CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
对大量精神分裂症样本进行的拷贝数变异（CNV）分析表明，16p12.1 和 SLC1A1 位点存在缺失，1p36.33 和 CGNL1 位点存在重复。
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddt540
Rees, Elliott; Walters, James T R; Chambert, Kimberly D; O'Dushlaine, Colm; Szatkiewicz, Jin; Richards, Alexander L; Georgieva, Lyudmila; Mahoney-Davies, Gerwyn; Legge, Sophie E; Moran, Jennifer L; Genovese, Giulio; Levinson, Douglas; Morris, Derek W; Cormican, Paul; Kendler, Kenneth S; O'Neill, Francis A; Riley, Brien; Gill, Michael; Corvin, Aiden; Sklar, Pamela; Hultman, Christina; Pato, Carlos; Pato, Michele; Sullivan, Patrick F; Gejman, Pablo V; McCarroll, Steven A; O'Donovan, Michael C; Owen, Michael J; Kirov, George
