The genetic basis of pulmonary arterial hypertension Lijiang MaWendy K. Chung Review Paper 21 January 2014 Pages: 471 - 479
Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA Madalene A. EarpLinda E. KelemenOn behalf of the Ovarian Cancer Association Consortium Original Investigation 05 November 2013 Pages: 481 - 497
BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3 Xin XiongChengqi XuQing K. Wang Original Investigation 05 November 2013 Pages: 499 - 508
A genome-wide association study of prostate cancer in West African men Michael Blaise CookZhaoming WangAfrican Ancestry Prostate Cancer GWAS Consortium Original Investigation 02 November 2013 Pages: 509 - 521
Erratum to: A genome-wide association study of prostate cancer in West African men Michael Blaise CookZhaoming WangStephen J. Chanock Erratum 03 December 2013 Pages: 523 - 523
A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer C. Fernandez-RozadillaJ. B. CazierC. Ruiz-Ponte Original Investigation 12 November 2013 Pages: 525 - 534
Comparative-high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations Pawel BorunLukasz KubaszewskiAndrzej Plawski Original Investigation Open access 15 November 2013 Pages: 535 - 545
Gene–gene and gene–environment interactions in ulcerative colitis Ming-Hsi WangClaudio FiocchiJean-Paul Achkar Original Investigation 17 November 2013 Pages: 547 - 558
Natural and orthogonal model for estimating gene–gene interactions applied to cutaneous melanoma Feifei XiaoJianzhong MaChristopher I. Amos Original Investigation 17 November 2013 Pages: 559 - 574
Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populations Shaolin WangAndrew D van der VaartMing D. Li Original Investigation 20 November 2013 Pages: 575 - 586
Common DNA variants predict tall stature in Europeans Fan LiuA. Emile J. HendriksManfred Kayser Original Investigation 20 November 2013 Pages: 587 - 597
COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal lamina Juan ArredondoMarian LaraRicardo A. Maselli Original Investigation 27 November 2013 Pages: 599 - 616
Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variants Can YangCong LiJoel Gelernter Original Investigation 03 December 2013 Pages: 617 - 624
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome R. S. MøllerL. R. JensenT. Kleefstra Original Investigation 11 December 2013 Pages: 625 - 638
Improving genetic risk prediction by leveraging pleiotropy Cong LiCan YangHongyu Zhao Original Investigation 13 December 2013 Pages: 639 - 650
Case–control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy Larry BaumBatoul Sadat HaerianPatrick Kwan Original Investigation 13 December 2013 Pages: 651 - 659
Identification of BACH2 as a susceptibility gene for Graves’ disease in the Chinese Han population based on a three-stage genome-wide association study Wei LiuHai-Ning WangThe China Consortium for the Genetics of Autoimmune Thyroid Disease Original Investigation 12 December 2013 Pages: 661 - 671
Does variation in NIPA2 contribute to genetic generalized epilepsy? Michael S. HildebrandJohn A. DamianoSamuel F. Berkovic Letter to the Editor 10 January 2014 Pages: 673 - 674
NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population Yuwu JiangYuehua ZhangXiru Wu Letter to the Editor 06 February 2014 Pages: 675 - 676
Erratum to: RET and NRG1 interplay in Hirschsprung disease Hongsheng GuiWai-Kiu TangMaria-Mercè Garcia-Barceló Erratum 15 February 2014 Pages: 677 - 677
