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Nature Communications
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May 10, 2019
Author Correction: Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects
Phuong A Nguyen, David A Born, Aimee M Deaton, et al.
Nature Communications
|
April 7, 2019
Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects
Phuong A Nguyen, David A Born, Aimee M Deaton, et al.
Trends in Pharmacological Sciences
|
December 16, 2017
Modernizing Human Cancer Risk Assessment of Therapeutics
Mark R Fielden, Lucas D Ward, Sheroy Minocherhomji, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
October 23, 2018
Rationalizing Secondary Pharmacology Screening Using Human Genetic and Pharmacological Evidence
Aimee M Deaton, Fan Fan, Wei Zhang, et al.
Scientific Reports
|
August 5, 2021
A proteomic platform to identify off-target proteins associated with therapeutic modalities that induce protein degradation or gene silencing
Xin Liu, Ye Zhang, Lucas D Ward, et al.
HGG Advances
|
May 2, 2022
Rare coding variants in DNA damage repair genes associated with timing of natural menopause
Lucas D Ward, Margaret M Parker, Aimee M Deaton, et al.
Biorxiv : the Preprint Server for Biology
|
February 27, 2026
Ancestry-specific performance of variant effect predictors in clinical variant classification
Rachel Hoffing, Daniel Zeiberg, Sarah L Stenton, et al.
The Journal of Biological Chemistry
|
February 9, 2024
AAV-mediated hepatic expression of SLC30A10 and the Thr95Ile variant attenuates manganese excess and other phenotypes in Slc30a10-deficient mice
Milankumar Prajapati, Chelsea B Quenneville, Jared Z Zhang, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 31, 2023
Transcript-aware analysis of rare predicted loss-of-function variants in the UK Biobank elucidate new isoform-trait associations
Rachel A Hoffing, Aimee M Deaton, Aaron M Holleman, et al.
Scientific Reports
|
November 4, 2021
Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
Aimee M Deaton, Margaret M Parker, Lucas D Ward, et al.
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of 5
Search research articles
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Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Nature Communications
|
May 10, 2019
Author Correction: Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects
Phuong A Nguyen, David A Born, Aimee M Deaton, et al.
Nature Communications
|
April 7, 2019
Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects
Phuong A Nguyen, David A Born, Aimee M Deaton, et al.
Trends in Pharmacological Sciences
|
December 16, 2017
Modernizing Human Cancer Risk Assessment of Therapeutics
Mark R Fielden, Lucas D Ward, Sheroy Minocherhomji, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
October 23, 2018
Rationalizing Secondary Pharmacology Screening Using Human Genetic and Pharmacological Evidence
Aimee M Deaton, Fan Fan, Wei Zhang, et al.
Scientific Reports
|
August 5, 2021
A proteomic platform to identify off-target proteins associated with therapeutic modalities that induce protein degradation or gene silencing
Xin Liu, Ye Zhang, Lucas D Ward, et al.
HGG Advances
|
May 2, 2022
Rare coding variants in DNA damage repair genes associated with timing of natural menopause
Lucas D Ward, Margaret M Parker, Aimee M Deaton, et al.
Biorxiv : the Preprint Server for Biology
|
February 27, 2026
Ancestry-specific performance of variant effect predictors in clinical variant classification
Rachel Hoffing, Daniel Zeiberg, Sarah L Stenton, et al.
The Journal of Biological Chemistry
|
February 9, 2024
AAV-mediated hepatic expression of SLC30A10 and the Thr95Ile variant attenuates manganese excess and other phenotypes in Slc30a10-deficient mice
Milankumar Prajapati, Chelsea B Quenneville, Jared Z Zhang, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
|
December 31, 2023
Transcript-aware analysis of rare predicted loss-of-function variants in the UK Biobank elucidate new isoform-trait associations
Rachel A Hoffing, Aimee M Deaton, Aaron M Holleman, et al.
Scientific Reports
|
November 4, 2021
Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
Aimee M Deaton, Margaret M Parker, Lucas D Ward, et al.
Page
of 5