Associated Papers
Rare genetic variants and severe COVID-19 in previously healthy admixed Latin American adults.
Rocha GD et al.
Scientific Reports, 2025
40595275 (PubMed )
Supplement: 41598_2025_8416_MOESM1_ESM.xlsx › S4
Rare Genetic Variants of NLRP12 in Admixed Latino-American Children With SARS-CoV-2-Related Multisystem Inflammatory Syndrome.
Barreto TMM et al.
The Journal of Infectious Diseases, 2024
In search of a function for human type III interferons: insights from inherited and acquired deficits.
Zhang Q et al.
Current Opinion in Immunology, 2024
Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes.
Subramanian DN et al.
Nature Communications, 2020
32242007 (PubMed )
Supplement: 41467_2020_15461_MOESM4_ESM.xlsx › Data_1
Exome sequencing reveals comprehensive genomic alterations across eight cancer cell lines.
Chang H et al.
Plos One, 2011
21701589 (PubMed )
Supplement: pone.0021097.s002.xls › mda-mb468_f40r3
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