(Q33904472)

29 July 2017

title

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

1 reference

29 July 2017

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Yujun Shao

1

1 reference

29 July 2017

M L Cuccaro

2

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29 July 2017

E R Hauser

3

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29 July 2017

K L Raiford

4

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29 July 2017

M M Menold

5

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29 July 2017

C M Wolpert

6

1 reference

29 July 2017

S A Ravan

7

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29 July 2017

L Elston

8

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29 July 2017

K Decena

9

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29 July 2017

S L Donnelly

10

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29 July 2017

R K Abramson

11

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29 July 2017

H H Wright

12

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29 July 2017

G R DeLong

13

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29 July 2017

J R Gilbert

14

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29 July 2017

M A Pericak-Vance

15

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29 July 2017

language of work or name

English

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publication date

3 February 2003

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American Journal of Human Genetics

29 July 2017

published in

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29 July 2017

volume

72

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29 July 2017

issue

3

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29 July 2017

page(s)

539-548

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Epidemiological trends in rates of autism.

29 July 2017

cites work

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

5 July 2018

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A family with a grand-maternally derived interstitial duplication of proximal 15q.

5 July 2018

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A genomewide screen for autism susceptibility loci

5 July 2018

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

5 July 2018

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Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

5 July 2018

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5 July 2018

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Three probands with autistic disorder and isodicentric chromosome 15.

5 July 2018

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5 July 2018

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Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Imprinting-mutation mechanisms in Prader-Willi syndrome

5 July 2018

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Autistic symptoms among children and young adults with isodicentric chromosome 15

5 July 2018

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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

5 July 2018

1 reference

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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

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

5 July 2018

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Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

5 July 2018

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Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation

5 July 2018

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The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

5 July 2018

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Allele-sharing models: LOD scores and accurate linkage tests

5 July 2018

1 reference

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Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autism in Angelman syndrome: a population-based study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Parametric and nonparametric linkage analysis: a unified multipoint approach

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

The neurobiology and genetics of infantile autism

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autism as a strongly genetic disorder: evidence from a British twin study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Behaviour problems in Angelman syndrome

5 July 2018

1 reference

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A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

5 July 2018

1 reference

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Strategies for multilocus linkage analysis in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Concordance for the syndrome of autism in 40 pairs of afflicted twins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autism and genetics. A decade of research

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Linkage strategies for genetically complex traits. I. Multilocus models

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Linkage of early-onset familial breast cancer to chromosome 17q21

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Etiology of autism: genetic influences

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Behavioral comparisons in autistic individuals from multiplex and singleton families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Genomic screen and follow-up analysis for autistic disorder.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Symptom domains in autism and related conditions: evidence for familiality

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

A comprehensive linkage analysis for myocardial infarction and its related risk factors

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

An autosomal genomic screen for autism.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Genetic studies in autistic disorder and chromosome 15.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Molecular genetic investigations of autism.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Genetics of autism: overview and new directions

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Autism and maternally derived aberrations of chromosome 15q.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

The Roscommon Family Study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

The Pre-Linguistic Autism Diagnostic Observation Schedule

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180230

Genetic Linkage Analysis of Complex Genetic Traits by Using Affected Sibling Pairs

29 October 2018

1 reference

12 December 2020

Genome-wide linkage analyses of systolic blood pressure using highly discordant siblings

1 reference

12 December 2020

PDD and Prader-Willi syndrome

1 reference

12 December 2020

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

12 December 2020

Identifiers

DOI

10.1086/367846

1 reference

29 July 2017

1 reference

29 July 2017

1 reference