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American Journal of Human Genetics|March 22, 2022
Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart StudyYanbing Wang, Han Chen, Gina M Peloso, et al.American Journal of Human Genetics|April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease riskJon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.American Journal of Human Genetics|September 18, 2018
Genetic Association of Albuminuria with Cardiometabolic Disease and Blood PressureMary E Haas, Krishna G Aragam, Connor A Emdin, et al.American Journal of Human Genetics|December 1, 1986
Linkage of cystic fibrosis locus and polymorphic DNA markers in 14 familiesS L Naylor, D R Barnett, J M Buchanan, et al.American Journal of Human Genetics|December 1, 1986
Inverted duplication of JH associated with chromosome 14 translocation and T-cell leukemia in ataxia-telangiectasiaJ P Johnson, R A Gatti, T S Sears, et al.American Journal of Human Genetics|March 24, 2022
Genetic modifiers of Huntington disease differentially influence motor and cognitive domainsJong-Min Lee, Yuan Huang, Michael Orth, et al.American Journal of Human Genetics|March 10, 2022
Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genesKathryn S Burch, Kangcheng Hou, Yi Ding, et al.American Journal of Human Genetics|February 23, 2022
The functional impact of BRCA1 BRCT domain variants using multiplexed DNA double-strand break repair assaysAleksandra I Adamovich, Mariame Diabate, Tapahsama Banerjee, et al.American Journal of Human Genetics|February 23, 2022
GWAS of longitudinal trajectories at biobank scaleSeyoon Ko, Christopher A German, Aubrey Jensen, et al.American Journal of Human Genetics|March 4, 2022
2021 ASHG presidential address-Imagination and daring: Past, present, and futureGail P JarvikPageof 979