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They could be genetic, associated with another gene in trans that also increases risk of parkinsonism, or could be epigenetic factors affecting expression of other genes that increase penetrance.
The aim of this study was to describe the spectrum of adaptive responses in humans exposed to graded EHH and identify factors (physiological and genetic) associated with inter-individual variation in these responses.
The overall objective of the study was to determine risk factors (cardiovascular, dialysis-related, environmental and genetic) associated with disordered cardiac autonomic regulation and ventricular conduction, as well as with incidence of SCD, in ESRD patients treated with hemodialysis.
The aim of our pilot study was to update the knee OA grading with further clinical and genetic associated data, since OA is nowadays considered a polygenic and multifactorial disease [ 47].
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Here we tackle the problem of distinguishing between genetic variations associated to cancer and variations associated to other genetic diseases.
We also used a genome-wide association approach to identify genetic markers associated with intron expression.
Genome wide association study shows the genetic variations associated with a particular disease.
For example, the query Select genetic variants associated with Abnormality of the Cerebellum should also return genetic variants associated with Ataxia and Arnold-Chiari type I malformation.
Recent genome-wide association studies have discovered several genetic variants associated with IOP and VCDR.
Some of the genetic complexity associated with CM can be attributed to environmental factors and genetic modifiers.
Recent genome-wide association studies have identified several novel genetic loci associated with these two traits.
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