1. Analysis of implantation and ongoing pregnancy rates following the transfer of mosaic diploid–aneuploid blastocysts

   • Elpida Fragouli
   • Samer Alfarawati
   • Dagan Wells

   Original Investigation 09 April 2017 Pages: 805 - 819

   

2. Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability

   • Nuria C. Bramswig
   • Hermann-Josef Lüdecke
   • Dagmar Wieczorek

   Original Investigation 09 April 2017 Pages: 821 - 834

   

3. A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism

   • Nir Pillar
   • Oren Pleniceanu
   • Noam Shomron

   Original Investigation Open access 25 April 2017 Pages: 835 - 845

   

4. Global skin colour prediction from DNA

   • Susan Walsh
   • Lakshmi Chaitanya
   • Manfred Kayser

   Original Investigation Open access 12 May 2017 Pages: 847 - 863

   

5. Erratum to: Global skin colour prediction from DNA

   • Susan Walsh
   • Lakshmi Chaitanya
   • Manfred Kayser

   Publisher's Erratum 03 June 2017 Pages: 865 - 866

6. Somatic mosaicism with reversion to normality of a mutated transthyretin allele related to a familial amyloidotic polyneuropathy

   • Concetta Federico
   • Ketty Dugo
   • Salvatore Saccone

   Original Investigation 15 May 2017 Pages: 867 - 873

   

7. CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice

   • Cong Huai
   • Chenqiang Jia
   • Daru Lu

   Original Investigation 15 May 2017 Pages: 875 - 883

   

8. An innovative strategy to clone positive modifier genes of defects caused by mtDNA mutations: MRPS18C as suppressor gene of m.3946G>A mutation in MT-ND1 gene

   • María Elena Rodríguez-García
   • Francisco Javier Cotrina-Vinagre
   • Francisco Martínez-Azorín

   Original Investigation 19 May 2017 Pages: 885 - 896

   

9. Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study

   • Sara Lindström
   • Marine Germain
   • for the INVENT Consortium

   Original Investigation 20 May 2017 Pages: 897 - 902

   

10. A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness

    • Ellen Knierim
    • Esther Gill
    • Markus Schuelke

    Original Investigation 24 May 2017 Pages: 903 - 910

    

11. Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants

    • Christina A. Markunas
    • Eric O. Johnson
    • Dana B. Hancock

    Original Investigation 31 May 2017 Pages: 911 - 919