Detalhe da pesquisa
1.
A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
Am J Med Genet B Neuropsychiatr Genet
; 165B(8): 619-26, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25228354
2.
Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2-p12.1 and two large chromosomal abnormalities at 16q22.3-q24.3 and Xq23-q28.
Clin Case Rep
; 3(4): 201-7, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25914809
3.
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism.
Psychiatr Genet
; 22(3): 137-40, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22157634
4.
Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia.
Arch Gen Psychiatry
; 69(9): 885-92, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22945618