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Audrey Ryback

@aryback.bsky.social
176 followers 48 following 20 posts

ME researcher at the University of Edinburgh.

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Reposted by Audrey Ryback
Action for ME @actionforme.bsky.social · 11/06/2026
Register for the PRIME International Symposium to explore emerging ME/CFS research with researchers, clinicians, charities and people with lived experience. 🗓️ 28 Sept 9am-29 Sept 2pm Find out more and register here 👇 www.actionforme.org.uk/register-for...
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Reposted by Audrey Ryback
Action for ME @actionforme.bsky.social · 12/05/2026
👉 Read more about the announcement on our website www.actionforme.org.uk/major-fundin...
actionforme.org.uk
Major funding secured for Sequence ME & Long Covid, a DecodeMe project
We are thrilled to announce that our landmark research study, Sequence ME & Long Covid, has received major funding (£4.75m) from the UK government, signalling a transformative...
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Audrey Ryback @aryback.bsky.social · 04/05/2026
It was a delight speaking to @davetuller1.bsky.social about our recent paper lead by @simonmcg.bsky.social with @charliehillier.bsky.social, @tschei.bsky.social, Joshua Dibble and Arild Angelsen. We discuss why this is solid evidence for two age peaks in ME/CFS onset and the biological implications.
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Reposted by Audrey Ryback
Simon McGrath @simonmcg.bsky.social · 15/04/2026
Blog about the recent study finding evidence across Europe for ME/CFS peaking at two different ages, a v unusual feature. The peak ages of 1about 6 and late 30s is a unique combo even among diseases with two, and could be a clue to the biology of ME/CFS. mecfsresearchreview.me/2026/04/15/m...
mecfsresearchreview.me
ME/CFS onset had two peaks, which may be a clue to causes
A new study strengthens the findings that ME/CFS is a disease with a highly unusual feature. Analysis of survey data on patients across Europe found there are two peak ages for getting ME/CFS, arou…
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Reposted by Audrey Ryback
Tom Kindlon @tomkindlon.bsky.social · 12/04/2026
ME Research UK: Researchers have looked at survey data from over 9,000 people across 10 European countries and observed two peaks in ME/CFS onset. Read more: tinyurl.com/3utbebt5 #MEcfs #PwME #CFS
Two distinct peaks in age of ME/CFS onset) 
"Our findings suggest that incidence of ME/CFS peaks in adolescence and early middle-age, and that early onset ME/CFS is more common in those with affected relatives, more often triggered by infection, and associated with more severe disease" 
(The first peak appeared in adolescence, with an average age of onset of 16 years. 


(-Fhe second peak was middle age, with onset age averaging 36.6 years. 
Note: Graph is is0 for illustrative purposes only Age of onset INFORM. INFLUENCE. INVEST. SCO36942 
RESoArH 
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McGrath S et al., Oxford Open Immunology (2026)
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Charlie Hillier @charliehillier.bsky.social · 31/03/2026
My good friend Tom Micklem who I first met back in university is running the London Marathon to raise money for Action for ME! @actionforme.bsky.social You can read about it and donate here, good luck Tom!: 2026tcslondonmarathon.enthuse.com/pf/tom-micklem
2026tcslondonmarathon.enthuse.com
Tom is running the London Marathon
Hello everyone Should all go to plan, I will be running the London marathon in April and I am taking the opportunity to raise some money for Action for M.E. Myalgic encephalomyelitis (M.E.), or chroni
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Reposted by Audrey Ryback
Action for ME @actionforme.bsky.social · 25/03/2026
This large-scale study analysed data from more than 9,000 people with ME/CFS, helping to build a clearer picture of the condition’s onset, potential triggers, and links to illness severity. Find out more here: www.actionforme.org.uk/me-onset-pat...
actionforme.org.uk
New study finds age peaks in ME onset
New research funded by Action for ME explores when ME develops, identifying two peak onset periods and links to triggers and severity.
