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Statistical power of transcriptome-wide association studies.
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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.
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OTTERS: a powerful TWAS framework leveraging summary-level reference data.
Nat Commun. 2023 Mar 7;14(1):1271. doi: 10.1038/s41467-023-36862-w.
4
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Cell. 2022 Nov 10;185(23):4409-4427.e18. doi: 10.1016/j.cell.2022.10.009.
5
KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design.
Am J Hum Genet. 2022 Oct 6;109(10):1761-1776. doi: 10.1016/j.ajhg.2022.08.013. Epub 2022 Sep 22.
6
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Nat Genet. 2022 Sep;54(9):1305-1319. doi: 10.1038/s41588-022-01148-2. Epub 2022 Aug 18.
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Identification of Immune Cells and Key Genes associated with Alzheimer's Disease.
Int J Med Sci. 2022 Jan 1;19(1):112-125. doi: 10.7150/ijms.66422. eCollection 2022.
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Powerful gene-based testing by integrating long-range chromatin interactions and knockoff genotypes.
Proc Natl Acad Sci U S A. 2021 Nov 23;118(47). doi: 10.1073/pnas.2105191118.

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