Detalhe da pesquisa
1.
Characterization of the TBR1 interactome: variants associated with neurodevelopmental disorders disrupt novel protein interactions.
Hum Mol Genet
; 32(9): 1497-1510, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36579832
2.
Neuroimaging genomics as a window into the evolution of human sulcal organization.
Cereb Cortex
; 34(3)2024 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38466113
3.
Using neuroimaging genomics to investigate the evolution of human brain structure.
Proc Natl Acad Sci U S A
; 119(40): e2200638119, 2022 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36161899
4.
Auditory discrimination learning and acoustic cue weighing in female zebra finches with localised FoxP1 knockdowns.
J Neurophysiol
; 2024 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38629163
5.
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Mol Psychiatry
; 28(4): 1647-1663, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36117209
6.
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Cell
; 137(5): 961-71, 2009 May 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-19490899
7.
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.
J Med Genet
; 60(6): 597-607, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328423
8.
The developmental genetic architecture of vocabulary skills during the first three years of life: Capturing emerging associations with later-life reading and cognition.
PLoS Genet
; 17(2): e1009144, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33577555
9.
Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals.
Proc Natl Acad Sci U S A
; 118(47)2021 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34785596
10.
Genetic variations within human gained enhancer elements affect human brain sulcal morphology.
Neuroimage
; 265: 119773, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36442731
11.
Understanding Language from a Genomic Perspective.
Annu Rev Genet
; 49: 131-60, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26442845
12.
Polygenic risk for mental disorder reveals distinct association profiles across social behaviour in the general population.
Mol Psychiatry
; 27(3): 1588-1598, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35228676
13.
Molecular networks of the FOXP2 transcription factor in the brain.
EMBO Rep
; 22(8): e52803, 2021 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34260143
14.
Language and reading impairments are associated with increased prevalence of non-right-handedness.
Child Dev
; 94(4): 970-984, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36780127
15.
Machine learning of large-scale multimodal brain imaging data reveals neural correlates of hand preference.
Neuroimage
; 262: 119534, 2022 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35931311
16.
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.
Am J Hum Genet
; 105(2): 403-412, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31303265
17.
Mapping brain asymmetry in health and disease through the ENIGMA consortium.
Hum Brain Mapp
; 43(1): 167-181, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32420672
18.
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Hum Brain Mapp
; 43(1): 300-328, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33615640
19.
Greater male than female variability in regional brain structure across the lifespan.
Hum Brain Mapp
; 43(1): 470-499, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33044802
20.
Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
Genet Med
; 24(6): 1283-1296, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35346573