The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes Dorota MoniesMohamed AbouelhodaFowzan S. Alkuraya Original Investigation Open access 09 June 2017 Pages: 921 - 939
Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma Meha KabraWei ZhangSubhabrata Chakrabarti Original Investigation 15 June 2017 Pages: 941 - 949
Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion Lam Opal HuangClaire Infante-RivardAurélie Labbe Original Investigation 19 June 2017 Pages: 951 - 961
Regulatory element-based prediction identifies new susceptibility regulatory variants for osteoporosis Shi YaoYan GuoTie-Lin Yang Original Investigation 20 June 2017 Pages: 963 - 974
Dosage effects of ZP2 and ZP3 heterozygous mutations cause human infertility Wenqiang LiuKunming LiShaorong Gao Original Investigation 24 June 2017 Pages: 975 - 985
A cis-eQTL genetic variant of the cancer–testis gene CCDC116 is associated with risk of multiple cancers Na QinCheng WangZhibin Hu Original Investigation 26 June 2017 Pages: 987 - 997
A genetic risk score is differentially associated with migraine with and without aura Claudia PisanuMartin PreisigHelgi B. Schiöth Original Investigation Open access 27 June 2017 Pages: 999 - 1008
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features Jing ZhangTomasz GambinPaweł Stankiewicz Erratum 28 June 2017 Pages: 1009 - 1011