Detalhe da pesquisa
1.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33864365
2.
Dyslexia-related loci are significantly associated with language and literacy in Chinese-English bilingual Hong Kong Chinese twins.
Hum Genet
; 142(10): 1519-1529, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37668838
3.
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
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.
Genomic Imprinting As a Window into Human Language Evolution.
Bioessays
; 41(6): e1800212, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31132171
6.
Hand preference and Mathematical Learning Difficulties: New data from Greece, the United Kingdom, and Germany and two meta-analyses of the literature.
Laterality
; 26(5): 485-538, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33823756
7.
Genome-wide association study and polygenic risk score analysis for hearing measures in children.
Am J Med Genet B Neuropsychiatr Genet
; 186(5): 318-328, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34476894
8.
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism.
FASEB J
; 33(10): 11284-11302, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31314595
9.
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.
Hum Mol Genet
; 25(9): 1771-9, 2016 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26908617
10.
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on.
Eur J Neurosci
; 48(10): 3212-3233, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30218584
11.
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
PLoS Genet
; 9(9): e1003751, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24068947
12.
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Dev Med Child Neurol
; 56(4): 346-53, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24117048
13.
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children.
NPJ Sci Learn
; 9(1): 26, 2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38538593
14.
PCSK6 is associated with handedness in individuals with dyslexia.
Hum Mol Genet
; 20(3): 608-14, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21051773
15.
Auditory Cortex Asymmetry Associations with Individual Differences in Language and Cognition.
Brain Sci
; 14(1)2023 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38248230
16.
Identification of loci involved in childhood visual acuity and associations with cognitive skills and educational attainment.
NPJ Sci Learn
; 8(1): 25, 2023 Jul 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37491545
17.
Elevated levels of mixed-hand preference in dyslexia: Meta-analyses of 68 studies.
Neurosci Biobehav Rev
; 154: 105420, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37783301
18.
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Am J Hum Genet
; 85(2): 264-72, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19646677
19.
A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
PLoS Genet
; 5(3): e1000436, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19325871
20.
Handedness in twins: meta-analyses.
BMC Psychol
; 10(1): 11, 2022 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35033205