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Paper Details

Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models.
Am J Hum Genet
12
2022
16p11, ASD, CNVs, CRISPR-engineered 16p11, Chromosome 16p11, GABAergic inhibitory neurons, GABAergic neurons, RNA, X messenger ribonucleoprotein, X messenger ribonucleoprotein target gene sets, autism spectrum disorder, calretinin, cerebral organoid models, copy-number variants, differentially expressed genes, excitatory, genomic, genomic disorder, human, human induced neurons, human neuronal models, induced neuron, intellectual disability, isogenic neural stem, isogenic neural stem cell, mouse, schizophrenia, syntenic 7qF3 region
Author NameAffiliation
Alex R Hastie
Roy H PerlisCenter for Quantitative Health, Division of Clinical Research, Massachusetts General Hospital, USA Center for Genomic Medicine, Massachusetts General Hospital and Harvard Medical School
Roy H PerlisCenter for Quantitative Health, Division of Clinical Research, Massachusetts General Hospital, USA Center for Genomic Medicine, Massachusetts General Hospital and Harvard Medical School
James F GusellaCenter for Genomic Medicine, Massachusetts General Hospital, Broad Institute of MIT and Harvard, Blavatnik Institute, Harvard Medical School, USA Harvard Stem Cell Institute, Harvard University
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