Steven Hart
0000-0001-7714-2734
13 papers found
Refreshing results…
Pitfalls in machine learning‐based assessment of tumor‐infiltrating lymphocytes in breast cancer: A report of the International Immuno‐Oncology Biomarker Working Group on Breast Cancer
Spatial analyses of immune cell infiltration in cancer: current methods and future directions: A report of the International Immuno‐Oncology Biomarker Working Group on Breast Cancer
Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C
Cybersecurity and Information Assurance for the Clinical Laboratory
An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance
Mutations in BRCA1/2 and Other Panel Genes in Patients With Metastatic Breast Cancer —Association With Patient and Disease Characteristics and Effect on Prognosis
Breast cancer risk factors and survival by tumor subtype: pooled analyses from the Breast Cancer Association Consortium
Whole‐exome sequencing of non‐ BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer
Effect of germline mutations in homologous recombination repair genes on overall survival of patients with pancreatic adenocarcinoma
Mutation prevalence tables for hereditary cancer derived from multigene panel testing
Contribution of Germline Predisposition Gene Mutations to Breast Cancer Risk in African American Women
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients
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