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Genetic Epidemiology
|
March 21, 2017
On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows
Heide Loehlein Fier, Dmitry Prokopenko, Julian Hecker, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
November 8, 2024
Assessing polyomic risk to predict Alzheimer's disease using a machine learning model
Tiffany Ngai, Julian Willett, Mohammad Waqas, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Polygenic risk scores associate with asthma phenotypes and proteomic analyses implicate IL1R1 in two family-based studies
Sanghun Lee, Matthew Moll, Kevin Mendez, et al.
Briefings in Bioinformatics
|
June 5, 2024
Prediction of disease-free survival for precision medicine using cooperative learning on multi-omic data
Georg Hahn, Dmitry Prokopenko, Julian Hecker, et al.
Bioinformatics (Oxford, England)
|
December 28, 2020
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests
Julian Hecker, F William Townes, Priyadarshini Kachroo, et al.
Journal of Personalized Medicine
|
January 27, 2026
A Categorical ANCOVA Approach to Severity Endophenotype-Specific Genome-Wide Association Studies in Childhood Asthma
Shraddha Piparia, Parham Hadikhani, John Ziniti, et al.
Briefings in Bioinformatics
|
December 31, 2022
A comparison between similarity matrices for principal component analysis to assess population stratification in sequenced genetic data sets
Sanghun Lee, Georg Hahn, Julian Hecker, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 27, 2026
Matching heterogeneous cohorts by projected principal components reveals two novel Alzheimer's disease-associated genes in the Hispanic population
Julian Daniel Sunday Willett, Mohamad Waqas, Serhiy Naumenko, et al.
Epigenetics
|
September 21, 2023
A consistent pattern of slide effects in Illumina DNA methylation BeadChip array data
Julian Hecker, Sanghun Lee, Priyadarshini Kachroo, et al.
BMC Bioinformatics
|
December 19, 2022
Unsupervised outlier detection applied to SARS-CoV-2 nucleotide sequences can identify sequences of common variants and other variants of interest
Georg Hahn, Sanghun Lee, Dmitry Prokopenko, et al.
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of 8
Search research articles
Search
Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
Genetic Epidemiology
|
March 21, 2017
On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows
Heide Loehlein Fier, Dmitry Prokopenko, Julian Hecker, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
November 8, 2024
Assessing polyomic risk to predict Alzheimer's disease using a machine learning model
Tiffany Ngai, Julian Willett, Mohammad Waqas, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Polygenic risk scores associate with asthma phenotypes and proteomic analyses implicate IL1R1 in two family-based studies
Sanghun Lee, Matthew Moll, Kevin Mendez, et al.
Briefings in Bioinformatics
|
June 5, 2024
Prediction of disease-free survival for precision medicine using cooperative learning on multi-omic data
Georg Hahn, Dmitry Prokopenko, Julian Hecker, et al.
Bioinformatics (Oxford, England)
|
December 28, 2020
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests
Julian Hecker, F William Townes, Priyadarshini Kachroo, et al.
Journal of Personalized Medicine
|
January 27, 2026
A Categorical ANCOVA Approach to Severity Endophenotype-Specific Genome-Wide Association Studies in Childhood Asthma
Shraddha Piparia, Parham Hadikhani, John Ziniti, et al.
Briefings in Bioinformatics
|
December 31, 2022
A comparison between similarity matrices for principal component analysis to assess population stratification in sequenced genetic data sets
Sanghun Lee, Georg Hahn, Julian Hecker, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 27, 2026
Matching heterogeneous cohorts by projected principal components reveals two novel Alzheimer's disease-associated genes in the Hispanic population
Julian Daniel Sunday Willett, Mohamad Waqas, Serhiy Naumenko, et al.
Epigenetics
|
September 21, 2023
A consistent pattern of slide effects in Illumina DNA methylation BeadChip array data
Julian Hecker, Sanghun Lee, Priyadarshini Kachroo, et al.
BMC Bioinformatics
|
December 19, 2022
Unsupervised outlier detection applied to SARS-CoV-2 nucleotide sequences can identify sequences of common variants and other variants of interest
Georg Hahn, Sanghun Lee, Dmitry Prokopenko, et al.
Page
of 8