News & Events

New pilot study investigating bilingualism and minimally-speaking children

Study new ways to measure thinking in minimally-speaking children

Dr Alfredo Gonzalez-Sulser, Dr Lindsey Mizen, Dr Damien Wright & PhD student Sydni Weissgold attended and presented at the Syngap1

Today (10th October) is International Fragile X Day. The SIDB and PWC work on this genetic condition, and we have

We are delighted to announce that alongside Fragile X UK we will be hosting another family get together next year.

We are currently looking for volunteers (3-45 years old) with full mutation fragile X syndrome to join our study that

We gathered for the annual research retreat to discuss latest developments in autism and neurodevelopmental conditions.

The European Research Council (ERC) funds SIDB Group Leader proposal for research on circuit mechanisms of cortical predictive learning.

SIDB and the PWC partnered up with ‘Fusion: Art meets Science’ to create an exhibition celebrating the brain.

Today is World Fragile X Day. SIDB PhD student Nawon Kim ‘shines a light’ on Fragile X with these illuminated

The SynGAP1 gene plays an important role in how our nerves function. The genetic address of Syngap is 6p21.32 (found

Dr. Lindsay Mizen, a PWC/SIDB member joined families and friends of people with SYNGAP1 Syndrome and did the Anfield Abseil

Patrick Wild Centre and SIDB researchers have found that those with SYNGAP1-ID generally had differing eye movement patterns compared with