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Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry.
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Supplement: 109_2024_2510_MOESM2_ESM.xlsx › Sheet1
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Frontiers in Cardiovascular Medicine, 2022
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Germline Mutation in MUS81 Resulting in Impaired Protein Stability is Associated with Familial Breast and Thyroid Cancer.
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Cancers, 2020
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Supplement: cancers-12-01289-s001.zip › cancers-768495_-Supplementary_Tables_.xlsx › Table_S2
Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer.
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Scientific Reports, 2017
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Supplement: srep37984-s2.xls › Exome_geMODERATE_variants
Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.
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Molecular Vision, 2016
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