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Author Details

Shannon K McDonnell
Mayo Clinic
1996
154
61
PMIDPaper TitleJournal TitlePublished Year
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
35353984Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk.Am J Hum Genet2022
35432445A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk.Front Genet2022
32800727Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer.Eur Urol2021
33436325Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.Eur Urol Oncol2021
33398198Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33473200Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
32514134The effect of sample size on polygenic hazard models for prostate cancer.Eur J Hum Genet2020
30622367Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.Nat Genet2019
30740785Familial recurrence risk with varying amount of family history.Genet Epidemiol2019
30739198Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.Acta Neuropathol2019
30958860An 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 One2019
29661148Identification of missing variants by combining multiple analytic pipelines.BMC Bioinformatics2018
29892050Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.Nat Commun2018
29892016Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.Nat Genet2018
30033362Risk SNP-Mediated Promoter-Enhancer Switching Drives Prostate Cancer through lncRNA PCAT19.Cell2018
30498369Association of mitochondrial DNA copy number with self-rated health status.Appl Clin Genet2018
27916600Mapping Complex Traits in a Diversity Outbred F1 Mouse Population Identifies Germline Modifiers of Metastasis in Human Prostate Cancer.Cell Syst2017
28211093gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.Genet Epidemiol2017
29156765Network-directed cis-mediator analysis of normal prostate tissue expression profiles reveals downstream regulatory associations of prostate cancer susceptibility loci.Oncotarget2017
28961785FIRE: functional inference of genetic variants that regulate gene expression.Bioinformatics2017
28944238Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.Mol Genet Genomic Med2017
27902461Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes.Oncotarget2017
27636879Germline miRNA DNA variants and the risk of colorectal cancer by subtype.Genes Chromosomes Cancer2017
27052111Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation.Nat Commun2016
27666373REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.Am J Hum Genet2016
27655946Incorporating Functional Annotations for Fine-Mapping Causal Variants in a Bayesian Framework Using Summary Statistics.Genetics2016
27262462Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.Hum Genet2016
27312771Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.Genet Epidemiol2016
27432226Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.Cancer Discov2016
25715684Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.Hum Genet2015
26611117Identification of candidate genes for prostate cancer-risk SNPs utilizing a normal prostate tissue eQTL data set.Nat Commun2015
26307654Genome-wide association study of prostate cancer-specific survival.Cancer Epidemiol Biomarkers Prev2015
26257771How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples.Front Genet2015
26034056A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.Cancer Discov2015
25983244Comprehensively evaluating cis-regulatory variation in the human prostate transcriptome by using gene-level allele-specific expression.Am J Hum Genet2015
26025378Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans.Hum Mol Genet2015
24162621Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease.Hum Genet2014
25217961A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.Nat Genet2014
25111073Mutational landscape of candidate genes in familial prostate cancer.Prostate2014
24687830Prospective validation of HLA-DRB1*07:01 allele carriage as a predictive risk factor for lapatinib-induced liver injury.J Clin Oncol2014
23064873HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).Hum Genet2013
23842950Detecting genomic clustering of risk variants from sequence data: cases versus controls.Hum Genet2013
23637064Identification of novel variants in colorectal cancer families by high-throughput exome sequencing.Cancer Epidemiol Biomarkers Prev2013
23650101Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data.Genet Epidemiol2013
23535732Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.Nat Genet2013
23548696Experimental designs for array comparative genomic hybridization technology.Cytogenet Genome Res2013
22945773Single-nucleotide polymorphism rs1052501 associated with monoclonal gammopathy of undetermined significance and multiple myeloma.Leukemia2013
23065704A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.Hum Mol Genet2013
21748754Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG.Prostate2012
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Collaborators

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Stephen N Thibodeau
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Co-authored papers 98
Janet L Stanford
Fred Hutchinson Cancer Research Center
Co-authored papers 43
Elaine A Ostrander
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Co-authored papers 38
Johanna Schleutker
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Co-authored papers 34
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Co-authored papers 31
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Walter A Rocca
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Co-authored papers 28
Douglas F Easton
University of Cambridge
Co-authored papers 28
Henrik Gr??nberg
Karolinska Institute
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William B Isaacs
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Jianfeng Xu
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John D Carpten
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Liang Wang
H. Lee Moffitt Cancer Center
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Ethan M Lange
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Judith A Clements
Co-authored papers 16
Sonja I Berndt
Co-authored papers 16
Freddie C Hamdy
University of Oxford
Co-authored papers 16
Christopher A Haiman
University of Southern California
Co-authored papers 16
Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers 15
Ruth C Travis
Co-authored papers 15
Stephen J Chanock
National Cancer Institute, National Institutes of Health
Co-authored papers 15
Loic Le Marchand
Co-authored papers 15
Børge G Nordestgaard
Co-authored papers 15
Alice S Whittemore
Co-authored papers 15
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