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Terence R. Flotte, MD

Celia and Isaac Haidak Professor, Dean of School of Medicine
Provost and Executive Deputy Chancellor
"This is an exciting time to be pursuing a career in medicine and applying to the University of Massachusetts Medical School"

 

About the Dean 

Terence R. Flotte, MD

Since joining UMass Medical School in 2007, Dean Flotte has led numerous successful initiatives elevating the academic stature of the institution, including establishing the Department of Quantitative Health Sciences; establishment of neurosurgery, urology and ophthalmology as academic departments; recruitment of numerous department chairs; and development of the Advanced Therapeutics Cluster. During Flotte’s time as dean of the School of Medicine, class size has increased from 103 to 162; a revised curriculum has been developed and implemented including “Learning Communities” guided by faculty mentors. in 2016, the medical school opened its first regional campus in Springfield, Mass. The research enterprise of the institution has grown to more than $280 million and a new 512,000-square-foot multiuse facility was built to accommodate the growing clinical and translational research laboratories as well as provide a new educational home for faculty and students.

An internationally known pioneer in human gene therapy, Flotte is currently investigating the use of gene therapy for genetic diseases, including alpha-1 antitrypsin deficiency and Tay-Sachs disease. In 1995, he led the team at Johns Hopkins that became the first to use the apparently harmless adeno-associated virus, or AAV, as a vehicle to deliver corrective genes to targeted sites in the body, including the damaged airways of adults with cystic fibrosis. He is the author of more than 250 scholarly papers and his research has been funded by the National Institutes of Health and the Alpha One Foundation. Since 2015, Flotte has also been editor-in-chief of gene therapy’s oldest journal family, Human Gene Therapy.Button - Learn More

  • Flotte lab to develop gene therapy models for genetic lung disease
    nov. 18, 2021

    Flotte lab to develop gene therapy models for genetic lung disease

    Researchers from UMass Chan Medical School have received a five-year $13.6 million program project grant from the National Heart, Lung and Blood Institute to develop new gene therapy models for alpha-1 antitrypsin deficiency, a chronic, debilitating genetic lung disease that shortens the lifespan.

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  • Alpha Omega Alpha Honor Medical Society at UMass Chan Medical School welcomes new members
    oct. 21, 2021

    Alpha Omega Alpha Honor Medical Society at UMass Chan Medical School welcomes new members

    UMass Chan Medical School welcomed 36 School of Medicine students into the Delta chapter of the Alpha Omega Alpha Honor Medical Society during an induction ceremony on Wednesday, Oct. 20.

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  • Riaan Research Initiative funds Cockayne syndrome gene replacement therapy research at UMass Chan Medical School
    oct. 4, 2021

    Riaan Research Initiative funds Cockayne syndrome gene replacement therapy research at UMass Chan Medical School

    Riaan Research Initiative, a non-profit organization, and UMass Chan Medical School are entering into an agreement to fund, research and develop a gene replacement therapy to combat Cockayne syndrome, a fatal autosomal recessive disorder.

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  • Chancellor Collins welcomes SOM Class of 2025 to ‘an exciting time to be coming into medicine’
    ago. 10, 2021

    Chancellor Collins welcomes SOM Class of 2025 to ‘an exciting time to be coming into medicine’

    Chancellor Michael F. Collins told the 162-member School of Medicine Class of 2025 that each encounter the future MDs have with their patients will be unique and profound.

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  • Gold Humanism Honor Society inducts 36 new members at UMMS
    jun. 10, 2021

    Gold Humanism Honor Society inducts 36 new members at UMMS

    The UMass Medical School chapter of the Gold Humanism Honor Society inducted 26 students, six residents and four faculty members on June 2.

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  • Alpha Omega Alpha Honor Medical Society at UMMS inducts largest, most diverse class
    jun. 10, 2021

    Alpha Omega Alpha Honor Medical Society at UMMS inducts largest, most diverse class

    New criteria was used to select the newest members of the Alpha Omega Alpha Honor Medical Society. The Class of 2021 is the largest and most diverse class of AOA inductees in the history of UMass Medical School.

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  • Chancellor Collins to Class of 2021: ‘You are scientists, nurses and doctors at their best’
    jun. 6, 2021

    Chancellor Collins to Class of 2021: ‘You are scientists, nurses and doctors at their best’

    The 48th annual UMass Medical School Commencement was held on Sunday, June 6, at Worcester State University following lifting of COVID-19 restrictions in recent weeks. Many graduates reflected on the unusual year in which they completed their studies.

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  • School of Medicine graduating students commended for resilience in year-end ceremony
    jun. 4, 2021

    School of Medicine graduating students commended for resilience in year-end ceremony

    Members of the School of Medicine Class of 2021 were recognized for their resilience and commitment as they completed their studies in the depths of the worst global pandemic in a century at the annual UMass Medical School Alumni Association breakfast.

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  • USA Today reports on first baby in gene therapy clinical trial for Sandhoff, Tay-Sachs diseases
    abr. 27, 2021

    USA Today reports on first baby in gene therapy clinical trial for Sandhoff, Tay-Sachs diseases

    Thomas Feldborg and Daria Rokina, of Denmark, chose to enroll their baby daughter, Alissa, in an investigational gene therapy for the treatment of GM2 gangliosidosis, which causes Tay-Sachs and Sandhoff diseases, to “let hope conquer the fears,” according to a report in USA Today chronicling their journey.

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  • Innovative neurosurgical technique used in Tay-Sachs gene therapy clinical trial
    mar. 3, 2021

    Innovative neurosurgical technique used in Tay-Sachs gene therapy clinical trial

    Oguz Cataltepe, MD, describes the innovative neurosurgical procedure used to treat patients in the new clinical trial for a gene therapy targeting infantile Tay-Sachs and Sandhoff diseases.

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