Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.
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| Title: | Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. |
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| Authors: | Adams AK; Department of Genetics, Yale University, New Haven, CT, USA., Smith SD; Munroe Meyer Institute, University of Nebraska Medical Center, Omaha, NE, USA., Truong DT; Department of Pediatrics, Yale University, New Haven, CT, USA., Willcutt EG; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA., Olson RK; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA., DeFries JC; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA., Pennington BF; Department of Psychology, University of Denver, Denver, CO, USA., Gruen JR; Department of Genetics, Yale University, New Haven, CT, USA. jeffrey.gruen@yale.edu.; Department of Pediatrics and the Investigative Medicine Program, Yale University, New Haven, CT, USA. jeffrey.gruen@yale.edu. |
| Source: | Human genetics [Hum Genet] 2017 Nov; Vol. 136 (11-12), pp. 1395-1405. Date of Electronic Publication: 2017 Sep 02. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 28866788 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Adams+AK%22">Adams AK</searchLink>; Department of Genetics, Yale University, New Haven, CT, USA.<br /><searchLink fieldCode="AU" term="%22Smith+SD%22">Smith SD</searchLink>; Munroe Meyer Institute, University of Nebraska Medical Center, Omaha, NE, USA.<br /><searchLink fieldCode="AU" term="%22Truong+DT%22">Truong DT</searchLink>; Department of Pediatrics, Yale University, New Haven, CT, USA.<br /><searchLink fieldCode="AU" term="%22Willcutt+EG%22">Willcutt EG</searchLink>; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.<br /><searchLink fieldCode="AU" term="%22Olson+RK%22">Olson RK</searchLink>; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.<br /><searchLink fieldCode="AU" term="%22DeFries+JC%22">DeFries JC</searchLink>; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.<br /><searchLink fieldCode="AU" term="%22Pennington+BF%22">Pennington BF</searchLink>; Department of Psychology, University of Denver, Denver, CO, USA.<br /><searchLink fieldCode="AU" term="%22Gruen+JR%22">Gruen JR</searchLink>; Department of Genetics, Yale University, New Haven, CT, USA. jeffrey.gruen@yale.edu.; Department of Pediatrics and the Investigative Medicine Program, Yale University, New Haven, CT, USA. jeffrey.gruen@yale.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227613873%22">Human genetics</searchLink> [Hum Genet] 2017 Nov; Vol. 136 (11-12), pp. 1395-1405. <i>Date of Electronic Publication: </i>2017 Sep 02. – 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="%22Springer+Verlag%22">Springer Verlag </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>7613873 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-1203 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203406717%22">03406717 </searchLink><i>NLM ISO Abbreviation: </i>Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=28866788 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00439-017-1838-z Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1395 Titles: – TitleFull: Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Adams AK – PersonEntity: Name: NameFull: Smith SD – PersonEntity: Name: NameFull: Truong DT – PersonEntity: Name: NameFull: Willcutt EG – PersonEntity: Name: NameFull: Olson RK – PersonEntity: Name: NameFull: DeFries JC – PersonEntity: Name: NameFull: Pennington BF – PersonEntity: Name: NameFull: Gruen JR IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: 2017 Nov Type: published Y: 2017 Identifiers: – Type: issn-electronic Value: 1432-1203 Numbering: – Type: volume Value: 136 – Type: issue Value: 11-12 Titles: – TitleFull: Human genetics Type: main |
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