15q11.2

A chromosome band present on 15q.
National Institutes of Health

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Highly Cited
2015
Highly Cited
2015
Analysis of de novo CNVs (dnCNVs) from the full Simons Simplex Collection (SSC) (N = 2,591 families) replicates prior findings of… (More)
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Highly Cited
2014
Highly Cited
2014
In a small fraction of patients with schizophrenia or autism, alleles of copy-number variants (CNVs) in their genomes are… (More)
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Highly Cited
2012
Highly Cited
2012
A small number of rare, recurrent genomic copy number variants (CNVs) are known to substantially increase susceptibility to… (More)
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Highly Cited
2012
Highly Cited
2012
Previous studies have shown that copy-number variants (CNVs) contribute to the risk of complex developmental phenotypes. However… (More)
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Highly Cited
2011
Highly Cited
2011
We have undertaken a genome-wide analysis of rare copy-number variation (CNV) in 1124 autism spectrum disorder (ASD) families… (More)
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Highly Cited
2011
Highly Cited
2011
The proximal long arm of chromosome 15 has segmental duplications located at breakpoints BP1–BP5 that mediate the generation of… (More)
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Highly Cited
2010
Highly Cited
2010
Prader–Willi syndrome (PWS) is a neurobehavioral disorder manifested by infantile hypotonia and feeding difficulties in infancy… (More)
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Highly Cited
2010
Highly Cited
2010
Epilepsy is one of the most common neurological disorders in humans with a prevalence of 1% and a lifetime incidence of 3… (More)
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Highly Cited
2009
Highly Cited
2009
Behavioural differences have been described in patients with type I deletions (between breakpoints 1 and 3 (BP1-BP3)) or type II… (More)
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Highly Cited
2009
Highly Cited
2009
We investigated the involvement of rare (<1%) copy number variants (CNVs) in 471 cases of schizophrenia and 2792 controls that… (More)
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