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Risk SNP-Mediated Promoter-Enhancer Switching Drives Prostate Cancer through lncRNA PCAT19

Cell, 2018-07, Vol.174 (3), p.564-575.e18

2018

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Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

Genetics (Austin), 2016-11, Vol.204 (3), p.933-958

2016

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An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set

PloS one, 2019-04, Vol.14 (4), p.e0214588-e0214588

2019

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A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk

Frontiers in genetics, 2022-03, Vol.13, p.836841-836841

2022

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Identification of missing variants by combining multiple analytic pipelines

BMC bioinformatics, 2018-04, Vol.19 (1), p.139-139, Article 139

2018

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Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

PloS one, 2009-06, Vol.4 (6), p.e5878-e5878

2009

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Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk

American journal of human genetics, 2022-05, Vol.109 (5), p.900-908

2022

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Confirmation of a Positive Association between Prostate Cancer Risk and a Locus at Chromosome 8q24

Cancer epidemiology, biomarkers & prevention, 2007-04, Vol.16 (4), p.809-814

2007

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The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas

American journal of human genetics, 2001-10, Vol.69 (4), p.780-790

2001

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Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

Cancer epidemiology, biomarkers & prevention, 2007-05, Vol.16 (5), p.969-978

2007

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Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci

American journal of human genetics, 2004-12, Vol.75 (6), p.948-965

2004

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Efficacy of Contralateral Prophylactic Mastectomy in Women With a Personal and Family History of Breast Cancer

Journal of clinical oncology, 2001-10, Vol.19 (19), p.3938-3943

2001

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Polymorphisms in Mitochondrial Genes and Prostate Cancer Risk

Cancer epidemiology, biomarkers & prevention, 2008-12, Vol.17 (12), p.3558-3566

2008

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Association between Kidney Stones and CKD: A Bidirectional Mendelian Randomization Study

Journal of the American Society of Nephrology, 2024-08

2024

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Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer

European urology, 2021-03, Vol.79 (3), p.353-361

2021

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Multiple Genetic Variant Association Testing by Collapsing and Kernel Methods With Pedigree or Population Structured Data

Genetic epidemiology, 2013-07, Vol.37 (5), p.409-418

2013

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Familial aggregation of Parkinson's disease: The Mayo Clinic family study

Annals of neurology, 2004-10, Vol.56 (4), p.495-502

2004

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Prospective Validation of HLA-DRB107:01 Allele Carriage As a Predictive Risk Factor for Lapatinib-Induced Liver Injury

Journal of clinical oncology, 2014-08, Vol.32 (22), p.2296-2303

2014

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Familial recurrence risk with varying amount of family history

Genetic epidemiology, 2019-06, Vol.43 (4), p.440-448

2019

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FIRE: functional inference of genetic variants that regulate gene expression

Bioinformatics (Oxford, England), 2017-12, Vol.33 (24), p.3895-3901

2017

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Role of the Nijmegen Breakage Syndrome 1 Gene in Familial and Sporadic Prostate Cancer

Cancer epidemiology, biomarkers & prevention, 2006-05, Vol.15 (5), p.935-938

2006

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Frequency of Defective DNA Mismatch Repair in Colorectal Cancer among the Alaska Native People

Cancer epidemiology, biomarkers & prevention, 2007-11, Vol.16 (11), p.2344-2350

2007

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Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990

Neurology, 1999-04, Vol.52 (6), p.1214-1214

1999

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Detecting genomic clustering of risk variants from sequence data: cases versus controls

Human genetics, 2013-11, Vol.132 (11), p.1301-1309

2013

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Risk SNP-Mediated Promoter-Enhancer Switching Drives Prostate Cancer through lncRNA PCAT19

Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics

An expanded variant list and assembly annotation identifies multiple novel coding and noncoding genes for prostate cancer risk using a normal prostate tissue eQTL data set

A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk

Identification of missing variants by combining multiple analytic pipelines

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk

Confirmation of a Positive Association between Prostate Cancer Risk and a Locus at Chromosome 8q24

The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal Carcinomas

Evaluation of Genetic Variations in the Androgen and Estrogen Metabolic Pathways as Risk Factors for Sporadic and Familial Prostate Cancer

Comparison of Microsatellites Versus Single-Nucleotide Polymorphisms in a Genome Linkage Screen for Prostate Cancer–Susceptibility Loci

Efficacy of Contralateral Prophylactic Mastectomy in Women With a Personal and Family History of Breast Cancer

Polymorphisms in Mitochondrial Genes and Prostate Cancer Risk

Association between Kidney Stones and CKD: A Bidirectional Mendelian Randomization Study

Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer

Multiple Genetic Variant Association Testing by Collapsing and Kernel Methods With Pedigree or Population Structured Data

Familial aggregation of Parkinson's disease: The Mayo Clinic family study

Prospective Validation of HLA-DRB107:01 Allele Carriage As a Predictive Risk Factor for Lapatinib-Induced Liver Injury

Familial recurrence risk with varying amount of family history

FIRE: functional inference of genetic variants that regulate gene expression

Role of the Nijmegen Breakage Syndrome 1 Gene in Familial and Sporadic Prostate Cancer

Frequency of Defective DNA Mismatch Repair in Colorectal Cancer among the Alaska Native People

Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990

Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia

Detecting genomic clustering of risk variants from sequence data: cases versus controls

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