Detalhe da pesquisa
1.
Pubertal maturation and timing effects on resting state electroencephalography in autistic and comparison youth.
Dev Psychobiol
; 65(7): e22415, 2023 11.
Artigo
Inglês
| MEDLINE | ID: mdl-37860899
2.
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.
Hum Mutat
; 43(4): 461-470, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35094443
3.
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
Genet Med
; 24(8): 1753-1760, 2022 08.
Artigo
Inglês
| MEDLINE | ID: mdl-35579625
4.
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
Genet Med
; 25(2): 100004, 2023 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-36745127
5.
Infant social attention: an endophenotype of ASD-related traits?
J Child Psychol Psychiatry
; 58(3): 270-281, 2017 03.
Artigo
Inglês
| MEDLINE | ID: mdl-27861851
6.
Developmental changes in infant brain activity during naturalistic social experiences.
Dev Psychobiol
; 57(7): 842-53, 2015 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-26219834
7.
Characterizing Sensory Phenotypes of Subgroups with a Known Genetic Etiology Pertaining to Diagnoses of Autism Spectrum Disorder and Intellectual Disability.
J Autism Dev Disord
; 2023 Apr 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37031308
8.
Characterizing the autism spectrum phenotype in DYRK1A-related syndrome.
Autism Res
; 16(8): 1488-1500, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37497568
9.
Genetic Ablation of GIGYF1, Associated With Autism, Causes Behavioral and Neurodevelopmental Defects in Zebrafish and Mice.
Biol Psychiatry
; 94(10): 769-779, 2023 11 15.
Artigo
Inglês
| MEDLINE | ID: mdl-36924980
10.
GIGYF1 disruption associates with autism and impaired IGF-1R signaling.
J Clin Invest
; 132(19)2022 10 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35917186
11.
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology.
Am J Psychiatry
; 179(3): 189-203, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35236119
12.
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders.
Sci Adv
; 8(33): eabo7112, 2022 08 19.
Artigo
Inglês
| MEDLINE | ID: mdl-35977029
13.
Sleep Problems in Children with ASD and Gene Disrupting Mutations.
J Genet Psychol
; 182(5): 317-334, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33998396
14.
Brief Report: Associations Between Self-injurious Behaviors and Abdominal Pain Among Individuals with ASD-Associated Disruptive Mutations.
J Autism Dev Disord
; 51(9): 3365-3373, 2021 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-33175317
15.
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects.
Sci Adv
; 7(23)2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-34088660
16.
Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Nat Genet
; 53(8): 1125-1134, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34312540
17.
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Nat Commun
; 11(1): 4932, 2020 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33004838
18.
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Nat Commun
; 11(1): 5398, 2020 Oct 21.
Artigo
Inglês
| MEDLINE | ID: mdl-33087701
19.
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency.
Mol Autism
; 8: 54, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-29034068
20.
The promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disorders.
OMICS
; 19(4): 197-208, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25831060