Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The contribution of rare diseases to understanding the epidemiology of neurodevelopmental disabilities.

Advances in experimental medicine and biology - 1 Jan 2010

Schendel Diana, Rice Catherine, Cunniff Christopher

Abstract excerpt

Our objective is to describe the contribution of rare diseases to our understanding of the epidemiology of neurodevelopmental disabilities (NDDs) by comparing and contrasting the epidemiologic features of NDDs classified according to key characteristics of developmental delay or deviance in such...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child Development Disorders, Pervasive
Share to Child, Preschool
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 22

Share to Developmental Disabilities

Share to Fragile X Syndrome

Share to Intellectual Disability

Share to Rare Diseases

Source

Identifiers

PMID: 20824459
DOI: 10.1007/978-90-481-9485-8_24

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-20824459-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The contribution of rare diseases to understanding the epidemiology of neurodevelopmental disabilities.PMID 20824459Read ↗

The frontiers of sequencing in undiagnosed neurodevelopmental diseases.Semantic proximity Read ↗

Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.Semantic proximity Read ↗

Genomic Diagnosis for Neurodevelopmental Disorders: Revolution, Evolution, And Current Reflections on the “Rational Diagnostic Evaluation”Semantic proximity Read ↗

Neurodevelopmental Phenotyping and Genotyping in the Pediatric National Institute of Health Undiagnosed Disease Program.Semantic proximity Read ↗

The genetics of neurodevelopmental disease.Semantic proximity Read ↗

The emerging face of FOXG1 Syndrome: a rare, genetically defined neurodevelopmental disorder coming of age in the genomics era.Semantic proximity Read ↗

Brief Report: Risk Variants Could Inform Early Neurodevelopmental Outcome in Children with Developmental Disabilities.Semantic proximity Read ↗

A Robust and Comprehensive Study of the Molecular and Genetic Basis of Neurodevelopmental Delay in a Sample of 3244 Patients, Evaluated by Exome Analysis in a Latin PopulationSemantic proximity Read ↗

Intellectual Disability & Rare Disorders: A Diagnostic Challenge.Semantic proximity Read ↗

NeuroDev: etiology and experience of neurodevelopmental disorders in Kenya and South AfricaSemantic proximity Read ↗

Genetic influences on neurodevelopmental disorders and their overlap with co-occurring conditions in childhood and adolescence: A meta-analysisSemantic proximity Read ↗

Neurodevelopmental assessments of rare genetic conditions.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.