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UnknownLevel of evidence used in recommendations by the National Comprehensive Cancer Network (NCCN) guidelines beyond Food and Drug Administration approvals.
Not available
S-EPMC6857604 | biostudies-literature
UnknownKidney Cancer, Version 3.2022, NCCN Clinical Practice Guidelines in Oncology.
Not available
S-EPMC10191161 | biostudies-literature
UnknownExome sequencing and analysis of 454,787 UK Biobank participants.
Not available
S-EPMC8596853 | biostudies-literature
UnknownPMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients.
Not available
S-EPMC11613782 | biostudies-literature
UnknownANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma.
Not available
S-EPMC9529959 | biostudies-literature
UnknownAssessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies.
Not available
S-EPMC9535845 | biostudies-literature
UnknownA large meta-analysis identifies genes associated with anterior uveitis.
Not available
S-EPMC10638276 | biostudies-literature
UnknownExclusion-based exome sequencing in critically ill adults 18-40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing.
Not available
S-EPMC12414659 | biostudies-literature
UnknownInference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions.
Not available
S-EPMC10111435 | biostudies-literature
UnknownPopulation-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Not available
S-EPMC9166757 | biostudies-literature
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