Detalhe da pesquisa
1.
Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability.
J Med Genet
; 59(5): 511-516, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34183358
2.
Clinical and neurocognitive issues associated with Bosch-Boonstra-Schaaf optic atrophy syndrome: A case study.
Am J Med Genet A
; 182(1): 213-218, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31729143
3.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature
; 515(7526): 209-15, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363760
4.
De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.
Am J Med Genet A
; 173(6): 1656-1662, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28407363
5.
Escitalopram pharmacogenetics: CYP2C19 relationships with dosing and clinical outcomes in autism spectrum disorder.
Pharmacogenet Genomics
; 25(11): 548-54, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26313485
6.
An ontology for Autism Spectrum Disorder (ASD) to infer ASD phenotypes from Autism Diagnostic Interview-Revised data.
J Biomed Inform
; 56: 333-47, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26151311
7.
Individual common variants exert weak effects on the risk for autism spectrum disorders.
Hum Mol Genet
; 21(21): 4781-92, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22843504
8.
A genome-wide scan for common alleles affecting risk for autism.
Hum Mol Genet
; 19(20): 4072-82, 2010 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20663923
9.
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Hum Genet
; 131(4): 565-79, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21996756
10.
Whole Blood Serotonin Levels and Platelet 5-HT2A Binding in Autism Spectrum Disorder.
J Autism Dev Disord
; 49(6): 2417-2425, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30927179
11.
Vocabulary comprehension in adults with fragile X syndrome (FXS).
J Neurodev Disord
; 11(1): 25, 2019 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31619160
12.
Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder.
J Am Acad Child Adolesc Psychiatry
; 57(11): 867-875, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30392628
13.
Case Report: Association of Comorbid Psychiatric Disorders and Sigmoid Prolapse with de novo POGZ Mutation.
J Autism Dev Disord
; 52(3): 1408-1411, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33909211
14.
Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Mol Autism
; 8: 14, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28344757
15.
Is there sexual dimorphism of hyperserotonemia in autism spectrum disorder?
Autism Res
; 10(8): 1417-1423, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28401654
16.
A prospective, open-label trial of memantine in the treatment of cognitive, behavioral, and memory dysfunction in pervasive developmental disorders.
J Child Adolesc Psychopharmacol
; 16(5): 517-24, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17069541
17.
ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-AVPR1A, AVPR1B, and OXTR.
Front Neurosci
; 10: 516, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27920663
18.
Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes.
Front Neurosci
; 10: 195, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27242401
19.
An open-label trial of escitalopram in pervasive developmental disorders.
J Am Acad Child Adolesc Psychiatry
; 44(4): 343-8, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15782081
20.
Pharmacogenetic Study of Serotonin Transporter and 5HT2A Genotypes in Autism.
J Child Adolesc Psychopharmacol
; 25(6): 467-74, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26262902