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By using a genetic variant associated with smoking heaviness as a proxy for smoking heaviness, bias from confounding is minimised and findings are not affected by reverse causality.
By using a genetic variant associated with smoking heaviness as a proxy for smoking heaviness, bias from confounding is minimised and findings not affected by reverse causality.
Mendelian randomization using a genetic variant related to alcohol intake (ADH1B rs1229984) was used to obtain unbiased estimates of the association between alcohol intake and cognitive performance.
As an additional exploratory analysis, we performed a Mendelian randomization analysis, using a genetic variant associated with smoking behaviour as a proxy for smoking during pregnancy.
35 Thus, a simple interpretation of a mendelian randomisation analysis using a genetic variant in an alcohol metabolising enzyme is that it is akin to a long term randomised trial of more versus less alcohol exposure.
Mendelian randomisation meta-analyses using a genetic variant (rs16969968/rs1051730) as a proxy for smoking heaviness, and observational meta-analyses of the associations of smoking status and smoking heaviness with depression, anxiety and psychological distress.
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The NeuroIDgenetix® test uses a genetic variant panel of ten genes, along with concomitant medications, to make medication management recommendations based on gene-drug and drug-drug interactions for over 40 medications used in the treatment of depression and anxiety.
We have used a genetic variant that influences circulating folate levels to test whether low folate availability is a risk factor for obesity.
In the absence of a viable randomised trial to confirm or refute the cardioprotective effect of light to moderate alcohol consumption, an alternative approach is to use a genetic variant that serves as a proxy for alcohol consumption.
In their original report on the C2/CFB locus in ARM, Gold et al. [60] did not include LOC387715 variants and, using a genetic algorithm search approach, they arrived at a genetic risk model of two CFH variants and three C2/CFB variants.
For this purpose, a native soluble form of the HA50 274 protein was produced by expression in E. coli BL21 (DE3) pLysS variant C41, using a genetic construct that included a peptide signal for periplasmic expression.
More suggestions(15)
using a restricted variant
using a new variant
using a genetic cross
using a dense variant
using a customised variant
using a genetic algorithm
using a genetic trigger
using a genetic engineering
using a velocimetric variant
using a probabilistic variant
using a standard variant
using a genetic mouse
using a reversed variant
using a motile variant
using a special variant
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