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M Borthwick

Showing results (91-100 of 101) with videos related to

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International Journal of Biomedical Data Mining|April 8, 2016
ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner WorkflowKenneth M Borthwick, Diane T Smelser, Jonathan A Bock, et al.
Human Mutation|February 12, 2019
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytesRichard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, et al.
The Lancet. Gastroenterology & Hepatology|July 9, 2026
Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trialJohn Burn, Gillian M Borthwick, Faye Elliott, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
Nature Communications|September 1, 2018
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkersJonathan D Mosley, QiPing Feng, Quinn S Wells, et al.
Genes and Immunity|October 10, 2014
Genetic variation in the HLA region is associated with susceptibility to herpes zosterD R Crosslin, D S Carrell, A Burt, et al.
Gastroenterology|December 31, 2022
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair DeficiencyRichard Gallon, Rachel Phelps, Christine Hayes, et al.
Circulation|December 21, 2018
Probing the Virtual Proteome to Identify Novel Disease BiomarkersJonathan D Mosley, Mark D Benson, J Gustav Smith, et al.
Medrxiv : the Preprint Server for Health Sciences|January 16, 2026
COMPREHENSIVE GENETIC INVESTIGATION REVEALS HETEROGENEOUS PATHWAYS TO OBSTRUCTIVE SLEEP APNEAAnne E Justice, Brendan T Keenan, Geetha Chittoor, et al.
The Pharmacogenomics Journal|July 15, 2015
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced coughJ D Mosley, C M Shaffer, S L Van Driest, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
International Journal of Biomedical Data Mining|April 8, 2016
ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner WorkflowKenneth M Borthwick, Diane T Smelser, Jonathan A Bock, et al.
Human Mutation|February 12, 2019
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytesRichard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, et al.
The Lancet. Gastroenterology & Hepatology|July 9, 2026
Aspirin for cancer prevention in individuals with Lynch syndrome: first results from the CaPP3 multicentre, randomised, double-blind, non-inferiority trialJohn Burn, Gillian M Borthwick, Faye Elliott, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
Nature Communications|September 1, 2018
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkersJonathan D Mosley, QiPing Feng, Quinn S Wells, et al.
Genes and Immunity|October 10, 2014
Genetic variation in the HLA region is associated with susceptibility to herpes zosterD R Crosslin, D S Carrell, A Burt, et al.
Gastroenterology|December 31, 2022
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair DeficiencyRichard Gallon, Rachel Phelps, Christine Hayes, et al.
Circulation|December 21, 2018
Probing the Virtual Proteome to Identify Novel Disease BiomarkersJonathan D Mosley, Mark D Benson, J Gustav Smith, et al.
Medrxiv : the Preprint Server for Health Sciences|January 16, 2026
COMPREHENSIVE GENETIC INVESTIGATION REVEALS HETEROGENEOUS PATHWAYS TO OBSTRUCTIVE SLEEP APNEAAnne E Justice, Brendan T Keenan, Geetha Chittoor, et al.
The Pharmacogenomics Journal|July 15, 2015
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced coughJ D Mosley, C M Shaffer, S L Van Driest, et al.
Pageof 11