Sutin named to Academy of Science, Engineering and Medicine of Florida

Jul 18, 2025

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Sutin named to Academy of Science, Engineering and Medicine of Florida

Angelina Sutin, Ph.D., a professor in the Department of Behavioral Sciences and Social Medicine at the College of Medicine, is one of six Florida State University faculty members named to the Academy of Science, Engineering and Medicine of Florida in recognition of their extraordinary research accomplishments.Headshot of Angelina Sutin, Ph.D.

 

Sutin studies the psychological and social factors that contribute to the risk of Alzheimer’s disease and related dementias. She has brought in more than $11 million in funding from the National Institutes of Health and is a fellow of the Association for Psychological Science, the Society for Personality and Social Psychology, and the Gerontological Society of America.

 

The other five FSU researchers are Christopher Patrick, Department of Psychology; Richard Liang, FAMU-FSU College of Engineering; and three faculty from the Department of Chemistry and Biochemistry: Igor Alabugin; Joseph Schlenoff, and Robert Schurko.

 

“These six researchers are outstanding faculty members who have made significant contributions to their fields,” said FSU Vice President for Research Stacey S. Patterson. “We are incredibly proud of their accomplishments and congratulate them on being named to the Academy of Science, Engineering and Medicine of Florida.” 

 

Founded in 2018, the academy studies issues in science, engineering and medicine of interest to the people of Florida and provides unbiased, expert advice related to these issues.

 

To be selected, individuals must live and work in Florida, be nominated by a current academy member, and have an outstanding record of accomplishments of international significance.

 

The researchers will be inducted into the academy at the organization’s annual conference in November.

 

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Jul 11, 2025
News Service of Florida

A key lawmaker and Florida State University leaders Wednesday touted a new law that includes offering free genetic screening for newborns and bolstering research on rare
pediatric diseases.

Gov. Ron DeSantis last month signed the law (HB 907), which was unanimously passed by the Legislature in April and is dubbed the Sunshine Genetics Act.

The law creates a pilot program led by the Florida Institute for Pediatric Rare Diseases at Florida State University, with families able to choose to have their babies’ full genetic
codes sequenced.

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Jul 09, 2025
Florida Phoenix

The Florida State University community gathered Wednesday to showcase the creation of an institute in its College of Medicine anda pilot program that will provide free genetic screening to newborns, established by HB 907, passed this spring.

The Florida Institute for Pediatric Rare Diseases was a “labor of love” for state Rep. Adam Anderson, the Palm Harbor Republican first elected to the House in 2022. It memorializes his late son Andrew, felled by Tay-Sachs disease, a deadly genetic malady.

Anderson called the project a “truly a historic milestone that’s giving Florida a once-in-a generation opportunity to lead the nation in genetic and precision medicine,” adding that “half-a-dozen” states have reached out to him about the idea.

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Jul 10, 2025
Tallahassee Democrat

Florida State University’s efforts to address pediatric rare diseases have reached greater heights.

Gov. Ron DeSantis recently signed HB 907 – the Sunshine Genetics Act – which establishes a pilot program for newborns through the Florida Institute for Pediatric Rare Diseases
at FSU. And with the initiative, families can have their baby’s full genetic code sequenced at no cost to identify potentially serious conditions.

“This not only marks the beginning of the next generation of healthcare for Floridians, but it also ensures thatIPRD (Institute for Pediatric Rare Diseases) will go on to live longer than anybody here in this room,” Rep.Adam Anderson, R-Palm Harbor – whose son Andrew died from Tay-Sachs disease – said July 9 at a ceremonial check presentation at the FSU College of Medicine.

As the new Sunshine Genetics law was made effective July 1 and kicks off the pilot program with $3 million, the Institute for Pediatric Rare Diseases at FSU – launched in
February 2024 – has received an additional $4.5 million from Florida’s 2025-2026 budget to boost research, which totals the state’s allocation toward the overall initiative to $7.5 million.

 

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