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The role of BAF (mSWI/SNF) complexes in mammalian neural development

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Vulnerabilities of Mutant SWI/SNF Complexes in Cancer

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SWI/SNF Factors Required for Cellular Resistance to DNA Damage Include ARID1A and ARID1B and Show Interdependent Protein Stability

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Requirement for PBAF in Transcriptional Repression and Repair at DNA Breaks in Actively Transcribed Regions of Chromatin

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The contribution of de novo coding mutations to autism spectrum disorder

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Swi/Snf chromatin remodeling/tumor suppressor complex establishes nucleosome occupancy at target promoters

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Haploinsufficiency of ARID1B , a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability

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A Landscape of Driver Mutations in Melanoma

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A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease

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An integrated map of genetic variation from 1,092 human genomes

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

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Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

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Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome

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Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma

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Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

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Genetic and Epigenetic Networks in Intellectual Disabilities

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Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B

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Essential Role of ARID2 Protein-containing SWI/SNF Complex in Tissue-specific Gene Expression

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A framework for variation discovery and genotyping using next-generation DNA sequencing data

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A Balanced Translocation t(6;14)(q25.3;q13.2) Leading to Reciprocal Fusion Transcripts in a Patient with Intellectual Disability and Agenesis of Corpus Callosum

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SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution

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CHD7 cooperates with PBAF to control multipotent neural crest formation

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A de novo paradigm for mental retardation

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Fast and accurate short read alignment with Burrows-Wheeler transform

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ATP-dependent chromatin remodeling in neural development

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