Detalhe da pesquisa
1.
Base-resolution analyses of sequence and parent-of-origin dependent DNA methylation in the mouse genome.
Cell
; 148(4): 816-31, 2012 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22341451
2.
Integrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneity.
Proc Natl Acad Sci U S A
; 120(20): e2210991120, 2023 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37155843
3.
Identification of brain cell types underlying genetic association with word reading and correlated traits.
Mol Psychiatry
; 28(4): 1719-1730, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36750735
4.
EGFR Mutation Promotes Glioblastoma through Epigenome and Transcription Factor Network Remodeling.
Mol Cell
; 60(2): 307-18, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26455392
5.
Language and reading impairments are associated with increased prevalence of non-right-handedness.
Child Dev
; 94(4): 970-984, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36780127
6.
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
PLoS Genet
; 9(10): e1003864, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24204291
7.
The Dyslexia-associated gene KIAA0319L is involved in neuronal migration in the developing chick visual system.
Int J Dev Biol
; 67(2): 49-56, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37410671
8.
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
Transl Psychiatry
; 12(1): 495, 2022 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36446759
9.
Language Difficulties in School-Age Children With Developmental Dyslexia.
J Learn Disabil
; 55(3): 200-212, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-33890525
10.
Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia.
Behav Genet
; 41(1): 77-89, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21207242
11.
Synaptic processes and immune-related pathways implicated in Tourette syndrome.
Transl Psychiatry
; 11(1): 56, 2021 01 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33462189
12.
Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.
Am J Med Genet B Neuropsychiatr Genet
; 153B(2): 447-462, 2010 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19588467
13.
No evidence of an association between two genes, EDN1 and ACE, and childhood-onset mood disorders.
Am J Med Genet B Neuropsychiatr Genet
; 153B(1): 341-6, 2010 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19475602
14.
DNA Variant in the RPGRIP1L Gene Influences Alternative Splicing.
Mol Neuropsychiatry
; 5(Suppl 1): 97-106, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32399473
15.
Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders.
Genes Brain Behav
; 19(6): e12648, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32108986
16.
Further genetic evidence implicates the vasopressin system in childhood-onset mood disorders.
Eur J Neurosci
; 30(8): 1615-9, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19821843
17.
Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region.
Am J Med Genet B Neuropsychiatr Genet
; 150B(1): 95-103, 2009 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18454440
18.
Association of SLITRK1 to Gilles de la Tourette Syndrome.
Am J Med Genet B Neuropsychiatr Genet
; 150B(4): 483-6, 2009 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18698576
19.
Tagging SNP association study of the IL-1beta gene (IL1B) and childhood-onset mood disorders.
Am J Med Genet B Neuropsychiatr Genet
; 150B(5): 653-9, 2009 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19016479
20.
G72/G30 (DAOA) and juvenile-onset mood disorders.
Am J Med Genet B Neuropsychiatr Genet
; 150B(7): 1007-12, 2009 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19089835