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Nature Genetics|May 23, 2017
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney diseaseHao Lu, Maria C Rondón Galeano, Elisabeth Ott, et al.Nature Genetics|May 23, 2017
The complex genetics of hypoplastic left heart syndromeXiaoqin Liu, Hisato Yagi, Shazina Saeed, et al.Nature Genetics|April 27, 2017
A SMARCD2-containing mSWI/SNF complex is required for granulopoiesisBrittany C Michel, Cigall KadochNature Genetics|May 23, 2018
Multiplex assessment of protein variant abundance by massively parallel sequencingKenneth A Matreyek, Lea M Starita, Jason J Stephany, et al.Nature Genetics|July 4, 2018
Publisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseasesMarie Verbanck, Chia-Yen Chen, Benjamin Neale, et al.Nature Genetics|July 11, 2018
Enhancer hubs and loop collisions identified from single-allele topologiesAmin Allahyar, Carlo Vermeulen, Britta A M Bouwman, et al.Nature Genetics|June 30, 2018
Genome-scale analysis identifies paralog lethality as a vulnerability of chromosome 1p loss in cancerSrinivas R Viswanathan, Marina F Nogueira, Colin G Buss, et al.Nature Genetics|July 18, 2018
Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migrationAshleigh E Schaffer, Martin W Breuss, Ahmet Okay Caglayan, et al.Nature Genetics|June 13, 2018
An interactome perturbation framework prioritizes damaging missense mutations for developmental disordersSiwei Chen, Robert Fragoza, Lambertus Klei, et al.Nature Genetics|June 13, 2018
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility lociFredrick R Schumacher, Ali Amin Al Olama, Sonja I Berndt, et al.Pageof 744