1. Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives

   • Jia Xu
   • Pengwei Yang
   • Baiju Parikh

   Review Open access 22 January 2019 Pages: 109 - 124

   

2. New insights into the genetics of spermatogenic failure: a review of the literature

   • Rossella Cannarella
   • Rosita A. Condorelli
   • Aldo E. Calogero

   Review 17 January 2019 Pages: 125 - 140

   

3. Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus

   • Jonas Carlsson Almlöf
   • Sara Nystedt
   • Ann-Christine Syvänen

   Original Investigation Open access 01 February 2019 Pages: 141 - 150

   

4. LncRNA ZBTB40-IT1 modulated by osteoporosis GWAS risk SNPs suppresses osteogenesis

   • Bing Mei
   • Ya Wang
   • Qingyang Huang

   Original Investigation 19 January 2019 Pages: 151 - 166

   

5. Integrative genomic analysis predicts novel functional enhancer-SNPs for bone mineral density

   • Chuan Qiu
   • Hui Shen
   • Hongwen Deng

   Original Investigation 17 January 2019 Pages: 167 - 185

   

6. 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 Fichera
   • Pinella Failla
   • Maurizio Elia

   Original Investigation 17 January 2019 Pages: 187 - 198

   

7. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

   • Karen Y. He
   • Xiaoyin Li
   • Xiaofeng Zhu

   Original Investigation 22 January 2019 Pages: 199 - 210