1. Leprosy as a genetic model for susceptibility to common infectious diseases

   • Andrea Alter
   • Alexandre Alcaïs
   • Erwin Schurr

   Review Article 05 February 2008 Pages: 227 - 235

   

2. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity

   • Ali Jalali
   • Kimberly A. Aldinger
   • Alexander G. Bassuk

   Original Investigation 19 January 2008 Pages: 237 - 245

   

3. Genetic variation in IGFBP2 and IGFBP5 is associated with breast cancer in populations of African descent

   • Chad P. Garner
   • Yuan C. Ding
   • Susan L. Neuhausen

   Original Investigation 22 January 2008 Pages: 247 - 255

   

4. Exploring gene-environment interactions in Parkinson’s disease

   • Colin C. McCulloch
   • Denise M. Kay
   • Haydeh Payami

   Original Investigation 22 January 2008 Pages: 257 - 265

5. A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9

   • Insaf Bel Hadj Ali
   • Melissa Thys
   • Guy Van Camp

   Original Investigation 26 January 2008 Pages: 267 - 272

   

6. Haplotypic analysis of Wellcome Trust Case Control Consortium data

   • Brian L. Browning
   • Sharon R. Browning

   Original Investigation 26 January 2008 Pages: 273 - 280

   

7. Protein C -1641A/-1654C haplotype is associated with organ dysfunction and the fatal outcome of severe sepsis in Chinese Han population

   • Qi Xing Chen
   • Shui Jing Wu
   • Xiang Ming Fang

   Original Investigation 05 February 2008 Pages: 281 - 287

8. An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women

   • Anna Stanisławska-Sachadyn
   • Karen S. Brown
   • Alexander S. Whitehead

   Original Investigation 05 February 2008 Pages: 289 - 295

   

9. A genome-wide association scan for asthma in a general Australian population

   • J. Hui
   • A. Oka
   • H. Inoko

   Original Investigation 06 February 2008 Pages: 297 - 306

   

10. Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease

    • Steven Wiltshire
    • Brenda L. Powell
    • John P. Beilby

    Original Investigation 21 February 2008 Pages: 307 - 313

11. William Reardon: The Bedside Dysmorphologist

    • Jill Clayton-Smith

    Book Review 29 January 2008 Pages: 315 - 316

12. W.A. Schultz: Molecular biology of human cancers. An advanced student’s textbook

    • Shirley Hodgson

    Book Review 05 February 2008 Pages: 317 - 318

13. Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16

    • Marcella Zollino
    • Rosetta Lecce
    • Giovanni Neri

    Erratum 15 February 2008 Pages: 319 - 319