outcome of Childhood Acute Lymphoblastic Leukemia

Causes of Clonal Hematopoiesis: a Review

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