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Journal of Open Source Software @joss-openjournals.bsky.social · 24/03/2026
Just published in JOSS: 'TarGene: A Nextflow pipeline for the estimation of genetic effects on human traits via semi-parametric methods.' doi.org/10.21105/joss.09603
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Reposted by Audrey Ryback
Institute of Genetics and Cancer @uoe-igc.bsky.social · 24/03/2026
Did you know there is strong evidence that people are most likely to develop ME/CFS at two points in life - at an average of age of 16 or 37? Read more about this new study led by @aryback.bsky.social 👉 edin.ac/4v3uIv0
edin.ac
Incidence of ME peaks in adolescence or early middle age | Institute of Genetics and Cancer | Institute of Genetics and Cancer
Researchers have found strong evidence that people are most likely to develop ME/CFS at two points in life, in a study that could help uncover causes of the disease and point to ways to prevent it.
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Reposted by Audrey Ryback
ME/CFS Science @mecfsscience.org · 23/03/2026
1) Two age peaks: a fascinating paper confirmed two peaks for when people get ME/CFS: around 16 years old and in the mid thirties. The early onset in adolescence was associated with severe ME/CFS, an infectious onset, and having relatives with the disease. A brief summary...
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Simon McGrath @simonmcg.bsky.social · 21/03/2026
Patients were central to the team that found ME/CFS is most likely to start in the teens and early middle age. Two age peaks is unusual for any disease and might help unravel ME's causes. academic.oup.com/ooim/advance... 1/ team credits to follow
academic.oup.com
Incidence age is bimodal for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, with higher severity burden for early onset disease
Abstract. Myalgic Encephalomyelitis, or Chronic Fatigue Syndrome (ME/CFS), is a disease of uncertain origin. Studies of Norwegian health records have sugge
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Reposted by Audrey Ryback
Charlie Hillier @charliehillier.bsky.social · 21/03/2026
Read our paper with @simonmcg.bsky.social @aryback.bsky.social here! We report that ME/CFS has a bimodal age onset pattern with peaks in adolescence and early middle age. It is unusual for a disease to have more than one onset peak, a feature that may provide a clue into the causes of the illness.
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Audrey Ryback @aryback.bsky.social · 23/03/2026
1/7 Excited to share our new paper co-produced with @simonmcg.bsky.social. We found that previous reports of ME having two age peaks in Norway replicates in two different datasets and across 7/10 European countries we examined, suggesting this is a generalisable- and distinctive- feature of ME.
Three onset age distributions for ME/CFS, one for Norway, one for the combined 9 other countries, and one for a DecodeME subcohort, with fitted splines.
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Chris Ponting @cgatist.bsky.social · 18/03/2026
PhD project to identify ME/CFS diagnostic markers @edinburgh-uni.bsky.social Interdisciplinary #MEcfs science involving #ML #AI Fully funded if eligible for home fees Contact us: @aryback.bsky.social @avakhamseh.bsky.social @sjoerdvbeentjes.bsky.social www.findaphd.com/phds/project...
findaphd.com
Precision medicine biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) using multi-modal AI/ML at University of Edinburgh on FindAPhD.com
PhD Project - Precision medicine biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) using multi-modal AI/ML at University of Edinburgh, listed on FindAPhD.com
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Audrey Ryback @aryback.bsky.social · 04/02/2026
1/3 Now published: We performed a large-scale replication testing the effect of serum from 67 pwME and 53 healthy donors on muscle cell mitochondria, revealing no significant differences. This suggests earlier results may not be true for people with ME in general. doi.org/10.1371/jour...
doi.org
Indistinguishable mitochondrial phenotypes after exposure of healthy myoblasts to myalgic encephalomyelitis/chronic fatigue syndrome or control serum
Myalgic Encephalomyelitis (ME) / Chronic Fatigue Syndrome is a disease of uncertain aetiology that affects up to 400,000 individuals in the UK. Exposure of cultured cells to the sera of people with ME...
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Reposted by Audrey Ryback
Action for ME @actionforme.bsky.social · 26/01/2026
⌛ The Big Survey closes tomorrow! Your responses directly shape our work and help us to illustrate the impact of ME. If you're thinking about taking part, please do. 🔗 Take part today: www.actionforme.org.uk/research-cam...
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Audrey Ryback @aryback.bsky.social · 22/01/2026
Calling pwME in the UK- please fill out this survey if you haven't yet! I'll be using data from this survey to better understand at what ages people develop ME and from what types of triggers. Thanks to everyone who has taken part so far!
