Detalhe da pesquisa
1.
Recommendations for accelerating open preprint peer review to improve the culture of science.
PLoS Biol
; 22(2): e3002502, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38421949
2.
Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication.
Cereb Cortex
; 26(5): 1957-64, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25678630
3.
Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications.
Hum Brain Mapp
; 37(8): 2833-48, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27219475
4.
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
5.
Opposing brain differences in 16p11.2 deletion and duplication carriers.
J Neurosci
; 34(34): 11199-211, 2014 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25143601
6.
Aberrant white matter microstructure in children with 16p11.2 deletions.
J Neurosci
; 34(18): 6214-23, 2014 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-24790192
7.
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
J Med Genet
; 49(10): 660-8, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23054248
8.
Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region.
Neurol Genet
; 8(5): e200018, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36531974
9.
16p11.2 deletion syndrome.
Curr Opin Genet Dev
; 68: 49-56, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667823
10.
Progress in Understanding and Treating SCN2A-Mediated Disorders.
Trends Neurosci
; 41(7): 442-456, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29691040
11.
Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
Biol Psychiatry
; 84(4): 253-264, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29778275
12.
Leaving the Bench and Finding Your Foundation.
Cold Spring Harb Perspect Biol
; 9(12)2017 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29196435
13.
Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.
J Autism Dev Disord
; 46(8): 2734-2748, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27207092
14.
Abnormal auditory and language pathways in children with 16p11.2 deletion.
Neuroimage Clin
; 9: 50-7, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26413471
15.
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
JAMA Psychiatry
; 72(2): 119-26, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25493922
16.
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
17.
SCIENTIFIC COMMUNITY. Preprints for the life sciences.
Science
; 352(6288): 899-901, 2016 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27199406