Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.

Saved in:
Bibliographic Details
Title: Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Authors: Addis L; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK., Ahn JW; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK., Dobson R; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Dixit A; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Ogilvie CM; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK., Pinto D; Departments of Psychiatry, and Genetics and Genomic Sciences, Seaver Autism Center, The Mindich Child Health & Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York., Vaags AK; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada., Coon H; Department of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah., Chaste P; Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania., Wilson S; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.; School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia, Australia., Parr JR; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Andrieux J; Institut de Génétique Médicale, Hopital Jeanne de Flandre, CHRU de Lille, France., Lenne B; Centre de Génétique Chromosomique, GHICL, Hôpital Saint Vincent de Paul, Lille, France., Tumer Z; Applied Human Molecular Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark., Leuzzi V; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza Università di Roma, Rome, Italy., Aubell K; Institute of Human Genetics, Medical University of Graz, Graz, Austria., Koillinen H; Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland., Curran S; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK., Marshall CR; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada., Scherer SW; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.; McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada., Strug LJ; Program in Genetics and Genome Biology, The Hospital for Sick Children, Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada., Collier DA; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK.; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK., Pal DK; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Source: Human mutation [Hum Mutat] 2015 Sep; Vol. 36 (9), pp. 842-50. Date of Electronic Publication: 2015 Jun 30.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 26010655
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Addis+L%22">Addis L</searchLink>; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK.<br /><searchLink fieldCode="AU" term="%22Ahn+JW%22">Ahn JW</searchLink>; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.<br /><searchLink fieldCode="AU" term="%22Dobson+R%22">Dobson R</searchLink>; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Dixit+A%22">Dixit A</searchLink>; Department of Biostatistics and NIHR BRC for Mental Health, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Ogilvie+CM%22">Ogilvie CM</searchLink>; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.<br /><searchLink fieldCode="AU" term="%22Pinto+D%22">Pinto D</searchLink>; Departments of Psychiatry, and Genetics and Genomic Sciences, Seaver Autism Center, The Mindich Child Health & Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York.<br /><searchLink fieldCode="AU" term="%22Vaags+AK%22">Vaags AK</searchLink>; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Coon+H%22">Coon H</searchLink>; Department of Psychiatry, University of Utah School of Medicine, Salt Lake City, Utah.<br /><searchLink fieldCode="AU" term="%22Chaste+P%22">Chaste P</searchLink>; Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.<br /><searchLink fieldCode="AU" term="%22Wilson+S%22">Wilson S</searchLink>; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia.; School of Medicine and Pharmacology, University of Western Australia, Nedlands, Western Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Parr+JR%22">Parr JR</searchLink>; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.<br /><searchLink fieldCode="AU" term="%22Andrieux+J%22">Andrieux J</searchLink>; Institut de Génétique Médicale, Hopital Jeanne de Flandre, CHRU de Lille, France.<br /><searchLink fieldCode="AU" term="%22Lenne+B%22">Lenne B</searchLink>; Centre de Génétique Chromosomique, GHICL, Hôpital Saint Vincent de Paul, Lille, France.<br /><searchLink fieldCode="AU" term="%22Tumer+Z%22">Tumer Z</searchLink>; Applied Human Molecular Genetics, Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.<br /><searchLink fieldCode="AU" term="%22Leuzzi+V%22">Leuzzi V</searchLink>; Department of Pediatrics, Child Neurology and Psychiatry, Sapienza Università di Roma, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Aubell+K%22">Aubell K</searchLink>; Institute of Human Genetics, Medical University of Graz, Graz, Austria.<br /><searchLink fieldCode="AU" term="%22Koillinen+H%22">Koillinen H</searchLink>; Department of Clinical Genetics, Helsinki University Hospital, Helsinki, Finland.<br /><searchLink fieldCode="AU" term="%22Curran+S%22">Curran S</searchLink>; Department of Cytogenetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.<br /><searchLink fieldCode="AU" term="%22Marshall+CR%22">Marshall CR</searchLink>; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.; Department of Molecular Genetics, Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Scherer+SW%22">Scherer SW</searchLink>; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.; McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Strug+LJ%22">Strug LJ</searchLink>; Program in Genetics and Genome Biology, The Hospital for Sick Children, Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Collier+DA%22">Collier DA</searchLink>; Neuroscience Discovery Research, Eli Lilly and Company, Erl Wood, Surrey, UK.; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Pal+DK%22">Pal DK</searchLink>; Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2015 Sep; Vol. 36 (9), pp. 842-50. <i>Date of Electronic Publication: </i>2015 Jun 30.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, Non-U.S. Gov't
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26010655
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/humu.22816
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 842
    Titles:
      – TitleFull: Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Addis L
      – PersonEntity:
          Name:
            NameFull: Ahn JW
      – PersonEntity:
          Name:
            NameFull: Dobson R
      – PersonEntity:
          Name:
            NameFull: Dixit A
      – PersonEntity:
          Name:
            NameFull: Ogilvie CM
      – PersonEntity:
          Name:
            NameFull: Pinto D
      – PersonEntity:
          Name:
            NameFull: Vaags AK
      – PersonEntity:
          Name:
            NameFull: Coon H
      – PersonEntity:
          Name:
            NameFull: Chaste P
      – PersonEntity:
          Name:
            NameFull: Wilson S
      – PersonEntity:
          Name:
            NameFull: Parr JR
      – PersonEntity:
          Name:
            NameFull: Andrieux J
      – PersonEntity:
          Name:
            NameFull: Lenne B
      – PersonEntity:
          Name:
            NameFull: Tumer Z
      – PersonEntity:
          Name:
            NameFull: Leuzzi V
      – PersonEntity:
          Name:
            NameFull: Aubell K
      – PersonEntity:
          Name:
            NameFull: Koillinen H
      – PersonEntity:
          Name:
            NameFull: Curran S
      – PersonEntity:
          Name:
            NameFull: Marshall CR
      – PersonEntity:
          Name:
            NameFull: Scherer SW
      – PersonEntity:
          Name:
            NameFull: Strug LJ
      – PersonEntity:
          Name:
            NameFull: Collier DA
      – PersonEntity:
          Name:
            NameFull: Pal DK
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 09
              Text: 2015 Sep
              Type: published
              Y: 2015
          Identifiers:
            – Type: issn-electronic
              Value: 1098-1004
          Numbering:
            – Type: volume
              Value: 36
            – Type: issue
              Value: 9
          Titles:
            – TitleFull: Human mutation
              Type: main
ResultId 1