1. U-statistics in genetic association studies

   • Hongzhe Li

   Review Paper 20 May 2012 Pages: 1395 - 1401

2. Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients

   • Richard B. Kennedy
   • Inna G. Ovsyannikova
   • Gregory A. Poland

   Original Investigation 19 May 2012 Pages: 1403 - 1421

   

3. Recommendations for ethical approaches to genotype-driven research recruitment

   • Laura M. Beskow
   • Stephanie M. Fullerton
   • Benjamin S. Wilfond

   Original Investigation 24 May 2012 Pages: 1423 - 1431

   

4. Genome-wide genetic associations with IFNγ response to smallpox vaccine

   • Richard B. Kennedy
   • Inna G. Ovsyannikova
   • Gregory A. Poland

   Original Investigation 03 June 2012 Pages: 1433 - 1451

   

5. Promoter variants in the MSMB gene associated with prostate cancer regulate MSMB/NCOA4 fusion transcripts

   • Hong Lou
   • Hongchuan Li
   • Michael Dean

   Original Investigation 04 June 2012 Pages: 1453 - 1466

   

6. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

   • Virginie J. M. Verhoeven
   • Pirro G. Hysi
   • Caroline C. W. Klaver

   Original Investigation Open access 05 June 2012 Pages: 1467 - 1480

   

7. Identification of germline genomic copy number variation in familial pancreatic cancer

   • Wigdan Al-Sukhni
   • Sarah Joe
   • Steven Gallinger

   Original Investigation 05 June 2012 Pages: 1481 - 1494

   

8. Genome-wide association analysis of circulating vitamin D levels in children with asthma

   • Jessica Lasky-Su
   • Nancy Lange
   • Augusto A. Litonjua

   Original Investigation 07 June 2012 Pages: 1495 - 1505

   

9. Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma

   • Yanhong Liu
   • Beatrice S. Melin
   • Melissa L. Bondy

   Original Investigation 12 June 2012 Pages: 1507 - 1517

   

10. Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction

    • Christelle Borel
    • Fanny Cheung
    • Andrew J. Sharp

    Short Report 30 May 2012 Pages: 1519 - 1524