(Q24795638)

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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

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scholarly article

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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates (English)

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James S. Sutcliffe

object named as

James S Sutcliffe

9

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Jonathan L Haines

8

object named as

Jonathan L Haines

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author name string

Jacob L McCauley

1

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Chun Li

2

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Lan Jiang

3

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Lana M Olson

4

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Genea Crockett

5

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Kimberly Gainer

6

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Susan E Folstein

7

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language of work or name

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publication date

12 January 2005

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BMC Medical Genetics

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6

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1

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1

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https://scigraph.springernature.com/pub.10.1186/1471-2350-6-1

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Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

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Chromosome 7q: where autism meets language disorder?

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A genomic screen of autism: evidence for a multilocus etiology

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The genetics of autism

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An autosomal genomic screen for autism. Collaborative linkage study of autism

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7 April 2017

Genetic studies of autistic disorder and chromosome 7

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7 April 2017

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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

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Infantile autism: a genetic study of 21 twin pairs

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7 April 2017

Autism as a paradigmatic complex genetic disorder

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28 September 2017

Molecular genetics of autism spectrum disorder.

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28 September 2017

Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.

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A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

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28 September 2017

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

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28 September 2017

Prevalence of autism in a US metropolitan area

1 reference

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28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=546213

28 September 2017

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

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28 September 2017

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=546213

28 September 2017

A genomewide screen for autism susceptibility loci

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28 September 2017

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

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28 September 2017

Effects of misclassification on estimates of relative risk in family history studies

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28 September 2017

Diagnosing autism: analyses of data from the Autism Diagnostic Interview.

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28 September 2017

Sex differences in higher functioning people with autism

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28 September 2017

Sex differences in pervasive developmental disorders

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28 September 2017

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

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28 September 2017

Genetic factors in child psychiatric disorders--II. Empirical findings

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28 September 2017

Linkage thresholds for two-stage genome scans

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30 May 2018

Diagnostic uses of the Vineland Adaptive Behavior Scales

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30 May 2018

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30 May 2018

Stoppage rules and genetic studies of autism

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30 May 2018

Genomic screen and follow-up analysis for autistic disorder.

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21 January 2018

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.

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https://api.crossref.org/works/10.1186%2F1471-2350-6-1

21 January 2018

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

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21 January 2018

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

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21 January 2018

Incorporating language phenotypes strengthens evidence of linkage to autism.

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21 January 2018

The pre-linguistic autism diagnostic observation schedule.

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Empirical genomewide significance levels established by whole genome simulations.

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21 January 2018

A principal components analysis of the Autism Diagnostic Interview-Revised.

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21 January 2018

Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R

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21 January 2018

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

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21 January 2018

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

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21 January 2018

Computer programs for multilocus haplotyping of general pedigrees.

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28 November 2018

Ordered subset analysis in genetic linkage mapping of complex traits

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Optimal allele-sharing statistics for genetic mapping using affected relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/15647115

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2350-6-1

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