Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
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| Title: | Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. |
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| Authors: | Villanueva P; Human Genetics Program, Institute of Biomedical Sciences (ICBM), Faculty of Medicine, University of Chile, Santiago, Chile; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile; Department of Child and Dental Maxillary Orthopedics, Faculty of Dentistry, University of Chile, Santiago, Chile; Doctoral Program of Psychology, Graduate School, University of Granada, Granada, Spain., Nudel R; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Hoischen A; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands., Fernández MA; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile., Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Gilissen C; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands., Reader RH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom., Jara L; Human Genetics Program, Institute of Biomedical Sciences (ICBM), Faculty of Medicine, University of Chile, Santiago, Chile., Echeverry MM; Grupo de Citogenetica, Filogenia y Evolucion de las Poblaciones, Facultades de Ciencias y de Ciencias de la Salud, Universidad del Tolima, Ibague, Colombia., Francks C; Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands., Baird G; Newcomen Centre, the Evelina Children's Hospital, London, United Kingdom., Conti-Ramsden G; School of Psychological Sciences, University of Manchester, Manchester, United Kingdom., O'Hare A; Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh, United Kingdom., Bolton PF; Departments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom., Hennessy ER; University Child Health and DMDE, University of Aberdeen, Aberdeen, United Kingdom., Palomino H; Department of Child and Dental Maxillary Orthopedics, Faculty of Dentistry, University of Chile, Santiago, Chile., Carvajal-Carmona L; Grupo de Citogenetica, Filogenia y Evolucion de las Poblaciones, Facultades de Ciencias y de Ciencias de la Salud, Universidad del Tolima, Ibague, Colombia; UC Davis Genome Center, Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Davis, California, United States of America., Veltman JA; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands., Cazier JB; Department of Oncology, University of Oxford, Oxford, United Kingdom; Centre for Computational Biology, University of Birmingham, Edgbaston, United Kingdom., De Barbieri Z; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile., Fisher SE; Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom; St Johns College, University of Oxford, Oxford, United Kingdom. |
| Corporate Authors: | SLI Consortium |
| Source: | PLoS genetics [PLoS Genet] 2015 Mar 17; Vol. 11 (3), pp. e1004925. Date of Electronic Publication: 2015 Mar 17 (Print Publication: 2015). |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 25781923 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Villanueva+P%22">Villanueva P</searchLink>; Human Genetics Program, Institute of Biomedical Sciences (ICBM), Faculty of Medicine, University of Chile, Santiago, Chile; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile; Department of Child and Dental Maxillary Orthopedics, Faculty of Dentistry, University of Chile, Santiago, Chile; Doctoral Program of Psychology, Graduate School, University of Granada, Granada, Spain.<br /><searchLink fieldCode="AU" term="%22Nudel+R%22">Nudel R</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hoischen+A%22">Hoischen A</searchLink>; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Fernández+MA%22">Fernández MA</searchLink>; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Simpson+NH%22">Simpson NH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Gilissen+C%22">Gilissen C</searchLink>; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Reader+RH%22">Reader RH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Jara+L%22">Jara L</searchLink>; Human Genetics Program, Institute of Biomedical Sciences (ICBM), Faculty of Medicine, University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Echeverry+MM%22">Echeverry MM</searchLink>; Grupo de Citogenetica, Filogenia y Evolucion de las Poblaciones, Facultades de Ciencias y de Ciencias de la Salud, Universidad del Tolima, Ibague, Colombia.<br /><searchLink fieldCode="AU" term="%22Francks+C%22">Francks C</searchLink>; Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Baird+G%22">Baird G</searchLink>; Newcomen Centre, the Evelina Children's Hospital, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Conti-Ramsden+G%22">Conti-Ramsden G</searchLink>; School of Psychological Sciences, University of Manchester, Manchester, United Kingdom.<br /><searchLink fieldCode="AU" term="%22O'Hare+A%22">O'Hare A</searchLink>; Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Bolton+PF%22">Bolton PF</searchLink>; Departments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Hennessy+ER%22">Hennessy ER</searchLink>; University Child Health and DMDE, University of Aberdeen, Aberdeen, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Palomino+H%22">Palomino H</searchLink>; Department of Child and Dental Maxillary Orthopedics, Faculty of Dentistry, University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Carvajal-Carmona+L%22">Carvajal-Carmona L</searchLink>; Grupo de Citogenetica, Filogenia y Evolucion de las Poblaciones, Facultades de Ciencias y de Ciencias de la Salud, Universidad del Tolima, Ibague, Colombia; UC Davis Genome Center, Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Davis, California, United States of America.<br /><searchLink fieldCode="AU" term="%22Veltman+JA%22">Veltman JA</searchLink>; Department of Human Genetics, Radboud Institute for Molecular Life Sciences and Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Cazier+JB%22">Cazier JB</searchLink>; Department of Oncology, University of Oxford, Oxford, United Kingdom; Centre for Computational Biology, University of Birmingham, Edgbaston, United Kingdom.<br /><searchLink fieldCode="AU" term="%22De+Barbieri+Z%22">De Barbieri Z</searchLink>; School of Speech and Hearing Therapy, Faculty of Medicine, University of Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Fisher+SE%22">Fisher SE</searchLink>; Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands.<br /><searchLink fieldCode="AU" term="%22Newbury+DF%22">Newbury DF</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom; St Johns College, University of Oxford, Oxford, United Kingdom. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22SLI+Consortium%22">SLI Consortium</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101239074%22">PLoS genetics</searchLink> [PLoS Genet] 2015 Mar 17; Vol. 11 (3), pp. e1004925. <i>Date of Electronic Publication: </i>2015 Mar 17 (<i>Print Publication: </i>2015). – 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="%22Public+Library+of+Science%22">Public Library of Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101239074 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1553-7404 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215537390%22">15537390 </searchLink><i>NLM ISO Abbreviation: </i>PLoS Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=25781923 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1371/journal.pgen.1004925 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e1004925 Titles: – TitleFull: Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Villanueva P – PersonEntity: Name: NameFull: Nudel R – PersonEntity: Name: NameFull: Hoischen A – PersonEntity: Name: NameFull: Fernández MA – PersonEntity: Name: NameFull: Simpson NH – PersonEntity: Name: NameFull: Gilissen C – PersonEntity: Name: NameFull: Reader RH – PersonEntity: Name: NameFull: Jara L – PersonEntity: Name: NameFull: Echeverry MM – PersonEntity: Name: NameFull: Francks C – PersonEntity: Name: NameFull: Baird G – PersonEntity: Name: NameFull: Conti-Ramsden G – PersonEntity: Name: NameFull: O'Hare A – PersonEntity: Name: NameFull: Bolton PF – PersonEntity: Name: NameFull: Hennessy ER – PersonEntity: Name: NameFull: Palomino H – PersonEntity: Name: NameFull: Carvajal-Carmona L – PersonEntity: Name: NameFull: Veltman JA – PersonEntity: Name: NameFull: Cazier JB – PersonEntity: Name: NameFull: De Barbieri Z – PersonEntity: Name: NameFull: Fisher SE – PersonEntity: Name: NameFull: Newbury DF IsPartOfRelationships: – BibEntity: Dates: – D: 17 M: 03 Text: 2015 Mar 17 Type: published Y: 2015 Identifiers: – Type: issn-electronic Value: 1553-7404 Numbering: – Type: volume Value: 11 – Type: issue Value: 3 Titles: – TitleFull: PLoS genetics Type: main |
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