Absent CNKSR2 causes seizures and intellectual, attention, and language deficits

eXclusion: Toward Integrating the X Chromosome in Genome-wide Association Analyses

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Clinical genetic study of the epilepsy-aphasia spectrum

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The Database of Genomic Variants: a curated collection of structural variation in the human genome

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What causes attention deficit hyperactivity disorder?

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

(2011) Josephine Elia et al.   NATURE GENETICS

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

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Characterization of the proteome, diseases and evolution of the human postsynaptic density

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Proteomic characterization of the dynamic KSR-2 interactome, a signaling scaffold complex in MAPK pathway

(2009) Lin Liu et al.   BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS

Defining mechanisms of actin polymerization and depolymerization during dendritic spine morphogenesis

(2009) Pirta Hotulainen et al.   JOURNAL OF CELL BIOLOGY

Organization and dynamics of PDZ-domain-related supramodules in the postsynaptic density

(2009) Wei Feng et al.   NATURE REVIEWS NEUROSCIENCE

CNK and HYP form a discrete dimer by their SAM domains to mediate RAF kinase signaling

(2008) T. Rajakulendran et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA