Detalhe da pesquisa
1.
Comparative Flavivirus-Host Protein Interaction Mapping Reveals Mechanisms of Dengue and Zika Virus Pathogenesis.
Cell
; 175(7): 1931-1945.e18, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30550790
2.
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
Cell
; 174(3): 505-520, 2018 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30053424
3.
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
Cell
; 155(5): 997-1007, 2013 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24267886
4.
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.
Nat Rev Neurosci
; 23(6): 323-341, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35440779
5.
Pleiotropy of autism-associated chromatin regulators.
Development
; 150(14)2023 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37366052
6.
The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos.
Development
; 147(21)2020 06 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32467234
7.
The contribution of de novo coding mutations to autism spectrum disorder.
Nature
; 515(7526): 216-21, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363768
8.
Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos.
Development
; 147(23)2020 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33288503
9.
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Nature
; 485(7397): 237-41, 2012 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22495306
10.
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.
PLoS Genet
; 11(1): e1004852, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25621974
11.
Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation.
Am J Hum Genet
; 92(4): 530-46, 2013 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23541343
12.
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Circ Res
; 115(10): 884-896, 2014 Oct 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25205790
13.
The developmental transcriptome of the human brain: implications for neurodevelopmental disorders.
Curr Opin Neurol
; 27(2): 149-56, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24565942
14.
Autism genes converge on microtubule biology and RNA-binding proteins during excitatory neurogenesis.
bioRxiv
; 2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38187634
15.
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD.
Nat Commun
; 14(1): 8077, 2023 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38057346
16.
Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome.
Biol Psychiatry
; 2023 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36738982
17.
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
; 109(5): 788-804.e8, 2021 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33497602
18.
Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.
Cell Rep
; 31(2): 107495, 2020 04 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32294447
19.
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
Biol Psychiatry
; 87(12): 1035-1044, 2020 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31771860
20.
Human 3D cellular model of hypoxic brain injury of prematurity.
Nat Med
; 25(5): 784-791, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31061540