My last visit with Friedrich Vogel: a personal remembrance Gudrun Rappold Obituary 06 December 2006 Pages: 749 - 750
Obituary: Prof. Dr. med. Dr. h. c. Friedrich Vogel (1925–2006) Karl Sperling Obituary 06 December 2006 Pages: 755 - 757
Structural divergence between the human and chimpanzee genomes Hildegard Kehrer-SawatzkiDavid N. Cooper Review 26 October 2006 Pages: 759 - 778
A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence? Catherine J. E. IngramMohamed F. ElaminDallas M. Swallow Original Investigation 21 November 2006 Pages: 779 - 788
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3 Shahid Y. KhanSaima RiazuddinSheikh Riazuddin Original Investigation 26 October 2006 Pages: 789 - 793
Cytogenetically balanced translocations are associated with focal copy number alterations Spencer K. WatsonRonald J. deLeeuwWan L. Lam Original Investigation 19 October 2006 Pages: 795 - 805
Admixture in Mexico City: implications for admixture mapping of Type 2 diabetes genetic risk factors Veronica L. Martinez-MarignacAdan ValladaresEsteban J. Parra Original Investigation 26 October 2006 Pages: 807 - 819
The possible role of 10398A and 16189C mtDNA variants in providing susceptibility toT2DM in two North Indian populations: a replicative study Audesh BhatAnil KoulR. N. K. Bamezai Original Investigation 26 October 2006 Pages: 821 - 826
Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males Yutaka NishigakiYoshiji YamadaMasashi Tanaka Original Investigation 11 October 2006 Pages: 827 - 836
Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome Rosanna WeksbergAndrea C. StachonAnne S. Bassett Original Investigation 07 October 2006 Pages: 837 - 845
Sequence variant in the laminin γ1 (LAMC1) gene associated with familial pelvic organ prolapse Ganka NikolovaHane LeeLarissa V. Rodríguez Original Investigation 05 October 2006 Pages: 847 - 856
The LRRK2 Gly2385Arg variant is associated with Parkinson’s disease: genetic and functional evidence E. K. TanY. ZhaoJ. J. Liu Original Investigation 30 September 2006 Pages: 857 - 863
Subsets of SNPs define rare genotype classes that predict ischemic heart disease Ruth Frikke-SchmidtCharles F. SingAnne Tybjærg-Hansen Original Investigation 28 September 2006 Pages: 865 - 877
Identification of a regulatory SNP in the retinol binding protein 4 gene associated with type 2 diabetes in Mongolia Lkhagvasuren MunkhtulgaKazuhiro NakayamaSadahiko Iwamoto Original Investigation 28 September 2006 Pages: 879 - 888
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. NicodemusBhaskar S. KolachanaDaniel R. Weinberger Original Investigation 28 September 2006 Pages: 889 - 906