Detalhe da pesquisa
1.
Bridge-building between communities: Imagining the future of biomedical autism research.
Cell;
186(18): 3747-3752, 2023 08 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37657415
2.
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
Cell;
180(3): 568-584.e23, 2020 02 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31981491
3.
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
4.
How does genetic variation modify ND-CNV phenotypes?
Trends Genet;
38(2): 140-151, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34364706
5.
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium.
Mol Psychiatry;
27(4): 2114-2125, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35136228
6.
Australian, Irish, and Swedish women's comfort levels when breastfeeding in public.
BMC Public Health;
23(1): 2535, 2023 12 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38110935
7.
Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure.
Hum Brain Mapp;
43(1): 37-55, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32420680
8.
NRXN1α+/- is associated with increased excitability in ASD iPSC-derived neurons.
BMC Neurosci;
22(1): 56, 2021 09 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34525970
9.
A novel non-viral delivery method that enables efficient engineering of primary human T cells for ex vivo cell therapy applications.
Cytotherapy;
23(9): 852-860, 2021 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33941482
10.
The clinical relevance of intragenic NRXN1 deletions.
J Med Genet;
57(5): 347-355, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31932357
11.
Autism spectrum disorder genomics: The progress and potential of genomic technologies.
Genomics;
112(6): 5136-5142, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32941983
12.
Parental stress and adjustment in the context of rare genetic syndromes: A scoping review.
J Intellect Disabil;
: 1744629521995378, 2021 Apr 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33866895
13.
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.
Br J Psychiatry;
216(5): 275-279, 2020 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31964429
14.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature;
515(7526): 209-15, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25363760
15.
Four priorities for new links between conservation science and accounting research.
Conserv Biol;
33(4): 972-975, 2019 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30456769
16.
Complexity based measures of postural stability provide novel evidence of functional decline in fragile X premutation carriers.
J Neuroeng Rehabil;
16(1): 87, 2019 07 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31299981
17.
Abnormal fronto-parietal white matter organisation in the superior longitudinal fasciculus branches in autism spectrum disorders.
Eur J Neurosci;
47(6): 652-661, 2018 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28741714
18.
Disrupted prediction errors index social deficits in autism spectrum disorder.
Brain;
140(1): 235-246, 2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28031223
19.
Effect of frenotomy on breastfeeding variables in infants with ankyloglossia (tongue-tie): a prospective before and after cohort study.
BMC Pregnancy Childbirth;
17(1): 373, 2017 Nov 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29132414
20.
Child Health Care in Ireland.
J Pediatr;
177S: S87-S106, 2016 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27666279