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I wrote an article for the BPS psych magazine reflecting on the importance of the inclusion of people with learning disability in the neurodiversity movement. I hope it helps unmask the diversity seen across people w/ LD whom are so much more than their lvl of cog ability

Participate in the Checklist Project. A tool for parents to understand behaviours that challenge. For parents of children aged 4-18 with a moderate-profound learning disability. #disabilityresearch #geneticsyndromes Warwick Med School University of Warwick Neurodevelopmental_conditions_research@WMS Cerebra Network

IT's OUT! A gaze following paradigm w/ autistic ppts & ppts w/ genetic syndromes (#FXS #CdLS) w/ unique profiles of autism characteristics in CORTEX for the neurodevelopmental neurodiversity issue! 🥳 tinyurl.com/2s4npec9 Jo Moss Sarah J White Malwina 1/6

Huge congratulations to Lauren Jenner who passed her viva with flying colours yesterday! It has been an honor and a privilege to be your supervisor! Emily Farran Cerebra Network @cer

I’ve passed my PhD viva! A heartfelt thank you to my supervisors Jo Moss Emily Farran for their encouragement, my examiners @AllyGrandison Charlotte Tye who made the viva such a positive experience, and to those who supported me on this journey Cerebra Network Cerebra

📚Help us improve our teacher training resource (findteacherresources.co.uk)📚 Are you a parent/caregiver of a person with a genetic syndrome? Are you a person with a genetic syndrome? If the answer is yes, please contact Dr Katherine Ellis at [email protected] for more info.

Can’t believe it’s already been a week since Gatlinburg Conference! 🇺🇸 Such a pleasure to be able to present alongside Kat Ellis, Gillian Hughes, Sarah-Marie Feighan, and Prof Jane Roberts in our symposium exploring social cognition using eye-tracking in genetic syndromes.

So great to see members of the Cerebra Network Team (representing University of Surrey) at the 56th Gatlinburg Conference in Kansas City showcasing research conducted across the Network. You can learn more about research at University of Surrey here: ndevresearchlab.com

Well done to Lauren Jenner Kat Ellis and Gillian Hughes for delivering a great symposium at Gatlinburg Conference last week on exploring social cognition using eye-tracking in genetic syndromes.

Jane Margetson reviews the Cerebra webinar talk on ‘Diagnostic overshadowing for children with a genetic condition associated with an intellectual disability’, led by Dr Jo Moss and Debbie Austin on 21st November 2023. buff.ly/3U72wpq

Wonderful to have Gillian Hughes presenting our work on females with the fragile X premutation at International Society for Autism Research, INSAR conference this year. Academy of Medical Sciences Fragile X Society, UK

#ShapeResearchChangeLives Report launch: Shape Research, Change Lives: setting priorities in genetic syndrome research. Gaia Scerif Liz Pellicano Jo Van Herwegen Laura Cristescu To download our report: shorturl.at/X6V75

The exclusively inclusive landscape of autism research Comment by Lauren Jenner & Joanna Moss go.nature.com/3LqPU8D

Such a pleasure to work with Jo Moss on this commentary on the representation of autistic people with intellectual disability in research. You can access the full paper here: rdcu.be/dN5Uv

Great working with Lauren Jenner on this commentary about the inclusion of people with intellectual disability in autism research. You can read the full article here: rdcu.be/dN5Uv Nature Reviews Psychology Cerebra Network Surrey [email protected]

Delighted to share that I’ve started my role as a Postdoctoral Fellow at USC Arnold School of Public Health, funded by LivJoy Foundation, to further research focused on representing girls and women with fragile X syndrome. Learn more about their story and mission here: livjoy.org 🦋💗

Thomas Christensen helps people age-in-place. His goal is to support adults with neurodevelopmental disabilities stay where they are, and he's using communication sciences and disorders to do it. ow.ly/bJuF50TA2tE #IAmPublicHealth #ArnoldSchoolProud

New paper out! We present a longitudinal analysis of depression symptoms in mothers with the FMR1 premutation from ages 20 to 75, revealing how both genetic and environmental factors shape vulnerability. doi.org/10.1002/ajmg.b…