Anticipation in hereditary disease: the history of a biomedical concept Judith E. Friedman Review Paper 12 June 2011 Pages: 705 - 714
A mutation screen in patients with Kabuki syndrome Yun LiNina BögershausenBernd Wollnik Original Investigation 24 May 2011 Pages: 715 - 724
Two-marker association tests yield new disease associations for coronary artery disease and hypertension Thomas P. SlavinTao FengRobert C. Elston Original Investigation 28 May 2011 Pages: 725 - 733
Alterations of ATM and CADM1 in chromosomal 11q22.3–23.2 region are associated with the development of invasive cervical carcinoma Dipanjana Mazumder IndraSraboni MitraChinmay Kumar Panda Original Investigation 05 June 2011 Pages: 735 - 748
A miRNA-492 binding-site polymorphism in BSG (basigin) confers risk to psoriasis in Central South Chinese population Li-Sha WuFang-Fang LiXiang Chen Original Investigation 08 June 2011 Pages: 749 - 757
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p Atteeq U. RehmanKhitab GulThomas B. Friedman Original Investigation 10 June 2011 Pages: 759 - 765
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer risk Chang SunDezheng HuoAnna Di Rienzo Original Investigations 10 June 2011 Pages: 767 - 775
The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions Minire HasiBridgette SoileauJannine D. Cody Original Investigation 14 June 2011 Pages: 777 - 787
Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers Shenying FangRalf KraheLouise C. Strong Original Investigation 19 June 2011 Pages: 789 - 794
Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD Jessica RossJudith BadnerCarol A. Mathews Original Investigation 21 June 2011 Pages: 795 - 805
MHC region and risk of systemic lupus erythematosus in African American women Edward A. Ruiz-NarvaezPatricia A. FraserLynn Rosenberg Original Investigation 22 June 2011 Pages: 807 - 815
Novel variant Pro143Ala in HTRA2 contributes to Parkinson’s disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria Chin-Hsien LinMeng-Ling ChenRuey-Meei Wu Original Investigation Open access 24 June 2011 Pages: 817 - 827
John C. Avise: Inside the human genome: a case for non-intelligent design Peter S. Harper Book Review 08 July 2011 Pages: 829 - 830
