Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
Research Articles
An epigenetically distinct subset of children with autism spectrum disorder resulting from differences in blood cell composition.
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
MVP predicts the pathogenicity of missense variants by deep learning.
‘There and back again’-forward genetics and reverse phenotyping in pulmonary arterial hypertension.
Patterns and correlates of two-year changes in depressive symptoms for autistic adults.
Evaluating two common strategies for research participant recruitment into autism studies: Observational study.
Measuring depression in autistic adults: Psychometric validation of the Beck Depression Inventory-II.
Homozygous deletions implicate non-coding epigenetic marks in autism spectrum disorder.
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