Evidence map›Paper›PMID 21193955›Full record

ArticleBehavior genetics2011

Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment.

Jessica Logan, Stephen A Petrill, Judy Flax, Laura M Justice, Liping Hou, Anne S Bassett, Paula Tallal, Linda M Brzustowicz, Christopher W Bartlett

Abstract read
In one paragraph

Article in Behavior genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Genome-wide association study of receptive language ability of 12-year-olds.Journal of speech, language, and hearing research : JSLHR · 2014
    Article
  7. Article
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Jessica LoganDepartment of Human Development and Family Science, The Ohio State University, Columbus, OH 43205, USA.
Stephen A Petrill
Judy Flax
Laura M Justice
Liping Hou
Anne S Bassett
Paula Tallal
Linda M Brzustowicz
Christopher W Bartlett

Funding

Molecular Genetics of Language and Related Cognition in FamiliesR01DC009453 · NIDCD · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BARTLETT, CHRISTOPHER WILIAM · 2010 to 2014
$3.3M
DETECTION OF PERILYMPHATIC FISTULAR01DC001654 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI WALL, CONRAD · 1993 to 1995
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NIDCD NIH HHS R01 DC009453NIDCD NIH HHS R01 DC01654
6 · The paper itself

Abstract

Specific language impairment is a developmental language disorder characterized by failure to develop language normally in the absence of a specific cause. Previous twin studies have documented the heritability of reading and language measures as well as the genetic correlation between those measures. This paper presents results from an alternative to the classical twin designs by estimating heritability from extended pedigrees. These pedigrees were previously studied as part of series of molecular genetic studies of specific language impairment where the strongest genetic findings were with reading phenotypes rather than language despite selecting pedigrees based on language impairments. To explore the relationship between reading and language in these pedigrees, variance components estimates of heritability of reading and language measures were conducted showing general agreement with the twin literature, as were genetics correlations between reading and language. Phonological short-term memory, phonological awareness and auditory processing were evaluated as candidate mediators of the reading-language genetic correlations. Only phonological awareness showed significant genetic correlations with all reading measures and several language measures while phonological short-term memory and auditory processing did not.

Indexed as

LanguageReadingCanadaChildChild, PreschoolFamily HealthFemaleHumansLanguage DisordersMaleMemory DisordersMemory, Short-TermModels, GeneticPedigreePhenotypeUnited States

Identifiers

PMID21193955
PMCPMC3129390

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Registered trials

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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.