Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing.
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| Title: | Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing. |
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| Authors: | Reuter CM; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Kohler JN; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Bonner D; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Zastrow D; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Fernandez L; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Dries A; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Marwaha S; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Davidson J; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA., Brokamp E; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN., Herzog M; Department of Human Genetics, University of California Los Angeles, Los Angeles, CA., Hong J; Department of Medicine, Brigham and Women's Hospital, Boston, MA., Macnamara E; Undiagnosed Diseases Program, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX., Schoch K; Department of Pediatrics, Duke University Medical Center, Durham, NC., Spillmann R; Department of Pediatrics, Duke University Medical Center, Durham, NC., Loscalzo J; Department of Medicine, Brigham and Women's Hospital, Boston, MA., Krier J; Department of Medicine, Brigham and Women's Hospital, Boston, MA., Stoler J; Division of Genetics, Boston Children's Hospital, Boston, MA., Sweetser D; Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA., Palmer CGS; Department of Human Genetics, University of California Los Angeles, Los Angeles, CA.; Psychiatry & Biobehavioral Sciences, University of California Los Angeles, Los Angeles, CA.; Institute for Society & Genetics, University of California Los Angeles, Los Angeles, CA., Phillips JA; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN., Shashi V; Department of Pediatrics, Duke University Medical Center, Durham, NC., Adams DA; Undiagnosed Diseases Program, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD., Yang Y; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX., Ashley EA; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.; Department of Genetics, Stanford University School of Medicine, Stanford, CA., Fisher PG; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA.; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA., Mulvihill JJ; Division of Genomic Medicine, National Human Genome Research Institute, Bethesda, MD., Bernstein JA; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA., Wheeler MT; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA. |
| Corporate Authors: | Undiagnosed Diseases Network |
| Source: | Journal of genetic counseling [J Genet Couns] 2019 Dec; Vol. 28 (6), pp. 1107-1118. Date of Electronic Publication: 2019 Sep 03. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Wiley Country of Publication: United States NLM ID: 9206865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-3599 (Electronic) Linking ISSN: 10597700 NLM ISO Abbreviation: J Genet Couns Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 31478310 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Reuter+CM%22">Reuter CM</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Kohler+JN%22">Kohler JN</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Bonner+D%22">Bonner D</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Zastrow+D%22">Zastrow D</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Fernandez+L%22">Fernandez L</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Dries+A%22">Dries A</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Marwaha+S%22">Marwaha S</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Davidson+J%22">Davidson J</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Brokamp+E%22">Brokamp E</searchLink>; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN.<br /><searchLink fieldCode="AU" term="%22Herzog+M%22">Herzog M</searchLink>; Department of Human Genetics, University of California Los Angeles, Los Angeles, CA.<br /><searchLink fieldCode="AU" term="%22Hong+J%22">Hong J</searchLink>; Department of Medicine, Brigham and Women's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Macnamara+E%22">Macnamara E</searchLink>; Undiagnosed Diseases Program, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD.<br /><searchLink fieldCode="AU" term="%22Rosenfeld+JA%22">Rosenfeld JA</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.<br /><searchLink fieldCode="AU" term="%22Schoch+K%22">Schoch K</searchLink>; Department of Pediatrics, Duke University Medical Center, Durham, NC.<br /><searchLink fieldCode="AU" term="%22Spillmann+R%22">Spillmann R</searchLink>; Department of Pediatrics, Duke University Medical Center, Durham, NC.<br /><searchLink fieldCode="AU" term="%22Loscalzo+J%22">Loscalzo J</searchLink>; Department of Medicine, Brigham and Women's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Krier+J%22">Krier J</searchLink>; Department of Medicine, Brigham and Women's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Stoler+J%22">Stoler J</searchLink>; Division of Genetics, Boston Children's Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Sweetser+D%22">Sweetser D</searchLink>; Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, MA.<br /><searchLink fieldCode="AU" term="%22Palmer+CGS%22">Palmer CGS</searchLink>; Department of Human Genetics, University of California Los Angeles, Los Angeles, CA.; 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Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA.; Department of Genetics, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Fisher+PG%22">Fisher PG</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA.; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Mulvihill+JJ%22">Mulvihill JJ</searchLink>; Division of Genomic Medicine, National Human Genome Research Institute, Bethesda, MD.<br /><searchLink fieldCode="AU" term="%22Bernstein+JA%22">Bernstein JA</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA.<br /><searchLink fieldCode="AU" term="%22Wheeler+MT%22">Wheeler MT</searchLink>; Center for Undiagnosed Diseases, Stanford University School of Medicine, Stanford, CA.; Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22Undiagnosed+Diseases+Network%22">Undiagnosed Diseases Network</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229206865%22">Journal of genetic counseling</searchLink> [J Genet Couns] 2019 Dec; Vol. 28 (6), pp. 1107-1118. <i>Date of Electronic Publication: </i>2019 Sep 03. – 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="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9206865 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1573-3599 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597700%22">10597700 </searchLink><i>NLM ISO Abbreviation: </i>J Genet Couns <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=31478310 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/jgc4.1161 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1107 Titles: – TitleFull: Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Reuter CM – PersonEntity: Name: NameFull: Kohler JN – PersonEntity: Name: NameFull: Bonner D – PersonEntity: Name: NameFull: Zastrow D – PersonEntity: Name: NameFull: Fernandez L – PersonEntity: Name: NameFull: Dries A – PersonEntity: Name: NameFull: Marwaha S – PersonEntity: Name: NameFull: Davidson J – PersonEntity: Name: NameFull: Brokamp E – PersonEntity: Name: NameFull: Herzog M – PersonEntity: Name: NameFull: Hong J – PersonEntity: Name: NameFull: Macnamara E – PersonEntity: Name: NameFull: Rosenfeld JA – PersonEntity: Name: NameFull: Schoch K – PersonEntity: Name: NameFull: Spillmann R – PersonEntity: Name: NameFull: Loscalzo J – PersonEntity: Name: NameFull: Krier J – PersonEntity: Name: NameFull: Stoler J – PersonEntity: Name: NameFull: Sweetser D – PersonEntity: Name: NameFull: Palmer CGS – PersonEntity: Name: NameFull: Phillips JA – PersonEntity: Name: NameFull: Shashi V – PersonEntity: Name: NameFull: Adams DA – PersonEntity: Name: NameFull: Yang Y – PersonEntity: Name: NameFull: Ashley EA – PersonEntity: Name: NameFull: Fisher PG – PersonEntity: Name: NameFull: Mulvihill JJ – PersonEntity: Name: NameFull: Bernstein JA – PersonEntity: Name: NameFull: Wheeler MT IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2019 Dec Type: published Y: 2019 Identifiers: – Type: issn-electronic Value: 1573-3599 Numbering: – Type: volume Value: 28 – Type: issue Value: 6 Titles: – TitleFull: Journal of genetic counseling Type: main |
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