1. A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

   • Claire J. Sineni
   • Muzeyyen Yildirim-Baylan
   • Mustafa Tekin

   Original Investigation 07 June 2019 Pages: 1071 - 1075

   

2. Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3

   • Xueshan Xiao
   • Wenmin Sun
   • Qingjiong Zhang

   Original Investigation Open access 06 June 2019 Pages: 1077 - 1090

   

3. Genetic associations of breast and prostate cancer are enriched for regulatory elements identified in disease-related tissues

   • Hongjie Chen
   • Gleb Kichaev
   • Sara Lindström

   Original Investigation 22 June 2019 Pages: 1091 - 1104

   

4. COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans

   • Thomas M. Kitzler
   • Ronen Schneider
   • Friedhelm Hildebrandt

   Original Investigation 22 June 2019 Pages: 1105 - 1115

   

5. Autosomal recessive diseases among the Israeli Arabs

   • Joël Zlotogora

   Original Investigation 26 June 2019 Pages: 1117 - 1122

6. Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic histories

   • Francisco C. Ceballos
   • Scott Hazelhurst
   • Michèle Ramsay

   Original Investigation 16 July 2019 Pages: 1123 - 1142

   

7. Correction to: Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic histories

   • Francisco C. Ceballos
   • Scott Hazelhurst
   • Michèle Ramsay

   Correction 29 July 2019 Pages: 1143 - 1144

   

8. The rare 13q33–q34 microdeletions: eight new patients and review of the literature

   • Lena Sagi-Dain
   • Yael Goldberg
   • Idit Maya

   Original Investigation 18 July 2019 Pages: 1145 - 1153

   

9. Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations

   • Kathryn E. Hatchell
   • Qiongshi Lu
   • Corinne D. Engelman

   Original Investigation 24 July 2019 Pages: 1155 - 1169

   

10. Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish

    • Andrea R. Waksmunski
    • Robert P. Igo Jr.
    • Jonathan L. Haines

    Original Investigation Open access 31 July 2019 Pages: 1171 - 1182

    

11. GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

    • Qing Ouyang
    • Brian C. Kavanaugh
    • Eric M. Morrow

    Original Investigation 30 August 2019 Pages: 1183 - 1200