Molecular genetics and epigenetics of the cytochrome P450 gene family and its relevance for cancer risk and treatment Cristina Rodriguez-AntonaAlvin GomezMagnus Ingelman-Sundberg Review Article 08 October 2009 Pages: 1 - 17
Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35) Kerry K. BrownJacob A. ReissCynthia C. Morton Original Investigation 26 August 2009 Pages: 19 - 31
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes David P. DimasiJern Y. ChenJamie E. Craig Original Investigation 28 August 2009 Pages: 33 - 44
Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency Véronique PicardJian-Min ChenMartine Alhenc-Gelas Original Investigation 17 September 2009 Pages: 45 - 53
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes Janniche TorsvikStefan JohanssonPål R. Njølstad Original Investigation 17 September 2009 Pages: 55 - 64
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans Digna Rosa VelezChristian WejseWilliam K. Scott Original Investigation 22 September 2009 Pages: 65 - 73
An intronic polymorphism in the corticotropin-releasing hormone receptor 2 gene increases susceptibility to HBV-related hepatocellular carcinoma in Chinese population Xing GuPeng QiChunfang Gao Original Investigation 08 October 2009 Pages: 75 - 81
A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia Adriana Huertas-VazquezChristopher L. PlaisierPäivi Pajukanta Original Investigation Open access 09 October 2009 Pages: 83 - 89
A comprehensive resequence analysis of the KLK15–KLK3–KLK2 locus on chromosome 19q13.33 Hemang ParikhZuoming DengLaufey Amundadottir Original Investigation Open access 13 October 2009 Pages: 91 - 99
The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies Sonny DandonaLi ChenAlexandre F. R. Stewart Original Investigation 03 November 2009 Pages: 101 - 105
H Kehrer-sawatzki and DN Cooper (eds): Copy number variation and disease F. Lucy Raymond Book Review 03 November 2009 Pages: 107 - 108