Article

Potential Association of Sickle Cell Disease Genotypes (Ss, as, Sβ Thalassemia) With Abo Blood Groups: In Indian Population

2026-05-19

Abstract excerpt

<title>Abstract</title> <p>Sickle cell disease (SCD) exhibits marked clinical and hematological heterogeneity influenced by genetic and biological modifiers. The ABO blood group system has been implicated in vascular and thrombotic pathways relevant to SCD pathophysiology; however, dataassociated with SCD genotypes and hematological severity in Indian population remains unexplored. The association between SCD gen...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: bd2c0aa1-7ea7-59e1-9e62-44114b3cf879
DOI: 10.21203/rs.3.rs-9298884/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Potential Association of Sickle Cell Disease Genotypes (Ss, as, Sβ Thalassemia) With Abo Blood Groups: In Indian PopulationDOI 10.21203/rs.3.rs-9298884/v1Read

Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profilesSemantic proximity Read

Clinical and genetic ancestry profile of a large multi-centre sickle cell disease cohort in Brazil.Semantic proximity Read

Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC).Semantic proximity Read

Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.Semantic proximity Read

Demographic Profiling of Haemoglobinopathies-A Rzetrospective Study at Thalassemia and Sickle Cell Society, TelanganaSemantic proximity Read

Burdwan University Thalassemia Severity (BUTS) Scoring System: A numerical Method For Defining the Clinicopathological status of Thalassaemia PatientSemantic proximity Read

Updated Worldwide Epidemiology of Inherited Erythrocyte DisordersSemantic proximity Read

Red Blood Cell Antigen Genotyping for Sickle Cell Disease, Thalassemia, and Other Transfusion Complications.Semantic proximity Read

ßs-Gene-Cluster Haplotypes in Sickle Cell Anemia: Clinical and Hematologic FeaturesSemantic proximity Read

Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.Semantic proximity Read

Sickle cell disease in Middle East Arab countriesSemantic proximity Read

The phenotypes of sickle cell disease: strategies to aid the identification of undiagnosed patients in the Italian landscapeSemantic proximity Read