Evidence map›Paper›PMID 41186445›Full record

ArticleJournal of speech, language, and hearing research : JSLHR2025

Deciphering the Language in Our DNA and Leveraging the Discoveries Toward Improved Outcomes: Introduction to the Forum.

Beate Peter

Abstract read
In one paragraph

Article in Journal of speech, language, and hearing research : JSLHR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Beate PeterCollege of Health Solutions, Arizona State University, Tempe.ORCID 0000-0002-9083-8522

Funding

Research Symposium in Communication Sciences and DisordersR13DC003383 · NIDCD · AMERICAN SPEECH-LANGUAGE-HEARING ASSN · PI MARGARET A. ROGERS · 1997 to 2026
$727k
NIDCD NIH HHS R13 DC003383
6 · The paper itself

Abstract

purposeInvestigating genetic influences on speech and language development is a fairly new field fueled by interprofessional collaborations among investigators trained in genomics, communication sciences and disorders, or, in rare cases, both. The 2024 Research Symposium, titled "Genetics in Communication Sciences and Disorders," aimed to provide updates on cutting-edge research findings in disorders of speech sound production, speech fluency, spoken language, and written language. A second important goal was to make research methods and findings of genetics studies in speech and language disorders accessible to an audience with expertise in communication sciences and disorders. The articles in this forum are based on the symposium presentations.

conclusionThe authors trace the history of investigating genotype-phenotype associations in their areas of specialty and discuss how technological advances have fueled recent insights in large participant samples. In addition, we show how insights from genetic studies of spoken and written language can be leveraged toward novel interventions based on principles of precision medicine, namely personalized and proactive approaches, with the goal of improved outcomes. A disclaimer is that genetic changes reflect only one of many sources of influence on the human capacity of verbal communication; many others-for instance microbiomes and the physical, social, and cultural environments-should also be acknowledged.

Indexed as

LanguageLanguage DisordersHumans

Identifiers

PMID41186445
PMCPMC12614921

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.