Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition Gemma L. Moir-MeyerJohn F. PearsonLogan C. Walker Original Investigation 09 November 2014 Pages: 269 - 278
Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C Etsuko IioKentaro MatsuuraYasuhito Tanaka Original Investigation 17 December 2014 Pages: 279 - 289
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs Margus PutkuMart KalsMaris Laan Original Investigation Open access 28 December 2014 Pages: 291 - 303
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5 Daniella MagenAyala OfirHanna Mandel Original Investigation 06 January 2015 Pages: 305 - 314
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5 Daniella MagenAyala OfirHanna Mandel Erratum 22 January 2015 Pages: 315 - 315
Genome-wide methylation analysis in Silver–Russell syndrome patients A. R. PrickettM. IshidaR. J. Oakey Original Investigation 07 January 2015 Pages: 317 - 332
Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA) H. Dean Hosgood IIIMinsun SongQing Lan Original Investigation 08 January 2015 Pages: 333 - 341
A systematic heritability analysis of the human whole blood transcriptome Tianxiao HuanChunyu LiuDaniel Levy Original Investigation 14 January 2015 Pages: 343 - 358
Is there a male-specific effect on hypertension? Theresa DankowskiArne SchillertAndreas Ziegler Letter to the Editor 06 January 2015 Pages: 359 - 360
