Index of /cdrom2025/5.2.RareVariantAssociation_DuncanPalmer/refs

	Name	Last modified	Size	Description
	Parent Directory		-
	Jurgens et al. 2024 - Rare coding variant analysis for human diseases across biobanks and ancestries.pdf	2025-02-24 14:29	7.8M
	Zhou et al. 2020 - Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts.pdf	2025-02-24 14:30	4.5M
	Zhou et al. 2022 - SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests.pdf	2025-02-24 14:31	3.9M
	Karczewski et al. 2020 - The mutational constraint spectrum quantified from variation in 141,456 humans.pdf	2025-02-24 14:30	3.2M
	Karczewski et al. 2023 - Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes.pdf	2025-02-24 14:30	3.1M
	Cirulli et al. 2020 - Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.pdf	2025-02-24 14:29	1.2M
	Lee et al. 2012 - Optimal unified approach for rare-variant association ... plication to small-sample case-control whole-exome sequencing studies.pdf	2025-02-24 14:30	630K
	Neale et al. 2011 - Testing for an unusual distribution of rare variants.pdf	2025-02-24 14:30	402K
	Wu et al. 2011 - Rare-variant association testing for sequencing data with the sequence kernel association test.pdf	2025-02-24 14:30	276K