Publications by authors named "Murat Kantarcıoglu"

Objectives: To determine the extent to which current Large Language Models (LLMs) can serve as substitutes for traditional machine learning (ML) as clinical predictors using data from electronic health records (EHRs), we investigated various factors that can impact their adoption, including overall performance, calibration, fairness, and resilience to privacy protections that reduce data fidelity.

Materials And Methods: We evaluated GPT-3.5, GPT-4, and ML (as gradient-boosting trees) on clinical prediction tasks in EHR data from Vanderbilt University Medical Center and MIMIC IV.

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Data access limitations have stifled COVID-19 disparity investigations in the United States. Though federal and state legislation permits publicly disseminating de-identified data, methods for de-identification, including a recently proposed dynamic policy approach to pandemic data sharing, remain unproved in their ability to support pandemic disparity studies. Thus, in this paper, we evaluate how such an approach enables timely, accurate, and fair disparity detection, with respect to potential adversaries with varying prior knowledge about the population.

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Scientific and clinical studies have a long history of bias in recruitment of underprivileged and minority populations. This underrepresentation leads to inaccurate, inapplicable, and non-generalizable results. Electronic medical record (EMR) systems, which now drive much research, often poorly represent these groups.

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As recreational genomics continues to grow in its popularity, many people are afforded the opportunity to share their genomes in exchange for various services, including third-party interpretation (TPI) tools, to understand their predisposition to health problems and, based on genome similarity, to find extended family members. At the same time, these services have increasingly been reused by law enforcement to track down potential criminals through family members who disclose their genomic information. While it has been observed that many potential users shy away from such data sharing when they learn that their privacy cannot be assured, it remains unclear how potential users' valuations of the service will affect a population's behavior.

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Background: As direct-to-consumer genetic testing services have grown in popularity, the public has increasingly relied upon online forums to discuss and share their test results. Initially, users did so anonymously, but more recently, they have included face images when discussing their results. Various studies have shown that sharing images on social media tends to elicit more replies.

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Background: Regular coffee consumption has beneficial and preventative effects on liver and chronic neurodegenerative diseases. However, the studies performed with the ingredients found in coffee beverages have not clarified the responsible mechanisms. Exosomes are small, membrane-coated cargo packages secreted by prokaryote and eukaryote cells.

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Blockchain is an emerging technology that has enabled many applications, from cryptocurrencies to digital asset management and supply chains. Due to this surge of popularity, analyzing the data stored on blockchains poses a new critical challenge in data science. To assist data scientists in various analytic tasks for a blockchain, in this tutorial, we provide a systematic and comprehensive overview of the fundamental elements of blockchain network models.

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Transparency has become a critical need in machine learning (ML) applications. Designing transparent ML models helps increase trust, ensure accountability, and scrutinize fairness. Some organizations may opt-out of transparency to protect individuals' privacy.

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Numerous studies have shown that a person's health status is closely related to their socioeconomic status. It is evident that incorporating socioeconomic data associated with a patient's geographic area of residence into clinical datasets will promote medical research. However, most socioeconomic variables are unique in combination and are affiliated with small geographical regions (e.

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Recent developments in a variety of sectors, including health care, research and the direct-to-consumer industry, have led to a dramatic increase in the amount of genomic data that are collected, used and shared. This state of affairs raises new and challenging concerns for personal privacy, both legally and technically. This Review appraises existing and emerging threats to genomic data privacy and discusses how well current legal frameworks and technical safeguards mitigate these concerns.

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Objective: Supporting public health research and the public's situational awareness during a pandemic requires continuous dissemination of infectious disease surveillance data. Legislation, such as the Health Insurance Portability and Accountability Act of 1996 and recent state-level regulations, permits sharing deidentified person-level data; however, current deidentification approaches are limited. Namely, they are inefficient, relying on retrospective disclosure risk assessments, and do not flex with changes in infection rates or population demographics over time.

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Person-specific biomedical data are now widely collected, but its sharing raises privacy concerns, specifically about the re-identification of seemingly anonymous records. Formal re-identification risk assessment frameworks can inform decisions about whether and how to share data; current techniques, however, focus on scenarios where the data recipients use only one resource for re-identification purposes. This is a concern because recent attacks show that adversaries can access multiple resources, combining them in a stage-wise manner, to enhance the chance of an attack’s success.

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Background: Blockchain has emerged as a decentralized and distributed framework that enables tamper-resilience and, thus, practical immutability for stored data. This immutability property is important in scenarios where auditability is desired, such as in maintaining access logs for sensitive healthcare and biomedical data. However, the underlying data structure of blockchain, by default, does not provide capabilities to efficiently query the stored data.

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To accelerate medical knowledge discovery, an increasing number of research programs are gathering and sharing data on a large number of participants. Due to the privacy concerns and legal restrictions on data sharing, these programs apply various strategies to mitigate privacy risk. However, the activities of participants and research program sponsors, particularly on social media, might reveal an individual's membership in a study, making it easier to recognize participants' records and uncover the information they have yet to disclose.

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As the quantity and detail of association studies between clinical phenotypes and genotypes grows, there is a push to make summary statistics widely available. Genome wide summary statistics have been shown to be vulnerable to the inference of a targeted individual's presence. In this paper, we show that presence attacks are feasible with phenome wide summary statistics as well.

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Biomedical data continues to grow in quantity and quality, creating new opportunities for research and data-driven applications. To realize these activities at scale, data must be shared beyond its initial point of collection. To maintain privacy, healthcare organizations often de-identify data, but they assume worst-case adversaries, inducing high levels of data corruption.

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Objective: Biomedical science is driven by datasets that are being accumulated at an unprecedented rate, with ever-growing volume and richness. There are various initiatives to make these datasets more widely available to recipients who sign Data Use Certificate agreements, whereby penalties are levied for violations. A particularly popular penalty is the temporary revocation, often for several months, of the recipient's data usage rights.

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Objective: Non-Hodgkin's lymphomas arising from tissues other than primary lymphatic sites are classified as primary extranodal lymphomas (PEL). PELs of the gastrointestinal system (PGISL) originate from the lymphatic tissues within the gastrointestinal tract. The prognostic value of F-FDG PET/CT in lymphomas is high in terms of both overall survival (OS) and disease-free survival (DFS).

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Background: Genomic data is increasingly collected by a wide array of organizations. As such, there is a growing demand to make summary information about such collections available more widely. However, over the past decade, a series of investigations have shown that attacks, rooted in statistical inference methods, can be applied to discern the presence of a known individual's DNA sequence in the pool of subjects.

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Emerging scientific endeavors are creating big data repositories of data from millions of individuals. Sharing data in a privacy-respecting manner could lead to important discoveries, but high-profile demonstrations show that links between de-identified genomic data and named persons can sometimes be reestablished. Such re-identification attacks have focused on worst-case scenarios and spurred the adoption of data-sharing practices that unnecessarily impede research.

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Objective. The aim of the present study was to investigate whether pentraxin 3 (PTX3) can be a new noninvasive marker for prediction of liver fibrosis in patients with NAFLD. We also aimed to evaluate the relationship between PTX3 and atherosclerosis in patients with NAFLD.

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