Ever stuttered?
Help us better understand the causes of stuttering by joining our genetics study today!
The Murdoch Children’s Research Institute is appealing for volunteers aged 7+ with experience of stuttering (past or present) to participate in the NHMRC Centre of Research Excellence in Speech and Language’s ‘Genetics of Stuttering Study’.
Study News
End of 2019 update!
2019 has been a busy year for the Genetics of Stuttering Study! As the year draws to a close, we thought it a good time to provide an update on how the study is progressing, and our plans into the new year.
Spotlight: Participant Rich talks about his experiences with stuttering
Rich Stephens talks about his experiences with stuttering, and the power of not feeling alone. He feels strongly that “stuttering should never be a taboo subject”. He believes that “to understand anything you need to start at the beginning. Which is why The Genetics of Stuttering Study is so important for the future generations of people who stutter.”
Genetics of Stuttering Study in the media!
What an exciting day we had on Friday! The Genetics of Stuttering team spent the day speaking to the media about the study, and put a call out for anybody who has ever experienced stuttering to volunteer for our study.
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Aged 8 to 18?
Interested in meeting others in the #stuttering #community?
Want to show off your #creative skills?
Enrolment is now open for @sayorg Australia's Confident Voices program. Check out the programs on offer!
https://t.co/nsLCE7JBBF
#FunFact - 7 out of 10 people who have signed up so far for the Genetics Of Stuttering study are male.
Find out more about who has volunteered for the study in our last blog post: https://t.co/hSiANRUNoA #scicomm #research https://t.co/uGqwSjNsBT
#Didyouknow As well as investigating the genetics of #stuttering, our study team are involved in research into other speech disorders, and several neurological conditions.
Here is one example of some of this exciting other work from study investigator @MelanieBahlo ! #scicomm https://t.co/gCKr7aEfB8
A decades-long global study involving WEHI bioinformaticians Mark Bennett @HaloomRafehi and @MelanieBahlo revealed two new gene mutations that cause a rare type of #epilepsy.
The research was published in @NatureComms in December.
https://t.co/98FnTVijmO https://t.co/Tsmr1H2FGR
Can you spare 5 mins to share your experiences of #stuttering with @callumschof ? #awareness https://t.co/iPArQsLVVF
Did you hear study investigator, Prof Angela Morgan ( @speechneuro) talk about #stuttering on @ABCaustralia's Summer Sunday Mornings radio show yesterday? Our study got a mention, with a further call for people to take part!
See our website for more: https://t.co/7kcho3tXM0
About the 'Genetics of Stuttering Study’
The 'Genetics of Stuttering Study’ aims to pinpoint the genes that predispose individuals to stuttering, which could revolutionise future research into the causes, treatment and prevention of the disorder.
Stuttering or stammering affects verbal communication – particularly the rhythm or flow of communication.
Although the exact cause of stuttering is yet to be determined, genetics does play a role in stuttering, and a number of genetic variants having been identified to date.
The study involves 15 investigators at eight sites in Australia, the UK, the USA and The Netherlands.
Study researchers are working to recruit 3,000 volunteers from Australia, aged 7+ with a history of stuttering (past or present).
Please see http://www.geneticavanstotteren.nl/ for more information about recruitment in the Netherlands and Belgium. We will be starting to recruit from other countries very soon - watch this space!
Participating in this study could make a genuine contribution to the understanding of stuttering.
How can you help?
If you currently live with, or have a history of stuttering, we encourage you to volunteer for our groundbreaking research study by completing the 10 minute core component of our online survey. Depending on your responses to our survey, you may be asked to donate a saliva sample.
To help us meet our target of 3,000 participants by 31 December 2020, volunteer for our study today
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