1. The genetics of kidney transplantation

   • Nicolas Pallet
   • Eric Thervet

   Review Paper 16 September 2011 Pages: 317 - 323

2. Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?

   • Mark Richards
   • Frédérique Coppée
   • Meena Upadhyaya

   Review Paper 09 October 2011 Pages: 325 - 340

   

3. Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population

   • Xin Liu
   • Guoying Wang
   • Xiaobin Wang

   Original Investigation 17 August 2011 Pages: 341 - 351

   

4. Sex differences in disease risk from reported genome-wide association study findings

   • Linda Y. Liu
   • Marc A. Schaub
   • Atul J. Butte

   Original Investigation 20 August 2011 Pages: 353 - 364

   

5. The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations

   • Myung-Ju Ahn
   • Hong-Hee Won
   • Keunchil Park

   Original Investigation 25 August 2011 Pages: 365 - 372

   

6. Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing

   • Kathleen Askland
   • Cynthia Read
   • Jason H. Moore

   Original Investigation 25 August 2011 Pages: 373 - 391

   

7. Expression signature of epidermolysis bullosa simplex

   • Mbarka Bchetnia
   • Marie-Lou Tremblay
   • Catherine Laprise

   Original Investigation 30 August 2011 Pages: 393 - 406

   

8. Novel Alu retrotransposon insertion leading to Alström syndrome

   • Mustafa Taşkesen
   • Gayle B. Collin
   • Jürgen K. Naggert

   Original Investigation 30 August 2011 Pages: 407 - 413

   

9. Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3–q21.2 and screening of the candidate genes

   • Umm-e-Kalsoom
   • Sulman Basit
   • Wasim Ahmad

   Original Investigation 30 August 2011 Pages: 415 - 422

   

10. High altitude adaptation in Daghestani populations from the Caucasus

    • Luca Pagani
    • Qasim Ayub
    • Chris Tyler-Smith

    Original Investigation Open access 09 September 2011 Pages: 423 - 433

    

11. Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

    • Jose Felix Marti-Masso
    • Javier Ruiz-Martínez
    • Coro Paisán-Ruiz

    Original Investigation 13 September 2011 Pages: 435 - 442

    

12. Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population

    • Kazuo Yamada
    • Yoshimi Iwayama
    • Takeo Yoshikawa

    Original Investigation Open access 17 September 2011 Pages: 443 - 451

    

13. SLC39A2 and FSIP1 polymorphisms as potential modifiers of arsenic-related bladder cancer

    • Margaret R. Karagas
    • Angeline S. Andrew
    • Karl T. Kelsey

    Original Investigation 25 September 2011 Pages: 453 - 461

    

14. Genome-wide association study identifies HMGN3 locus for spine bone size variation in Chinese

    • Shu-Feng Lei
    • Hui Shen
    • Hong-Wen Deng

    Original Investigation 25 September 2011 Pages: 463 - 469

    

15. Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height

    • Jae-Jung Kim
    • Young-Mi Park
    • Jong-Keuk Lee

    Original Investigation 29 September 2011 Pages: 471 - 478

    

16. Fine mapping of 14q24.1 breast cancer susceptibility locus

    • Phoebe Lee
    • Yi-Ping Fu
    • Stephen J. Chanock

    Original Investigation 30 September 2011 Pages: 479 - 490

    

17. Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II

    • Hua Zhang
    • Hongsheng Chen
    • Yong Feng

    Original Investigation 01 October 2011 Pages: 491 - 503

    

18. Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese Hans

    • Ling Lu
    • Hongguang Sheng
    • Xu Lin

    Original Investigation 05 October 2011 Pages: 505 - 512

    

19. Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

    • Lluís Armengol
    • Julián Nevado
    • Luis Alberto Pérez-Jurado

    Original Investigation Open access 06 October 2011 Pages: 513 - 523

20. Review of Aaron Gillette, Eugenics and the nature–nurture debate in the twentieth century 2007, paperback edition, 2011, New York: Palgrave Macmillan

    • John Dupré

    Book Review 29 September 2011 Pages: 525 - 526