{ "items": [ "\n\n
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\n Whole-Brain Image Analysis and Anatomical Atlas 3D Generation Using MagellanMapper\n

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Young DM. et al, (2020), Current Protocols in Neuroscience, 94

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\n Not All Autism Genes Are Created Equal: A Response to Myers et al.\n

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Buxbaum JD. et al, (2020), American Journal of Human Genetics, 107, 1000 - 1003

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\n Exome sequencing for prenatal diagnosis in nonimmune hydrops fetalis\n

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Sparks TN. et al, (2020), New England Journal of Medicine, 383, 1746 - 1756

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\n A Chromatin Accessibility Atlas of the Developing Human Telencephalon\n

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Markenscoff-Papadimitriou E. et al, (2020), Cell, 182, 754 - 769.e18

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\n Homeostatic plasticity fails at the intersection of autism-gene mutations and a novel class of common genetic modifiers\n

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Gen\u00e7 \u00d6. et al, (2020), eLife, 9, 1 - 32

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\n Clinical impact of splicing in neurodevelopmental disorders\n

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Sanders SJ. et al, (2020), Genome Medicine, 12

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\n Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex\n

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Werling DM. et al, (2020), Cell Reports, 31

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\n Constructing and Optimizing 3D Atlases From 2D Data With Application to the Developing Mouse Brain\n

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Young DM. et al, (2020)

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\n Biological concepts in human sodium channel epilepsies and their relevance in clinical practice\n

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Brunklaus A. et al, (2020), Epilepsia, 61, 387 - 399

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\n Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.\n

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Satterstrom FK. et al, (2020), Cell, 180, 568 - 584.e23

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\n Homeostatic Plasticity Commonly Fails at the Intersection of Autism-Gene Mutations and a Novel Class of Common Phenotypic Modifier\n

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Gen\u00e7 \u00d6. et al, (2020)

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\n CHARACTERIZATION OF DE NOVO AND TRANSMITTED GENETIC VARIATION ASSOCIATED WITH CHILDHOOD-ONSET SCHIZOPHRENIA\n

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Quick VS. et al, (2020), JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 59, S261 - S261

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\n Differential excitatory vs inhibitory SCN expression at single cell level regulates brain sodium channel function in neurodevelopmental disorders\n

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Du J. et al, (2020), European Journal of Paediatric Neurology, 24, 129 - 133

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\n HyDROPS study: Exome sequencing identifies genetic disorders causing non-immune hydrops fetalis\n

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Sparks TN. et al, (2020), AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 222, S68 - S69

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\n Whole-Exome Sequencing in Fetuses with Congenital Diaphragmatic Hernias: Known and Novel Genetic Mutation\n

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Schwab ME. et al, (2020), JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 231, S217 - S217

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\n Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.\n

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Cross-Disorder Group of the Psychiatric Genomics Consortium. Electronic address: plee0@mgh.harvard.edu None. and Cross-Disorder Group of the Psychiatric Genomics Consortium None., (2019), Cell, 179, 1469 - 1482.e11

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\n A Chromatin Accessibility Atlas of the Developing Human Telencephalon\n

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Markenscoff-Papadimitriou E. et al, (2019)

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\n A framework for the investigation of rare genetic disorders in neuropsychiatry\n

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Sanders SJ. et al, (2019), Nature Medicine, 25, 1477 - 1487

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\n The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex\n

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Spratt PWE. et al, (2019), Neuron, 103, 673 - 685.e5

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\n Next-generation sequencing in autism spectrum disorder\n

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Sanders SJ., (2019), Cold Spring Harbor Perspectives in Medicine, 9

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