Detalhe da pesquisa
1.
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Mol Psychiatry
; 26(11): 6125-6148, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34188164
2.
Correction: Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.
Mol Psychiatry
; 26(12): 7852, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34282265
3.
Impact of patient education videos on genetic counseling outcomes after exome sequencing.
Patient Educ Couns
; 103(1): 127-135, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31521424
4.
In vivo epigenetic editing of Sema6a promoter reverses transcallosal dysconnectivity caused by C11orf46/Arl14ep risk gene.
Nat Commun
; 10(1): 4112, 2019 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31511512
5.
DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition.
Biol Psychiatry
; 80(10): 765-774, 2016 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27184921