Beta2-adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndrome.
De novo truncating variants in the AHDC1 gene encoding the AT-hook DNA-binding motif-containing protein 1 are associated with intellectual disability and developmental delay.
In tribute to Bob Blanchard: Divergent behavioral phenotypes of 16p11.2 deletion mice reared in same-genotype versus mixed-genotype cages.
16p11.2 deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks.
16p11.2 deletion syndrome mice display sensory and ultrasonic vocalization deficits during social interactions.
The autism inpatient collection: Methods and preliminary sample description.
Clustering autism: Using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity.
Smarca4 ATPase mutations disrupt direct eviction of PRC1 from chromatin.
Dynamics of BAF-Polycomb complex opposition on heterochromatin in normal and oncogenic states.
Paul Wang, M.D.
Paul Wang joined Clinical Research Associates (CRA) and the Simons Foundation in 2016. He helps to oversee portions of SFARI's clinical research portfolio, and CRA's work with the experimental drug arbaclofen.
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