Tina Pesaran
0000-0001-9807-4304
7 papers found
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Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C
An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance
Classification of the canonical splice alteration MUTYH c.934-2A > G is likely benign based on RNA and clinical data
Racial and ethnic differences in multigene hereditary cancer panel test results for women with breast cancer
Genotype-phenotype correlations among TP53 carriers: literature review and analysis of probands undergoing multi-gene panel testing and single-gene testing
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort
Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes
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