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Women who test positive for a BRCA genetic mutation are at a higher risk of developing hereditary breast and ovarian cancer, which impacts their health, reproductive choices, and identity [10,11]. Within their lifetime, individuals with a BRCA mutation have up to a 75% increased risk in developing breast or ovarian cancer [12].
J Med Internet Res 2025;27:e67794
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Perceived neighborhood racial composition (PNRC) is an investigator-adapted and self-reported measure of the racial composition of a participant’s community [14]. The PNRC measure is limited in several ways. First, it focuses on a single neighborhood aspect [15]. Second, it does not address the difference that an individual may experience on a daily basis when moving between their home and school (or work) [16].
JMIR Public Health Surveill 2024;10:e55461
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changed to:
Algorithms were developed based on the National Comprehensive Cancer Network (NCCN) guidelines for genetic testing for hereditary breast, ovarian, pancreatic, and colorectal cancers.
(2) Textbox 1 has been revised for clarity and accuracy, and to comply with the citation guidelines of the National Comprehensive Cancer Network (NCCN).
(3) In the originally published paper, the following sentence was present in the Background section:
The National Comprehensive Cancer Network (NCCN) has published a
JMIR Med Inform 2022;10(9):e42533
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Current EHR systems often provide a dedicated FHH section, in which FHH assertions can be captured using a combination of structured (eg, coded disease, relationship, and age of onset) and unstructured data (ie, the comments field).
JMIR Med Inform 2022;10(8):e37842
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Natural language processing was used to answer the questions, if possible, from a library of prescripted responses. This created a real-time communication experience with immediately answered inquires that did not require additional effort from a provider for a response.
J Med Internet Res 2021;23(11):e29447
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Each time a user logged on to the tool, a unique session ID was generated, which enabled each visit to be tracked. Each time a page on the tool was accessed, a tracking database stored the session ID, date and time, as well as user actions (ie, whether they logged in, logged out, viewed the page, or redirected). Session IDs were randomly generated and created so that users could not be identified.
Knowledge was measured using eight questions in the Let’s Review section.
J Med Internet Res 2018;20(6):e209
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However, the Internet gives engaged individuals a direct method of accessing health information on a breadth of topics, and represents one of the most frequent reasons that individuals consult the Internet. A 2012 Pew Research Center Survey found that most general Internet users (66% of Hispanics; 73% of non-Hispanic whites) used the Internet to find health information [76]. A recent study indicated that Hispanics are highly receptive to online cancer information [77].
JMIR Res Protoc 2017;6(4):e52
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Although previous studies have examined Web-based searching for health information in general, limited information is available about the Web-based searching experience of people who are living with a rare or genetic disease. A 2001 study on use of the Internet for genetics-related information found that a majority of individuals surveyed searched the Internet for genetics-related information after visiting a genetics clinic.
JMIR Res Protoc 2014;3(1):e10
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