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Reposted by Audrey Ryback
Institute of Genetics and Cancer @uoe-igc.bsky.social · 04/12/2025
Find a great project with the @uoe-eid.bsky.social Future Medicine PhD fellowships 2026, including with #IGC's @cgatist.bsky.social, @aryback.bsky.social, Sara Brown and Liz Patton, and IGC affiliates Kelly Blacklock, @avakhamseh.bsky.social and @sjoerdvbeentjes.bsky.social 👇 edin.ac/3MDRZle
edin.ac
Future Medicine PhD fellowships 2026 | Edinburgh Infectious Diseases | Edinburgh Infectious Diseases
New PhD opportunity to explore the role of infectious agents in chronic disease. 4 fully-funded PhD places are available for UK/home fee students. Apply by 16 January 2026 for entry in October 2026.
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Audrey Ryback @aryback.bsky.social · 28/10/2025
Want to join our amazing team for a PhD in ME/CFS research as part of a funded Future Medicine PhD Fellowship? See: www.findaphd.com/phds/project... We offer: Exciting and rigorous science, PPI, truly interdisciplinary and fantastic research culture! Please contact us to discuss before applying!
findaphd.com
Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh on FindAPhD.com
PhD Project - Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh, listed on FindAPhD.com
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Reposted by Audrey Ryback
Chris Ponting @cgatist.bsky.social · 28/10/2025
Interested in ME/CFS research? Want to do a PhD with @aryback.bsky.social, @avakhamseh.bsky.social, @sjoerdvbeentjes.bsky.social & @cgatist.bsky.social? Then apply for a *funded* Future Medicine PhD Fellowship. See: www.findaphd.com/phds/project... Please contact us to discuss before applying.
findaphd.com
Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh on FindAPhD.com
PhD Project - Personalised blood-based biomarkers for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS) symptom severity at University of Edinburgh, listed on FindAPhD.com
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Katharine Cheston @kacheston.bsky.social · 13/10/2025
The Big Survey is now live! It has been such a privilege to get to work on this with such a wonderful, inspiring team at @actionforme.bsky.social, including our brilliant Patient and Public Involvement Group, made up of people with lived experience of ME and Long Covid.
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Tom Kindlon @tomkindlon.bsky.social · 12/10/2025
UK Action for ME Big Survey 2025 The 5 yearly survey of people in the UK with ME/CFS will open on Monday 13th October. It has been developed by AfME in collaboration with @kacheston.bsky.social Dr Katherine Cheston at Durham University. www.actionforme.org.uk/research-cam... #MEcfs #PwME #CFS
actionforme.org.uk
2025 Big Survey
Find out how you can contribute to our 2025 Big Survey - a vital research project aiming to illustrate the impact of ME and long Covid.
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Reposted by Audrey Ryback
Durham Institute for Medical Humanities @durhamimh.bsky.social · 13/10/2025
🎉 We are delighted to launch this year’s Big Survey in collaboration with @actionforme.bsky.social! If you are in the UK living with ME or Long Covid with ME symptoms, we want to hear from you! tinyurl.com/2s4dbrkx 🧵
tinyurl.com
2025 Big Survey
Find out how you can contribute to our 2025 Big Survey - a vital research project aiming to illustrate the impact of ME and long Covid.
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Reposted by Audrey Ryback
Chris Ponting @cgatist.bsky.social · 08/10/2025
The research used to claim reliability of a ME/CFS blood test has important limitations, shown here. www.theguardian.com/society/2025...
Three possible confounders in a study proposing an ME/CFS blood test : sex/age, batch and inactivity/severity. Better designed studies by independent researchers are necessary.
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Chris Ponting @cgatist.bsky.social · 01/09/2025
Seeking a Project Manager for the PRIME project: "Building Infrastructure for Patients, Researchers and Industry for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)". Closing date for applications is 15 September 2025. #pwME #MEcfs elxw.fa.em3.oraclecloud.com/hcmUI/Candid...
elxw.fa.em3.oraclecloud.com
PRIME Project Manager
The PRIME project is looking for an experienced and dedicated project manager. This role will be crucial to the successful delivery of PRIME, with the post holder responsible for the strategic executi...
