Shafali Jeste

The paper identifies 253 autism-associated genes using rare variation from 62,429 individuals and finds pleiotropy across physiological systems and developmental disorders.

Among infant siblings of autistic children, greater trial-to-trial variability in visual P1 latency at 6 and 12 months tracked higher 24-month cognitive and language scores; mean P1 measures did not.

The paper investigates altered aperiodic EEG spectral power during speech perception in youths with ASD, linking increased neural noise to lower verbal communication skills.

The paper introduces a novel metric, estimated axonal latency, to measure neuronal processing speed in autism spectrum disorder using MRI and EEG data.

This study evaluates a genomics-informed multidisciplinary clinic for neurodevelopmental disorders, finding that genetic diagnoses lead to significant clinical management changes in most patients.

This paper reviews US professional society guidelines for genetic testing in neurodevelopmental disorders and highlights the need for unified, updated, and accessible cross-specialty guidelines.

The paper examines altered Salience Network connectivity in 6-week-old infants at risk for autism, finding that stronger sensorimotor connectivity predicts ASD symptomatology.

The paper examines thalamocortical connectivity in infants at high familial risk for ASD and finds altered functional and structural connectivity predicting later social development.

This study finds that adults with autism spectrum disorder show accelerated age-related oscillatory slowing in peak alpha frequency compared to neurotypical controls.

The paper assesses the test-retest reliability of EEG PSD profiles in children with ASD and TD controls using two analytical approaches, showing stable individual signatures across sessions.

The paper uses EEG data from infants to predict later ASD symptoms using multivariate pattern analysis, finding specific connectivity differences associated with ASD.

The paper uses EEG to identify early functional brain differences in infants with tuberous sclerosis complex (TSC) that predict later autism spectrum disorder (ASD) development.