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16p11.2

A chromosome band present on 16p
National Institutes of Health

Related topics

Related topics

17 relations
CD19 wt AlleleCD2BP2 wt AlleleChromosome 16 Short ArmChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome
▪ A heterozygous interstitial duplication of ~551Kb at chromosome 16p11.2 (Chr16:29,647,342 30,198,151) was detected by SNP array… 
2019
2019
[Adolescent with a schizophreniform disorder and recurrent 16p11.2 duplication].
Genetic factors play an important role in the development of psychotic disorders. With increasing evidence, several rare copy… 
2017
2017
Chapter 11 Genetic Etiology of Autism
2017
2017
Deep Insight Into YPEL3
Deep insight into YPEL3. YPEL3 identification The Yippee gene was first identified in Drosophila through a yeast interaction trap… 
2017
2017
Dosage-Dependent Phenotypes in Models of Human 16 p 11 . 2 Lesions Found in Autism
Recurrent copy number variations (CNVs) of human 16p11.2 have been associated with a variety of developmental/neurocognitive… 
2014
2014
The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained
Results: Individuals with the 16p11.2 deletion presented with a high frequency of psychiatric and developmental disorders (90… 
2014
2014
Correction: Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders
Copyright: 2014 The PLOS ONE Staff. This is an open-access article distributed under the terms of the Creative Commons… 
2013
2013
16p11.2 is required for neuronal polarity
Since Autism Spectrum Disorder (ASD) is strongly associated with chromosomal abnormalities of 16p11.2, and Autism has been… 
2011
2011
Genetic insights beginning to divide autism diagnosis
Review
2011
Review
2011
PLK1 (polo-like kinase 1 (Drosophila))
Review on PLK1 (polo-like kinase 1 (Drosophila)), with data on DNA, on the protein encoded, and where the gene is implicated. 
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