Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population (Q35030971)

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20 January 2020

title

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population (English)

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20 January 2020

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9

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20 January 2020

Dianne F Newbury

2

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20 January 2020

Jean-Baptiste Cazier

8

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20 January 2020

author name string

Pia Villanueva

1

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20 January 2020

Lilian Jara

3

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20 January 2020

Zulema De Barbieri

4

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20 January 2020

Ghazala Mirza

5

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20 January 2020

Hernán M Palomino

6

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20 January 2020

María Angélica Fernández

7

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Hernán Palomino

10

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20 January 2020

publication date

19 January 2011

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European Journal of Human Genetics

20 January 2020

published in

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20 January 2020

volume

19

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issue

6

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20 January 2020

page(s)

687-695

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Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

20 January 2020

copyright license

start time

19 January 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

A functional genetic link between distinct developmental language disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Runs of homozygosity in European populations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

High prevalence of specific language impairment in Robinson Crusoe Island. A possible founder effect

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

PLINK: a tool set for whole-genome association and population-based linkage analyses

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Haploview: analysis and visualization of LD and haplotype maps

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Semantic verbal fluency of animals: a normative and predictive study in a Spanish population

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

A major susceptibility locus for specific language impairment is located on 13q21.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

A genomewide scan identifies two novel loci involved in specific language impairment

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Genetic and environmental risks for specific language impairment in children

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

The genealogic approach to human genetics of disease.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Prevalence and natural history of primary speech and language delay: findings from a systematic review of the literature

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Clinical characteristics of children referred to a child development center for evaluation of speech, language, and communication disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Neuropathology of thiamine deficiency: an update on the comparative analysis of human disorders and experimental models

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Incorrect specification of marker allele frequencies: effects on linkage analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

Familial aggregation in specific language impairment.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

The token test: A sensitive test to detect receptive disturbances in aphasics.

8 July 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2010.251

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2010.251

Incorporating language phenotypes strengthens evidence of linkage to autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038/EJHG.2010.251

An autosomal genomic screen for autism

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110042

GRR: graphical representation of relationship errors

25 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21248734

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Heritability of Language: A Review and Metaanalysis of Twin, Adoption, and Linkage Studies

1 reference

https://api.crossref.org/works/10.1038/EJHG.2010.251

inferred from DOI database lookup

7 January 2021

based on heuristic

The Effect of Thiamine Deficiency in Infancy on the Development of Syntactic and Lexical Abilities

1 reference

https://api.crossref.org/works/10.1038/EJHG.2010.251

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/EJHG.2010.251

1 reference

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20 January 2020

0 references

1 reference

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20 January 2020

PubMed publication ID

21248734

1 reference