Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency Kenichiro ShiraoSatoshi OkadaMasao Kobayashi Review Article 08 April 2010 Pages: 619 - 628
West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica Edward A. Ruiz-NarváezLance BareHannia Campos Original Investigation 06 March 2010 Pages: 629 - 638
Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts David A. NielsenSara HamonMary Jeanne Kreek Original Investigation 18 March 2010 Pages: 639 - 649
Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes Yan V. SunStephen T. TurnerSharon L. R. Kardia Original Investigation 18 March 2010 Pages: 651 - 658
Two-stage case–control designs for rare genetic variants Daniel J. SchaidJason P. Sinnwell Original Investigation 30 March 2010 Pages: 659 - 668
Heritability of chronic venous disease Andreas FiebigPetra KruscheStefan Schreiber Original Investigation Open access 31 March 2010 Pages: 669 - 674
Fine mapping of the 9q31 Hirschsprung’s disease locus C. S. TangY. SribudianiM. M. Garcia-Barceló Original Investigation Open access 02 April 2010 Pages: 675 - 683
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 NakayamaTumenbayer BayasgalanJichi Medical University Promotion Team of a Large-scale Human Genome Bank for All over Japan Original Investigation 03 April 2010 Pages: 685 - 690
Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers Jinxue WeiJennie Z. MaMing D. Li Original Investigation 10 April 2010 Pages: 691 - 698
Power analysis for case–control association studies of samples with known family histories Bo PengBiao LiChristopher I. Amos Original Investigation 11 April 2010 Pages: 699 - 704
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families Ellen M. WijsmanJoseph H. RothsteinGail P. Jarvik Original Investigation 11 April 2010 Pages: 705 - 719
A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency Liat Ashkenazi-HoffnungYael LebenthalGalia Gat-Yablonski Original Investigation 16 April 2010 Pages: 721 - 729
Evidence for inheritance in patients with VACTERL association Benjamin D. SolomonDaniel E. Pineda-AlvarezDerek A. T. Cummings Short Report 06 April 2010 Pages: 731 - 733
Philippe Collas (ed): Chromatin immunoprecipitation assays: methods and protocols Ray Waters Book Review 09 March 2010 Pages: 735 - 735
Malcolm Collins: Medicine and Sports Science, Vol. 54: Genetics and Sports Jaikirty Singh Rawal Book Review 04 April 2010 Pages: 737 - 737