Detalhe da pesquisa
1.
Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
Brain
; 146(4): 1686-1696, 2023 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36059063
2.
Rare copy number variation in posttraumatic stress disorder.
Mol Psychiatry
; 27(12): 5062-5069, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36131047
3.
Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
Mol Psychiatry
; 26(6): 2663-2676, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33414497
4.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
; 26(7): 3004-3017, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057169
5.
Estimating the effects of copy-number variants on intelligence using hierarchical Bayesian models.
Genet Epidemiol
; 44(8): 825-840, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32783248
6.
Cannabinoids and psychotic symptoms: A potential role for a genetic variant in the P2X purinoceptor 7 (P2RX7) gene.
Brain Behav Immun
; 88: 573-581, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32330591
7.
Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics.
Adv Anat Embryol Cell Biol
; 224: 1-25, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28551748
8.
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
PLoS Genet
; 10(9): e1004580, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25188300
9.
The genetic landscapes of autism spectrum disorders.
Annu Rev Genomics Hum Genet
; 14: 191-213, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23875794
10.
SHANK1 Deletions in Males with Autism Spectrum Disorder.
Am J Hum Genet
; 90(5): 879-87, 2012 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22503632
11.
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
Am J Med Genet A
; 167A(12): 3019-30, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26334118
12.
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
PLoS Genet
; 8(2): e1002521, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22346768
13.
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Hum Genet
; 133(6): 781-92, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24442360
14.
Clinical correlates of diagnostic certainty in children and youths with Autistic Disorder.
Mol Autism
; 15(1): 15, 2024 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38570867
15.
Genetic and phenotypic similarity across major psychiatric disorders: a systematic review and quantitative assessment.
Transl Psychiatry
; 14(1): 171, 2024 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38555309
16.
Using rare genetic mutations to revisit structural brain asymmetry.
Nat Commun
; 15(1): 2639, 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38531844
17.
Heterozygous FA2H mutations in autism spectrum disorders.
BMC Med Genet
; 14: 124, 2013 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24299421
18.
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.
J Pineal Res
; 54(1): 46-57, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22775292
19.
A Heat Diffusion Perspective on Geodesic Preserving Dimensionality Reduction.
ArXiv
; 2023 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37396618
20.
GEODESIC SINKHORN FOR FAST AND ACCURATE OPTIMAL TRANSPORT ON MANIFOLDS.
ArXiv
; 2023 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37808090