1. Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency

   • Kenichiro Shirao
   • Satoshi Okada
   • Masao Kobayashi

   Review Article 08 April 2010 Pages: 619 - 628

   

2. West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica

   • Edward A. Ruiz-Narváez
   • Lance Bare
   • Hannia Campos

   Original Investigation 06 March 2010 Pages: 629 - 638

   

3. Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts

   • David A. Nielsen
   • Sara Hamon
   • Mary Jeanne Kreek

   Original Investigation 18 March 2010 Pages: 639 - 649

4. Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes

   • Yan V. Sun
   • Stephen T. Turner
   • Sharon L. R. Kardia

   Original Investigation 18 March 2010 Pages: 651 - 658

   

5. Two-stage case–control designs for rare genetic variants

   • Daniel J. Schaid
   • Jason P. Sinnwell

   Original Investigation 30 March 2010 Pages: 659 - 668

   

6. Heritability of chronic venous disease

   • Andreas Fiebig
   • Petra Krusche
   • Stefan Schreiber

   Original Investigation Open access 31 March 2010 Pages: 669 - 674

7. Fine mapping of the 9q31 Hirschsprung’s disease locus

   • C. S. Tang
   • Y. Sribudiani
   • M. M. Garcia-Barceló

   Original Investigation Open access 02 April 2010 Pages: 675 - 683

   

8. A single nucleotide polymorphism in the FADS1/FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyle

   • Kazuhiro Nakayama
   • Tumenbayer Bayasgalan
   • Jichi Medical University Promotion Team of a Large-scale Human Genome Bank for All over Japan

   Original Investigation 03 April 2010 Pages: 685 - 690

   

9. Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers

   • Jinxue Wei
   • Jennie Z. Ma
   • Ming D. Li

   Original Investigation 10 April 2010 Pages: 691 - 698

   

10. Power analysis for case–control association studies of samples with known family histories

    • Bo Peng
    • Biao Li
    • Christopher I. Amos

    Original Investigation 11 April 2010 Pages: 699 - 704

    

11. Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families

    • Ellen M. Wijsman
    • Joseph H. Rothstein
    • Gail P. Jarvik

    Original Investigation 11 April 2010 Pages: 705 - 719

    

12. A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency

    • Liat Ashkenazi-Hoffnung
    • Yael Lebenthal
    • Galia Gat-Yablonski

    Original Investigation 16 April 2010 Pages: 721 - 729

    

13. Evidence for inheritance in patients with VACTERL association

    • Benjamin D. Solomon
    • Daniel E. Pineda-Alvarez
    • Derek A. T. Cummings

    Short Report 06 April 2010 Pages: 731 - 733

    

14. Philippe Collas (ed): Chromatin immunoprecipitation assays: methods and protocols

    • Ray Waters

    Book Review 09 March 2010 Pages: 735 - 735

15. Malcolm Collins: Medicine and Sports Science, Vol. 54: Genetics and Sports

    • Jaikirty Singh Rawal

    Book Review 04 April 2010 Pages: 737 - 737