SLNSW-Rare copy number variants in over 100,000 Europea...-TN_cdi_proquest_journals_2342502509

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Full title: Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Author/creator: Li, Yun Rose, Glessner, Joseph T, Coe, Bradley P, Li, Jin, Mohebnasab, Maede, Chang, Xiao, Connolly, John, Kao, Charlly, Wei, Zhi, Bradfield, Jonathan, Kim, Cecilia, Hou, Cuiping, Khan, Munir, Mentch, Frank, Qiu, Haijun, Bakay, Marina, Cardinale, Christopher, Lemma, Maria, Abrams, Debra, Bridglall-Jhingoor, Andrew, Behr, Meckenzie, Harrison, Shanell, Otieno, George, Thomas, Alexandria, Wang, Fengxiang, Chiavacci, Rosetta, Wu, Lawrence, Hadley, Dexter, Goldmuntz, Elizabeth, Elia, Josephine, Maris, John, Grundmeier, Robert, Devoto, Marcella, Keating, Brendan, March, Michael, Pellagrino, Renata, Grant, Struan F A, Sleiman, Patrick M A, Li, Mingyao, Eichler, Evan E, Hakonarson, Hakon.

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Record Identifier: TN_cdi_proquest_journals_2342502509

Language: English

Formats: Articles

Publishers: England: Nature Publishing Group

Permalink: https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2342502509

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    Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

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    TN_cdi_proquest_journals_2342502509

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2342502509

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    Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2342502509

    Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

    Full title

    Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

    Author / Creator

    Li, Yun Rose ; Glessner, Joseph T ; Coe, Bradley P ; Li, Jin ; Mohebnasab, Maede ; Chang, Xiao ; Connolly, John ; Kao, Charlly ; Wei, Zhi ; Bradfield, Jonathan ; Kim, Cecilia ; Hou, Cuiping ; Khan, Munir ; Mentch, Frank ; Qiu, Haijun ; Bakay, Marina ; Cardinale, Christopher ; Lemma, Maria ; Abrams, Debra ; Bridglall-Jhingoor, Andrew ; Behr, Meckenzie ; Harrison, Shanell ; Otieno, George ; Thomas, Alexandria ; Wang, Fengxiang ; Chiavacci, Rosetta ; Wu, Lawrence ; Hadley, Dexter ; Goldmuntz, Elizabeth ; Elia, Josephine ; Maris, John ; Grundmeier, Robert ; Devoto, Marcella ; Keating, Brendan ; March, Michael ; Pellagrino, Renata ; Grant, Struan F A ; Sleiman, Patrick M A ; Li, Mingyao ; Eichler, Evan E ; Hakonarson, Hakon

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    England: Nature Publishing Group

    Journal title

    Nature communications, 2020, Vol.11 (1), p.255-255

    Record Identifier

    TN_cdi_proquest_journals_2342502509

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    English

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    Arrays Bias Binding sites Child & adolescent psychiatry Coding Comparative Genomic Hybridization Copy number Databases, Genetic Deletion Disease Diseases DNA Copy Number Variations Environmental impact European Continental Ancestry Group - genetics Exons Gene deletion Genes Genetic Loci Genetic predisposition to disease Genetic Predisposition to Disease - ethnology Genetic Predisposition to Disease - genetics Genome, Human - genetics Genome-wide association studies Genome-Wide Association Study Genomes Genomics Hospitals Humans Hybridization Medicine Mental disorders Metabolism Molecular Sequence Annotation Non-coding RNA Phenotypes Polymorphism, Single Nucleotide Quality control Single-nucleotide polymorphism Structural variation

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    TN_cdi_proquest_journals_2342502509

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2342502509

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