Emma L Meaburn
Overview
Explore the profile of Emma L Meaburn including associated specialties, affiliations and a list of published articles.
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21
Citations
712
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Recent Articles
1.
Gui A, Meaburn E, Tye C, Charman T, Johnson M, Jones E
JAMA Pediatr
. 2021 Jun;
175(9):968-970.
PMID: 34096992
No abstract available.
2.
Donati G, Dumontheil I, Pain O, Asbury K, Meaburn E
Sci Rep
. 2021 Feb;
11(1):3851.
PMID: 33594131
How well one does at school is predictive of a wide range of important cognitive, socioeconomic, and health outcomes. The last few years have shown marked advancement in our understanding...
3.
Saffari A, Arno M, Nasser E, Ronald A, Wong C, Schalkwyk L, et al.
Mol Autism
. 2019 Nov;
10:38.
PMID: 31719968
Background: A gap exists in our mechanistic understanding of how genetic and environmental risk factors converge at the molecular level to result in the emergence of autism symptoms. We compared...
4.
Donati G, Dumontheil I, Meaburn E
Mind Brain Educ
. 2019 Oct;
13(3):224-233.
PMID: 31598132
Individual differences in executive functions (EF) are heritable and predictive of academic attainment (AA). However, little is known about genetic contributions to EFs or their genetic relationship with AA and...
5.
Saffari A, Silver M, Zavattari P, Moi L, Columbano A, Meaburn E, et al.
Genet Epidemiol
. 2017 Oct;
42(1):20-33.
PMID: 29034560
Epigenome-wide association studies (EWAS) are designed to characterise population-level epigenetic differences across the genome and link them to disease. Most commonly, they assess DNA-methylation status at cytosine-guanine dinucleotide (CpG) sites,...
6.
Marzi S, Meaburn E, Dempster E, Lunnon K, Paya-Cano J, Smith R, et al.
Epigenetics
. 2016 Jan;
11(1):24-35.
PMID: 26786711
While DNA methylation is usually thought to be symmetrical across both alleles, there are some notable exceptions. Genomic imprinting and X chromosome inactivation are two well-studied sources of allele-specific methylation...
7.
St Pourcain B, Cents R, Whitehouse A, Haworth C, Davis O, OReilly P, et al.
Nat Commun
. 2014 Sep;
5:4831.
PMID: 25226531
Twin studies suggest that expressive vocabulary at ~24 months is modestly heritable. However, the genes influencing this early linguistic phenotype are unknown. Here we conduct a genome-wide screen and follow-up...
8.
Davis O, Band G, Pirinen M, Haworth C, Meaburn E, Kovas Y, et al.
Nat Commun
. 2014 Jul;
5:4204.
PMID: 25003214
Dissecting how genetic and environmental influences impact on learning is helpful for maximizing numeracy and literacy. Here we show, using twin and genome-wide analysis, that there is a substantial genetic...
9.
Sieradzka D, Power R, Freeman D, Cardno A, McGuire P, Plomin R, et al.
PLoS One
. 2014 Apr;
9(4):e94398.
PMID: 24718684
Psychosis has been hypothesised to be a continuously distributed quantitative phenotype and disorders such as schizophrenia and bipolar disorder represent its extreme manifestations. Evidence suggests that common genetic variants play...
10.
Harlaar N, Meaburn E, Hayiou-Thomas M, Davis O, Docherty S, Hanscombe K, et al.
J Speech Lang Hear Res
. 2014 Apr;
57(1):96-105.
PMID: 24687471
Purpose: Researchers have previously shown that individual differences in measures of receptive language ability at age 12 are highly heritable. In the current study, the authors attempted to identify some...