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Rare-variant association testing for sequencing data with the sequence kernel association test.
Am J Hum Genet. 2011 Jul 15;89(1):82-93. doi: 10.1016/j.ajhg.2011.05.029. Epub 2011 Jul 7.
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A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.
Genet Epidemiol. 2016 Dec;40(8):702-721. doi: 10.1002/gepi.21984. Epub 2016 Jul 4.
4
Sequence kernel association tests for the combined effect of rare and common variants.
Am J Hum Genet. 2013 Jun 6;92(6):841-53. doi: 10.1016/j.ajhg.2013.04.015. Epub 2013 May 16.
5
Generalized functional linear models for gene-based case-control association studies.
Genet Epidemiol. 2014 Nov;38(7):622-637. doi: 10.1002/gepi.21840. Epub 2014 Sep 9.
6
On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant Set.
Ann Hum Genet. 2016 Mar;80(2):123-35. doi: 10.1111/ahg.12144. Epub 2016 Jan 12.
7
Optimal tests for rare variant effects in sequencing association studies.
Biostatistics. 2012 Sep;13(4):762-75. doi: 10.1093/biostatistics/kxs014. Epub 2012 Jun 14.
8
Functional linear models for association analysis of quantitative traits.
Genet Epidemiol. 2013 Nov;37(7):726-42. doi: 10.1002/gepi.21757.
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Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.
Genet Epidemiol. 2014 Jul;38(5):447-56. doi: 10.1002/gepi.21813. Epub 2014 May 21.
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On Robust Association Testing for Quantitative Traits and Rare Variants.
G3 (Bethesda). 2016 Dec 7;6(12):3941-3950. doi: 10.1534/g3.116.035485.

引用本文的文献

4
Winner's curse in rare variant analysis: effect size estimation bias depends on effect direction and the association method used.
Front Genet. 2025 Aug 8;16:1416673. doi: 10.3389/fgene.2025.1416673. eCollection 2025.
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Leveraging multimodal neuroimaging and GWAS for identifying modality-level causal pathways to Alzheimer's disease.
Imaging Neurosci (Camb). 2025 May 16;3. doi: 10.1162/imag_a_00580. eCollection 2025.
7
Spatial-extent inference for testing variance components in reliability and heritability studies.
Imaging Neurosci (Camb). 2024 Jan 9;2. doi: 10.1162/imag_a_00058. eCollection 2024.
8
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Towards improved fine-mapping of candidate causal variants.
Nat Rev Genet. 2025 Jul 28. doi: 10.1038/s41576-025-00869-4.

本文引用的文献

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Testing for an unusual distribution of rare variants.
PLoS Genet. 2011 Mar;7(3):e1001322. doi: 10.1371/journal.pgen.1001322. Epub 2011 Mar 3.
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Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes.
Am J Hum Genet. 2010 Nov 12;87(5):604-17. doi: 10.1016/j.ajhg.2010.10.012.
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Rare variant association analysis methods for complex traits.
Annu Rev Genet. 2010;44:293-308. doi: 10.1146/annurev-genet-102209-163421.
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A map of human genome variation from population-scale sequencing.
Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534.
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Challenges in the identification and use of rare disease-associated predisposition variants.
Curr Opin Genet Dev. 2010 Jun;20(3):277-81. doi: 10.1016/j.gde.2010.05.005.
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Powerful SNP-set analysis for case-control genome-wide association studies.
Am J Hum Genet. 2010 Jun 11;86(6):929-42. doi: 10.1016/j.ajhg.2010.05.002.
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Pooled association tests for rare variants in exon-resequencing studies.
Am J Hum Genet. 2010 Jun 11;86(6):832-8. doi: 10.1016/j.ajhg.2010.04.005. Epub 2010 May 13.
9
A data-adaptive sum test for disease association with multiple common or rare variants.
Hum Hered. 2010;70(1):42-54. doi: 10.1159/000288704. Epub 2010 Apr 23.
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Accurate detection and genotyping of SNPs utilizing population sequencing data.
Genome Res. 2010 Apr;20(4):537-45. doi: 10.1101/gr.100040.109. Epub 2010 Feb 11.

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