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Jane Hankins

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Professor

University of Tennessee Health Science Center

United States

Research Interests

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Professors in United States

Recent Grants

Grant: Open

Novel therapeutic gene editing to induce fetal hemoglobin for sickle cell disease

Open Date: 2023-09-01

Close Date: 2028-08-31

Grant: Close

Measuring Lifelong Multimorbidity with Patient Perspectives: Implementing and Visualizing the Cumulative Burden Methodology Across Cohorts

Open Date: 2022-03-11

Close Date: 2026-02-28

Grant: Close

RE-aiming at Hydroxyurea Adherence for Sickle cell with mHealth (RE-HASH)

Open Date: 2016-08-08

Close Date: 2023-06-30

Grant: Close

Sparing Conversion to Abnormal TCD Elevation

Open Date: 2010-09-05

Close Date: 2014-11-30

Grant: Close

Massive Iron Deposit Assessment (MIDAS)

Open Date: 2010-08-01

Close Date: 2015-04-30

Articles (20)

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UNITED STATES

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George Goshua

UNITED STATES

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Heather Conklin

Chief, Division of Neuropsychology

St. Jude Children's Research Hospital

UNITED STATES

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Alexis Thompson

Division Chief

Children's Hospital of Philadelphia

UNITED STATES

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Jane Hankins

Research Interests

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Recent Grants

Articles (20)

Beyond mistrust: Diverse biobanking preferences among parents and adolescents with sickle cell disease

Acute Exercise Challenge and Airway Dynamics in Youth With Sickle Cell Anemia: A Multicenter Study

Early onset and worse pain in adolescents and young adults with sickle cell disease during health care transition

Hydroxyurea therapy in sickle cell disease: evaluating health care costs and use in a Brazilian tertiary setting

Relation of Adverse Childhood Experiences to Clinical and Patient‐Reported Outcomes for Adults With Sickle Cell Disease: A Registry Study

Sickle cell care in Lusophone countries: proceedings from the 1st International Lusophone Specialists’ Alliance in Sickle Cell Disease (ALUA) Conference

Accelerating Novel Therapies for Sickle Cell Disease with RWE: ASH RC Data Hub as a Strategically Coordinated Registry Network

Statewide Academic Performance of High School Students With Sickle Cell Disease

User Perceptions of a Multilevel mHealth Intervention to Boost Adherence to Hydroxyurea in Sickle Cell Disease

Utility of caregiver signaling questions to detect neurocognitive impairment in children with sickle cell disease

A Novel One-Sample Mendelian Randomization Approach for Count-Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic Effects

Investigation of Sickle Cell Retinopathy in Pediatric and Adolescent Patients Enrolled in a Large Cohort Study

Caregiver and provider perspectives on developmental services for children with sickle cell disease: a mixed methods analysis.

Single-cell transcriptomics reveals heterocellular g-globin gene expression in Agdb-thalassemia.

Neurocognitive functioning of patients with sickle cell disease in low- and middle-income countries

Normalization of Cerebral Hemodynamics After Gene Therapy in Adults With Sickle Cell Disease

A clinical evaluation program to monitor neurocognitive risk in children and adolescents with sickle cell disease

Variability in Health Outcomes According to Pediatric to Adult Transfer-of-Care Status Among Young Adults With Sickle Cell Disease.

Pediatric Hematology–Oncology or Pediatric Hematology and Pediatric Oncology: A Need for Further Discussion

Reply to: Comment on: Perinatal risk factors and neurocognitive outcomes in children and adolescents with sickle cell disease

Collaborators (10)

Eunyoung Kang

William Wood

Robert W. Gibson

Santiago Molina

Robyn Cohen

Guolian Kang

Kelly Harris

George Goshua

Heather Conklin

Alexis Thompson

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