Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.

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2 octobre 2014

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info:eu-repo/semantics/altIdentifier/doi/10.1038/nature13545

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info:eu-repo/semantics/altIdentifier/pmid/25231870

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info:eu-repo/semantics/altIdentifier/eissn/1476-4687

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_7816C9E4E3E58

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J.R. Perry et al., « Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. », Serveur académique Lausannois, ID : 10.1038/nature13545


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Age at menarche is a marker of timing of puberty in females. It varies widely between individuals, is a heritable trait and is associated with risks for obesity, type 2 diabetes, cardiovascular disease, breast cancer and all-cause mortality. Studies of rare human disorders of puberty and animal models point to a complex hypothalamic-pituitary-hormonal regulation, but the mechanisms that determine pubertal timing and underlie its links to disease risk remain unclear. Here, using genome-wide and custom-genotyping arrays in up to 182,416 women of European descent from 57 studies, we found robust evidence (P 

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