ArticleEuropean journal of human genetics : EJHG2013
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
Article in European journal of human genetics : EJHG, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 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
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Who cites it
25 citing papers in PubMed.
- Three Unrelated Children With Childhood Apraxia of Speech: Exome Sequencing and Functional Gene Analysis Imply a Role of Laminin-511 in Early Neurodevelopment.Case reports in genetics · 2026Article
- Genomic Investigations of Spoken and Written Language Abilities: A Guide to Advances in Approaches, Technologies, and Discovery.Journal of speech, language, and hearing research : JSLHR · 2025Review
- Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review.Journal of applied genetics · 2024Review
- The Genetic and Molecular Basis of Developmental Language Disorder: A Review.Children (Basel, Switzerland) · 2022Review
- Differences and Commonalities in Children with Childhood Apraxia of Speech and Comorbid Neurodevelopmental Disorders: A Multidimensional Perspective.Journal of personalized medicine · 2022Article
- Genome-Wide Association Study of Motor Coordination.Frontiers in human neuroscience · 2021Article
- Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.European journal of human genetics : EJHG · 2018Article
- Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis.Wellcome open research · 2018Article
- Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.Wellcome open research · 2018Article
- A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.European journal of human genetics : EJHG · 2016Article
- Investigating the effects of copy number variants on reading and language performance.Journal of neurodevelopmental disorders · 2016Article
- Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.PloS one · 2016Article
- Genome-wide analysis identifies a role for common copy number variants in specific language impairment.European journal of human genetics : EJHG · 2015Article
- New genes for focal epilepsies with speech and language disorders.Current neurology and neuroscience reports · 2015Review
- Insights into the genetic foundations of human communication.Neuropsychology review · 2015Review
- Pure interstitial dup(6)(q22.31q22.31) - a case report.Italian journal of pediatrics · 2015Article
- Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.European journal of human genetics : EJHG · 2014Article
- Article
- Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain.Epigenetics · 2014Article
- Late breaking chromosomes.Molecular syndromology · 2014Article
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Abstract
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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.