selected publications
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academic article
- X-chromosome-wide association study for Alzheimer's disease.. Molecular psychiatry. 2024
- Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study.. American journal of human genetics. 109:738-749. 2022
- Exploiting family history in aggregation unit-based genetic association tests.. European journal of human genetics : EJHG. 30:1355-1362. 2021
- Cerebral small vessel disease genomics and its implications across the lifespan.. Nature communications. 11:-. 2020
- Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association.. American journal of respiratory and critical care medicine. 199:631-642. 2019
- Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.. American journal of human genetics. 103:691-706. 2018
- Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.. Molecular psychiatry. 25:1859-1875. 2018
- Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.. Genomics. 111:808-818. 2018
- Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.. Dementia and geriatric cognitive disorders. 45:1-17. 2018
- Whole genome sequence analyses of brain imaging measures in the Framingham Study.. Neurology. 90:e188-e196. 2017
- Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.. Nature genetics. 49:1373-1384. 2017
- Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.. Neurology. 86:351-9. 2015
- Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases.. European journal of human genetics : EJHG. 24:1029-34. 2015
- Directional dominance on stature and cognition in diverse human populations.. Nature. 523:459-462. 2015
- The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.. BMC medical genetics. 8 Suppl 1:-. 2007