Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic studies of stuttering in a founder population.

Journal of fluency disorders - 1 Jan 2007

Wittke-Thompson Jacqueline K, Ambrose Nicoline, Yairi Ehud, Roe Cheryl, Cook Edwin H, Ober Carole, Cox Nancy J

Abstract excerpt

UNLABELLED: Genome-wide linkage and association analyses were conducted to identify genetic determinants of stuttering in a founder population in which 48 individuals affected with stuttering are connected in a single 232-person genealogy. A novel approach was devised to account for all necessary relationships to enable multipoint linkage analysis. Regions with nominal evidence for linkage were found on...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Chromosomes, Human, Pair 13
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 3

Share to Genetic Linkage

Share to Genotype

Share to Pedigree

Share to Population Surveillance

Source

Open in PubMed Open full text

Identifiers

PMID: 17276504
DOI: 10.1016/j.jfludis.2006.12.002
PMCID: PMC2128723

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic studies of stuttering in a founder population.PMID 17276504Read ↗

Challenges and Opportunities in Characterizing the Genetics of Stuttering: From Sample Acquisition to Functional Interpretation of the Genome.Semantic proximity Read ↗

Genetic bases of stuttering: the state of the art, 2011.Semantic proximity Read ↗

Large-scale genome-wide analyses of stuttering.Semantic proximity Read ↗

A genetic linkage study in Brazil identifies a new locus for persistent developmental stuttering on chromosome 10.Semantic proximity Read ↗

Functionally Oriented Genetic Analyses Reveal Potential Transcriptomic and Neurological Mechanisms of Stuttering.Semantic proximity Read ↗

Genetic analyses of a large consanguineous south Indian family reveal novel variants in NAGPA and four hitherto unreported genes in developmental stuttering.Semantic proximity Read ↗

Evidence for a major gene influence on persistent developmental stuttering.Semantic proximity Read ↗

Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation.Semantic proximity Read ↗

Variants in GNPTAB, GNPTG and NAGPA genes are associated with stutterers.Semantic proximity Read ↗

De novo protein-coding gene variants in developmental stuttering.Semantic proximity Read ↗

Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance.Semantic proximity Read ↗

Genetics in speech disorders.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.