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Article

Streamlining Inherited Cancer Identification via an EMR-Integrated Risk Assessment Platform: A Nonrandomized Clinical Trial.

JAMA network open - 1 Apr 2026

Orlando Lori A, Mittendorf Kathleen F, Bihlmeyer Nathan A, Bland Harris T, Myers Rachel A, Pratap Siddharth, Celaya-Cobbs Natasha, Andujar Justin, Gerhart Meredith, Sadeghpour Azita, Hooker Gillian, Wu R Ryanne, Marshall Dana R, Edwards Clasherrol, Frederickson Katie L, Leegon Jeff, Jones Sarah H, Rosenbloom S Trent, Peterson Josh F, Wiesner Georgia L

Abstract excerpt

Importance: Approximately 10% of cancers are attributable to heritable germline variants, yet identification of individuals at risk remains suboptimal. Objective: To assess the feasibility of personal history and family health history (FHH) risk assessment technology via the electronic medical record (EMR) to enhance identification of patients at risk for a broad array of inherited cancer syndromes. Design,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42054024
DOI: 10.1001/jamanetworkopen.2026.9816
PMCID: PMC13129876

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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