Complex segregation analysis of autism (Q35197040)

7 August 2017

title

Complex segregation analysis of autism (English)

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7 August 2017

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L B Jorde

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7 August 2017

S J Hasstedt

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7 August 2017

E R Ritvo

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7 August 2017

A Mason-Brothers

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7 August 2017

B J Freeman

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7 August 2017

C Pingree

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7 August 2017

W M McMahon

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7 August 2017

B Petersen

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7 August 2017

W R Jenson

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7 August 2017

A Mo

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7 August 2017

language of work or name

English

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publication date

1 November 1991

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

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7 August 2017

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7 August 2017

page(s)

932-938

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Genetic distances between the Utah Mormons and related populations

7 August 2017

cites work

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A General Model for the Genetic Analysis of Pedigree Data

13 July 2018

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Analysis of family resemblance. 3. Complex segregation of quantitative traits

13 July 2018

1 reference

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Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism

13 July 2018

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

13 July 2018

1 reference

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Familial heterogeneity in infantile autism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Gene mapping studies with the syndrome of autism

13 July 2018

1 reference

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Fenfluramine treatment of autism: UCLA collaborative study of 81 patients at nine medical centers

13 July 2018

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Fragile X and autism: a multicenter survey.

13 July 2018

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Electroretinograms in autism: a pilot study of b-wave amplitudes

13 July 2018

1 reference

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Fenfluramine treatment of autism

13 July 2018

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Autism and genetics. A decade of research

13 July 2018

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Elevated blood serotonin in autistic probands and their first-degree relatives

13 July 2018

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The UCLA-University of Utah epidemiologic survey of autism: prevalence

13 July 2018

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Electroretinograms (ERGs) in four autistic probands and six first-degree relatives.

13 July 2018

1 reference

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The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling

13 July 2018

1 reference

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The fragile X marker and autism in perspective

13 July 2018

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Chromosome findings in twins with early-onset autistic disorder

13 July 2018

1 reference

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Review of fenfluramine in the treatment of the developmental disabilities

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Inbreeding in the Utah Mormons: an evaluation of estimates based on pedigrees, isonymy, and migration matrices

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

The UCLA-University of Utah epidemiologic survey of autism: genealogical analysis of familial aggregation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Mixed-model segregation analysis of schizophrenia in the Lindelius Swedish pedigrees

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

The UCLA-University of Utah epidemiologic survey of autism: prenatal, perinatal, and postnatal factors

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Deficiency of suppressor-inducer (CD4+CD45RA+) T cells in autism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Genetic analyses of pyloric stenosis suggesting a specific maternal effect

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Infantile autism: a genetic study of 21 twin pairs

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

Continuous variation caused by genes with graduated effects

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683259

A goodness-of-fit test for the polygenic threshold model: Application to pyloric stenosis

13 July 2018

1 reference

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Genetics of common disorders

13 July 2018

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12 December 2020

Multifactorial qualitative traits: genetic analysis and prediction of recurrence risks

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12 December 2020

Recurrence risks in the presence of single gene susceptibility to environmental agents

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12 December 2020

Segregation analysis of leprosy in families of northern Thailand

1 reference

12 December 2020

Identifiers

PMC publication ID

1683259

1 reference

7 August 2017

1 reference