Detalhe da pesquisa
1.
Evaluation of polygenic risks for narcolepsy and essential hypersomnia.
J Hum Genet
; 61(10): 873-878, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27305985
2.
Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population.
J Hum Genet
; 55(3): 137-41, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20094064
3.
Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene.
Int J Neuropsychopharmacol
; 13(4): 443-9, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19895723
4.
Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.
BMC Med Genomics
; 13(1): 55, 2020 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32223758
5.
No association between the neuronal pentraxin II gene polymorphism and autism.
Prog Neuropsychopharmacol Biol Psychiatry
; 31(4): 940-3, 2007 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-17408830
6.
Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study.
Brain Dev
; 29(8): 510-3, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17376622
7.
Erratum: Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals.
Hum Genome Var
; 3: 15046, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27082423
8.
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Autism Res
; 9(3): 340-9, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26314684
9.
Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals.
Hum Genome Var
; 2: 15024, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-27081536
10.
Impaired prefrontal hemodynamic maturation in autism and unaffected siblings.
PLoS One
; 4(9): e6881, 2009 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-19727389
11.
Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism.
Int J Neuropsychopharmacol
; 12(1): 1-10, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18664314