Genetic syndromes caused by mutations in epigenetic genes María BerdascoManel Esteller Review Paper 31 January 2013 Pages: 359 - 383
Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance M. Hashim RazaE. Michael GertzDennis Drayna Original Investigation 13 December 2012 Pages: 385 - 396
Ordered subset linkage analysis based on admixture proportion identifies new linkage evidence for alcohol dependence in African-Americans Shizhong HanJoel GelernterBao-Zhu Yang Original Investigation 13 December 2012 Pages: 397 - 403
Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity Alexis C. Frazier-WoodAni ManichaikulDonna K. Arnett Original Investigation 22 December 2012 Pages: 405 - 413
Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio Adam J. Lawrance-OwenGary BargaryJ. D. Mollon Original Investigation 22 December 2012 Pages: 415 - 421
Genome-wide association study identified novel genetic variant on SLC45A3 gene associated with serum levels prostate-specific antigen (PSA) in a Chinese population Jielin SunSha TaoZengnan Mo Original Investigation 27 December 2012 Pages: 423 - 429
Dissecting direct and indirect genetic effects on chronic obstructive pulmonary disease (COPD) susceptibility Mateusz SiedlinskiDustin Tingleyand the COPDGene and ECLIPSE Investigators Original Investigation 09 January 2013 Pages: 431 - 441
Increased paternal age and the influence on burden of genomic copy number variation in the general population Jacobine E. Buizer-VoskampHylke M. BlauwRoel A. Ophoff Original Investigation 13 January 2013 Pages: 443 - 450
Functional polymorphisms in NFκB1/IκBα predict risks of chronic obstructive pulmonary disease and lung cancer in Chinese Dongsheng HuangLei YangJiachun Lu Original Investigation 16 January 2013 Pages: 451 - 460
Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients Stella-Amrei KundeNils RademacherSarah A. Shoichet Original Investigation 18 January 2013 Pages: 461 - 471
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita Bari J. BallewMeredith YeagerSharon A. Savage Original Investigation 18 January 2013 Pages: 473 - 480