1. The genetic basis of pulmonary arterial hypertension

   • Lijiang Ma
   • Wendy K. Chung

   Review Paper 21 January 2014 Pages: 471 - 479

   

2. Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA

   • Madalene A. Earp
   • Linda E. Kelemen
   • On behalf of the Ovarian Cancer Association Consortium

   Original Investigation 05 November 2013 Pages: 481 - 497

   

3. BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3

   • Xin Xiong
   • Chengqi Xu
   • Qing K. Wang

   Original Investigation 05 November 2013 Pages: 499 - 508

   

4. A genome-wide association study of prostate cancer in West African men

   • Michael Blaise Cook
   • Zhaoming Wang
   • African Ancestry Prostate Cancer GWAS Consortium

   Original Investigation 02 November 2013 Pages: 509 - 521

   

5. Erratum to: A genome-wide association study of prostate cancer in West African men

   • Michael Blaise Cook
   • Zhaoming Wang
   • Stephen J. Chanock

   Erratum 03 December 2013 Pages: 523 - 523

6. A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer

   • C. Fernandez-Rozadilla
   • J. B. Cazier
   • C. Ruiz-Ponte

   Original Investigation 12 November 2013 Pages: 525 - 534

   

7. Comparative-high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations

   • Pawel Borun
   • Lukasz Kubaszewski
   • Andrzej Plawski

   Original Investigation Open access 15 November 2013 Pages: 535 - 545

   

8. Gene–gene and gene–environment interactions in ulcerative colitis

   • Ming-Hsi Wang
   • Claudio Fiocchi
   • Jean-Paul Achkar

   Original Investigation 17 November 2013 Pages: 547 - 558

   

9. Natural and orthogonal model for estimating gene–gene interactions applied to cutaneous melanoma

   • Feifei Xiao
   • Jianzhong Ma
   • Christopher I. Amos

   Original Investigation 17 November 2013 Pages: 559 - 574

   

10. Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populations

    • Shaolin Wang
    • Andrew D van der Vaart
    • Ming D. Li

    Original Investigation 20 November 2013 Pages: 575 - 586

    

11. Common DNA variants predict tall stature in Europeans

    • Fan Liu
    • A. Emile J. Hendriks
    • Manfred Kayser

    Original Investigation 20 November 2013 Pages: 587 - 597

    

12. COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal lamina

    • Juan Arredondo
    • Marian Lara
    • Ricardo A. Maselli

    Original Investigation 27 November 2013 Pages: 599 - 616

    

13. Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variants

    • Can Yang
    • Cong Li
    • Joel Gelernter

    Original Investigation 03 December 2013 Pages: 617 - 624

    

14. X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome

    • R. S. Møller
    • L. R. Jensen
    • T. Kleefstra

    Original Investigation 11 December 2013 Pages: 625 - 638

    

15. Improving genetic risk prediction by leveraging pleiotropy

    • Cong Li
    • Can Yang
    • Hongyu Zhao

    Original Investigation 13 December 2013 Pages: 639 - 650

    

16. Case–control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy

    • Larry Baum
    • Batoul Sadat Haerian
    • Patrick Kwan

    Original Investigation 13 December 2013 Pages: 651 - 659

    

17. 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 Liu
    • Hai-Ning Wang
    • The China Consortium for the Genetics of Autoimmune Thyroid Disease

    Original Investigation 12 December 2013 Pages: 661 - 671

    

18. Does variation in NIPA2 contribute to genetic generalized epilepsy?

    • Michael S. Hildebrand
    • John A. Damiano
    • Samuel F. Berkovic

    Letter to the Editor 10 January 2014 Pages: 673 - 674

19. NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population

    • Yuwu Jiang
    • Yuehua Zhang
    • Xiru Wu

    Letter to the Editor 06 February 2014 Pages: 675 - 676

20. Erratum to: RET and NRG1 interplay in Hirschsprung disease

    • Hongsheng Gui
    • Wai-Kiu Tang
    • Maria-Mercè Garcia-Barceló

    Erratum 15 February 2014 Pages: 677 - 677