Detalhe da pesquisa
1.
Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder.
Am J Hum Genet
; 108(6): 1069-1082, 2021 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34022130
2.
Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders.
J Hum Genet
; 67(2): 95-101, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34400773
3.
A Domain-General Developmental "Do-GooD" Network Model of Prosocial Cognition in Adolescence: A Systematic Review.
Front Behav Neurosci
; 16: 815811, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35350389
4.
A Feasibility Study of a Remotely-Delivered Mindfulness-Based Training for Adolescents During the COVID-19 Pandemic.
Front Psychiatry
; 13: 838694, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35633797
5.
Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis.
Dev Cell
; 57(20): 2381-2396.e13, 2022 10 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36228617
6.
ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infection.
Ann Clin Transl Neurol
; 9(8): 1276-1288, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35871307
7.
Reduced anxiety and changes in amygdala network properties in adolescents with training for awareness, resilience, and action (TARA).
Neuroimage Clin
; 29: 102521, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33316764