(Q34507264)

2 August 2017

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

1 reference

2 August 2017

1 reference

8

Edwin H Cook

1 reference

2 August 2017

13

Nancy J Cox

1 reference

2 August 2017

Rathi Suresh

1

1 reference

2 August 2017

Nicoline Ambrose

2

1 reference

2 August 2017

Cheryl Roe

3

1 reference

2 August 2017

Anna Pluzhnikov

4

1 reference

2 August 2017

Jacqueline K Wittke-Thompson

5

1 reference

2 August 2017

Maggie C-Y Ng

6

1 reference

2 August 2017

Xiaolin Wu

7

1 reference

2 August 2017

Cecilia Lundstrom

9

1 reference

2 August 2017

Marie Garsten

10

1 reference

2 August 2017

Ruth Ezrati

11

1 reference

2 August 2017

Ehud Yairi

12

1 reference

2 August 2017

language of work or name

English

0 references

publication date

1 February 2006

1 reference

American Journal of Human Genetics

2 August 2017

1 reference

2 August 2017

78

1 reference

2 August 2017

4

1 reference

2 August 2017

554-563

1 reference

Replication of autism linkage: fine-mapping peak at 17q21.

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Genomewide significant linkage to stuttering on chromosome 12.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Evidence for sex-specific risk alleles in autism spectrum disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Molecular genetics of autism spectrum disorder.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Enhanced pedigree error detection

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

A forkhead-domain gene is mutated in a severe speech and language disorder

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Genomewide scans of complex human diseases: true linkage is hard to find

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Improved inference of relationship for pairs of individuals

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Chromosome 7q: where autism meets language disorder?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Allegro, a new computer program for multipoint linkage analysis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Early childhood stuttering I: persistency and recovery rates

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Allele-sharing models: LOD scores and accurate linkage tests

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

The genetic basis of persistence and recovery in stuttering.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Genetics of stuttering: a critical review

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Genetic Factors in Stuttering Confirmed

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Evidence for a major gene influence on persistent developmental stuttering.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Segregation analyses of stuttering

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1424690

Results of a genome-wide linkage scan for stuttering

9 December 2018

1 reference

12 December 2020

Familial stuttering patterns are not related to one measure of severity

1 reference

12 December 2020

Concordance for stuttering in monozygotic and dizygotic twin pairs

1 reference

12 December 2020

Genetic aspects of early childhood stuttering

1 reference

12 December 2020

The use of a genetic map of biallelic markers in linkage studies

1 reference

12 December 2020

The sex-specific genetic architecture of quantitative traits in humans

1 reference

12 December 2020

Genome-wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early-onset, major depression

1 reference

12 December 2020

Identifiers

DOI

10.1086/501370

1 reference

2 August 2017

1 reference

2 August 2017

1 reference