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Jonathan D Mosley

Showing results (121-130 of 142) with videos related to

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Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Circulation. Genomic and Precision Medicine|July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> VariantsKrystian Kozek, Yuko Wada, Luca Sala, et al.
JCI Insight|February 16, 2021
Proteomic profiling reveals biomarkers and pathways in type 2 diabetes riskDebby Ngo, Mark D Benson, Jonathan Z Long, et al.
HGG Advances|June 7, 2024
Transcriptome-wide association analysis identifies candidate susceptibility genes for prostate-specific antigen levels in men without prostate cancerDorothy M Chen, Ruocheng Dong, Linda Kachuri, et al.
Pharmacogenetics and Genomics|May 26, 2017
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adultsQuinn S Wells, Olivia J Veatch, Joshua P Fessel, et al.
Bioinformatics (Oxford, England)|November 6, 2023
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomicsMegan M Shuey, William W Stead, Ida Aka, et al.
Scientific Reports|May 7, 2020
The polygenic architecture of left ventricular mass mirrors the clinical epidemiologyJonathan D Mosley, Rebecca T Levinson, Eric Farber-Eger, et al.
Nature Communications|February 1, 2017
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancerThomas J Hoffmann, Michael N Passarelli, Rebecca E Graff, et al.
Circulation|March 7, 2013
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia riskMarylyn D Ritchie, Joshua C Denny, Rebecca L Zuvich, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count geneticsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
Pageof 15

Showing results (121-130 of 142) with videos related to

Sort By:
Pageof 15
Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Circulation. Genomic and Precision Medicine|July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> VariantsKrystian Kozek, Yuko Wada, Luca Sala, et al.
JCI Insight|February 16, 2021
Proteomic profiling reveals biomarkers and pathways in type 2 diabetes riskDebby Ngo, Mark D Benson, Jonathan Z Long, et al.
HGG Advances|June 7, 2024
Transcriptome-wide association analysis identifies candidate susceptibility genes for prostate-specific antigen levels in men without prostate cancerDorothy M Chen, Ruocheng Dong, Linda Kachuri, et al.
Pharmacogenetics and Genomics|May 26, 2017
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adultsQuinn S Wells, Olivia J Veatch, Joshua P Fessel, et al.
Bioinformatics (Oxford, England)|November 6, 2023
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomicsMegan M Shuey, William W Stead, Ida Aka, et al.
Scientific Reports|May 7, 2020
The polygenic architecture of left ventricular mass mirrors the clinical epidemiologyJonathan D Mosley, Rebecca T Levinson, Eric Farber-Eger, et al.
Nature Communications|February 1, 2017
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancerThomas J Hoffmann, Michael N Passarelli, Rebecca E Graff, et al.
Circulation|March 7, 2013
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia riskMarylyn D Ritchie, Joshua C Denny, Rebecca L Zuvich, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count geneticsJonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
Pageof 15