Results 221 to 230 of about 6,414,238 (349)
Dichotomous transformations for statistical inference about odds ratios [PDF]
Xiangning Huang, Baibing Li
openalex +1 more source
ABSTRACT Objective Substance use right before or during work (hereinafter, “substance use in the workplace”) poses significant health risks to users, colleagues, and the public in the workplace. However, less clear are figures on recent prevalence, characteristics of those engaging in such behaviors, and variations across occupations.
Sehun Oh+2 more
wiley +1 more source
Using the properties of the odds ratio to improve precision in meta-analysis: an update on the benefits of targeted deployment of physician-led interprofessional pre-hospital teams on the care of critically ill and injured patients. [PDF]
McHenry RD.
europepmc +1 more source
A comparison of marginal odds ratio estimators
T. Loux, C. Drake, J. Smith-Gagen
semanticscholar +1 more source
ABSTRACT Background Benzene is an established Group 1 carcinogen due to its leukemogenic properties. Recent studies suggest that occupational benzene exposure may be associated with solid cancers. However, little is known about its association with male genital cancers.
Alessandro Godono+5 more
wiley +1 more source
The association between healthy diet indicator and phytochemical index with prostate cancer odds ratio: a case-control study. [PDF]
Mahmoodi M+6 more
europepmc +1 more source
The odds ratio: calculation, usage, and interpretation [PDF]
Mary L. McHugh
openalex +1 more source
ABSTRACT The missense SNP NC_000004.12:g.102267552C>T (also known as SLC39A8.p.(Ala391Thr), rs13107325) in SLC39A8 encodes a zinc transporter. This SNP has been linked to schizophrenia and is the likely causal variant for one of the genome‐wide association loci associated with the disorder. Using regression analyses, we tested whether the schizophrenia‐
Sophie E. Smart+12 more
wiley +1 more source
Odds ratios are not conditional risk ratios [PDF]
openaire +3 more sources
Genome‐Wide Insights and Polygenic Risk Scores in Common Epilepsies: A Narrative Review
ABSTRACT The research of single gene‐related disorders or pathogenic copy‐number variations (CNVs) has given a significant impetus to the shift from a diagnostic work‐up focused on epileptic syndromes to genomic approaches in individuals with severe pediatric‐onset epilepsies and in developmental and epileptic encephalopathies.
Mario Mastrangelo+5 more
wiley +1 more source