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February 2, 2026Indian Journal of Hematology and Blood Transfusion

Genetic Landscape and Linkage Analysis of Factor VIII Gene Markers in Indian Women: Improving Carrier Detection for Haemophilia A

Chanda Hemaliya Arun Kumar Singh Anju Bharti Lalit Prashant Meena Ajeet Kumar Akhtar Ali

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Key Points

Carrier detection for haemophilia A can be improved using genetic markers related to factor VIII.
Analysis conducted on the genetic landscape of factor VIII gene markers specifically in Indian women.
Linkage analysis illustrates significant relationships between certain markers and haemophilia A inheritance.
Findings may enhance screening methods for healthy carriers, facilitating better management of haemophilia A.

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Implication

Analysis reveals genetic markers linked to haemophilia A in Indian women, suggesting improved carrier detection strategies.

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Cite This Study

Hemaliya et al. (2026) studied this question.

synapsesocial.com/papers/69a76639badf0bb9e87dc318 https://doi.org/10.1007/s12288-026-02326-6

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Compound heterozygous hemophilia A in a female patient and the identification of a novel missense mutation, p.Met1093IleOriginal Research · 2013 · 8 citations
2Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 gene combined with skewed X-chromosome inactivationOriginal Research · 2015 · 10 citations
3Spectrum and origin of mutations in sporadic cases of haemophilia A in ChinaOriginal Research · 2018 · 31 citations
4Prevalence of sporadic and familial haemophiliaRetrospective Study · 2006 · 90 citations
5Origin of mutation in sporadic cases of severe haemophilia A in SwedenOriginal Research · 2015 · 30 citations

More related papers

Haemophilia A: molecular insights2007
Linkage analysis in haemophilia A: simultaneous genotyping of two polymorphisms of the human factor VIII gene using induced heteroduplex formation1998
Polymorphisms associated with the FVIII and FIX genes in the Turkish population1995

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