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Medrxiv : the Preprint Server for Health Sciences
|
November 14, 2023
Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score
Elisabeth A Rosenthal, Li Hsu, Minta Thomas, et al.
Genetic Epidemiology
|
September 24, 2024
Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score
Elisabeth A Rosenthal, Li Hsu, Minta Thomas, et al.
Geroscience
|
August 21, 2023
Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome
Fuki M Hisama, Renuka Kandhaya Pillai, Julia Sidorova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2018
Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model
Seung-Been Lee, Marsha M Wheeler, Karynne Patterson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 13, 2024
Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome
Clémence Vanlerberghe, Anne Sophie Jourdain, Frédéric Frenois, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us Participants
Andrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology
|
February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Communications Biology
|
June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 22, 2024
Defining and Reducing Variant Classification Disparities
Moez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Genome Medicine
|
December 4, 2024
Using multiplexed functional data to reduce variant classification inequities in underrepresented populations
Moez Dawood, Shawn Fayer, Sriram Pendyala, et al.
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Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Medrxiv : the Preprint Server for Health Sciences
|
November 14, 2023
Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score
Elisabeth A Rosenthal, Li Hsu, Minta Thomas, et al.
Genetic Epidemiology
|
September 24, 2024
Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score
Elisabeth A Rosenthal, Li Hsu, Minta Thomas, et al.
Geroscience
|
August 21, 2023
Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome
Fuki M Hisama, Renuka Kandhaya Pillai, Julia Sidorova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 8, 2018
Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model
Seung-Been Lee, Marsha M Wheeler, Karynne Patterson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 13, 2024
Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome
Clémence Vanlerberghe, Anne Sophie Jourdain, Frédéric Frenois, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us Participants
Andrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology
|
February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Communications Biology
|
June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 22, 2024
Defining and Reducing Variant Classification Disparities
Moez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Genome Medicine
|
December 4, 2024
Using multiplexed functional data to reduce variant classification inequities in underrepresented populations
Moez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Page
of 2