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Medrxiv : the Preprint Server for Health Sciences
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January 5, 2021
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19
Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Nature Communications
|
May 21, 2015
Erratum: Whole-genome sequence-based analysis of thyroid function
Peter N Taylor, Eleonora Porcu, Shelby Chew, et al.
Nature Communications
|
March 7, 2015
Whole-genome sequence-based analysis of thyroid function
Peter N Taylor, Eleonora Porcu, Shelby Chew, et al.
The Journal of Clinical Investigation
|
May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19
Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Clinical Proteomics
|
September 28, 2022
The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals
Guillaume Butler-Laporte, Edgar Gonzalez-Kozlova, Chen-Yang Su, et al.
American Journal of Human Genetics
|
December 12, 2018
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Despoina Manousaki, Tom Dudding, Simon Haworth, et al.
Clinical Proteomics
|
November 15, 2022
Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals
Guillaume Butler-Laporte, Edgar Gonzalez-Kozlova, Chen-Yang Su, et al.
Scientific Reports
|
April 17, 2023
Circulating proteins to predict COVID-19 severity
Chen-Yang Su, Sirui Zhou, Edgar Gonzalez-Kozlova, et al.
American Journal of Human Genetics
|
August 1, 2017
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Despoina Manousaki, Tom Dudding, Simon Haworth, et al.
Nature Genetics
|
April 17, 2019
Author Correction: An atlas of genetic influences on osteoporosis in humans and mice
John A Morris, John P Kemp, Scott E Youlten, et al.
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of 9
Search research articles
Search
Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 9
Medrxiv : the Preprint Server for Health Sciences
|
January 5, 2021
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19
Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Nature Communications
|
May 21, 2015
Erratum: Whole-genome sequence-based analysis of thyroid function
Peter N Taylor, Eleonora Porcu, Shelby Chew, et al.
Nature Communications
|
March 7, 2015
Whole-genome sequence-based analysis of thyroid function
Peter N Taylor, Eleonora Porcu, Shelby Chew, et al.
The Journal of Clinical Investigation
|
May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19
Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.
Clinical Proteomics
|
September 28, 2022
The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals
Guillaume Butler-Laporte, Edgar Gonzalez-Kozlova, Chen-Yang Su, et al.
American Journal of Human Genetics
|
December 12, 2018
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Despoina Manousaki, Tom Dudding, Simon Haworth, et al.
Clinical Proteomics
|
November 15, 2022
Correction: The dynamic changes and sex differences of 147 immune-related proteins during acute COVID-19 in 580 individuals
Guillaume Butler-Laporte, Edgar Gonzalez-Kozlova, Chen-Yang Su, et al.
Scientific Reports
|
April 17, 2023
Circulating proteins to predict COVID-19 severity
Chen-Yang Su, Sirui Zhou, Edgar Gonzalez-Kozlova, et al.
American Journal of Human Genetics
|
August 1, 2017
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Despoina Manousaki, Tom Dudding, Simon Haworth, et al.
Nature Genetics
|
April 17, 2019
Author Correction: An atlas of genetic influences on osteoporosis in humans and mice
John A Morris, John P Kemp, Scott E Youlten, et al.
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