1. Anticipation in hereditary disease: the history of a biomedical concept

   • Judith E. Friedman

   Review Paper 12 June 2011 Pages: 705 - 714

   

2. A mutation screen in patients with Kabuki syndrome

   • Yun Li
   • Nina Bögershausen
   • Bernd Wollnik

   Original Investigation 24 May 2011 Pages: 715 - 724

   

3. Two-marker association tests yield new disease associations for coronary artery disease and hypertension

   • Thomas P. Slavin
   • Tao Feng
   • Robert C. Elston

   Original Investigation 28 May 2011 Pages: 725 - 733

   

4. Alterations of ATM and CADM1 in chromosomal 11q22.3–23.2 region are associated with the development of invasive cervical carcinoma

   • Dipanjana Mazumder Indra
   • Sraboni Mitra
   • Chinmay Kumar Panda

   Original Investigation 05 June 2011 Pages: 735 - 748

   

5. A miRNA-492 binding-site polymorphism in BSG (basigin) confers risk to psoriasis in Central South Chinese population

   • Li-Sha Wu
   • Fang-Fang Li
   • Xiang Chen

   Original Investigation 08 June 2011 Pages: 749 - 757

   

6. Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p

   • Atteeq U. Rehman
   • Khitab Gul
   • Thomas B. Friedman

   Original Investigation 10 June 2011 Pages: 759 - 765

   

7. A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer risk

   • Chang Sun
   • Dezheng Huo
   • Anna Di Rienzo

   Original Investigations 10 June 2011 Pages: 767 - 775

   

8. The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions

   • Minire Hasi
   • Bridgette Soileau
   • Jannine D. Cody

   Original Investigation 14 June 2011 Pages: 777 - 787

   

9. Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers

   • Shenying Fang
   • Ralf Krahe
   • Louise C. Strong

   Original Investigation 19 June 2011 Pages: 789 - 794

   

10. Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD

    • Jessica Ross
    • Judith Badner
    • Carol A. Mathews

    Original Investigation 21 June 2011 Pages: 795 - 805

    

11. MHC region and risk of systemic lupus erythematosus in African American women

    • Edward A. Ruiz-Narvaez
    • Patricia A. Fraser
    • Lynn Rosenberg

    Original Investigation 22 June 2011 Pages: 807 - 815

    

12. Novel variant Pro143Ala in HTRA2 contributes to Parkinson’s disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria

    • Chin-Hsien Lin
    • Meng-Ling Chen
    • Ruey-Meei Wu

    Original Investigation Open access 24 June 2011 Pages: 817 - 827

    

13. John C. Avise: Inside the human genome: a case for non-intelligent design

    • Peter S. Harper

    Book Review 08 July 2011 Pages: 829 - 830