(Q36691668)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239121%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance (English)

1 reference

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20 February 2020

1 reference

2

1 reference

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20 February 2020

6

Alejandro A Schäffer

1 reference

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20 February 2020

author name string

M Hashim Raza

1

1 reference

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20 February 2020

Jennifer Mundorff

3

1 reference

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20 February 2020

Joseph Lukong

4

1 reference

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20 February 2020

Judith Kuster

5

1 reference

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20 February 2020

Dennis Drayna

7

1 reference

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20 February 2020

publication date

13 December 2012

1 reference

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20 February 2020

number of pages

12

1 reference

inferred from page(s)

published in

Human Genetics

1 reference

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20 February 2020

volume

132

1 reference

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20 February 2020

issue

4

1 reference

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20 February 2020

page(s)

385-396

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239121%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-012-1252-5

20 February 2020

exact match

0 references

cites work

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1 reference

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Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees

30 September 2017

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Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

30 September 2017

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Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

30 September 2017

1 reference

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Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79

30 September 2017

1 reference

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Mutations in the lysosomal enzyme-targeting pathway and persistent stuttering

30 September 2017

1 reference

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Exome sequencing identifies the cause of a mendelian disorder

30 September 2017

1 reference

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A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart

30 September 2017

1 reference

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A second-generation combined linkage physical map of the human genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Genetic etiology in cases of recovered and persistent stuttering in an unselected, longitudinal sample of young twins

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Genetic studies of stuttering in a founder population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

New complexities in the genetics of stuttering: significant sex-specific linkage signals

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Genomewide significant linkage to stuttering on chromosome 12.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Epidemiology of stuttering in the community across the entire life span

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Finding susceptibility genes for developmental disorders of speech: the long and winding road

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Genotyping for human whole-genome scans: past, present, and future

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Power comparison of parametric and nonparametric linkage tests in small pedigrees

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Epidemiological and offspring analyses of developmental speech disorders using data from the Colorado Adoption Project

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Computer-simulation methods in human linkage analysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Online system for faster multipoint linkage analysis via parallel execution on thousands of personal computers

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

The sex ratio in familial persistent stuttering

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Genetic Factors in Stuttering Confirmed

28 June 2018

1 reference

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Stuttering and tics in twins.

28 June 2018

1 reference

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Heritability and environmental effects for self-reported periods with stuttering: a twin study from Denmark.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Genetic and environmental influences on stuttering and tics in Japanese twin children.

5 September 2018

1 reference

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Evidence for a major gene influence on persistent developmental stuttering.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemia

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Exact genetic linkage computations for general pedigrees.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

A study of the genetic and environmental etiology of stuttering in a selected twin sample.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

The power to detect linkage in complex disease by means of simple LOD-score analyses

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3600087

Concordance for stuttering in monozygotic and dizygotic twin pairs

5 September 2018

1 reference

12 December 2020

Stuttering in families of adopted stutterers

1 reference

12 December 2020

A study of familial stuttering

1 reference

12 December 2020

Bivariate genetic analyses of stuttering and nonfluency in a large sample of 5-year-old twins

1 reference

12 December 2020

Multilingual children who stutter: clinical issues

1 reference

12 December 2020

Results of a genome-wide linkage scan for stuttering

1 reference

12 December 2020

How to model a complex trait. 2. Analysis with two disease loci

1 reference

12 December 2020

10.1007/S00439-012-1252-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239121%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239121%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23239121%20AND%20SRC:MED&resulttype=core&format=json