Opportunity to shape future research in genetic syndromes including #fragilexsyndrome
10-minute survey. 👇

Delighted to produce these alongside Kirsten Johnson, FRSA Gaia Scerif Kayla Smith jonathan herring Hayley Crawford and Angus Clarke The All Wales Medical Genomics Service. Guidelines help professionals and empower those affected by fragile X and their families. Fragile X Society, UK Fragile X International (FraXI)

doi.org/10.1111/jar.13…

CHANGES study of behaviour in SYNGAP1 goes on tour!
Book now - dates available in York, Manchester, Luton and Bristol
patrickwildcentre.com/news/book-date…

Our first Winefride and Booth Smith lecture, celebrating our new PhD studentships. Peter Kind will discuss some of the latest research in understanding genetic conditions associated with intellectual disabilities. Register here:
eventbrite.co.uk/e/winefride-an…

Fantastic photos!! Thank you all so much for all the hard work that has gone into the Lighting Up!! We are incredibly grateful for your support of the Charity. It is very much appreciated.

😍Beautiful updated #SYNGAP1 poster shared by Jillian McKee at Child Neurology Society #CNSAM . This is so valuable for families explaining #SynGAP to clinicians.

‼️Note: #Autism & behaviors vs #Rett and #Angelman in fig 2⃣. #Seizures vs #SCN2A & #STXBP1 in fig 3⃣. Meds in Fig 4⃣.

Sydni Weissgold presenting her PhD plans to families at the UK #SYNGAP1 family meet-up. Longitudinal naturalistic studies will be so valuable in understanding behavior and developing better therapies.

Delighted to be hosting the UK #SYNGAP1 family meet up today.

Congratulations, Peter - this is great news!
To find out more about Peter’s work or SIDB, visit:
sidb.org.uk/news-events/pe…

Great to be at this yesterday. Wonderful involvement of the #fragilex community in the service development process. Heartily supported from all of us in Edinburgh Patrick Wild Centre

Wooohoo!!! Our new pre-print on #EEF1A2 epileptic encephalopathy is here. Thanks so much for involving me Cathy Abbott, and huge effort from Grant F. Marshall and Melissa Fasol!

PWC clinical research director carid_pwc presenting findings from their SIDB funded #SYNGAP research on Thursday!

Sign up now to our UK SYNGAP1 family day!
eventbrite.com/e/662291390377…

Super important work examining sensitivity to touch in #FragileX , by members of CARID, Patrick Wild Centre and SIDB. Congratulations to Damien on becoming a FRAXA postdoctoral fellow!
fraxa.org/somatosensory-…

Fantastic research on show for the SIDB research retreat. Patrick Wild Centre

Tonight we are lighting up the castle in teal for World Fragile X Day.

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disabilities worldwide and is often associated with anxiety, autism and ADHD.

SIDB carid_pwc

Today is International SYNGAP1 day! Very proud to be doing clinical research about SYNGAP1 for my PhD 🧬🧠💜

We are pleased to be running this trial which is now recruiting in Edinburgh. Also taking place in other UK sites. Visit the website below for more details.

Congratulations to our students for their lightening talks on #EdNeuroDay 😃
It was a great hit among the delegates!
Well done 👏

L-R: Kelly Panichnantakul, Arish Mudra Rakshasa, Nithya Nair, Michael Sewell, Philip Braaker, Emma Wilson
#neuroscience #PhDtalk

Andrew McKechanie presenting on what makes a quality service. Deliberate design so important - we need to get the environment right first of all. Who knew there was a British Standard on designing buildings for neurodiversity? ITAKOM Patrick Wild Centre #ITAKOM