Reader, Rose H
223  Ergebnisse:
Personensuche X
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Genome-wide analysis identifies a role for common copy numb..:

the SLI Consortium ; Simpson, Nuala H ; Ceroni, Fabiola...
European Journal of Human Genetics.  23 (2015)  10 - p. 1370-1377 , 2015
 
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6

Genome-Wide Studies of Specific Language Impairment:

Reader, Rose H. ; Covill, Laura E. ; Nudel, Ron.
Current Behavioral Neuroscience Reports.  1 (2014)  4 - p. 242-250 , 2014
 
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8

Next-generation DNA sequencing identifies novel gene varian..:

Chen, Xiaowei Sylvia ; Reader, Rose H ; Hoischen, Alexander...
Chen , X S , Reader , R H , Hoischen , A , Veltman , J A , Simpson , N H , Francks , C , Newbury , D F & Fisher , S E 2017 , ' Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment ' , Scientific Reports , vol. 7 , 46105 . https://doi.org/10.1038/srep46105.  , 2017
 
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Genome-wide analysis identifies a role for common copy numb..:

Simpson, Nuala H ; Ceroni, Fabiola ; Reader, Rose H...
Simpson , N H , Ceroni , F , Reader , R H , Covill , L E , Knight , J C , Hennessy , E R , Bolton , P F , Conti-Ramsden , G , O'Hare , A , Baird , G , Fisher , S E , Newbury , D F , Nudel , R , Monaco , A P , Simonoff , E , Bolton , P F , Pickles , A , Slonims , V , Dworzynski , K , Everitt , A , Clark , A , Watson , J , Seckl , J , Cowie , H , Cohen , W , Nasir , J , Bishop , D V M & Simkin , Z 2015 , ' Genome-wide analysis identifies a role for common copy number variants in specific language impairment ' , European journal of human genetics : EJHG , vol. 23 , no. 10 , pp. 1370-1377 . https://doi.org/10.1038/ejhg.2014.296.  , 2015
 
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14

Genome-wide analysis identifies a role for common copy numb..:

Simpson, Nuala H ; Ceroni, Fabiola ; Reader, Rose H...
Simpson , N H , Ceroni , F , Reader , R H , Covill , L E , Knight , J C , Hennessy , E R , Bolton , P F , Conti-Ramsden , G , O'Hare , A , Baird , G , Fisher , S E , Newbury , D F , Nudel , R , Monaco , A P , Simonoff , E , Bolton , P F , Pickles , A , Slonims , V , Dworzynski , K , Everitt , A , Clark , A , Watson , J , Seckl , J , Cowie , H , Cohen , W , Nasir , J , Bishop , D V M & Simkin , Z 2015 , ' Genome-wide analysis identifies a role for common copy number variants in specific language impairment ' , European journal of human genetics : EJHG , vol. 23 , no. 10 , pp. 1370-1377 . https://doi.org/10.1038/ejhg.2014.296.  , 2015
 
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15

Exome Sequencing in an Admixed Isolated Population Indicate..:

Villanueva, Pía ; Nudel, Ron ; Hoischen, Alexander...
Villanueva , P , Nudel , R , Hoischen , A , Fernández , M A , Simpson , N H , Gilissen , C , Reader , R H , Jara , L , Echeverry , M M , Francks , C , Baird , G , Conti-Ramsden , G , O'Hare , A , Bolton , P F , Hennessy , E R , Palomino , H , Carvajal-Carmona , L , Veltman , J A , Cazier , J B , De Barbieri , Z , Fisher , S E , Newbury , D F , Slonims , V , Clark , A , Watson , J , Simonoff , E , Pickles , A , Everitt , A , Seckl , J , Cowie , H , Cohen , W , Nasir , J , Bishop , D V M & Simkin , Z 2015 , ' Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment ' , PL o S Genetics , vol. 11 , no. 3 , e1004925 . https://doi.org/10.1371/journal.pgen.1004925.  , 2015
 
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