But what are the limits?

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In this vast border region, tuberculosis control is a high-stakes game of chase. Some patients infected with the disease frequently cross into Mexico for work or to visit family, slipping off the radar of public health workers who must verify they are taking their medicines

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Without any public scrutiny, insurers and data brokers are predicting your health costs based on data about things like race, marital status, how much TV you watch, whether you pay your bills on time or even buy plus-size clothing

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Electronic medical records are everywhere – annoying to doctors and intrusive to patients. But now researchers are looking to see if they can plow through the vast amount of data that’s gathered in those records, along with insurance billing information, to tease out the bits that could be useful in refining treatments and identifying new uses for drugs.

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Why you aren’t as anonymous as you think online. So-called ‘anonymous’ data can be easily used to identify everything from our medical records to purchase histories

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Genetic diagnosis is getting ever more sophisticated. But as doctors uncover diseases that are hereditary, who needs to know? Shaun Raviv explores the rights – and duties – of doctors, patients and families

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The advent of social media technology has opened many new avenues of research in population health, demographics, psychology, and the social sciences

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In a letter to the Baltimore Sun, a group of geneticists, genetic counselors, and ethicists, including our Debra Mathews, supports efforts to reunite immigrant families as quickly as possible, while raising serious concerns about the use of DNA testing as a means of achieving this goal

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