1. CRISPR/Cas9 in zebrafish: an efficient combination for human genetic diseases modeling

   • Jiaqi Liu
   • Yangzhong Zhou
   • Nan Wu

   Review Open access 02 November 2016 Pages: 1 - 12

   

2. Copy number variability in Parkinson’s disease: assembling the puzzle through a systems biology approach

   • Valentina La Cognata
   • Giovanna Morello
   • Sebastiano Cavallaro

   Review Open access 28 November 2016 Pages: 13 - 37

   

3. Atlas of human diseases influenced by genetic variants with extreme allele frequency differences

   • Arvis Sulovari
   • Yolanda H. Chen
   • Dawei Li

   Original Investigation 03 October 2016 Pages: 39 - 54

   

4. Network analysis of mitonuclear GWAS reveals functional networks and tissue expression profiles of disease-associated genes

   • Simon C. Johnson
   • Brenda Gonzalez
   • Yousin Suh

   Original Investigation Open access 04 October 2016 Pages: 55 - 65

   

5. Preferential use of minor codons in the translation initiation region of human genes

   • Jung-Ho Park
   • Munjin Kwon
   • Masayori Inouye

   Original Investigation 11 October 2016 Pages: 67 - 74

   

6. Genetic factor common to schizophrenia and HIV infection is associated with risky sexual behavior: antagonistic vs. synergistic pleiotropic SNPs enriched for distinctly different biological functions

   • Qian Wang
   • Renato Polimanti
   • Joel Gelernter

   Original Investigation 17 October 2016 Pages: 75 - 83

   

7. Complete mitochondrial genomes of Thai and Lao populations indicate an ancient origin of Austroasiatic groups and demic diffusion in the spread of Tai–Kadai languages

   • Wibhu Kutanan
   • Jatupol Kampuansai
   • Mark Stoneking

   Original Investigation Open access 11 November 2016 Pages: 85 - 98

   

8. KDF1, encoding keratinocyte differentiation factor 1, is mutated in a multigenerational family with ectodermal dysplasia

   • Hanan E. Shamseldin
   • Ola Khalifa
   • Fowzan S. Alkuraya

   Original Investigation 12 November 2016 Pages: 99 - 105

   

9. A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect

   • Justin A. Pater
   • Tammy Benteau
   • Terry-Lynn Young

   Original Investigation Open access 12 November 2016 Pages: 107 - 118

   

10. Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders

    • R. Holt
    • S. A. Ugur Iseri
    • Nicola Ragge

    Original Investigation 14 November 2016 Pages: 119 - 127