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1.
Day, F.R.* et al.: Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat. Genet. 49, 834-841 (2017)
2.
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat. Genet. 47, 1294-1303 (2015)
3.
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility, and BRCA1-mediated DNA repair. Obstet. Gynecol. 70, 758-762 (2015)
4.
Lunetta, K.L.* et al.: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:7756 (2015)
5.
Lunetta, K.L.* et al.: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat. Commun. 6:10257 (2015)
6.
Perry, J.R.B.* et al.: Parent-of-origin specific allelic associations among 106 genomic1 loci for age at menarche. Nature 514, 92-97 (2014)
7.
Fernández-Rhodes, L.* et al.: Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am. J. Epidemiol. 178, 451-460 (2013)
8.
Stolk, L.* et al.: Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat. Genet. 44, 260-268 (2012)
9.
Dupuis, J.* et al.: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat. Genet. 42, 105-116 (2010)
10.
Elks, C.E.* et al.: Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat. Genet. 42, 1077-1085 (2010)
11.
Pfeufer, A. et al.: Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat. Genet. 41, 407-414 (2009)
12.
Prokopenko, I.* et al.: Variants in MTNR1B influence fasting glucose levels. Nat. Genet. 41, 77-81 (2009)