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Showing results (81-90 of 101) with videos related to
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Human Mutation
|
September 1, 2019
Sequencing-based microsatellite instability testing using as few as six markers for high-throughput clinical diagnostics
Richard Gallon, Harsh Sheth, Christine Hayes, et al.
Plos One
|
September 29, 2015
A GWAS Study on Liver Function Test Using eMERGE Network Participants
Bahram Namjou, Keith Marsolo, Todd Lingren, et al.
BMC Infectious Diseases
|
November 19, 2016
Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies
Kathryn L Jackson, Michael Mbagwu, Jennifer A Pacheco, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
January 30, 2020
Multisite validation of a simple electronic health record algorithm for identifying diagnosed obstructive sleep apnea
Brendan T Keenan, H Lester Kirchner, Olivia J Veatch, et al.
Cancer Prevention Research (Philadelphia, Pa.)
|
July 25, 2022
Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up
John C Mathers, Faye Elliott, Finlay Macrae, et al.
Lancet (London, England)
|
June 15, 2020
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial
John Burn, Harsh Sheth, Faye Elliott, et al.
Scientific Reports
|
April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network
Jacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.
International Journal of Cancer
|
October 10, 2022
Is HLA type a possible cancer risk modifier in Lynch syndrome?
Aysel Ahadova, Johannes Witt, Saskia Haupt, et al.
Plos One
|
May 17, 2023
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Yoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Scientific Reports
|
May 7, 2020
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology
Jonathan D Mosley, Rebecca T Levinson, Eric Farber-Eger, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 101) with videos related to
Sort By:
Page
of 11
Human Mutation
|
September 1, 2019
Sequencing-based microsatellite instability testing using as few as six markers for high-throughput clinical diagnostics
Richard Gallon, Harsh Sheth, Christine Hayes, et al.
Plos One
|
September 29, 2015
A GWAS Study on Liver Function Test Using eMERGE Network Participants
Bahram Namjou, Keith Marsolo, Todd Lingren, et al.
BMC Infectious Diseases
|
November 19, 2016
Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies
Kathryn L Jackson, Michael Mbagwu, Jennifer A Pacheco, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
January 30, 2020
Multisite validation of a simple electronic health record algorithm for identifying diagnosed obstructive sleep apnea
Brendan T Keenan, H Lester Kirchner, Olivia J Veatch, et al.
Cancer Prevention Research (Philadelphia, Pa.)
|
July 25, 2022
Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up
John C Mathers, Faye Elliott, Finlay Macrae, et al.
Lancet (London, England)
|
June 15, 2020
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial
John Burn, Harsh Sheth, Faye Elliott, et al.
Scientific Reports
|
April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network
Jacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.
International Journal of Cancer
|
October 10, 2022
Is HLA type a possible cancer risk modifier in Lynch syndrome?
Aysel Ahadova, Johannes Witt, Saskia Haupt, et al.
Plos One
|
May 17, 2023
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Yoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Scientific Reports
|
May 7, 2020
The polygenic architecture of left ventricular mass mirrors the clinical epidemiology
Jonathan D Mosley, Rebecca T Levinson, Eric Farber-Eger, et al.
Page
of 11