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Author Details

Daniel J Schaid
Mayo Clinic
1982
438
90
PMIDPaper TitleJournal TitlePublished Year
37620596Principles and methods for transferring polygenic risk scores across global populations.Nat Rev Genet2024
37752310A linear weighted combination of polygenic scores for a broad range of traits improves prediction of coronary heart disease.Eur J Hum Genet2024
36540998Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.Pac Symp Biocomput2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
37778899Genome-wide determinants of cellular immune responses to mumps vaccine.Vaccine2023
37609230A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization.medRxiv2023
37645766Broadcasters, receivers, functional groups of metabolites and the link to heart failure progression using polygenic factors.Res Sq2023
37536808Clinical Trials Overview: From Explanatory to Pragmatic Clinical Trials.Mayo Clin Proc2023
37536801Introduction to Thematic Reviews on Forward Thinking on Clinical Trials in Clinical Practice.Mayo Clin Proc2023
37292833Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry.medRxiv2023
37311464Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.Am J Hum Genet2023
37205333Genome-Wide Determinants of Cellular Immune Responses to Mumps Vaccine.medRxiv2023
37223852Implementing Reporting Standards for Polygenic Risk Scores for Atherosclerotic Cardiovascular Disease.Curr Atheroscler Rep2023
37028392Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.Am J Hum Genet2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
34664742Penalized mediation models for multivariate data.Genet Epidemiol2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35653140Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer.Clin Cancer Res2022
35545612A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes.Nat Commun2022
35796859Use of Polygenic Risk Scores for Coronary Heart Disease in Ancestrally Diverse Populations.Curr Cardiol Rep2022
35765100Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.Genome Med2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35432445A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk.Front Genet2022
35353984Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk.Am J Hum Genet2022
36186433From classical mendelian randomization to causal networks for systematic integration of multi-omics.Front Genet2022
35226188Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.Hum Genet2022
34968746Mumps virus-specific immune response outcomes and sex-based differences in a cohort of healthy adolescents.Clin Immunol2022
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
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
33818775Transcriptional signatures associated with rubella virus-specific humoral immunity after a third dose of MMR vaccine in women of childbearing age.Eur J Immunol2021
33667396Response to Li and Hopper.Am J Hum Genet2021
33802509Genetic Predictors of Chemotherapy-Induced Peripheral Neuropathy from Paclitaxel, Carboplatin and Oxaliplatin: NCCTG/Alliance N08C1, N08CA and N08CB Study.Cancers (Basel)2021
33578652Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.Cancers (Basel)2021
34140684A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts.Nat Genet2021
342568182dFDR: a new approach to confounder adjustment substantially increases detection power in omics association studies.Genome Biol2021
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
33159444Antimullerian Hormone as a Serum Biomarker for Risk of Chemotherapy-Induced Amenorrhea.J Natl Cancer Inst2021
33473200Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33097489Impact of Personalized Genetic Breast Cancer Risk Estimation With Polygenic Risk Scores on Preventive Endocrine Therapy Intention and Uptake.Cancer Prev Res (Phila)2021
32342572Penalized models for analysis of multiple mediators.Genet Epidemiol2020
33463755Penalized variance components for association of multiple genes with traits.Genet Epidemiol2020
33154747Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses.Front Immunol2020
32758450Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.Am J Hum Genet2020
32386537Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.Am J Hum Genet2020
32514134The effect of sample size on polygenic hazard models for prostate cancer.Eur J Hum Genet2020
32226016Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.PLoS Genet2020
29267957Multivariate generalized linear model for genetic pleiotropy.Biostatistics2019
31371054Genetic predictors of chemotherapy-related amenorrhea in women with breast cancer.Fertil Steril2019
31070467Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease-Brief Report.Arterioscler Thromb Vasc Biol2019
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Collaborators

Mayo Clinic
Co-authored papers 126
Mayo Clinic
Co-authored papers 121
Fred Hutchinson Cancer Research Center
Co-authored papers 48
Institute of Biomedicine, University of Turku
Co-authored papers 40
National Cancer Institute
Co-authored papers 39
Mayo Clinic
Co-authored papers 37
Mayo Clinic
Co-authored papers 36
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University of Cambridge
Co-authored papers 34
Karolinska Institute
Co-authored papers 32
The Institute of Cancer Research
Co-authored papers 31
The Institute of Cancer Research
Co-authored papers 31
The Brady Urological Institute, The Johns Hopkins School of Medicine
Co-authored papers 30
Co-authored papers 29
Marshfield Clinic Research Institute
Co-authored papers 27
Mayo Clinic Vaccine Research Group
Co-authored papers 26
University of Oxford, John Radcliffe Hospital
Co-authored papers 23
Duke University School of Medicine, and the Duke Cancer Institute
Co-authored papers 23
Kaiser Permanente Southern California
Co-authored papers 22
Co-authored papers 22
Mayo Clinic
Co-authored papers 22
University of Southern California
Co-authored papers 21
International Hereditary Cancer Center, Pomeranian Medical University
Co-authored papers 20
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National Cancer Institute, National Institutes of Health
Co-authored papers 20
Mayo Clinic
Co-authored papers 20
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Mayo Clinic
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