Marsha Treadwell

3.7k total citations
120 papers, 2.4k citations indexed

About

Marsha Treadwell is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marsha Treadwell has authored 120 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Genetics, 65 papers in Hematology and 46 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marsha Treadwell's work include Hemoglobinopathies and Related Disorders (102 papers), Iron Metabolism and Disorders (63 papers) and Prenatal Screening and Diagnostics (26 papers). Marsha Treadwell is often cited by papers focused on Hemoglobinopathies and Related Disorders (102 papers), Iron Metabolism and Disorders (63 papers) and Prenatal Screening and Diagnostics (26 papers). Marsha Treadwell collaborates with scholars based in United States, United Kingdom and South Africa. Marsha Treadwell's co-authors include Elliott Vichinsky, Christine Miaskowski, Kathryn L. Hassell, San Keller, Eufémia Jacob, Judith Beyer, Lori Styles, Keith Quirolo, Marilyn Savedra and Robert W. Gibson and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Marsha Treadwell

116 papers receiving 2.3k citations

Peers

Marsha Treadwell
Carlton Dampier United States
Susan D. Roseff United States
Diana Rofail United States
Johanna H. van der Lee Netherlands
Miriam O. Ezenwa United States
Lubna Daraz United States
Suzanne Ameringer United States
Patricia E. Hershberger United States
Alicia Kunin‐Batson United States
Jennifer Klima United States
Carlton Dampier United States
Marsha Treadwell
Citations per year, relative to Marsha Treadwell Marsha Treadwell (= 1×) peers Carlton Dampier

Countries citing papers authored by Marsha Treadwell

Since Specialization
Citations

This map shows the geographic impact of Marsha Treadwell's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marsha Treadwell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marsha Treadwell more than expected).

Fields of papers citing papers by Marsha Treadwell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marsha Treadwell. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marsha Treadwell. The network helps show where Marsha Treadwell may publish in the future.

Co-authorship network of co-authors of Marsha Treadwell

This figure shows the co-authorship network connecting the top 25 collaborators of Marsha Treadwell. A scholar is included among the top collaborators of Marsha Treadwell based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marsha Treadwell. Marsha Treadwell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Crosby, Lori E., Allison A. King, Jerlym S. Porter, et al.. (2025). Recommended measurement protocols for sickle cell disease in the PhenX toolkit: psychosocial factors and social determinants of health. PubMed. 2(1). yoaf019–yoaf019.
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Pugh, Norma, Donald Brambilla, Barbara L. Kroner, et al.. (2024). Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registry. American Journal of Hematology. 99(5). 900–909. 9 indexed citations
4.
King, Allison A., Cathy L. Melvin, Christopher R. Carpenter, et al.. (2024). Impact of an individualized pain plan to treat sickle cell disease vaso-occlusive episodes in the emergency department. Blood Advances. 8(20). 5330–5338. 2 indexed citations
5.
Howell, Kristen E., Jerlym S. Porter, Marsha Treadwell, et al.. (2024). 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 Consortium. British Journal of Haematology. 206(3). 944–953. 1 indexed citations
6.
Munung, Nchangwi Syntia, et al.. (2024). Perceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania. European Journal of Human Genetics. 32(10). 1307–1313. 6 indexed citations
7.
Treadwell, Marsha. (2023). Mental health and psychological resilience in sickle cell disease. The Lancet Haematology. 10(8). e569–e571. 1 indexed citations
8.
Lamont, Andrea, Lewis L. Hsu, Sara Jacobs, et al.. (2022). What does it mean to be affiliated with care?: Delphi consensus on the definition of “unaffiliation” and “specialist” in sickle cell disease. PLoS ONE. 17(11). e0272204–e0272204. 6 indexed citations
9.
Phillips, Shannon, Yumei Chen, Rita Masese, et al.. (2022). Perspectives of individuals with sickle cell disease on barriers to care. PLoS ONE. 17(3). e0265342–e0265342. 32 indexed citations
10.
Smeltzer, Matthew P., Kristen E. Howell, Marsha Treadwell, et al.. (2021). 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 USA. BMJ Open. 11(11). e050880–e050880. 25 indexed citations
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Hankins, Jane S., Nirmish Shah, Lisa DiMartino, et al.. (2020). Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization: Protocol for an Efficacy and Implementation Study. JMIR Research Protocols. 9(7). e16319–e16319. 19 indexed citations
13.
Porter, Jerlym S., Kathryn Russell, Marsha Treadwell, et al.. (2017). Provider Perspectives of Necessary Factors in Sickle Cell Disease Health Care Transition: Results from an Online Survey. Blood. 130. 2140–2140. 1 indexed citations
14.
Treadwell, Marsha, Julie Makani, Kwaku Ohene‐Frempong, et al.. (2017). Stakeholder Perspectives on Public Health Genomics Applications for Sickle Cell Disease: A Methodology for a Human Heredity and Health in Africa (H3Africa) Qualitative Research Study. OMICS A Journal of Integrative Biology. 21(6). 323–332. 8 indexed citations
15.
Treadwell, Marsha, Shirley Johnson, India Sisler, et al.. (2015). Development of a sickle cell disease readiness for transition assessment. International Journal of Adolescent Medicine and Health. 28(2). 193–201. 26 indexed citations
16.
Treadwell, Marsha, Shirley Johnson, India Sisler, et al.. (2015). Self-efficacy and readiness for transition from pediatric to adult care in sickle cell disease. International Journal of Adolescent Medicine and Health. 28(4). 381–388. 32 indexed citations
17.
Gold, Jeffrey I., et al.. (2011). The mediating effects of family functioning on psychosocial outcomes in healthy siblings of children with sickle cell disease. Pediatric Blood & Cancer. 57(6). 1055–1061. 24 indexed citations
18.
Stotts, Nancy A., et al.. (2011). A Biopsychosocial-Spiritual Model of Chronic Pain in Adults with Sickle Cell Disease. Pain Management Nursing. 14(4). 287–301. 31 indexed citations
19.
Pakbaz, Zahra, Marsha Treadwell, Hae‐Young Kim, et al.. (2010). Education and employment status of children and adults with thalassemia in North America. Pediatric Blood & Cancer. 55(4). 678–683. 12 indexed citations
20.
Beyer, Judith, et al.. (1999). Practice Guidelines for the Assessment of Children With Sickle Cell Pain. Journal for Specialists in Pediatric Nursing. 4(2). 61–73. 14 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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