Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how? Caroline Fiona WrightMark Kroese Review Article 20 November 2009 Pages: 125 - 134
Transposable elements in disease-associated cryptic exons Igor Vorechovsky Original Investigation 10 October 2009 Pages: 135 - 154
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations Isabelle SchrauwenMegan EalyGuy Van Camp Original Investigation 22 October 2009 Pages: 155 - 162
Malaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypes Marc C. LevesqueMaurine R. HobbsJ. Brice Weinberg Original Investigation 27 October 2009 Pages: 163 - 182
Genetic variation in PARL influences mitochondrial content Joanne E. CurranJeremy B. M. JowettAhmed H. Kissebah Original Investigation 28 October 2009 Pages: 183 - 190
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss Hui-Mei HongJiann-Jou YangShuan-Yow Li Original Investigation 30 October 2009 Pages: 191 - 199
Common CFTR gene variants influence body composition and survival in rural Ghana Maris KuningasDavid van BodegomRudi G. J. Westendorp Original Investigation Open access 05 November 2009 Pages: 201 - 206
Rubella vaccine-induced cellular immunity: evidence of associations with polymorphisms in the Toll-like, vitamin A and D receptors, and innate immune response genes Inna G. OvsyannikovaNeelam DhimanGregory A. Poland Original Investigation 10 November 2009 Pages: 207 - 221
Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines Hung-Pin TuAlbert Min-Shan KoYing-Chin Ko Original Investigation 14 November 2009 Pages: 223 - 229
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia Fiona ConnellKamini KalidasLymphoedema Consortium Original Investigation 13 November 2009 Pages: 231 - 241
Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia Fiona ConnellKamini KalidasLymphoedema Consortium Erratum 05 December 2009 Pages: 243 - 243
Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population Binbin WangZhimin MiaoXu Ma Short Report 17 November 2009 Pages: 245 - 246
R. C. Elston and W. D. Johnson: Basic biostatistics for geneticists and epidemiologists Peter HolmansLesley Jones Book Review 26 November 2009 Pages: 247 - 248