Structural Variants May Be a Source of Missing Heritability in sALS.

Saved in:
Bibliographic Details
Title: Structural Variants May Be a Source of Missing Heritability in sALS.
Authors: Theunissen F; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Human Sciences, University of Western Australia, Nedlands, WA, Australia., Flynn LL; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia., Anderton RS; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; School of Health Sciences, Institute for Health Research, University of Notre Dame Australia, Fremantle, WA, Australia., Mastaglia F; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia., Pytte J; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Human Sciences, University of Western Australia, Nedlands, WA, Australia., Jiang L; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Biological Sciences, University of Western Australia, Nedlands, WA, Australia., Hodgetts S; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Human Sciences, University of Western Australia, Nedlands, WA, Australia., Burns DK; Zinfandel Pharmaceuticals, Chapel Hill, NC, United States., Saunders A; Zinfandel Pharmaceuticals, Chapel Hill, NC, United States., Fletcher S; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia., Wilton SD; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia., Akkari PA; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia.
Source: Frontiers in neuroscience [Front Neurosci] 2020 Jan 31; Vol. 14, pp. 47. Date of Electronic Publication: 2020 Jan 31 (Print Publication: 2020).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101478481 Publication Model: eCollection Cited Medium: Print ISSN: 1662-4548 (Print) Linking ISSN: 1662453X NLM ISO Abbreviation: Front Neurosci Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 32082115
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Structural Variants May Be a Source of Missing Heritability in sALS.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Theunissen+F%22">Theunissen F</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Human Sciences, University of Western Australia, Nedlands, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Flynn+LL%22">Flynn LL</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Anderton+RS%22">Anderton RS</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; School of Health Sciences, Institute for Health Research, University of Notre Dame Australia, Fremantle, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Mastaglia+F%22">Mastaglia F</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Pytte+J%22">Pytte J</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Human Sciences, University of Western Australia, Nedlands, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Jiang+L%22">Jiang L</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Biological Sciences, University of Western Australia, Nedlands, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Hodgetts+S%22">Hodgetts S</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; School of Human Sciences, University of Western Australia, Nedlands, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Burns+DK%22">Burns DK</searchLink>; Zinfandel Pharmaceuticals, Chapel Hill, NC, United States.<br /><searchLink fieldCode="AU" term="%22Saunders+A%22">Saunders A</searchLink>; Zinfandel Pharmaceuticals, Chapel Hill, NC, United States.<br /><searchLink fieldCode="AU" term="%22Fletcher+S%22">Fletcher S</searchLink>; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Wilton+SD%22">Wilton SD</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia.<br /><searchLink fieldCode="AU" term="%22Akkari+PA%22">Akkari PA</searchLink>; Perron Institute for Neurological and Translational Science, Nedlands, WA, Australia.; Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, WA, Australia.; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, WA, Australia.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%22101478481%22">Frontiers in neuroscience</searchLink> [Front Neurosci] 2020 Jan 31; Vol. 14, pp. 47. <i>Date of Electronic Publication: </i>2020 Jan 31 (<i>Print Publication: </i>2020).
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation%22">Frontiers Research Foundation </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101478481 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>1662-4548 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%221662453X%22">1662453X </searchLink><i>NLM ISO Abbreviation: </i>Front Neurosci <i>Subsets: </i>PubMed not MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32082115
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.3389/fnins.2020.00047
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 47
    Titles:
      – TitleFull: Structural Variants May Be a Source of Missing Heritability in sALS.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Theunissen F
      – PersonEntity:
          Name:
            NameFull: Flynn LL
      – PersonEntity:
          Name:
            NameFull: Anderton RS
      – PersonEntity:
          Name:
            NameFull: Mastaglia F
      – PersonEntity:
          Name:
            NameFull: Pytte J
      – PersonEntity:
          Name:
            NameFull: Jiang L
      – PersonEntity:
          Name:
            NameFull: Hodgetts S
      – PersonEntity:
          Name:
            NameFull: Burns DK
      – PersonEntity:
          Name:
            NameFull: Saunders A
      – PersonEntity:
          Name:
            NameFull: Fletcher S
      – PersonEntity:
          Name:
            NameFull: Wilton SD
      – PersonEntity:
          Name:
            NameFull: Akkari PA
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 31
              M: 01
              Text: 2020 Jan 31
              Type: published
              Y: 2020
          Identifiers:
            – Type: issn-print
              Value: 1662-4548
          Numbering:
            – Type: volume
              Value: 14
          Titles:
            – TitleFull: Frontiers in neuroscience
              Type: main
ResultId 1