Analysis of implantation and ongoing pregnancy rates following the transfer of mosaic diploid–aneuploid blastocysts Elpida FragouliSamer AlfarawatiDagan Wells Original Investigation 09 April 2017 Pages: 805 - 819
Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability Nuria C. BramswigHermann-Josef LüdeckeDagmar Wieczorek Original Investigation 09 April 2017 Pages: 821 - 834
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism Nir PillarOren PleniceanuNoam Shomron Original Investigation Open access 25 April 2017 Pages: 835 - 845
Global skin colour prediction from DNA Susan WalshLakshmi ChaitanyaManfred Kayser Original Investigation Open access 12 May 2017 Pages: 847 - 863
Erratum to: Global skin colour prediction from DNA Susan WalshLakshmi ChaitanyaManfred Kayser Publisher's Erratum 03 June 2017 Pages: 865 - 866
Somatic mosaicism with reversion to normality of a mutated transthyretin allele related to a familial amyloidotic polyneuropathy Concetta FedericoKetty DugoSalvatore Saccone Original Investigation 15 May 2017 Pages: 867 - 873
CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice Cong HuaiChenqiang JiaDaru Lu Original Investigation 15 May 2017 Pages: 875 - 883
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-GarcíaFrancisco Javier Cotrina-VinagreFrancisco Martínez-Azorín Original Investigation 19 May 2017 Pages: 885 - 896
Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study Sara LindströmMarine Germainfor the INVENT Consortium Original Investigation 20 May 2017 Pages: 897 - 902
A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness Ellen KnierimEsther GillMarkus Schuelke Original Investigation 24 May 2017 Pages: 903 - 910
Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants Christina A. MarkunasEric O. JohnsonDana B. Hancock Original Investigation 31 May 2017 Pages: 911 - 919