Swati S. Kulkarni - Publications

The silent threat: a true Bombay phenotype with unexpected tolerance to group O-positive incidental transfusion.

Journal: Laboratory medicine

Published: May 25, 2026

Molecular characterization of rare S-s-U- phenotype in antenatal woman producing anti-U and anti-D and presenting HDFN during twin pregnancy: First report from India.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: June 20, 2025

D-- phenotype in a South Indian family: A multicentric approach to workup and management.

Journal: Transfusion medicine (Oxford, England)

Published: January 07, 2025

Unveiling Novel and Rare Variants in the α-1,4-Galactosyltransferase Gene Leading to Rare p Phenotype in Indian Patients.

Journal: Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie

Published: December 31, 2024

Weak or partial D: Importance of molecular characterization of D variants.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: September 05, 2024

Alloimmunization Due to Multiple Red Cell Antibodies in a RhD Positive Pregnancy: Lessons to be Learnt.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: July 30, 2024

Identification of novel FUT1 gene mutation 346A>G in an Indian Bombay phenotype patient.

Journal: Transfusion

Published: May 29, 2024

Autoimmune anti-D in an RhD-positive young infant: Learning from a rare case.

Journal: Vox sanguinis

Published: September 07, 2023

ACKR1 gene polymorphisms in Bombay blood group (Oh) individuals of Indian origin.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: July 14, 2023

Challenges in the transfusion management of a 15-month-old pediatric patient with Bombay blood group phenotype.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: February 05, 2023

Phenotyping and Genotyping of HNA: Prevalence, Risk of Alloimmunization, and HNA Incompatibilities in Indians.

Journal: Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie

Published: March 14, 2022

D--phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17(Hrₒ) antibodies.

Journal: Transfusion medicine (Oxford, England)

Published: May 04, 2021