Melissa Parisi

9PUBLICATIONS
16CO-AUTHORS
Disease surveillanceDevelopment cooperationGene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapyNeonatology
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Publications (9)

|Mar 26, 2026
Challenges and opportunities for the use of telehealth in rare disease diagnosis, treatment, research, and education: key opinion leader interviews by the IRDiRC telehealth task force.

Melissa A Parisi, Adam L Hartman, Mary Catherine V Letinturier

|Jan 10, 2024
The National Institutes of Health INvestigation of Co-occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan.

Sujata Bardhan, Huiqing Li, Erika Tarver

|Mar 06, 2023
When is the best time to screen and evaluate for treatable genetic disorders?: A lifespan perspective.

Melissa A Parisi, Michele Caggana, Jennifer L Cohen

|Mar 03, 2023
Gene-targeted therapies: Overview and implications.

P J Brooks, Tiina K Urv, Melissa A Parisi

|Jan 24, 2023
Are we prepared to deliver gene-targeted therapies for rare diseases?

Timothy W Yu, Stephen F Kingsmore, Robert C Green

|Sep 14, 2022
Newborn screening research sponsored by the NIH: From diagnostic paradigms to precision therapeutics.

Mollie A Minear, Megan N Phillips, Alice Kau

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Frequent Collaborators

3 joint publications

Tiina K Urv

2 joint publications

Jasmine Knoll

2 joint publications

Jill A Morris

1 joint publications

Daniel A Doherty