Identifying barriers to evidence-based care for sickle cell disease: results from the Sickle Cell Disease Implementation Consortium cross-sectional survey of healthcare providers in the USAMatthew P. Smeltzer, Jane S. Hankins, Robert W. Gibson et al.|BMJ Open|2021Cited by 56
Transition care continuity promotes long‐term retention in adult care among young adults with sickle cell diseaseKristen E. Howell, Jane S. Hankins, Sheila Anderson et al.|Pediatric Blood & Cancer|2021Cited by 13
Gaps during pediatric to adult care transfer escalate acute resource utilization in sickle cell diseaseKristen E. Howell, Jane S. Hankins, Mariam Kayle et al.|Blood Advances|2024Cited by 9
Depression, sleep and pain affect instrumental activities of daily living through cognitive functioning in adults with sickle cell disease: A report from the Sickle Cell Disease Implementation ConsortiumJennifer Longoria, Andrew M. Heitzer, Kristen E. Howell et al.|British Journal of Haematology|2024Cited by 5
Assessment of transition readiness to predict health care utilization during transition to adult care in sickle cell diseaseKristen E. Howell, Jerlym S. Porter, Andrew M. Heitzer et al.|Expert Review of Hematology|2022Cited by 5