Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity

Obesity is a multifactorial condition that is highly heritable. There have been ~60 susceptibility loci identified, but they only account for a fraction of cases. As copy number variations (CNVs) have been implicated in the etiology of a multitude of human disorders including obesity, here, we inves...

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Gepubliceerd in:Eur J Hum Genet
Hoofdauteurs: Selvanayagam, Thanuja, Walker, Susan, Gazzellone, Matthew J., Kellam, Barbara, Cytrynbaum, Cheryl, Stavropoulos, Dimitri J., Li, Ping, Birken, Catherine S., Hamilton, Jill, Weksberg, Rosanna, Scherer, Stephen W.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Springer International Publishing 2018
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6189095/
https://ncbi.nlm.nih.gov/pubmed/29976977
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0189-0
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