1. My last visit with Friedrich Vogel: a personal remembrance

   • Gudrun Rappold

   Obituary 06 December 2006 Pages: 749 - 750

   

2. Friedrich Vogel 1925–2006

   • Peter Propping
   • Claus R. Bartram

   Obituary 06 December 2006 Pages: 751 - 753

3. Obituary: Prof. Dr. med. Dr. h. c. Friedrich Vogel (1925–2006)

   • Karl Sperling

   Obituary 06 December 2006 Pages: 755 - 757

4. Structural divergence between the human and chimpanzee genomes

   • Hildegard Kehrer-Sawatzki
   • David N. Cooper

   Review 26 October 2006 Pages: 759 - 778

   

5. A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?

   • Catherine J. E. Ingram
   • Mohamed F. Elamin
   • Dallas M. Swallow

   Original Investigation 21 November 2006 Pages: 779 - 788

   

6. Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

   • Shahid Y. Khan
   • Saima Riazuddin
   • Sheikh Riazuddin

   Original Investigation 26 October 2006 Pages: 789 - 793

   

7. Cytogenetically balanced translocations are associated with focal copy number alterations

   • Spencer K. Watson
   • Ronald J. deLeeuw
   • Wan L. Lam

   Original Investigation 19 October 2006 Pages: 795 - 805

   

8. Admixture in Mexico City: implications for admixture mapping of Type 2 diabetes genetic risk factors

   • Veronica L. Martinez-Marignac
   • Adan Valladares
   • Esteban J. Parra

   Original Investigation 26 October 2006 Pages: 807 - 819

   

9. The possible role of 10398A and 16189C mtDNA variants in providing susceptibility toT2DM in two North Indian populations: a replicative study

   • Audesh Bhat
   • Anil Koul
   • R. N. K. Bamezai

   Original Investigation 26 October 2006 Pages: 821 - 826

10. Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males

    • Yutaka Nishigaki
    • Yoshiji Yamada
    • Masashi Tanaka

    Original Investigation 11 October 2006 Pages: 827 - 836

11. Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome

    • Rosanna Weksberg
    • Andrea C. Stachon
    • Anne S. Bassett

    Original Investigation 07 October 2006 Pages: 837 - 845

    

12. Sequence variant in the laminin γ1 (LAMC1) gene associated with familial pelvic organ prolapse

    • Ganka Nikolova
    • Hane Lee
    • Larissa V. Rodríguez

    Original Investigation 05 October 2006 Pages: 847 - 856

    

13. The LRRK2 Gly2385Arg variant is associated with Parkinson’s disease: genetic and functional evidence

    • E. K. Tan
    • Y. Zhao
    • J. J. Liu

    Original Investigation 30 September 2006 Pages: 857 - 863

    

14. Subsets of SNPs define rare genotype classes that predict ischemic heart disease

    • Ruth Frikke-Schmidt
    • Charles F. Sing
    • Anne Tybjærg-Hansen

    Original Investigation 28 September 2006 Pages: 865 - 877

    

15. Identification of a regulatory SNP in the retinol binding protein 4 gene associated with type 2 diabetes in Mongolia

    • Lkhagvasuren Munkhtulga
    • Kazuhiro Nakayama
    • Sadahiko Iwamoto

    Original Investigation 28 September 2006 Pages: 879 - 888

    

16. Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia

    • Kristin K. Nicodemus
    • Bhaskar S. Kolachana
    • Daniel R. Weinberger

    Original Investigation 28 September 2006 Pages: 889 - 906

17. Novel human pathological mutations

    Human Gene Mutations 07 November 2006 Pages: 907 - 918