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As summarized by Berk et al. (2011), an increase in pro-inflammatory markers is associated with acute BD episodes of both depressive and manic polarity.
Furthermore, the use of multiple markers is associated with a significant increase in costs.
Carriage of specific growth-related genetic markers is associated with growth response in GHD and TS.
The performance of multiple markers is associated with relatively high costs (depending on the markers) [ 24].
EMT, as well as its related markers, is associated with cancer development and chemotherapy resistance [8], [9].
Furthermore, an increase in the number of expressed tumour markers is associated with worsening prognosis (Ardill and Erikkson, 2003).
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Population structure can result in spurious associations that result from unlinked markers being associated with causative loci [ 30].
Both markers were associated with birth weight in a term population in a recent genome-wide association study of Freathy et al.
None of these markers were associated with risk of late-onset cardiomyopathy.
Two of these markers were associated with differences in strength and rump angle on chromosomes 4 and 9, respectively.
A growing number of serum filtration markers are associated with mortality and end-stage renal disease (ESRD) in adults.
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