Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia.
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| Title: | Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. |
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| Authors: | Al Eissa MM; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Fiorentino A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.; Current address: Institute of Opthalmology, University College London, London, UK., Sharp SI; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., O'Brien NL; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Wolfe K; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Giaroli G; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., Curtis D; University College London Genetics Institute, University College London, London, UK., Bass NJ; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK., McQuillin A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK. |
| Source: | Annals of human genetics [Ann Hum Genet] 2018 Mar; Vol. 82 (2), pp. 88-92. Date of Electronic Publication: 2017 Nov 17. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0416661 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-1809 (Electronic) Linking ISSN: 00034800 NLM ISO Abbreviation: Ann Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 29148569 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Al+Eissa+MM%22">Al Eissa MM</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Fiorentino+A%22">Fiorentino A</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.; Current address: Institute of Opthalmology, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Sharp+SI%22">Sharp SI</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22O'Brien+NL%22">O'Brien NL</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Wolfe+K%22">Wolfe K</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Giaroli+G%22">Giaroli G</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Curtis+D%22">Curtis D</searchLink>; University College London Genetics Institute, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Bass+NJ%22">Bass NJ</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK.<br /><searchLink fieldCode="AU" term="%22McQuillin+A%22">McQuillin A</searchLink>; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220416661%22">Annals of human genetics</searchLink> [Ann Hum Genet] 2018 Mar; Vol. 82 (2), pp. 88-92. <i>Date of Electronic Publication: </i>2017 Nov 17. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>0416661 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1469-1809 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200034800%22">00034800 </searchLink><i>NLM ISO Abbreviation: </i>Ann Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29148569 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/ahg.12226 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 88 Titles: – TitleFull: Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Al Eissa MM – PersonEntity: Name: NameFull: Fiorentino A – PersonEntity: Name: NameFull: Sharp SI – PersonEntity: Name: NameFull: O'Brien NL – PersonEntity: Name: NameFull: Wolfe K – PersonEntity: Name: NameFull: Giaroli G – PersonEntity: Name: NameFull: Curtis D – PersonEntity: Name: NameFull: Bass NJ – PersonEntity: Name: NameFull: McQuillin A IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2018 Mar Type: published Y: 2018 Identifiers: – Type: issn-electronic Value: 1469-1809 Numbering: – Type: volume Value: 82 – Type: issue Value: 2 Titles: – TitleFull: Annals of human genetics Type: main |
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