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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

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Highly Cited
2018
Highly Cited
2018
Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human
Human genetic studies are rapidly identifying variants that increase risk for neurodevelopmental disorders. However, it remains… 
Highly Cited
2016
Highly Cited
2016
Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes
The 16p11.2 600 kb BP4-BP5 deletion and duplication syndromes have been associated with developmental delay; autism spectrum… 
Highly Cited
2015
Highly Cited
2015
16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions
Recurrent deletions and duplications at chromosomal region 16p11.2 are variably associated with speech delay, autism spectrum… 
Highly Cited
2014
Highly Cited
2014
The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity
Anatomical structures and mechanisms linking genes to neuropsychiatric disorders are not deciphered. Reciprocal copy number… 
Highly Cited
2012
Highly Cited
2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
Background The recurrent ∼600 kb 16p11.2 BP4-BP5 deletion is among the most frequent known genetic aetiologies of autism spectrum… 
Highly Cited
2012
Highly Cited
2012
Human-Specific Histone Methylation Signatures at Transcription Start Sites in Prefrontal Neurons
Mapping histone methylation landscapes in neurons from human, chimpanzee, and macaque brains reveals coordinated, human-specific… 
Highly Cited
2011
Highly Cited
2011
Rare copy number variants are an important cause of epileptic encephalopathies
Rare copy number variants (CNVs)—deletions and duplications—have recently been established as important risk factors for both… 
Highly Cited
2011
Highly Cited
2011
Gene and miRNA expression profiles in autism spectrum disorders
Highly Cited
2008
Highly Cited
2008
A nonsynonymous functional variant in integrin-αM (encoded by ITGAM) is associated with systemic lupus erythematosus
We identified and replicated an association between ITGAM (CD11b) at 16p11.2 and risk of systemic lupus erythematosus (SLE) in 3… 
Review
1995
Review
1995
Transcriptional regulation by MAP kinases
Tyrosine kinase growth factor receptors activate MAP kinase by a complex mechanism involving the SH2/3 protein Grb2, the exchange… 
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