Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives Jia XuPengwei YangBaiju Parikh Review Open access 22 January 2019 Pages: 109 - 124
New insights into the genetics of spermatogenic failure: a review of the literature Rossella CannarellaRosita A. CondorelliAldo E. Calogero Review 17 January 2019 Pages: 125 - 140
Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus Jonas Carlsson AlmlöfSara NystedtAnn-Christine Syvänen Original Investigation Open access 01 February 2019 Pages: 141 - 150
LncRNA ZBTB40-IT1 modulated by osteoporosis GWAS risk SNPs suppresses osteogenesis Bing MeiYa WangQingyang Huang Original Investigation 19 January 2019 Pages: 151 - 166
Integrative genomic analysis predicts novel functional enhancer-SNPs for bone mineral density Chuan QiuHui ShenHongwen Deng Original Investigation 17 January 2019 Pages: 167 - 185
Mutations in ACTL6B, coding for a subunit of the neuron-specific chromatin remodeling complex nBAF, cause early onset severe developmental and epileptic encephalopathy with brain hypomyelination and cerebellar atrophy Marco FicheraPinella FaillaMaurizio Elia Original Investigation 17 January 2019 Pages: 187 - 198
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data Karen Y. HeXiaoyin LiXiaofeng Zhu Original Investigation 22 January 2019 Pages: 199 - 210