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Reposted by Audrey Ryback
ME Association @meassociation.org.uk · 29/08/2025
The ME Association are pleased to announce that we have awarded Decode ME the Howes-Goudsmit Award 2025 for their extensive work and commitment to their genome-wide association study. Find out more: meassociation.org.uk/ir3e #MECFS #pwME #SevereME #MyalgicE #DecodeME #HowesGoudsmitAward
meassociation.org.uk
The ME Association awards Decode ME the Howes Goudsmit Award 2025 - The ME Association
The ME Association are pleased to announce that we have […]
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Reposted by Audrey Ryback
Ava Khamseh @avakhamseh.bsky.social · 12/08/2025
New course “EMBO Causality in Biomedicine”: We have organised the first EMBO course in *causal* stats/ML methods for quantitative biomedicine. @sjoerdvbeentjes.bsky.social @nimahejazi.org @pablormier.bsky.social @DariaSokolova @CarolineUhler Very much looking forward to teaching and discussing!
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DecodeME @decodemestudy.bsky.social · 12/08/2025
"DecodeME is now calling on researchers worldwide to join us in accelerating ME/CFS research.” - Prof Chris Ponting (DecodeME Investigator). We encourage researchers to explore and build on our findings. Apply for access to our rich dataset now shorturl.at/F8aOM
Image of Chris Ponting next to quote "This is a wakeup call. These extraordinary results speak the language of people with ME/CFS, often recounting people's ME/CFS symptoms. DecodeME is now calling on researchers worldwide to join us in accelerating ME/CFS research"
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Tom Kindlon @tomkindlon.bsky.social · 07/08/2025
New blog post from DecodeME team explaining new findings and discussing them in a bit more detail: "X marks the spot where ME/CFS biology can be discovered" www.decodeme.org.uk/x-marks-the-... #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME
DecodeME logo

Home > X marks the spot where ME/CFS biology can be discovered

X marks the spot where ME/CFS biology can be discovered
06 August 2025

Scientists, people with ME/CFS, and their charities came together to create DecodeME, the world's biggest ME/CFS study – and its results are striking. 18,000 people with ME/CFS gave their DNA, enabling DecodeME to reveal eightgenetic signals for the illness. These signals indicate that immune and neurological processes play a significant role in ME/CFS.
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ME/CFS Science @mecfsscience.org · 10/08/2025
1) Saw some skepticism about DecodeME, asking if it is overhyped. As an account that focuses on critically analyzing research (our name was 'ME/CFS Skeptic' for a reason!), we think it’s the real deal. Here are a couple of reasons why it stands out. 🧵
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Audrey Ryback @aryback.bsky.social · 07/08/2025
DecodeME results are out! So inspired by my incredible colleagues at UoE who have carried out this research to the highest standard. I hope these results will bring about a paradigm shift in ME/CFS research and attract more interest and investment to the field. shorturl.at/VwN3s #DecodeME
shorturl.at
Initial findings from the DecodeME genome-wide association study of myalgic encephalomyelitis/chronic fatigue syndrome
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DecodeME @decodemestudy.bsky.social · 06/08/2025
Our initial DNA results! DecodeME have discovered that people with an ME/CFS diagnosis have significant genetic differences compared to the general population. - Summary of our results: shorturl.at/pgsjk Check out our full preprint paper: shorturl.at/VwN3s
DecodeME: The Results announcement post. The graphic has a blue background with a DNA helix. In the centre of the graphic it says ‘We have released our initial DNA results! We have discovered that your genes contribute to your chances of developing ME/CFS.’ At the bottom left of the graphic is an image of a research paper.
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DecodeME @decodemestudy.bsky.social · 04/08/2025
The initial DNA results from DecodeME are coming this week! We will release them on our website on Wednesday 6th August at 7pm (approx). We're letting you know the timing in advance so you can pace beforehand. Thank you to our participants & supporters.
Dark blue background with image of DNA helix. At the top of the DecodeME ‘the results’ logo. Two spotlights shine on a speech bubble that says ‘Initial DNA results’. To the right of this is an image of a research paper. At the bottom of the graphic it says ‘Wednesday 7pm BST’.
