Detalhe da pesquisa
1.
Developmental trajectories for young children with 16p11.2 copy number variation.
Am J Med Genet B Neuropsychiatr Genet
; 174(4): 367-380, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28349640
2.
Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Genet Med
; 18(4): 341-9, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26066539
3.
Consistency of parent-report SLC6A1 data in Simons Searchlight with Provider-Based Publications.
J Neurodev Disord
; 14(1): 40, 2022 06 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35761184
4.
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Nat Genet
; 54(9): 1305-1319, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35982159
5.
16p11.2 deletion syndrome.
Curr Opin Genet Dev
; 68: 49-56, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667823
6.
Availability of Services and Caregiver Burden: Supporting Individuals With Neurogenetic Conditions During the COVID-19 Pandemic.
J Child Neurol
; 36(9): 760-767, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33829918
7.
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.
NPJ Genom Med
; 4: 19, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31452935
8.
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
JAMA Psychiatry
; 73(1): 20-30, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26629640
9.
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Biol Psychiatry
; 77(9): 785-93, 2015 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25064419