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Nature Genetics|April 25, 2017
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer riskFelix R Day, Deborah J Thompson, Hannes Helgason, et al.Nature Genetics|August 1, 1994
Cooperative tumorigenic effects of germline mutations in Rb and p53B O Williams, L Remington, D M Albert, et al.Nature Genetics|August 1, 1994
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalenceD C Rubinsztein, W Amos, J Leggo, et al.Nature Genetics|August 1, 1994
Methylation of the oestrogen receptor CpG island links ageing and neoplasia in human colonJ P Issa, Y L Ottaviano, P Celano, et al.Nature Genetics|August 1, 1994
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1S Kass, C MacRae, H L Graber, et al.Nature Genetics|February 1, 1995
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disordersG Dodt, N Braverman, C Wong, et al.Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.Nature Genetics|February 1, 1995
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndromeA O Wilkie, S F Slaney, M Oldridge, et al.Nature Genetics|March 4, 2008
LKB1 signaling in mesenchymal cells required for suppression of gastrointestinal polyposisPekka Katajisto, Kari Vaahtomeri, Niklas Ekman, et al.Nature Genetics|January 15, 2008
Common variants in the GDF5-UQCC region are associated with variation in human heightSerena Sanna, Anne U Jackson, Ramaiah Nagaraja, et al.Pageof 744