Detalhe da pesquisa
1.
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease.
Genet Med
; 21(5): 1121-1130, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30293986
2.
Whole exome sequencing in patients with white matter abnormalities.
Ann Neurol
; 79(6): 1031-1037, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27159321
3.
Factors Associated with Uptake of Genetics Services for Hypertrophic Cardiomyopathy.
J Genet Couns
; 24(5): 797-809, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25566741
4.
Inter-subject synchronization of brain responses during natural music listening.
Eur J Neurosci
; 37(9): 1458-69, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23578016
5.
Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy.
Epilepsia Open
; 4(3): 397-408, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31440721
6.
Brain organization underlying superior mathematical abilities in children with autism.
Biol Psychiatry
; 75(3): 223-30, 2014 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23954299
7.
Default mode network in childhood autism: posteromedial cortex heterogeneity and relationship with social deficits.
Biol Psychiatry
; 74(3): 212-9, 2013 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23375976
8.
Salience network-based classification and prediction of symptom severity in children with autism.
JAMA Psychiatry
; 70(8): 869-79, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23803651
9.
Brain hyperconnectivity in children with autism and its links to social deficits.
Cell Rep
; 5(3): 738-47, 2013 Nov 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-24210821
10.
Multivariate searchlight classification of structural magnetic resonance imaging in children and adolescents with autism.
Biol Psychiatry
; 70(9): 833-41, 2011 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21890111