A third linear association between Olduvai (DUF1220) copy number and severity of the classic symptoms of inherited autism.
Research Articles
Oligogenic effects of 16p11.2 copy number variation on craniofacial development.
Infraslow state fluctuations govern spontaneous fMRI network dynamics.
Paternal-age-related de novo mutations and risk for five disorders.
A genome-wide scan statistic framework for whole-genome sequence data analysis.
Gaining insights into aggressive behaviour in autism spectrum disorder using latent profile analysis.
Imaging striatal dopamine release using a nongenetically encoded near infrared fluorescent catecholamine nanosensor.
The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism individuals.
Habituation learning is a widely affected mechanism in Drosophila models of intellectual disability and autism spectrum disorders.
Sensorimotor cortical oscillations during movement preparation in 16p11.2 deletion carriers.
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