A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss Claire J. SineniMuzeyyen Yildirim-BaylanMustafa Tekin Original Investigation 07 June 2019 Pages: 1071 - 1075
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3 Xueshan XiaoWenmin SunQingjiong Zhang Original Investigation Open access 06 June 2019 Pages: 1077 - 1090
Genetic associations of breast and prostate cancer are enriched for regulatory elements identified in disease-related tissues Hongjie ChenGleb KichaevSara Lindström Original Investigation 22 June 2019 Pages: 1091 - 1104
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans Thomas M. KitzlerRonen SchneiderFriedhelm Hildebrandt Original Investigation 22 June 2019 Pages: 1105 - 1115
Autosomal recessive diseases among the Israeli Arabs Joël Zlotogora Original Investigation 26 June 2019 Pages: 1117 - 1122
Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic histories Francisco C. CeballosScott HazelhurstMichèle Ramsay Original Investigation 16 July 2019 Pages: 1123 - 1142
Correction to: Runs of homozygosity in sub-Saharan African populations provide insights into complex demographic histories Francisco C. CeballosScott HazelhurstMichèle Ramsay Correction 29 July 2019 Pages: 1143 - 1144
The rare 13q33–q34 microdeletions: eight new patients and review of the literature Lena Sagi-DainYael GoldbergIdit Maya Original Investigation 18 July 2019 Pages: 1145 - 1153
Ancestry-specific polygenic scores and SNP heritability of 25(OH)D in African- and European-ancestry populations Kathryn E. HatchellQiongshi LuCorinne D. Engelman Original Investigation 24 July 2019 Pages: 1155 - 1169
Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish Andrea R. WaksmunskiRobert P. Igo Jr.Jonathan L. Haines Original Investigation Open access 31 July 2019 Pages: 1171 - 1182
GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates Qing OuyangBrian C. KavanaughEric M. Morrow Original Investigation 30 August 2019 Pages: 1183 - 1200