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Human Heredity
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September 1, 2016
Accuracy of Gene Scores when Pruning Markers by Linkage Disequilibrium
Frank Dudbridge, Paul J Newcombe
Genetic Epidemiology
|
October 23, 2022
Statistical methods for cis-Mendelian randomization with two-sample summary-level data
Apostolos Gkatzionis, Stephen Burgess, Paul J Newcombe
Genetic Epidemiology
|
March 31, 2016
JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects
Paul J Newcombe, David V Conti, Sylvia Richardson
Statistics in Medicine
|
June 22, 2021
Bayesian variable selection with a pleiotropic loss function in Mendelian randomization
Apostolos Gkatzionis, Stephen Burgess, David V Conti, et al.
Biometrics
|
January 15, 2021
Two-stage penalized regression screening to detect biomarker-treatment interactions in randomized clinical trials
Jixiong Wang, Ashish Patel, James M S Wason, et al.
Genetic Epidemiology
|
July 23, 2019
A flexible and parallelizable approach to genome-wide polygenic risk scores
Paul J Newcombe, Christopher P Nelson, Nilesh J Samani, et al.
BMC Genomics
|
January 25, 2019
Fine mapping chromatin contacts in capture Hi-C data
Christiaan Q Eijsbouts, Oliver S Burren, Paul J Newcombe, et al.
American Journal of Epidemiology
|
January 6, 2021
A Hierarchical Approach Using Marginal Summary Statistics for Multiple Intermediates in a Mendelian Randomization or Transcriptome Analysis
Lai Jiang, Shujing Xu, Nicholas Mancuso, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 16, 2018
Development and External Validation of Prediction Models for 10-Year Survival of Invasive Breast Cancer. Comparison with PREDICT and CancerMath
Solon Karapanagiotis, Paul D P Pharoah, Christopher H Jackson, et al.
Biostatistics (Oxford, England)
|
August 7, 2021
Tailored Bayes: a risk modeling framework under unequal misclassification costs
Solon Karapanagiotis, Umberto Benedetto, Sach Mukherjee, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Human Heredity
|
September 1, 2016
Accuracy of Gene Scores when Pruning Markers by Linkage Disequilibrium
Frank Dudbridge, Paul J Newcombe
Genetic Epidemiology
|
October 23, 2022
Statistical methods for cis-Mendelian randomization with two-sample summary-level data
Apostolos Gkatzionis, Stephen Burgess, Paul J Newcombe
Genetic Epidemiology
|
March 31, 2016
JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects
Paul J Newcombe, David V Conti, Sylvia Richardson
Statistics in Medicine
|
June 22, 2021
Bayesian variable selection with a pleiotropic loss function in Mendelian randomization
Apostolos Gkatzionis, Stephen Burgess, David V Conti, et al.
Biometrics
|
January 15, 2021
Two-stage penalized regression screening to detect biomarker-treatment interactions in randomized clinical trials
Jixiong Wang, Ashish Patel, James M S Wason, et al.
Genetic Epidemiology
|
July 23, 2019
A flexible and parallelizable approach to genome-wide polygenic risk scores
Paul J Newcombe, Christopher P Nelson, Nilesh J Samani, et al.
BMC Genomics
|
January 25, 2019
Fine mapping chromatin contacts in capture Hi-C data
Christiaan Q Eijsbouts, Oliver S Burren, Paul J Newcombe, et al.
American Journal of Epidemiology
|
January 6, 2021
A Hierarchical Approach Using Marginal Summary Statistics for Multiple Intermediates in a Mendelian Randomization or Transcriptome Analysis
Lai Jiang, Shujing Xu, Nicholas Mancuso, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 16, 2018
Development and External Validation of Prediction Models for 10-Year Survival of Invasive Breast Cancer. Comparison with PREDICT and CancerMath
Solon Karapanagiotis, Paul D P Pharoah, Christopher H Jackson, et al.
Biostatistics (Oxford, England)
|
August 7, 2021
Tailored Bayes: a risk modeling framework under unequal misclassification costs
Solon Karapanagiotis, Umberto Benedetto, Sach Mukherjee, et al.
Page
of 3