ReviewGenome biology2013
Neurogenomics of speech and language disorders: the road ahead.
Review in Genome biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
19 citing papers in PubMed, 36 citations in OpenAlex.
- Review
- Impact of intermittent lead exposure on hominid brain evolution.Science advances · 2025Article
- Interindividual Variation Refuses to Go Away: A Bayesian Computer Model of Language Change in Communicative Networks.Frontiers in psychology · 2021Article
- Neurofilament-lysosomal genetic intersections in the cortical network of stuttering.Progress in neurobiology · 2020Article
- Developmental Perceptual Impairments: Cases When Tone-Deafness and Prosopagnosia Co-occur.Frontiers in human neuroscience · 2018Article
- Prevalence of congenital amusia.European journal of human genetics : EJHG · 2017Article
- Talking Convergence: Growing Evidence Links FOXP2 and Retinoic Acid in Shaping Speech-Related Motor Circuitry.Frontiers in neuroscience · 2017Article
- A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.European journal of human genetics : EJHG · 2016Article
- Risk Factors Associated With Language in Autism Spectrum Disorder: Clues to Underlying Mechanisms.Journal of speech, language, and hearing research : JSLHR · 2016Review
- Investigating the effects of copy number variants on reading and language performance.Journal of neurodevelopmental disorders · 2016Article
- A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.Frontiers in behavioral neuroscience · 2016Article
- Neurogenomics: An opportunity to integrate neuroscience, genomics and bioinformatics research in Africa.Applied & translational genomics · 2015Review
- Defining the biological bases of individual differences in musicality.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015Review
- Insights into the genetic foundations of human communication.Neuropsychology review · 2015Review
- Modification of spectral features by nonhuman primates.The Behavioral and brain sciences · 2014Article
- De novo TBR1 mutations in sporadic autism disrupt protein functions.Nature communications · 2014Article
- Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.Journal of visualized experiments : JoVE · 2014Article
- Assessing the effects of common variation in the FOXP2 gene on human brain structure.Frontiers in human neuroscience · 2014Article
- Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Journal of neurodevelopmental disorders · 2013Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Next-generation sequencing is set to transform the discovery of genes underlying neurodevelopmental disorders, and so offer important insights into the biological bases of spoken language. Success will depend on functional assessments in neuronal cell lines, animal models and humans themselves.
Indexed as
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.