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American Journal of Human Genetics|January 7, 2023
Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasetsSeyoon Ko, Benjamin B Chu, Daniel Peterson, et al.American Journal of Human Genetics|January 7, 2023
Fast, accurate local ancestry inference with FLARESharon R Browning, Ryan K Waples, Brian L BrowningAmerican Journal of Human Genetics|January 12, 2021
Multi-trait transcriptome-wide association studies with probabilistic Mendelian randomizationLu Liu, Ping Zeng, Fuzhong Xue, et al.American Journal of Human Genetics|June 8, 2021
De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsyMuhammad A Usmani, Zubair M Ahmed, Pamela Magini, et al.American Journal of Human Genetics|September 1, 1988
Cytogenetic studies in Dupuytren contractureD H Wurster-Hill, F Brown, J P Park, et al.American Journal of Human Genetics|September 1, 1988
Comparison of sequential and fixed-structure sampling of pedigrees in complex segregation analysis of a quantitative traitM Boehnke, M R Young, P P MollAmerican Journal of Human Genetics|June 1, 2022
A spectrum of recessiveness among Mendelian disease variants in UK BiobankAlison R Barton, Margaux L A Hujoel, Ronen E Mukamel, et al.American Journal of Human Genetics|November 30, 2022
Statistical phasing of 150,119 sequenced genomes in the UK BiobankBrian L Browning, Sharon R BrowningAmerican Journal of Human Genetics|June 6, 2022
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 studyLisanne van Prooyen Schuurman, Erik A Sistermans, Diane Van Opstal, et al.American Journal of Human Genetics|June 9, 2022
An epigenome-wide view of osteoarthritis in primary tissuesPeter Kreitmaier, Matthew Suderman, Lorraine Southam, et al.Pageof 979