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Blood Transfusion = Trasfusione Del Sangue|April 5, 2021
Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experienceDisha Parchure, Manisha Madkaikar, Swati KulkarniTransfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|January 20, 2025
Weak or partial D: Importance of molecular characterization of D variantsAkshaya Tomar, Rati Devendra, Disha Parchure, et al.Transfusion|May 5, 2017
First report of Rh<sub>null</sub> individuals in the Indian population and characterization of the underlying molecular mechanismsSwati S Kulkarni, Kasiviswanathan Vasantha, Harita Gogri, et al.Vox Sanguinis|November 6, 2023
Autoimmune anti-D in an RhD-positive young infant: Learning from a rare caseSheetal Malhotra, Manisha Roy, Disha Parchure, et al.Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|June 22, 2018
RHD-Positive Alleles among D- C/E+ Individuals from IndiaSwati S Kulkarni, Harita Gogri, Disha Parchure, et al.Transfusion|February 27, 2018
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD alleleYann Fichou, Disha Parchure, Harita Gogri, et al.Blood Transfusion = Trasfusione Del Sangue|December 2, 2020
Molecular characterization of rare D--/D-- variants in individuals of Indian originSwati Kulkarni, Garima Mishra, Harita Maru, et al.Pageof 1