1. A locus for juvenile myoclonic epilepsy maps to 2q33–q36

   • Rinki Ratnapriya
   • Joseph Vijai
   • Anuranjan Anand

   Original Investigation 14 May 2010 Pages: 123 - 130

   

2. Association between genome-wide association studies reported SNPs and pediatric-onset Crohn’s disease in Canadian children

   • Devendra K. Amre
   • David R. Mack
   • Emile Levy

   Original Investigation 16 May 2010 Pages: 131 - 135

3. Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population

   • Shufeng Chen
   • Hongwei Wang
   • Dongfeng Gu

   Original Investigation 16 May 2010 Pages: 137 - 143

   

4. Genome-wide analysis of the structure of the South African Coloured Population in the Western Cape

   • Erika de Wit
   • Wayne Delport
   • Eileen G. Hoal

   Original Investigation 20 May 2010 Pages: 145 - 153

   

5. Genetic determinants of autism in individuals with deletions of 18q

   • Louise O’Donnell
   • Bridgette Soileau
   • Jannine D. Cody

   Original Investigation 25 May 2010 Pages: 155 - 164

   

6. Self-reported ethnicity, genetic structure and the impact of population stratification in a multiethnic study

   • Hansong Wang
   • Christopher A. Haiman
   • Daniel O. Stram

   Original Investigation 25 May 2010 Pages: 165 - 177

   

7. Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics

   • Y. Qiao
   • C. Harvard
   • E. Rajcan-Separovic

   Original Investigation 29 May 2010 Pages: 179 - 194

   

8. Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA

   • Meredith A. Bostrom
   • Lingyi Lu
   • Barry I. Freedman

   Original Investigation 08 June 2010 Pages: 195 - 204

   

9. The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expression

   • Chih-Hsin Lin
   • Chiung-Mei Chen
   • Guey-Jen Lee-Chen

   Original Investigation 09 June 2010 Pages: 205 - 212

   

10. Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes

    • Sulman Basit
    • Ghazanfar Ali
    • Wasim Ahmad

    Original Investigation 11 June 2010 Pages: 213 - 220

    

11. Identification of HAVCR1 gene haplotypes associated with mRNA expression levels and susceptibility to autoimmune diseases

    • José Raúl García-Lozano
    • Cristina Abad
    • María Francisca González-Escribano

    Original Investigation 12 June 2010 Pages: 221 - 229

    

12. Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs, David J. Weatherall: Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management

    • Alison May

    Book Review 25 May 2010 Pages: 231 - 232