AI Model Reads Brain Scans to Spot Dyslexia in Children with 96% Accuracy
A new deep learning framework called MedFusionNet combines diffusion-based synthetic MRI generation with a fusion of three neural architectures to ...
Tag: Neurodevelopmental Disorders
Cleft palate genetics study finds no common variant link to neurodevelopmental risk
A large genomic study of children with cleft lip and/or palate finds that common genetic variants do not explain the ...
Family Support Emerges as a Powerful Shield Against Parental Burnout in Raising Children with Neurodevelopmental Disorders
A Brazilian study of 207 parents found that having a child with a neurodevelopmental disorder, female gender, and higher education ...
Statistical Imputation of Intelligence Scores Expands Genetic Discovery in UK Biobank
Researchers statistically imputed fluid intelligence scores for hundreds of thousands of UK Biobank participants, reducing ascertainment bias and uncovering 26 ...
Massive Parkinson’s Genetics Study Confirms Rare Gene Variants Raise Disease Risk
New data from the 8,660-participant ROPAD cohort corroborate that ITSN1 loss-of-function variants raise Parkinson's disease risk five- to fifteen-fold, while ...
Faulty Epigenetic Switch Disrupts Brain Cell Cycles and Drives White Matter Defects in Autism-Linked Disorders
New research shows that pathogenic variants in the chromatin regulator MSL2 disrupt oligodendrocyte precursor cell division and myelination through loss ...
Horse Therapy Shows Real Promise in Psychiatry, but the Evidence Remains Shaky
A systematic review of 107 studies finds equine-assisted services show substantial benefits for psychiatric patients, but low methodological quality and ...
Frontline Doctors in Palestine Miss Key Signs of Seizures That Devastate Infants
A survey of 419 physicians in the West Bank found that fewer than half had good knowledge of infantile epileptic ...
DNA Methylation Episignatures Emerge as a Powerful New Diagnostic Layer for Rare Disease
A new review explains how DNA methylation episignatures provide functional evidence of disease mechanism in rare genetic disorders, helping resolve ...
Shock Therapy Shows Promise for Mysterious Regression in Down Syndrome
A new systematic review and case series finds that electroconvulsive therapy significantly reduces catatonic symptoms in young people with Down ...
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Mothers who receive childcare support from maternal grandparents show more parental warmth, finds NTU Singapore study
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University of Seville Breaks 120-Year-Old Mystery, Revises a Key Einstein Concept
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Bee body mass, pathogens and local climate influence heat tolerance
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Researchers record first-ever images and data of a shark experiencing a boat strike
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Groundbreaking Clinical Trial Reveals Lubiprostone Enhances Kidney Function
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