Using iPSCs and genomics to catch CNVs in the act.

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Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.Pathophysiology of TFII-I: Old Guard Wearing New Hats.

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Using iPSCs and genomics to catch CNVs in the act.

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2015 nî lūn-bûn

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2015年の論文

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Using iPSCs and genomics to catch CNVs in the act.

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Using iPSCs and genomics to catch CNVs in the act.

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Using iPSCs and genomics to catch CNVs in the act.

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Using iPSCs and genomics to catch CNVs in the act.

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Alexander Eckehart Urban

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Carolin Purmann

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

CNVs: harbingers of a rare variant revolution in psychiatric genetics

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

Animal models of neuropsychiatric disorders

Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder.

Animal models relevant to schizophrenia and autism: validity and limitations.

Intrapatient variations in type 1 diabetes-specific iPS cell differentiation into insulin-producing cells.

Challenges and standards in integrating surveys of structural variation.

Origins and implications of pluripotent stem cell variability and heterogeneity.

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ng.3204

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scholarly article

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10.1038/NG.3204

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English

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2015-02-01T00:00:00Z

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Using iPSCs and genomics to catch CNVs in the act.

about

P2860

P2860

Using iPSCs and genomics to catch CNVs in the act.

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