The complex genetic landscape of familial breast cancer Lorenzo MelchorJavier BenÃtez Review Paper 05 April 2013 Pages: 845 - 863
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy Jan HalbritterJonathan D. PorathThe GPN Study Group Original Investigation 05 April 2013 Pages: 865 - 884
Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome J. C. CzeschikC. VoigtD. Wieczorek Original Investigation 09 April 2013 Pages: 885 - 898
Comprehensively identifying and characterizing the missing gene sequences in human reference genome with integrated analytic approaches Geng ChenCharles WangTieliu Shi Original Investigation 10 April 2013 Pages: 899 - 911
Exome sequencing reveals CCDC111 mutation associated with high myopia Fuxin ZhaoJinyu WuXiangtian Zhou Original Investigation 12 April 2013 Pages: 913 - 921
Mouse models of fukutin-related protein mutations show a wide range of disease phenotypes Anthony BlaeserElizabeth KeramarisQi Long Lu Original Investigation 17 April 2013 Pages: 923 - 934
Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth Jude J. McElroyCourtney E. GutmanLouis J. Muglia Original Investigation 17 April 2013 Pages: 935 - 942
BET1L and TNRC6B associate with uterine fibroid risk among European Americans Todd L. EdwardsKara A. MichelsDigna R. Velez Edwards Original Investigation 19 April 2013 Pages: 943 - 953
Nathaniel Comfort: The science of human perfection, how genes became the heart of American Medicine Shirley Hodgson Book Review 20 June 2013 Pages: 955 - 956
Erratum to: Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort Sharon R. BrowningBrian L. Browning Erratum 19 April 2013 Pages: 957 - 958