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1.
Trans-ancestry meta-analysis of genome wide association studies of inhibitory control.
Mol Psychiatry
; 28(10): 4175-4184, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37500827
2.
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.
Hum Mol Genet
; 30(12): 1160-1171, 2021 06 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33864365
3.
Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probands.
Mol Psychiatry
; 27(1): 710-730, 2022 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34002022
4.
Intensity Matters: High-intensity Interval Exercise Enhances Motor Cortex Plasticity More Than Moderate Exercise.
Cereb Cortex
; 30(1): 101-112, 2020 01 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31041988
5.
The role of cadherin genes in five major psychiatric disorders: A literature update.
Am J Med Genet B Neuropsychiatr Genet
; 177(2): 168-180, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28921840
6.
Dopamine transporter genotype is associated with a lateralized resistance to distraction during attention selection.
J Neurosci
; 34(47): 15743-50, 2014 Nov 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-25411502
7.
An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults.
Am J Med Genet B Neuropsychiatr Genet
; 168B(2): 89-96, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25656223
8.
Evaluating the regulatory function of non-coding autism-associated single nucleotide polymorphisms on gene expression in human brain tissue.
Autism Res
; 17(3): 467-481, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38323502
9.
Norepinephrine genes predict response time variability and methylphenidate-induced changes in neuropsychological function in attention deficit hyperactivity disorder.
J Clin Psychopharmacol
; 33(3): 356-62, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23609393
10.
Dissecting Schizotypy and Its Association With Cognition and Polygenic Risk for Schizophrenia in a Nonclinical Sample.
Schizophr Bull
; 49(5): 1217-1228, 2023 09 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36869759
11.
Integration of xeno-free single-cell cloning in CRISPR-mediated DNA editing of human iPSCs improves homogeneity and methodological efficiency of cellular disease modeling.
Stem Cell Reports
; 18(12): 2515-2527, 2023 12 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37977144
12.
Generation of induced pluripotent stem cell lines from three individuals with autism spectrum disorder.
Stem Cell Res
; 71: 103170, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37494850
13.
Potential role for immune-related genes in autism spectrum disorders: Evidence from genome-wide association meta-analysis of autistic traits.
Autism
; 26(2): 361-372, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34344231
14.
Evidence against benefits from cognitive training and transcranial direct current stimulation in healthy older adults.
Nat Hum Behav
; 5(1): 146-158, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33106629
15.
Genetic influences on hub connectivity of the human connectome.
Nat Commun
; 12(1): 4237, 2021 07 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34244483
16.
The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project design and methodologies: a dimensional approach to understanding neurobiological and genetic aetiology.
Mol Autism
; 12(1): 55, 2021 08 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-34353377
17.
Functional validation of CHMP7 as an ADHD risk gene.
Transl Psychiatry
; 10(1): 385, 2020 11 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33159045
18.
Impact of CYP2C19 genotype-predicted enzyme activity on hippocampal volume, anxiety, and depression.
Psychiatry Res
; 288: 112984, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32315880
19.
Generation of four iPSC lines from peripheral blood mononuclear cells (PBMCs) of an attention deficit hyperactivity disorder (ADHD) individual and a healthy sibling in an Australia-Caucasian family.
Stem Cell Res
; 34: 101353, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30622032
20.
Absence of the 7-repeat variant of the DRD4 VNTR is associated with drifting sustained attention in children with ADHD but not in controls.
Am J Med Genet B Neuropsychiatr Genet
; 147B(6): 927-37, 2008 Sep 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-18361436