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Author Details
Full Name
Daniel J Schaid
Affiliation
Mayo Clinic
ORCID
Career Start Year
1982
Papers
438
H Index
90
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37620596
Principles and methods for transferring polygenic risk scores across global populations.
Nat Rev Genet
2024
37752310
A linear weighted combination of polygenic scores for a broad range of traits improves prediction of coronary heart disease.
Eur J Hum Genet
2024
36540998
Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index.
Pac Symp Biocomput
2023
37945903
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Nat Genet
2023
37778899
Genome-wide determinants of cellular immune responses to mumps vaccine.
Vaccine
2023
37609230
A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization.
medRxiv
2023
37645766
Broadcasters, receivers, functional groups of metabolites and the link to heart failure progression using polygenic factors.
Res Sq
2023
37536808
Clinical Trials Overview: From Explanatory to Pragmatic Clinical Trials.
Mayo Clin Proc
2023
37536801
Introduction to Thematic Reviews on Forward Thinking on Clinical Trials in Clinical Practice.
Mayo Clin Proc
2023
37292833
Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry.
medRxiv
2023
37311464
Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.
Am J Hum Genet
2023
37205333
Genome-Wide Determinants of Cellular Immune Responses to Mumps Vaccine.
medRxiv
2023
37223852
Implementing Reporting Standards for Polygenic Risk Scores for Atherosclerotic Cardiovascular Disease.
Curr Atheroscler Rep
2023
37028392
Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.
Am J Hum Genet
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
34664742
Penalized mediation models for multivariate data.
Genet Epidemiol
2022
35710995
Genome-wide polygenic score to predict chronic kidney disease across ancestries.
Nat Med
2022
35653140
Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Patients with Breast Cancer.
Clin Cancer Res
2022
35545612
A rare variant analysis framework using public genotype summary counts to prioritize disease-predisposition genes.
Nat Commun
2022
35796859
Use of Polygenic Risk Scores for Coronary Heart Disease in Ancestrally Diverse Populations.
Curr Cardiol Rep
2022
35765100
Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations.
Genome Med
2022
35701404
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.
Nat Commun
2022
35432445
A microRNA Transcriptome-wide Association Study of Prostate Cancer Risk.
Front Genet
2022
35353984
Polygenic risk for prostate cancer: Decreasing relative risk with age but little impact on absolute risk.
Am J Hum Genet
2022
36186433
From classical mendelian randomization to causal networks for systematic integration of multi-omics.
Front Genet
2022
35226188
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.
Hum Genet
2022
34968746
Mumps virus-specific immune response outcomes and sex-based differences in a cohort of healthy adolescents.
Clin Immunol
2022
34930020
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
2022
32800727
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.
Eur Urol
2021
33818775
Transcriptional signatures associated with rubella virus-specific humoral immunity after a third dose of MMR vaccine in women of childbearing age.
Eur J Immunol
2021
33667396
Response to Li and Hopper.
Am J Hum Genet
2021
33802509
Genetic Predictors of Chemotherapy-Induced Peripheral Neuropathy from Paclitaxel, Carboplatin and Oxaliplatin: NCCTG/Alliance N08C1, N08CA and N08CB Study.
Cancers (Basel)
2021
33578652
Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.
Cancers (Basel)
2021
34140684
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts.
Nat Genet
2021
34256818
2dFDR: a new approach to confounder adjustment substantially increases detection power in omics association studies.
Genome Biol
2021
33436325
Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.
Eur Urol Oncol
2021
33398198
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
2021
33159444
Antimullerian Hormone as a Serum Biomarker for Risk of Chemotherapy-Induced Amenorrhea.
J Natl Cancer Inst
2021
33473200
Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
2021
33097489
Impact of Personalized Genetic Breast Cancer Risk Estimation With Polygenic Risk Scores on Preventive Endocrine Therapy Intention and Uptake.
Cancer Prev Res (Phila)
2021
32342572
Penalized models for analysis of multiple mediators.
Genet Epidemiol
2020
33463755
Penalized variance components for association of multiple genes with traits.
Genet Epidemiol
2020
33154747
Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses.
Front Immunol
2020
32758450
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Am J Hum Genet
2020
32386537
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.
Am J Hum Genet
2020
32514134
The effect of sample size on polygenic hazard models for prostate cancer.
Eur J Hum Genet
2020
32226016
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.
PLoS Genet
2020
29267957
Multivariate generalized linear model for genetic pleiotropy.
Biostatistics
2019
31371054
Genetic predictors of chemotherapy-related amenorrhea in women with breast cancer.
Fertil Steril
2019
31070467
Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease-Brief Report.
Arterioscler Thromb Vasc Biol
2019
1 - 50 of 438
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37
James N Ingle
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Co-authored papers
36
Graham G Giles
Co-authored papers
35
Douglas F Easton
University of Cambridge
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Henrik Gr??nberg
Karolinska Institute
Co-authored papers
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The Institute of Cancer Research
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31
Rosalind A Eeles
The Institute of Cancer Research
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31
William B Isaacs
The Brady Urological Institute, The Johns Hopkins School of Medicine
Co-authored papers
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Jianfeng Xu
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Scott J Hebbring
Marshfield Clinic Research Institute
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27
Gregory A Poland
Mayo Clinic Vaccine Research Group
Co-authored papers
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David E Neal
University of Oxford, John Radcliffe Hospital
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23
Kathleen A Cooney
Duke University School of Medicine, and the Duke Cancer Institute
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23
Steven J Jacobsen
Kaiser Permanente Southern California
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22
Sonja I Berndt
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