Matt Might's bio generator

You can use this page to generate a bio about me to suit your needs.

If you're going to read it out, please to generate a short version.

A recent CV is available: matthew-might-cv.pdf.

Please contact me if you need a recent NIH or NSF biosketch. (The next time someone requests one of these, I'll place them in a public Dropbox folder and link it here.)

Please contact me if you need a newer version of any of this material.

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Generated bio

INTRONAME has been the Director of the Hugh Kaul Precision Medicine Institute at the University of Alabama at Birmingham (UAB) since 2017. At UAB, NEXTNAME is the Hugh Kaul Kaul Endowed Chair of Personalized Medicine, a Professor of Internal Medicine and a Professor of Computer Science. At UAB, NEXTNAME's NIH and philanthropically funded research focuses on precision prevention, diagnosis and therapeutics across rare disease, cancer and common/chronic conditions. A principal theme in his research is the use of computer and data science to enhance clinical and academic medicine.

From 2016 to 2018, NEXTNAME was a Strategist in the Executive Office of the President in The White House. At The White House, NEXTNAME worked primarily on President Obama's Precision Medicine Initiative with both the NIH and the Departmant of Veterans Affairs. And, in 2015, NEXTNAME joined the faculty of the Department of Biomedical Informatics at the Harvard Medical School. At Harvard, NEXTNAME's research focuses on rare disease discovery and diagnosis, and on the development of personalized therapeutics for rare disease.

NEXTNAME's journey from computer science to medicine has been inspired by his son Bertrand. In 2012, Bertrand became the first patient in the world to be diagnosed with NGLY1 deficiency, and this inspired NEXTNAME to use social media to discover other patients and form a community. Through the community's efforts in science, two therapeutics for NGLY1 deficiency have been identified since its discovery, and more are under active development. NEXTNAME is co-founder and Chief Scientific Officer of, a non-profit dedicated to finding treatments for NGLY1 deficiency, and he is a co-founder and Scientific Advisor to Pairnomix, a start-up which identifies potential patient-specific therapies for rare disorders -- and genetic epilepsies in particular.

Prior to medicine, NEXTNAME spent nearly a decade as a professor of computer science at the University of Utah. In computer science, NEXTNAME's research focuses primarily on cybersecurityautomated detection of security vulnerabilities; scientific computingdomain-specific languages for scientific computing; and automated reasoning about programsstatic analysis of higher-order programs. His research has also included excursions into parsing (with derivatives) and purely functional algorithms and data structures. At Utah, his research was supported by the Department of Defense (via DARPA), the Department of Energy and the National Science Foundation, including an NSF CAREER Award in 2014. In 2014, he was named one of Utah's first six Presidential Scholars.

NEXTNAME received his B.S. (2001), M.S. (2005) and Ph.D. (2007) in computer science from Georgia Tech.

NEXTNAME tweets from @mattmight and blogs at

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