DE eng

Search in the Catalogues and Directories

Page: 1 2
Hits 1 – 20 of 24

1
Pathways from the early language and communication environment to literacy outcomes at the end of primary school; the roles of language development and social development ...
Gibson, Jenny; Newbury, DF; Durkin, K. - : Apollo - University of Cambridge Repository, 2021
BASE
Show details
2
Neural and behavioural indices of face processing in siblings of children with autism spectrum disorder (ASD): a longitudinal study from infancy to mid-childhood
BASE
Show details
3
Do emotional difficulties and peer problems hew together from childhood to adolescence? The case of children with a history of developmental language disorder (DLD)
Conti-Ramsden, G.; Mok, P.; Durkin, K.. - : Springer (part of Springer Nature), 2018
BASE
Show details
4
Randomised trial of a parent-mediated intervention for infants at high risk for autism: longitudinal outcomes to age 3 years
Green, J.; Pickles, A.; Pasco, G.. - : Wiley, 2017
BASE
Show details
5
The impact of nonverbal ability on prevalence and clinical presentation of language disorder: evidence from a population study
In: Journal of Child Psychology and Psychiatry (2016) (In press). (2016)
BASE
Show details
6
Predicting the rate of language development from early motor skills in at-risk infants who develop autism spectrum disorder
Leonard, H; Bedford, R; Pickles, A. - : Elsevier, 2015
BASE
Show details
7
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014)
BASE
Show details
8
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Abstract: Aim: Sex chromosome aneuploidies increase the risk of spoken or written language disorders but individuals with specific language impairment (SLI) or dyslexia do not routinely undergo cytogenetic analysis. We assess the frequency of sex chromosome aneuploidies in individuals with language impairment or dyslexia. Method: Genome-wide single nucleotide polymorphism genotyping was performed in three sample sets: a clinical cohort of individuals with speech and language deficits (87 probands: 61 males, 26 females; age range 4 to 23 years), a replication cohort of individuals with SLI, from both clinical and epidemiological samples (209 probands: 139 males, 70 females; age range 4 to 17 years), and a set of individuals with dyslexia (314 probands: 224 males, 90 females; age range 7 to 18 years). Results: In the clinical language-impaired cohort, three abnormal karyotypic results were identified in probands (proband yield 3.4%). In the SLI replication cohort, six abnormalities were identified providing a consistent proband yield (2.9%). In the sample of individuals with dyslexia, two sex chromosome aneuploidies were found giving a lower proband yield of 0.6%. In total, two XYY, four XXY (Klinefelter syndrome), three XXX, one XO (Turner syndrome), and one unresolved karyotype were identified. Interpretation: The frequency of sex chromosome aneuploidies within each of the three cohorts was increased over the expected population frequency (approximately 0.25%) suggesting that genetic testing may prove worthwhile for individuals with language and literacy problems and normal non-verbal IQ. Early detection of these aneuploidies can provide information and direct the appropriate management for individuals.
Keyword: Neuroscience. Biological psychiatry. Neuropsychiatry; Special aspects of education
URL: https://doi.org/10.1111/dmcn.12294
https://strathprints.strath.ac.uk/48936/
BASE
Hide details
9
Infant neural sensitivity to dynamic eye gaze is associated with later emerging autism
Elsabbagh, Mayada; Mercure, Evelyne; Hudry, K.. - : Cell Press, 2012
BASE
Show details
10
Individual common variants exert weak effects on the risk for autism spectrum disorders
Anney, R.; Klei, L.; Pinto, D.. - : Oxford University Press, 2012
BASE
Show details
11
Genetic copy number variation and general cognitive ability.
In: PLoS One , 7 (12) , Article e37385 . (2012) (2012)
BASE
Show details
12
Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef ; ORA review team (2012)
BASE
Show details
13
Genome-wide association studies establish that human intelligence is highly heritable and polygenic
In: MOL PSYCHIATR , 16 (10) 996 - 1005. (2011) (2011)
BASE
Show details
14
Genome-wide association studies establish that human intelligence is highly heritable and polygenic
Davies, G.; Tenesa, A.; Payton, A.. - : Nature Publishing Group, 2011
BASE
Show details
15
Speech perception and phonological short-term memory capacity in language impairment: preliminary evidence from adolescents with specific language impairment (SLI) and autism spectrum disorders (ASD)
In: International Journal of Language and Communication Disorders, May-June 2010 (2010)
BASE
Show details
16
Persistence of literacy problems: spelling in adolescence and at mid-life.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; CrossRef (2009)
BASE
Show details
17
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009)
BASE
Show details
18
Loss of language in early development of autism and specific language impairment
In: JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY , 50 (7) 843 - 852. (2009) (2009)
BASE
Show details
19
Persistence of literacy problems: spelling in adolescence and at mid-life
BASE
Show details
20
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment
BASE
Show details

Page: 1 2

Catalogues
0
0
0
0
0
0
0
Bibliographies
0
0
0
0
0
0
0
0
1
Linked Open Data catalogues
0
Online resources
0
0
0
0
Open access documents
23
0
0
0
0
© 2013 - 2024 Lin|gu|is|tik | Imprint | Privacy Policy | Datenschutzeinstellungen ändern