Area of research
Genetics · Cognitive Neuroscience
Research interest
Research interests include Autism Spectrum Disorder Research, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, and Genomics and Rare Diseases.
Risk Factors for Autism Spectrum Disorder in Individuals Born Preterm: A Systematic Review and Meta-Analysis of Population-Based Studies
Machine Learning Prediction of Autism Spectrum Disorder From a Minimal Set of Medical and Background Information
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder
Infants’ looking preferences for social versus non-social objects reflect genetic variation
Deficiency of the Heterogeneous Nuclear Ribonucleoprotein U locus leads to delayed hindbrain neurogenesis
Genetic correlates of phenotypic heterogeneity in autism
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium
Preferential looking to eyes versus mouth in early infancy: heritability and link to concurrent and later development
Presynaptic dysfunction in CASK-related neurodevelopmental disorders
Modeling SHH-driven medulloblastoma with patient iPS cell-derived neural stem cells
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders
Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder
Long-term social skills group training for children and adolescents with autism spectrum disorder: a randomized controlled trial
Fetal and postnatal metal dysregulation in autism
Social Skills Training for Children and Adolescents With Autism Spectrum Disorder: A Randomized Controlled Trial
A Novel Way to Measure and Predict Development: A Heuristic Approach to Facilitate the Early Detection of Neurodevelopmental Disorders
Genome-wide characteristics of de novo mutations in autism
Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay
Synaptic, transcriptional and chromatin genes disrupted in autism
The Roots of Autism and ADHD Twin Study in Sweden (RATSS)
Copy number variation in Han Chinese individuals with autism spectrum disorder
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes