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.
Cultural contributions to adults' self-rated mental health problems and strengths: 7 culture clusters, 28 societies, 16 906 adults.
Psychol Med
; 53(16): 7581-7590, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37203460
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.
Effects of maternal folic acid supplementation during the second and third trimesters of pregnancy on neurocognitive development in the child: an 11-year follow-up from a randomised controlled trial.
BMC Med
; 19(1): 73, 2021 03 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33750355
6.
Dynamic relationships between phonological memory and reading: A five year longitudinal study from age 4 to 9.
Dev Sci
; 24(1): e12986, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32412095
7.
Auditory frequency discrimination in developmental dyslexia: A meta-analysis.
Dyslexia
; 26(1): 36-51, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31877576
8.
Long-term Effects of Cholestatic Liver Disease in Childhood on Neuropsychological Outcomes and Neurochemistry.
J Pediatr Gastroenterol Nutr
; 69(2): 145-151, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31169662
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.
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
11.
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
12.
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
13.
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Nat Genet
; 30(1): 86-91, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11743577
14.
Morphology in autism spectrum disorders: local processing bias and language.
Cogn Neuropsychol
; 29(7-8): 584-600, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23521055
15.
Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet
; 54(11): 1621-1629, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36266505
16.
To Name or Not to Name: Eye Movements and Semantic Processing in RAN and Reading.
Brain Sci
; 11(7)2021 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34209779
17.
Symptoms of hyperactivity and inattention can mediate deficits of postural stability in developmental dyslexia.
Exp Brain Res
; 192(4): 627-33, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18830588
18.
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Transl Psychiatry
; 9(1): 77, 2019 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30741946
19.
Processing of structural neuroimaging data in young children: Bridging the gap between current practice and state-of-the-art methods.
Dev Cogn Neurosci
; 33: 206-223, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29033222
20.
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet
; 55(3): 520, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36823321