1. Molecular genetics and epigenetics of the cytochrome P450 gene family and its relevance for cancer risk and treatment

   • Cristina Rodriguez-Antona
   • Alvin Gomez
   • Magnus Ingelman-Sundberg

   Review Article 08 October 2009 Pages: 1 - 17

   

2. Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)

   • Kerry K. Brown
   • Jacob A. Reiss
   • Cynthia C. Morton

   Original Investigation 26 August 2009 Pages: 19 - 31

   

3. Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes

   • David P. Dimasi
   • Jern Y. Chen
   • Jamie E. Craig

   Original Investigation 28 August 2009 Pages: 33 - 44

   

4. Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency

   • Véronique Picard
   • Jian-Min Chen
   • Martine Alhenc-Gelas

   Original Investigation 17 September 2009 Pages: 45 - 53

   

5. Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

   • Janniche Torsvik
   • Stefan Johansson
   • Pål R. Njølstad

   Original Investigation 17 September 2009 Pages: 55 - 64

   

6. Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans

   • Digna Rosa Velez
   • Christian Wejse
   • William K. Scott

   Original Investigation 22 September 2009 Pages: 65 - 73

   

7. An intronic polymorphism in the corticotropin-releasing hormone receptor 2 gene increases susceptibility to HBV-related hepatocellular carcinoma in Chinese population

   • Xing Gu
   • Peng Qi
   • Chunfang Gao

   Original Investigation 08 October 2009 Pages: 75 - 81

8. A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia

   • Adriana Huertas-Vazquez
   • Christopher L. Plaisier
   • Päivi Pajukanta

   Original Investigation Open access 09 October 2009 Pages: 83 - 89

   

9. A comprehensive resequence analysis of the KLK15–KLK3–KLK2 locus on chromosome 19q13.33

   • Hemang Parikh
   • Zuoming Deng
   • Laufey Amundadottir

   Original Investigation Open access 13 October 2009 Pages: 91 - 99

   

10. The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies

    • Sonny Dandona
    • Li Chen
    • Alexandre F. R. Stewart

    Original Investigation 03 November 2009 Pages: 101 - 105

11. H Kehrer-sawatzki and DN Cooper (eds): Copy number variation and disease

    • F. Lucy Raymond

    Book Review 03 November 2009 Pages: 107 - 108

12. Novel human pathological mutations

    Human Gene Mutations 07 November 2009 Pages: 109 - 124