Detalhe da pesquisa
1.
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes
J Psychiatry Neurosci
; 44(5): 350-359, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31094488
2.
The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction and related behavioral traits.
Front Psychiatry
; 14: 1293663, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937232
3.
Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders.
Transl Psychiatry
; 12(1): 11, 2022 01 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35013130
4.
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention.
Genes (Basel)
; 13(1)2021 12 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35052433
5.
Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures.
Neuropsychopharmacology
; 45(7): 1188-1195, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31896117
6.
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses.
J Clin Med
; 9(6)2020 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32545830
7.
Lack of replication of previous autism spectrum disorder GWAS hits in European populations.
Autism Res
; 10(2): 202-211, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27417655
8.
A Highly Polymorphic Copy Number Variant in the NSF Gene is Associated with Cocaine Dependence.
Sci Rep
; 6: 31033, 2016 08 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27498889
9.
Common and rare variants of microRNA genes in autism spectrum disorders.
World J Biol Psychiatry
; 16(6): 376-386, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25903372
10.
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.
Eur J Hum Genet
; 23(12): 1694-701, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25782667
11.
Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.
Psychiatr Genet
; 23(2): 82-5, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23277129
12.
Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects.
Arch Neurol
; 68(5): 615-21, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21555636