(Q22242734)

Dimensions Publication ID

Dimensions

1044969063

7 February 2023

Nancy J Mendelsohn

series ordinal

author given names

Nancy J.

author last names

Mendelsohn

1 reference

Dimensions Publication ID

Dimensions

1044969063

Trajectory of development in adolescents and adults with autism

7 February 2023

language of work or name

English

0 references

publication date

January 2008

0 references

0 references

0 references

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4-12

0 references

cites work

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

21 January 2018

The prevalence of autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Pervasive Developmental Disorders in Preschool Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Obsessive-compulsive behaviors in parents of multiplex autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

21 January 2018

The genetics of autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Genetic counseling in autism and pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Genetic testing in autism: how much is enough?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

The diagnostic utility of a genetics evaluation in children with pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Genetic landmarks through philately - autism spectrum disorders: a genetic update

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

On the selection of patients with developmental delay/mental retardation and autism spectrum disorders for genetic studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Diagnostic evaluation of developmental delay/mental retardation: An overview

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Acquired epileptiform aphasia: a dimensional view of Landau-Kleffner syndrome and the relation to regressive autistic spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

American Academy of Pediatrics: The pediatrician's role in the diagnosis and management of autistic spectrum disorder in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

MECP2 abnormality phenotypes: clinicopathologic area with broad variability

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Etiologic yield of autistic spectrum disorders: a prospective study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

An investigation into sub-telomeric deletions of chromosome 22 and pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Subtle chromosomal rearrangements in children with unexplained mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Outcomes of genetic evaluation in children with pervasive developmental disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Laboratory evaluation of children with autistic spectrum disorders: a guide for primary care pediatricians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Identification of MeCP2 mutations in a series of females with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Head circumference measurements in children with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Macrocephaly in autism and other pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Obstetric complications in autism: consequences or causes of the condition?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

The near universal presence of autism spectrum disorders in children with Smith-Lemli-Opitz syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Abnormalities of cholesterol metabolism in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Autism and phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Autism in children with congenital rubella

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Teratogenicity of sodium valproate

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

21 January 2018

The teratology of autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

Detection of low-level mosaicism by array CGH in routine diagnostic specimens

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

The genetics of autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

The neurobiology and genetics of infantile autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

2-year-old boy who has been diagnosed with autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

Diagnostic yield in the clinical genetic evaluation of autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

Hypomelanosis of Ito in Three Cases with Autism and Autistic-like Conditions

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

Autism and hypomelanosis of Ito in twins

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

Autism in thalidomide embryopathy: a population study.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

Modern Views of Autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31815EFDD7

7 January 2021

10.1097/GIM.0B013E31815EFDD7

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1044969063

0 references

Fatcat ID

release_pvpg3ac6x5c5hirg7ikbzxdwqa

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/pvpg3ac6x5c5hirg7ikbzxdwqa

24 November 2022

mapped directly with Wikidata item

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

18197051

1 reference

Consolidated OpenCitations Corpus – April 2017