Detalhe da pesquisa
1.
A framework for an evidence-based gene list relevant to autism spectrum disorder.
Nat Rev Genet
; 21(6): 367-376, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32317787
2.
Gene copy number variation and pediatric mental health/neurodevelopment in a general population.
Hum Mol Genet
; 32(15): 2411-2421, 2023 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37154571
3.
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome.
Hum Brain Mapp
; 45(1): e26553, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38224541
4.
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome.
Mol Psychiatry
; 28(1): 341-353, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36192458
5.
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Mol Psychiatry
; 28(5): 2071-2080, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869225
6.
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
Am J Hum Genet
; 106(1): 26-40, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31870554
7.
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.
Genet Med
; 25(3): 100338, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36729053
8.
Support to caregivers who have received genetic information about neurodevelopmental and psychiatric vulnerability in their young children: A narrative review.
Clin Genet
; 104(2): 163-173, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37098443
9.
Autism genetics: opportunities and challenges for clinical translation.
Nat Rev Genet
; 18(6): 362-376, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28260791
10.
The concept of "metabolic jet lag" in the pathophysiology of bipolar disorder: implications for research and clinical care.
CNS Spectr
; 28(5): 571-580, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36503605
11.
Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels.
Genet Med
; 24(9): 1899-1908, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35616647
12.
Characterizing eating behavioral phenotypes in mood disorders: a narrative review.
Psychol Med
; 52(14): 2885-2898, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36004528
13.
Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model.
Psychol Med
; 52(14): 3184-3192, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33443009
14.
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Mol Psychiatry
; 26(8): 4496-4510, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32015465
15.
Pediatric Brain Tumor Survivors' Understanding of Friendships: A Qualitative Analysis of ADOS-2 Interview Responses.
J Pediatr Psychol
; 47(6): 662-673, 2022 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34981125
16.
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Hum Mol Genet
; 28(22): 3724-3733, 2019 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31884517
17.
Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Mol Psychiatry
; 25(11): 2818-2831, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31358905
18.
Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Mol Psychiatry
; 25(8): 1822-1834, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29895892
19.
Sleep phenotype of individuals with autism spectrum disorder bearing mutations in the PER2 circadian rhythm gene.
Am J Med Genet A
; 185(4): 1120-1130, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33474825
20.
Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.
Curr Psychiatry Rep
; 23(3): 13, 2021 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33625600