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A comprehensive approach for identifying filaggrin mutations and copy number variants by long-read sequencing.
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Phase separation as a possible mechanism for dosage sensitivity.
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38225666 (PubMed )
Supplement: 13059_2023_3128_MOESM3_ESM.xlsx › NMD-escaping_mutations
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.
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Deciphering genes associated with diffuse large B-cell lymphoma with lymphomatous effusions: A mutational accumulation scoring approach.
Abdollahi S et al.
Biomarker Research, 2021
34635181 (PubMed )
Supplement: 40364_2021_330_MOESM2_ESM.xlsx › ___1
Massively Parallel Sequencingof the Filaggrin Gene Reveals an Association Between FLG Loss-of-function Mutations and Leprosy.
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The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
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Cell Research, 2020
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Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
Novel recurrently mutated genes and a prognostic mutation signature in colorectal cancer.
Yu J et al.
Gut, 2015
24951259 (PubMed )
Supplement: gutjnl-2013-306620-s14.pdf
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