Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program.
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| Title: | Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program. |
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| Authors: | Venner E; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA. venner@bcm.edu., Muzny D; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA., Smith JD; Department of Genome Sciences, University of Washington, Seattle, WA, USA., Walker K; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA., Neben CL; Color Health, Burlingame, CA, USA., Lockwood CM; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA., Empey PE; Department of Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA., Metcalf GA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA., Kachulis C; Broad Institute of MIT and Harvard, Cambridge, MA, USA., Mian S; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA., Musick A; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA., Rehm HL; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA., Harrison S; Broad Institute of MIT and Harvard, Cambridge, MA, USA., Gabriel S; Broad Institute of MIT and Harvard, Cambridge, MA, USA., Gibbs RA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA., Nickerson D; Department of Genome Sciences, University of Washington, Seattle, WA, USA., Zhou AY; Color Health, Burlingame, CA, USA., Doheny K; Center for Inherited Disease Research, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Ozenberger B; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA., Topper SE; Color Health, Burlingame, CA, USA., Lennon NJ; Broad Institute of MIT and Harvard, Cambridge, MA, USA. |
| Corporate Authors: | All of Us Research Program Regulatory Working Group |
| Source: | Genome medicine [Genome Med] 2022 Mar 28; Vol. 14 (1), pp. 34. Date of Electronic Publication: 2022 Mar 28. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 35346344 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Venner+E%22">Venner E</searchLink>; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA. venner@bcm.edu.<br /><searchLink fieldCode="AU" term="%22Muzny+D%22">Muzny D</searchLink>; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Smith+JD%22">Smith JD</searchLink>; Department of Genome Sciences, University of Washington, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Walker+K%22">Walker K</searchLink>; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Neben+CL%22">Neben CL</searchLink>; Color Health, Burlingame, CA, USA.<br /><searchLink fieldCode="AU" term="%22Lockwood+CM%22">Lockwood CM</searchLink>; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Empey+PE%22">Empey PE</searchLink>; Department of Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.<br /><searchLink fieldCode="AU" term="%22Metcalf+GA%22">Metcalf GA</searchLink>; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Kachulis+C%22">Kachulis C</searchLink>; Broad Institute of MIT and Harvard, Cambridge, MA, USA.<br /><searchLink fieldCode="AU" term="%22Mian+S%22">Mian S</searchLink>; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Musick+A%22">Musick A</searchLink>; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Rehm+HL%22">Rehm HL</searchLink>; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Harrison+S%22">Harrison S</searchLink>; Broad Institute of MIT and Harvard, Cambridge, MA, USA.<br /><searchLink fieldCode="AU" term="%22Gabriel+S%22">Gabriel S</searchLink>; Broad Institute of MIT and Harvard, Cambridge, MA, USA.<br /><searchLink fieldCode="AU" term="%22Gibbs+RA%22">Gibbs RA</searchLink>; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Nickerson+D%22">Nickerson D</searchLink>; Department of Genome Sciences, University of Washington, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Zhou+AY%22">Zhou AY</searchLink>; Color Health, Burlingame, CA, USA.<br /><searchLink fieldCode="AU" term="%22Doheny+K%22">Doheny K</searchLink>; Center for Inherited Disease Research, Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.<br /><searchLink fieldCode="AU" term="%22Ozenberger+B%22">Ozenberger B</searchLink>; NIH All of Us Research Program, National Institutes of Health Office of the Director, Bethesda, MD, USA.<br /><searchLink fieldCode="AU" term="%22Topper+SE%22">Topper SE</searchLink>; Color Health, Burlingame, CA, USA.<br /><searchLink fieldCode="AU" term="%22Lennon+NJ%22">Lennon NJ</searchLink>; Broad Institute of MIT and Harvard, Cambridge, MA, USA. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22All+of+Us+Research+Program+Regulatory+Working+Group%22">All of Us Research Program Regulatory Working Group</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101475844%22">Genome medicine</searchLink> [Genome Med] 2022 Mar 28; Vol. 14 (1), pp. 34. <i>Date of Electronic Publication: </i>2022 Mar 28. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101475844 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1756-994X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%221756994X%22">1756994X </searchLink><i>NLM ISO Abbreviation: </i>Genome Med <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=35346344 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13073-022-01031-z Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 34 Titles: – TitleFull: Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Venner E – PersonEntity: Name: NameFull: Muzny D – PersonEntity: Name: NameFull: Smith JD – PersonEntity: Name: NameFull: Walker K – PersonEntity: Name: NameFull: Neben CL – PersonEntity: Name: NameFull: Lockwood CM – PersonEntity: Name: NameFull: Empey PE – PersonEntity: Name: NameFull: Metcalf GA – PersonEntity: Name: NameFull: Kachulis C – PersonEntity: Name: NameFull: Mian S – PersonEntity: Name: NameFull: Musick A – PersonEntity: Name: NameFull: Rehm HL – PersonEntity: Name: NameFull: Harrison S – PersonEntity: Name: NameFull: Gabriel S – PersonEntity: Name: NameFull: Gibbs RA – PersonEntity: Name: NameFull: Nickerson D – PersonEntity: Name: NameFull: Zhou AY – PersonEntity: Name: NameFull: Doheny K – PersonEntity: Name: NameFull: Ozenberger B – PersonEntity: Name: NameFull: Topper SE – PersonEntity: Name: NameFull: Lennon NJ IsPartOfRelationships: – BibEntity: Dates: – D: 28 M: 03 Text: 2022 Mar 28 Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1756-994X Numbering: – Type: volume Value: 14 – Type: issue Value: 1 Titles: – TitleFull: Genome medicine Type: main |
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