1. Mouse models of SMA: tools for disease characterization and therapeutic development

   • Thomas W. Bebee
   • Catherine E. Dominguez
   • Dawn S. Chandler

   Review Paper 29 April 2012 Pages: 1277 - 1293

   

2. Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events

   • Shuenn-Nan Chiu
   • Mei-Hwan Wu
   • Mohamed Chahine

   Original Investigation 11 March 2012 Pages: 1295 - 1304

   

3. Adaptive evolution of loci covarying with the human African Pygmy phenotype

   • Isabel Mendizabal
   • Urko M. Marigorta
   • David Comas

   Original Investigation Open access 11 March 2012 Pages: 1305 - 1317

   

4. A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher

   • Kathryn M. Meurs
   • Sunshine Lahmers
   • Kerstin Lindblad-Toh

   Original Investigation 25 March 2012 Pages: 1319 - 1325

   

5. Using graded response model for the prediction of prostate cancer risk

   • Shyh-Huei Chen
   • Edward H. Ip
   • Fang-Chi Hsu

   Original Investigation 30 March 2012 Pages: 1327 - 1336

   

6. Increased risk of stroke in oral contraceptive users carried replicated genetic variants: a population-based case–control study in China

   • Chun Wang
   • Ying Li
   • Jianling Bai

   Original Investigation 04 April 2012 Pages: 1337 - 1344

7. Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats

   • Lena M. Brueckner
   • Evgeny Sagulenko
   • Larissa Savelyeva

   Original Investigation 05 April 2012 Pages: 1345 - 1359

   

8. Further clarification of the contribution of the ADH1C gene to vulnerability of alcoholism and selected liver diseases

   • Dawei Li
   • Hongyu Zhao
   • Joel Gelernter

   Original Investigation 05 April 2012 Pages: 1361 - 1374

   

9. Reduced interferon (IFN)-α conditioned by IFNA2 (−173) and IFNA8 (−884) haplotypes is associated with enhanced susceptibility to severe malarial anemia and longitudinal all-cause mortality

   • Prakasha Kempaiah
   • Samuel B. Anyona
   • Douglas J. Perkins

   Original Investigation 09 May 2012 Pages: 1375 - 1391

   

10. McKinlay Gardner RJ, Sutherland GR, Shaffer LG: Chromosome abnormalities and genetic counselling

    • John C. K. Barber

    Book Review 07 April 2012 Pages: 1393 - 1394