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Action for ME @actionforme.bsky.social · 16/06/2025
@aryback.bsky.social is a Research Fellow at the Uni of Edinburgh, holds the first Clare Francis Postdoctoral Fellowship awarded by Action for ME. Audrey’s research will play an important part in understanding ME/CFS. Read the pre-print here 👇 www.actionforme.org.uk/research-upd... #MECFS #pwME
actionforme.org.uk
Research Update from Dr Audrey Ryback - Findings and Pre-Print Available - Action for ME
An update from Dr Audrey Ryback's research, testing the effect of serum from people with ME on muscle cell mitochondria, and findings.
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Chris Ponting @cgatist.bsky.social · 20/06/2025
📢 Now published: www.embopress.org/doi/full/10..... Since the preprint, we replicated 9 of 14 traits in All of Us & showed that #pwME with PEM-like symptoms have stronger biomarker differences. bsky.app/profile/cgat...
embopress.org
Replicated blood-based biomarkers for myalgic encephalomyelitis not explicable by inactivity | EMBO Molecular Medicine
imageimageThere are no cellular or molecular biomarkers diagnostic of myalgic encephalomyelitis (also known as chronic fatigue syndrome [ME/CFS]). We find hundreds of blood-based traits are different,...
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Audrey Ryback @aryback.bsky.social · 09/06/2025
1/2 New pre-print: We performed a large-scale replication testing the effect of serum from 67 pwME and 53 healthy donors on muscle cell mitochondria, revealing no significant differences. This suggests earlier results may not be true for people with ME in general. doi.org/10.1101/2025...
doi.org
Indistinguishable mitochondrial phenotypes after exposure of healthy myoblasts to myalgic encephalomyelitis or control serum
Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome is a disease of uncertain aetiology that affects up to 400,000 individuals in the UK. Exposure of cultured cells to the sera of people with ME has been proposed to cause phenotypic changes in these cells in vitro when compared to sera from healthy controls. ME serum factors causing these changes could inform the development of diagnostic tests. In this study, we performed a large-scale, pre-registered replication of an experiment from Fluge et al (2016) that reported an increase in maximal respiratory capacity in healthy myoblasts after treatment with serum from people with ME compared to serum from healthy controls. We replicated the original experiment with a larger sample size, using sera from 67 people with ME and 53 controls to treat healthy cultured myoblasts, and generated results from over 1,700 mitochondrial stress tests performed with a Seahorse Bioanalyser. We observed no significant differences between treatment with ME or healthy control sera for our primary outcome of interest, oxygen consumption rate at maximal respiratory capacity. Results from our study provide strong evidence against the hypothesis that ME blood factors differentially affect healthy myoblast mitochondrial phenotypes in vitro. ### Competing Interest Statement The authors have declared no competing interest. Action for ME, https://ror.org/0569v7v35, Clare Francis Research Fellowship
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Chris Ponting @cgatist.bsky.social · 22/04/2025
NEW: There are 400,000 people diagnosed with ME/CFS in the UK, at least there would be if access to diagnosis was equal. ME/CFS diagnosis however is a postcode lottery. It's much rarer in non-White communities and socioeconomically deprived areas, much worse than for other diseases rdcu.be/eiEeu
rdcu.be
Unequal access to diagnosis of myalgic encephalomyelitis in England
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Audrey Ryback @aryback.bsky.social · 17/02/2025
Pleased to share this research from my PhD in @graemecowan.bsky.social's lab! We replicated existing evidence of moderately increased IGHV3-30 usage in B cells of patients with mild/moderate, but not severe ME. www.frontiersin.org/journals/imm...
frontiersin.org
Frontiers | Deep sequencing of BCR heavy chain repertoires in myalgic encephalomyelitis/chronic fatigue syndrome
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Chris Ponting @cgatist.bsky.social · 07/02/2025
Significant replication of combinatorial genetic signatures for Long Covid risk www.medrxiv.org/content/10.1...
medrxiv.org
Reproducibility of Genetic Risk Factors Identified for Long COVID using Combinatorial Analysis Across US and UK Patient Cohorts with Diverse Ancestries
Background Long COVID is a major public health burden causing a diverse array of debilitating symptoms in tens of millions of patients globally. In spite of this overwhelming disease prevalence and st...
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