1. Resequencing and association analysis of the SP110 gene in adult pulmonary tuberculosis

   • Jeffrey S. Szeszko
   • Barry Healy
   • Sergey Nejentsev

   Original Investigation 06 December 2006 Pages: 155 - 160

2. Genetic polymorphisms in the oxidative stress pathway and susceptibility to non-Hodgkin lymphoma

   • Qing Lan
   • Tongzhang Zheng
   • Stephen Chanock

   Original Investigation 06 December 2006 Pages: 161 - 168

3. The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case–control studies

   • Klaus Berger
   • Florian Stögbauer
   • Harald Funke

   Original Investigation 13 December 2006 Pages: 169 - 178

4. A case of true hermaphroditism reveals an unusual mechanism of twinning

   • Vivienne L. Souter
   • Melissa A. Parisi
   • Grant W. Montgomery

   Original Investigation 13 December 2006 Pages: 179 - 185

   

5. High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications

   • Johan H. Gibcus
   • Klaas Kok
   • Ed Schuuring

   Original Investigation 15 December 2006 Pages: 187 - 201

   

6. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

   • Inga Ebermann
   • Hendrik P. N. Scholl
   • Hanno Bolz

   Original Investigation 15 December 2006 Pages: 203 - 211

   

7. Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population

   • Justine A. Ellis
   • Katrina J. Scurrah
   • Stephen B. Harrap

   Original Investigation 20 December 2006 Pages: 213 - 222

   

8. PD-1 gene haplotype is associated with the development of type 1 diabetes mellitus in Japanese children

   • Ronghua Ni
   • Kenji Ihara
   • Toshiro Hara

   Original Investigation 03 January 2007 Pages: 223 - 232

   

9. Genetic variation in the base excision repair pathway and bladder cancer risk

   • Jonine D. Figueroa
   • Núria Malats
   • Montserrat García-Closas

   Original Investigation 03 January 2007 Pages: 233 - 242

   

10. Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels

    • Ana M. Coutinho
    • Inês Sousa
    • Astrid M. Vicente

    Original Investigation 03 January 2007 Pages: 243 - 256

    

11. Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance

    • Sanna Pakkanen
    • Agnes B. Baffoe-Bonnie
    • Johanna Schleutker

    Original Investigation 03 January 2007 Pages: 257 - 267

    

12. A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33–34

    • B. Isidor
    • N. Dagoneau
    • V. Cormier-Daire

    Original Investigation 03 January 2007 Pages: 269 - 273

    

13. Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations

    • Lisa J. Martin
    • Vijaya Ramachandran
    • D. Woodrow Benson

    Original Investigation 04 January 2007 Pages: 275 - 284

    

14. Times of triumph, times of doubt and the battle for public trust

    • Peter S. Harper

    Book Review 13 December 2006 Pages: 285 - 285

15. Novel human pathological mutations

    Human Gene Mutations 08 February 2007 Pages: 287 - 299

16. Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

    • Daniel J. Schaid
    • Investigators of the International Consortium for Prostate Cancer Genetics

    Erratum 16 December 2006 Pages: 301 - 303