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Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.

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Title: Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.
Authors: Ben-David E; Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem,Edmond J. Safra campus, Jerusalem 91904, Israel., Granot-Hershkovitz E, Monderer-Rothkoff G, Lerer E, Levi S, Yaari M, Ebstein RP, Yirmiya N, Shifman S
Source: Human molecular genetics [Hum Mol Genet] 2011 Sep 15; Vol. 20 (18), pp. 3632-41. Date of Electronic Publication: 2011 Jun 16.
Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.
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  Data: <searchLink fieldCode="AU" term="%22Ben-David+E%22">Ben-David E</searchLink>; Department of Genetics, The Institute of Life Sciences, The Hebrew University of Jerusalem,Edmond J. Safra campus, Jerusalem 91904, Israel.<br /><searchLink fieldCode="AU" term="%22Granot-Hershkovitz+E%22">Granot-Hershkovitz E</searchLink><br /><searchLink fieldCode="AU" term="%22Monderer-Rothkoff+G%22">Monderer-Rothkoff G</searchLink><br /><searchLink fieldCode="AU" term="%22Lerer+E%22">Lerer E</searchLink><br /><searchLink fieldCode="AU" term="%22Levi+S%22">Levi S</searchLink><br /><searchLink fieldCode="AU" term="%22Yaari+M%22">Yaari M</searchLink><br /><searchLink fieldCode="AU" term="%22Ebstein+RP%22">Ebstein RP</searchLink><br /><searchLink fieldCode="AU" term="%22Yirmiya+N%22">Yirmiya N</searchLink><br /><searchLink fieldCode="AU" term="%22Shifman+S%22">Shifman S</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2011 Sep 15; Vol. 20 (18), pp. 3632-41. <i>Date of Electronic Publication: </i>2011 Jun 16.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1093/hmg/ddr283
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              Text: 2011 Sep 15
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