Closed UK: DecodeME updates, was recruitment thread.

Status
Not open for further replies.
@Andy im pretty close with several reporters in the U.S. who have covered ME & LC over the years. If these connections can help with any media coverage of this (if results dictate) just let me know and I can reach out to any to gauge interest
Thanks for the offer. At this stage the easiest thing I think would be if you sent them the preprint or a link to the DecodeME site once it is out.
 
Is it typical to do press for a preprint?? Usually this happens when a paper is published.

See here

Who are they to advise. They are just a bunch of political activists who got the ear of governments and spread the opinions of their cronies. Maybe they are miffed that MECFS researchers would prefer to have nothing to do with them.

It adds another good reason to put out a press release with the preprint - to stick some fingers up. Of course there is no doubt that some people put out preprintsc without due care but then the SMC has continually done that.
 
In these GWAS, we discovered eight loci that are significantly associated with ME/CFS, including three near BTN2A2, OLFM4, and RABGAP1L genes that act in the response to viral or bacterial infection. Four of the eight loci (RABGAP1L, FBXL4, OLFM4, CA10) were associated at p < 0.05 with cases ascertained using post-exertional malaise and fatigue in the UK Biobank and the Netherlands biobank Lifelines. We found no evidence of sex-bias among discovered associations, and replicated in males two genetic signals (ARFGEF2, CA10) discovered in females. The ME/CFS association near CA10 colocalises with a known association to multisite chronic pain. We found no evidence that the eight ME/CFS genetic signals share common causal genetic variants with depression or anxiety. Our findings suggest that both immunological and neurological processes are involved in the genetic risk of ME/CFS.
 
Status
Not open for further replies.
Back
Top Bottom