ArticleJournal of neurodevelopmental disorders2011
Dissection of genetic associations with language-related traits in population-based cohorts.
Article in Journal of neurodevelopmental disorders, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
15 citing papers in PubMed, 30 citations in OpenAlex.
- The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration.The Journal of comparative neurology · 2019Article
- The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on.The European journal of neuroscience · 2018Review
- The DCDC2 deletion is not a risk factor for dyslexia.Translational psychiatry · 2017Article
- The evolutionary history of genes involved in spoken and written language: beyond FOXP2.Scientific reports · 2016Article
- Investigating the effects of copy number variants on reading and language performance.Journal of neurodevelopmental disorders · 2016Article
- The interface between genetics and psychology: lessons from developmental dyslexia.Proceedings. Biological sciences · 2015Review
- Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.Genes, brain, and behavior · 2015Article
- Insights into the genetic foundations of human communication.Neuropsychology review · 2015Review
- Genome-wide screening for DNA variants associated with reading and language traits.Genes, brain, and behavior · 2014Article
- Genome-wide association study of receptive language ability of 12-year-olds.Journal of speech, language, and hearing research : JSLHR · 2014Article
- Language growth and genetics of specific language impairment.International journal of speech-language pathology · 2013Review
- Speech-evoked auditory brainstem responses reflect familial and cognitive influences.Developmental science · 2013Article
- Toward epigenetic and gene regulation models of specific language impairment: looking for links among growth, genes, and impairments.Journal of neurodevelopmental disorders · 2012Article
- Defining the genetic architecture of human developmental language impairment.Life sciences · 2012Review
- The shared neurobiological basis of developmental dyslexia and developmental stuttering: A meta-analysis of functional and structural MRI studies.International journal of clinical and health psychology : IJCHPArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
Abstract
Recent advances in the field of language-related disorders have led to the identification of candidate genes for specific language impairment (SLI) and dyslexia. Replication studies have been conducted in independent samples including population-based cohorts, which can be characterised for a large number of relevant cognitive measures. The availability of a wide range of phenotypes allows us to not only identify the most suitable traits for replication of genetic association but also to refine the associated cognitive trait. In addition, it is possible to test for pleiotropic effects across multiple phenotypes which could explain the extensive comorbidity observed across SLI, dyslexia and other neurodevelopmental disorders. The availability of genome-wide genotype data for such cohorts will facilitate this kind of analysis but important issues, such as multiple test corrections, have to be taken into account considering that small effect sizes are expected to underlie such associations.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.