1. Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?

   • Caroline Fiona Wright
   • Mark Kroese

   Review Article 20 November 2009 Pages: 125 - 134

   

2. Transposable elements in disease-associated cryptic exons

   • Igor Vorechovsky

   Original Investigation 10 October 2009 Pages: 135 - 154

   

3. Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations

   • Isabelle Schrauwen
   • Megan Ealy
   • Guy Van Camp

   Original Investigation 22 October 2009 Pages: 155 - 162

   

4. Malaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypes

   • Marc C. Levesque
   • Maurine R. Hobbs
   • J. Brice Weinberg

   Original Investigation 27 October 2009 Pages: 163 - 182

   

5. Genetic variation in PARL influences mitochondrial content

   • Joanne E. Curran
   • Jeremy B. M. Jowett
   • Ahmed H. Kissebah

   Original Investigation 28 October 2009 Pages: 183 - 190

   

6. A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss

   • Hui-Mei Hong
   • Jiann-Jou Yang
   • Shuan-Yow Li

   Original Investigation 30 October 2009 Pages: 191 - 199

   

7. Common CFTR gene variants influence body composition and survival in rural Ghana

   • Maris Kuningas
   • David van Bodegom
   • Rudi G. J. Westendorp

   Original Investigation Open access 05 November 2009 Pages: 201 - 206

   

8. 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. Ovsyannikova
   • Neelam Dhiman
   • Gregory A. Poland

   Original Investigation 10 November 2009 Pages: 207 - 221

   

9. Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines

   • Hung-Pin Tu
   • Albert Min-Shan Ko
   • Ying-Chin Ko

   Original Investigation 14 November 2009 Pages: 223 - 229

   

10. Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

    • Fiona Connell
    • Kamini Kalidas
    • Lymphoedema Consortium

    Original Investigation 13 November 2009 Pages: 231 - 241

    

11. Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

    • Fiona Connell
    • Kamini Kalidas
    • Lymphoedema Consortium

    Erratum 05 December 2009 Pages: 243 - 243

    

12. Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population

    • Binbin Wang
    • Zhimin Miao
    • Xu Ma

    Short Report 17 November 2009 Pages: 245 - 246

13. R. C. Elston and W. D. Johnson: Basic biostatistics for geneticists and epidemiologists

    • Peter Holmans
    • Lesley Jones

    Book Review 26 November 2009 Pages: 247 - 248