ResearchJan 28, 2020Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohortsNATURE COMMUNICATIONS
Press ReleasesJan 9, 2020Mayo Clinic to sequence 100K participants to build genomic database for improved care and research in collaboration with Helix
Press ReleasesJan 9, 2020Mayo Clinic to Sequence 100,000 Participants to Build Genomic Database for Improved Care and Research in Collaboration with Helix
ResearchOct 17, 2019Are we ready to implement polygenic risk score tests in the clinic? Expanding the utility of prostate cancer polygenic risk score in multiple ethnicities and clinical best practicesASHG 2019
ResearchOct 17, 2019Applying Confidence Intervals to Clinical Polygenic Risk Scores in 60,000 Exome+ Sequenced IndividualsASHG 2019
ResearchOct 17, 2019Genome-wide rare variant analysis for thousands of phenotypes in >70,000 exomesASHG 2019
ResearchOct 16, 2019A genetic retrospective study of Maturity-Onset Diabetes of the Young (MODY) in two population health studiesASHG 2019
ResearchOct 16, 2019The spectrum of mitochondrial genomic variation across 250,000 individualsASHG 2019
ResearchOct 8, 2019Selective constraints and pathogenicity of mitochondrial DNA variants inferred from a novel database of 196,554 unrelated individualsBIORXIV