(Q35751636)

10 August 2017

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title

Conducting genetic epidemiology studies of autism spectrum disorders: issues in matching (English)

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10 August 2017

autism spectrum disorder

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2

Lonnie Zwaigenbaum

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Peter Szatmari

series ordinal

1

object named as

Peter Szatmari

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10 August 2017

Susan Bryson

3

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PubMed ID

15098957

10 August 2017

language of work or name

English

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publication date

1 February 2004

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Journal of Autism and Developmental Disorders

10 August 2017

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10 August 2017

34

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10 August 2017

1

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10 August 2017

49-57

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https://scigraph.springernature.com/pub.10.1023/b:jadd.0000018074.74369.cd

10 August 2017

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cites work

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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

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Psychiatric disorder and the broad autism phenotype: evidence from a family study of multiple-incidence autism families.

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Recurrence risks in mental retardation

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

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The HGP: end of phase 1

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Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders.

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Psychosocial adaptation of fathers of children with autism, Down syndrome, and normal development

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Autism: the phenotype in relatives.

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Autism, affective and other psychiatric disorders: patterns of familial aggregation.

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The genetics of autism

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Personalized medicine.

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Autism: in search of susceptibility genes

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The endophenotype concept in psychiatry: etymology and strategic intentions

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Stoppage rules and genetic studies of autism

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The pattern of care in families of adults with a mental handicap: A comparison between families of autistic adults and Down syndrome adults

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

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The high-risk infant.

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Behaviour/mental health problems in young adults with intellectual disability: the impact on families

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Can standard measures identify subclinical markers of autism?

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A screening instrument for autism at 18 months of age: a 6-year follow-up study

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Autism, affective disorders, and social phobia

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The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study.

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The future of genetic studies of complex human diseases

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Heritable and nonheritable risk factors for autism spectrum disorders

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Endophenotypes as quantitative risk factors for psychiatric disease: rationale and study design.

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Non-pharmacological modification of cardiac risk factors: part 3. Smoking cessation and alcohol consumption

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Predictors of cognitive test patterns in autism families.

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

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Personality traits of the relatives of autistic probands.

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Endophenotypes and child psychiatry.

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Family history of cognitive disabilities in first-degree relatives of autistic and mentally retarded children

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Genes for human personality traits: "endophenotypes" of psychiatric disorders?

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Towards a cognitive phenotype for autism: increased prevalence of executive dysfunction and superior spatial span amongst siblings of children with autism

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Genetics of childhood disorders: XLVI. Autism, part 5: genetics of autism

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Growth, developmental milestones and health problems in the first 2 years in very preterm infants compared with term infants: a population based study

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Pervasive Developmental Disorders in Preschool Children

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Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives.

1 reference

12 December 2020

10.1023/B:JADD.0000018074.74369.CD

Identifiers

DOI

1 reference

PubMed ID

15098957

Dimensions Publication ID

10 August 2017

0 references

1 reference

PubMed ID

15098957