1. Genetic alterations of δ-catenin/NPRAP/Neurojungin (CTNND2): functional implications in complex human diseases

   • Qun Lu
   • Byron J. Aguilar
   • Yan-Hua Chen

   Review 05 July 2016 Pages: 1107 - 1116

   

2. Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

   • Lyndal Henden
   • Saskia Freytag
   • Melanie Bahlo

   Original Investigation 01 July 2016 Pages: 1117 - 1125

   

3. The genetic history of Cochin Jews from India

   • Yedael Y. Waldman
   • Arjun Biddanda
   • Alon Keinan

   Original Investigation Open access 04 July 2016 Pages: 1127 - 1143

   

4. Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry

   • Frank Qian
   • Ye Feng
   • Dezheng Huo

   Original Investigation 05 July 2016 Pages: 1145 - 1159

5. Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith–Magenis syndrome with evident peripheral neuropathy

   • Bo Yuan
   • Juanita Neira
   • James R. Lupski

   Original Investigation 07 July 2016 Pages: 1161 - 1174

   

6. Immunoglobulin G genotypes and the risk of schizophrenia

   • Janardan P. Pandey
   • Aryan M. Namboodiri
   • Robert C. Elston

   Original Investigation 08 July 2016 Pages: 1175 - 1179

7. Three novel missense mutations in the filamin B gene are associated with isolated congenital talipes equinovarus

   • Haiou Yang
   • Zhaojing Zheng
   • Qihua Fu

   Original Investigation 09 July 2016 Pages: 1181 - 1189

   

8. Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans

   • Ranad Shaheen
   • Amal Hashem
   • Fowzan S. Alkuraya

   Original Investigation 08 August 2016 Pages: 1191 - 1197

   

9. CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly

   • Sulman Basit
   • Khalid M. Al-Harbi
   • Mohammed I. Samman

   Original Investigation 12 August 2016 Pages: 1199 - 1207

   

10. A lethal phenotype associated with tissue plasminogen deficiency in humans

    • Hanan E. Shamseldin
    • Abdulrahman Aldeeri
    • Fowzan S. Alkuraya

    Short Communication 14 July 2016 Pages: 1209 - 1211