16p11.2

A chromosome band present on 16p
National Institutes of Health

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Highly Cited
2012
Highly Cited
2012
BACKGROUND The recurrent ~600 kb 16p11.2 BP4-BP5 deletion is among the most frequent known genetic aetiologies of autism spectrum… (More)
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Highly Cited
2011
Highly Cited
2011
Recurrent copy number variations (CNVs) of human 16p11.2 have been associated with a variety of developmental/neurocognitive… (More)
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Highly Cited
2011
Highly Cited
2011
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI… (More)
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Highly Cited
2010
Highly Cited
2010
BACKGROUND Deletion and the reciprocal duplication in 16p11.2 were recently associated with autism and developmental delay… (More)
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Highly Cited
2009
Highly Cited
2009
Recurrent microdeletions and microduplications of a 600-kb genomic region of chromosome 16p11.2 have been implicated in childhood… (More)
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Highly Cited
2009
Highly Cited
2009
Array CGH (comparative genomic hybridization) screening of large patient cohorts with mental retardation and/or multiple… (More)
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Highly Cited
2008
Highly Cited
2008
Autism is a childhood neurodevelopmental disorder with a strong genetic component, yet the identification of autism… (More)
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Highly Cited
2008
Highly Cited
2008
Structural variation (copy number variation [CNV] including deletion and duplication, translocation, inversion) of chromosomes… (More)
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Highly Cited
2008
Highly Cited
2008
Systemic lupus erythematosus (SLE) is a common systemic autoimmune disease with complex etiology but strong clustering in… (More)
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