CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
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2014Access:
openAccessCitation:
Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Sklar P, Hultman C, Pato C, Pato M, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1., Human molecular genetics, 23, 6, 2014, 1669-1676Download Item:
ddt540.pdf (Published (author's copy) - Peer Reviewed) 196.0Kb
Sponsor
Grant Number
European Union Framework Programme 7 (FP7)
HEALTH-F2-2010-241909 (Project EU-GEI)
Medical Research Council (MRC)
G0801418
Medical Research Council (MRC)
G0800509
Wellcome Trust
Author's Homepage:
http://people.tcd.ie/acorvinhttp://people.tcd.ie/morrisdw
http://people.tcd.ie/mgill
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PUBLISHEDType of material:
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Human molecular genetics23
6
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Full text availableKeywords:
schizophrenia, geneticsSubject (TCD):
Genes & Society , NeuroscienceDOI:
http://dx.doi.org/10.1093/hmg/ddt540Licences: