Divyaswathi Citla Sridhar Institution-verified
Sourced from institutional research profiles (UAMS TRI or ARA).
Researcher
faculty
Research Areas
Biography and Research Information
OverviewAI-generated summary
Divyaswathi Citla Sridhar's research focuses on hematologic disorders, particularly venous thromboembolism and bleeding conditions. She has investigated risk factors for joint bleeding in severe hemophilia A and B, analyzing data from the Community Counts longitudinal surveillance cohort. Her work also examines venous thromboembolism in individuals using hormonal contraceptives and the healthcare utilization and disparities in transplant care for Wiskott Aldrich syndrome patients. Sridhar has contributed to interdisciplinary management guidelines for gynecologic bleeding with anticoagulation and has studied bone health in hemophilia carriers and individuals with von Willebrand disease. Her research also touches upon parental adverse childhood experiences and their impact on healthcare use among children with sickle cell disease.
Metrics
- h-index: 7
- Publications: 53
- Citations: 612
Selected Publications
-
HTRS2025.P1.27 Prevalence Vitamin D deficiency and risk factors for poor bone health in persons with Hemophilia A and B in Arkansas – A retrospective single institution study (2025)
-
Characterising Glanzmann Thrombasthenia in the United States: Real‐World Data From the EPIC Cosmos Dataset (2025)
-
Venous thromboembolism in obese hormonal contraceptive users: a large national database study (2025)
-
Unclassified Versus Well-defined Platelet Function Disorders: A Multicenter Comparison of Bleeding Patterns and Treatment (2025)
-
Interdisciplinary management of gynecologic bleeding with anticoagulation: a recommended toolkit from the Foundation for Women and Girls with Blood Disorders+ Thrombosis Subcommittee (2025)
-
Parental Adverse Childhood Experiences and Health Care Use Among Children With Sickle Cell Disease (2025)
-
Bone Health Screening in Persons With Bleeding Disorders: A Survey of United States Haemophilia Treatment Centres (2025)
-
Evaluating the Burden of Glanzmann Thrombasthenia: A Systematic Literature Review to Identify Research Priorities (2024)
-
A case of bruising and joint hypermobility: The need to consider genetic testing for platelet disorders (2024)
-
Risk of Venous Thromboembolic Events Among Obese Hormonal Contraceptive Users (2023)
-
Poor School Performance As an Indicator of Severity of Sickle Cell Disease (2023)
-
Reproductive healthcare utilization in patients with bleeding disorders (2023)
-
Reproductive Health Needs in Patients with Bleeding Disorders (2022)
-
Thrombotic microangiopathies: An illustrated review (2022)
-
Bone health in haemophilia carriers and persons with von Willebrand disease: A large database analysis (2022)
Grants & Funding
Collaboration Network
Top Collaborators
- Thrombotic microangiopathies: An illustrated review
- Bone health in haemophilia carriers and persons with von Willebrand disease: A large database analysis
- Wiskott Aldrich syndrome: healthcare utilizations and disparities in transplant care
- Risk factors for joint bleeding in severe hemophilia A and B: analysis of the Community Counts longitudinal surveillance cohort
- Surgery-Associated Bleeding Risk in Patients with Platelet Function Disorders - a Cross Sectional Study with the American Thrombosis and Hemostasis Network Dataset (ATHNdataset)
Showing 5 of 11 shared publications
- Parental Adverse Childhood Experiences and Health Care Use Among Children With Sickle Cell Disease
- HTRS2023.P3.5 Screening for abnormal uterine bleeding in adolescents presenting to primary care clinics
- Poor School Performance As an Indicator of Severity of Sickle Cell Disease
- Mental health in persons with von Willebrand disease in the United States – a large national database study
- A case of bruising and joint hypermobility: The need to consider genetic testing for platelet disorders
Showing 5 of 9 shared publications
- Bone health in haemophilia carriers and persons with von Willebrand disease: A large database analysis
- Surgery-Associated Bleeding Risk in Patients with Platelet Function Disorders - a Cross Sectional Study with the American Thrombosis and Hemostasis Network Dataset (ATHNdataset)
- A Multi-Institution Retrospective Study to Assess Bleeding Phenotype Among Patients with Platelet Function Disorders
- Reproductive Health Needs in Patients with Bleeding Disorders
- Reproductive healthcare utilization in patients with bleeding disorders
Showing 5 of 7 shared publications
- Interdisciplinary management of gynecologic bleeding with anticoagulation: a recommended toolkit from the Foundation for Women and Girls with Blood Disorders+ Thrombosis Subcommittee
- Risk of Venous Thromboembolic Events Among Obese Hormonal Contraceptive Users
- Venous thromboembolism in obese hormonal contraceptive users: a large national database study
- Intravenous Estrogen for Acute Heavy Menstrual Bleeding: Commentary and Database Analysis
- Anticoagulation stewardship from menstruation to menopause: a toolkit for clinical management
- Parental Adverse Childhood Experiences and Health Care Use Among Children With Sickle Cell Disease
- Poor School Performance As an Indicator of Severity of Sickle Cell Disease
- Mental health in persons with von Willebrand disease in the United States – a large national database study
- Effects of Vitamin D Stoss Dosing in Patients with Sickle Cell Disease
- Risk of Venous Thromboembolic Events Among Obese Hormonal Contraceptive Users
- Venous thromboembolism in obese hormonal contraceptive users: a large national database study
- Intravenous Estrogen for Acute Heavy Menstrual Bleeding: Commentary and Database Analysis
- Interdisciplinary management of gynecologic bleeding with anticoagulation: a recommended toolkit from the Foundation for Women and Girls with Blood Disorders+ Thrombosis Subcommittee
- Risk of Venous Thromboembolic Events Among Obese Hormonal Contraceptive Users
- Venous thromboembolism in obese hormonal contraceptive users: a large national database study
- Risk factors for joint bleeding in severe hemophilia A and B: analysis of the Community Counts longitudinal surveillance cohort
- Risk Factors for Joint Bleeding in Severe Hemophilia a and B: Analysis of the Community Counts Longitudinal Surveillance Cohort
- Bone Health Screening in Persons With Bleeding Disorders: A Survey of United States Haemophilia Treatment Centres
- Risk factors for joint bleeding in severe hemophilia A and B: analysis of the Community Counts longitudinal surveillance cohort
- Risk Factors for Joint Bleeding in Severe Hemophilia a and B: Analysis of the Community Counts Longitudinal Surveillance Cohort
- Bone Health Screening in Persons With Bleeding Disorders: A Survey of United States Haemophilia Treatment Centres
- Risk factors for joint bleeding in severe hemophilia A and B: analysis of the Community Counts longitudinal surveillance cohort
- Risk Factors for Joint Bleeding in Severe Hemophilia a and B: Analysis of the Community Counts Longitudinal Surveillance Cohort
- Bone Health Screening in Persons With Bleeding Disorders: A Survey of United States Haemophilia Treatment Centres
- Risk factors for joint bleeding in severe hemophilia A and B: analysis of the Community Counts longitudinal surveillance cohort
- Risk Factors for Joint Bleeding in Severe Hemophilia a and B: Analysis of the Community Counts Longitudinal Surveillance Cohort
- Bone Health Screening in Persons With Bleeding Disorders: A Survey of United States Haemophilia Treatment Centres
- Surgery-Associated Bleeding Risk in Patients with Platelet Function Disorders - a Cross Sectional Study with the American Thrombosis and Hemostasis Network Dataset (ATHNdataset)
- A Multi-Institution Retrospective Study to Assess Bleeding Phenotype Among Patients with Platelet Function Disorders
- A Multi-Institution Retrospective Study to Assess Bleeding Phenotype Among Patients with Platelet Function Disorders
- Unclassified Versus Well-defined Platelet Function Disorders: A Multicenter Comparison of Bleeding Patterns and Treatment
- Poor School Performance As an Indicator of Severity of Sickle Cell Disease
- Effects of Vitamin D Stoss Dosing in Patients with Sickle Cell Disease
- Risk of Venous Thromboembolic Events Among Obese Hormonal Contraceptive Users
- Venous thromboembolism in obese hormonal contraceptive users: a large national database study
Similar Researchers
Based on overlapping research topics