1. Missing data imputation and haplotype phase inference for genome-wide association studies

   • Sharon R. Browning

   Review 11 October 2008 Pages: 439 - 450

   

2. The human pseudoxanthoma elasticum gene ABCC6 is transcriptionally regulated by PLAG family transcription factors

   • Marcin Ratajewski
   • Wim J. M. Van de Ven
   • Lukasz Pulaski

   Original Investigation 12 October 2008 Pages: 451 - 463

   

3. MMP-1 polymorphisms and the risk of idiopathic pulmonary fibrosis

   • Marco Checa
   • Víctor Ruiz
   • Annie Pardo

   Original Investigation 14 October 2008 Pages: 465 - 472

   

4. Gradual reduction of BUBR1 protein levels results in premature sister-chromatid separation then in aneuploidy

   • Elodie Bohers
   • Nasrin Sarafan-Vasseur
   • Thierry Frebourg

   Original Investigation 19 October 2008 Pages: 473 - 478

   

5. Male–female differences in the genetic regulation of t-PA and PAI-1 levels in a Ghanaian population

   • J. A. Schoenhard
   • F. W. Asselbergs
   • Scott M. Williams

   Original Investigation 25 October 2008 Pages: 479 - 488

6. Identification of copy number variants associated with BPES-like phenotypes

   • Antoinet C. J. Gijsbers
   • Barbara D’haene
   • Claudia A. L. Ruivenkamp

   Original Investigation Open access 25 October 2008 Pages: 489 - 498

   

7. Association of the GNAS locus with severe malaria

   • Sarah Auburn
   • Mahamadou Diakite
   • Dominic P. Kwiatkowski

   Original Investigation 26 October 2008 Pages: 499 - 506

   

8. Ataxia and pancytopenia caused by a mutation in TINF2

   • Elena Tsangaris
   • Sally-Lin Adams
   • Yigal Dror

   Original Investigation 01 November 2008 Pages: 507 - 513

   

9. Haplotypes of IL-10 promoter variants are associated with susceptibility to severe malarial anemia and functional changes in IL-10 production

   • Collins Ouma
   • Gregory C. Davenport
   • Douglas J. Perkins

   Original Investigation 30 October 2008 Pages: 515 - 524

   

10. The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts

    • Marie-José H. van den Boogaard
    • Dominique de Costa
    • Régine P. M. Steegers-Theunissen

    Original Investigation Open access 19 October 2008 Pages: 525 - 534

    

11. A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred

    • George S. Charames
    • Lily Ramyar
    • Bharati Bapat

    Original Investigation 04 November 2008 Pages: 535 - 541

    

12. Linkage mapping of CVD risk traits in the isolated Norfolk Island population

    • C. Bellis
    • H. C. Cox
    • L. R. Griffiths

    Original Investigation 31 October 2008 Pages: 543 - 552

    

13. MLXIPL variant in individuals with low and high triglyceridemia in white population in Central Europe

    • Michal Vrablik
    • Richard Ceska
    • Jaroslav A. Hubacek

    Short Report 23 October 2008 Pages: 553 - 555

14. Genetic variants in the renin-angiotensin system genes are associated with cardiovascular-renal-related risk factors in Mexican Americans

    • Farook Thameem
    • V. Saroja Voruganti
    • Nedal H. Arar

    Short Report 06 November 2008 Pages: 557 - 559