Nancy S. Green

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Professor

Columbia University Vagelos College of Physicians and Surgeons

United States

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About

Nancy S. Green is a Professor at Columbia University College of Physicians and Surgeons in the United States. Her research primarily focuses on sickle cell disease, exploring areas such as quality of life in affected youth, academic proficiency, neurocognitive outcomes, and adherence to hydroxyurea therapy. Recent publications include studies on the impacts of air pollution on respiratory events in children with sickle cell disease and the effectiveness of community health worker support in treatment adherence.

Recent Grants

Grant: Close

Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment: HABIT

Open Date: 2017-09-27

Close Date: 2021-06-30

Grant: Close

HYDROXYUREA ADHERENCE FOR PERSONAL BEST IN SICKLE CELL TREATMENT: HABIT

Open Date: 2017-09-01

Close Date: 2021-06-01

Grant: Close

Burden and Risk of Neurological and Cognitive Impairment in Pediatric Sickle Cell Anemia in Uganda

Open Date: 2016-08-18

Close Date: 2019-07-31

Grant: Close

Clinical and Translational Science Award

Open Date: 2016-07-01

Close Date: 2021-05-31

Grant: Close

Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment: HABIT

Open Date: 2013-05-08

Close Date: 2016-04-30

Articles (20)

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2020

Collaborators (3)

Arlene Smaldone

Columbia University School of Nursing

UNITED STATES

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Rhonda G. Kost

Clinical Research Officer/ Associate Professor

Rockefeller University

UNITED STATES

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Cristina Fernández

Assistant Professor

Columbia University Irving Medical Center

UNITED STATES

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Nancy S. Green

Research Interests

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About

Recent Grants

Articles (20)

HABIT Efficacy Trial Intervention Improves Elements of General and Disease‐Specific Quality of Life in Youth With Sickle Cell Disease

Academic Proficiency in Ugandan Children With Sickle Cell Anemia: A Cross-Sectional Study.

Neurocognitive Gains Among Ugandan Children with Sickle Cell Anemia on Hydroxyurea: 18-month trial interim results.

Standards and infrastructure for multisite deployment of the research participant perception survey

What research participants say about their research experiences in Empowering the Participant Voice: Outcomes and actionable data.

Comment on: “Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT) efficacy trial: Community health worker support may increase hydroxyurea adherence of youth with sickle cell disease”: Participant evaluation

Assessing multilevel barriers to hydroxyurea adherence in youth with sickle cell disease using pharmacy‐based refill records

Effects of Air Pollution on Respiratory Events and Pain Crises among Children with Sickle Cell Disease in New York City.

Hydroxyurea therapy for neurological and cognitive protection in pediatric sickle cell anemia in Uganda (BRAIN SAFE II): Protocol for a single-arm open label trial.

Neurocognitive impairment in Ugandan children with sickle cell anemia compared to sibling controls: a cross-sectional study.

Food insecurity, housing instability, and dietary quality among children with sickle cell disease: Assessment from a single urban center

Pediatric hematology providers' contraceptive practices for female adolescents and young adults with sickle cell disease: A national survey.

Anti-SARS-CoV-19 antibodies in children and adults with sickle cell disease: A single-site analysis in New York City.

Mental health assessment of youth with sickle cell disease and their primary caregivers during the COVID-19 pandemic.

Transition Preparation and Satisfaction of Care Among Adolescents and Young Adults With Sickle Cell Disease at the Ghana Institute of Clinical Genetics.

Brain Magnetic Resonance Imaging and Angiography in Children with Sickle Cell Anaemia in Uganda in a Cross-Sectional Sample.

Managing Human Subjects Research During a Global Pandemic at an Academic Center: Lessons Learned from COVID-19.

Administrative data identify sickle cell disease: A critical review of approaches in U.S. health services research.

Parental Notification Via Text Messaging for Infant Sickle Screening Programs: Exploration of Feasibility and Acceptability in Uganda.

Quality of Life of Latino and Non-Latino Youth With Sickle Cell Disease as Reported by Parents and Youth.

Collaborators (3)

Arlene Smaldone

Rhonda G. Kost

Cristina Fernández

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