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
em 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
em Inglês
| MEDLINE | ID: mdl-35094443
3.
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
Am J Hum Genet
; 105(5): 947-958, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31668704
4.
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
em Inglês
| MEDLINE | ID: mdl-35579625
5.
Nifedipine for primary dysmenorrhoea.
Cochrane Database Syst Rev
; 12: CD012912, 2021 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34921554
6.
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.
Genet Med
; 21(9): 2160-2161, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30696996
7.
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.
Genet Med
; 21(6): 1295-1307, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30349098
8.
Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.
Genet Med
; 25(2): 100004, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36745127
9.
Infant social attention: an endophenotype of ASD-related traits?
J Child Psychol Psychiatry
; 58(3): 270-281, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27861851
10.
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
11.
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
12.
Developmental changes in infant brain activity during naturalistic social experiences.
Dev Psychobiol
; 57(7): 842-53, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26219834
13.
Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions.
J Neurodev Disord
; 16(1): 15, 2024 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38622540
14.
Interventions for hyperthyroidism pre-pregnancy and during pregnancy.
Cochrane Database Syst Rev
; (11): CD008633, 2013 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24249524
15.
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
em Inglês
| MEDLINE | ID: mdl-37031308
16.
Characterizing the autism spectrum phenotype in DYRK1A-related syndrome.
Autism Res
; 16(8): 1488-1500, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37497568
17.
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
em Inglês
| MEDLINE | ID: mdl-36924980
18.
Transverse position. Using rotation to aid normal birth-OUTcomes following manual rotation (the TURN-OUT trial): a randomized controlled trial.
Am J Obstet Gynecol MFM
; 4(1): 100488, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34543751
19.
GIGYF1 disruption associates with autism and impaired IGF-1R signaling.
J Clin Invest
; 132(19)2022 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35917186
20.
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
em Inglês
| MEDLINE | ID: mdl-35236119