|| Title of the thesis
|| Bhatia HM
|| Study of blood groups substance H.
|| Baxi AJ
|| Biochemical effects of ionizing radiations.
|| Vyas GN
|| Studies on blood transfusion with special reference to blood volume and survival rates of erythrocytes.
|| Hakim SMA
|| Blood and serum groups and other genetical characters of some endogamous muslim groups.
|| Sathe MS
|| Variants of A and B antigens and Oh ( Bombay ) phenotype with reference to quantitative evaluations.
|| Gupte SC
|| Assessment of neonatal jaundice due to blood group incompatibilities and G6PD deficiency
|| Badakere SS
|| Studies on the blood group antigen (In a).
|| Bapat JP
|| Studies on the intracellular and membrane markers in the cases of hematological disorders.
|| Joshi SR
|| Studies on the I-i blood groups in health and disease with hematologic disorders
|| Joshi SH
|| Studies on hepatitis B surface antigens (HBsAg)
|| Pavri RS
|| Studies on the mechanism of oxidative injury to the red cell in some hematological disorders
|| Pourazar A
|| Changes in blood group ABH and I antigens in leukaemia and other hematologic malignancy patients
|| Iyer YS
|| Immunoglobulin studies in haematologic disorders
|| Mehta MM
|| HLA antigens and lymphocyte surface markers in health and diseases
|| Bhargava AB
|| Contribution of glycolytic enzymes. Intermediates and membrane markers to storage lesions of banked blood.
|| Anand T. Chablani
|| Correlation of Immunological profiles with clinical manifestations in various Autoimmune Diseases
|| Chablani UA
|| Studies on different aspects of HLA system
|| Rao VR
|| Population genetics of some important tribes in Vidarbha region of Maharashtra
|| Gorakshakar AC
|| Genetic studies in Bhils and other Bhil related tribes of Western India .
|| Mukherjee MB
|| Molecular genetics of sickle cell disease in Western India and its correlation with hematological and clinical profile.
|| Nadkarni AH
|| Biochemical studies on interrelationship between , and genes in clinical expression of thalassemia syndromes.
|| Shetty Shrimati
|| Detection of mutants and mutant carriers in hemophilia A and hemophilia B families.
||Dr. Aruna Pawar
||Molecular characterization of Indian beat thalassemia by DGGE and mismatched priming PCR
|| Mehta Yashesh
|| A study of the specificities of platelet antibodies and anti-idiotype antibodies in cases of autoimmune thrombocytopenic purpura.
|| Sukumar Sridevi
|| Molecular characterization of glucose-6-phosphate dehydrogenase in Indians.
|| Kulkarni Bipin
|| Study of platelet specific antigens in the Indian population and its association with neonatal alloimmune thromcytopenic purpura (NAITP).
|| Khare Amit
|| Genetic risk factors for coronary artery disease in the young.
|| Nair Sona
|| Molecular basis of hereditary platelet disorders in western India with special emphasis on glanzmanns thrombosis.
|| Kulkarni Swati
|| Population screening for detection and molecular characterization of partial D antigen and Rh variants.
|| Pradhan Vandana
|| Anti-neutrophil cytoplasmic antibodies in systemic vasculitides and other related disorders
|| Vora Sonal
|| Thrombophilia as an important predictor…… loss in India .
|| Kedar Prabhakar
|| Pyruvate kinase deficiency Escherichia Coli, Human erythrocytes and mice:Genomic and proteomic application to study metabolic regulation.
|| Vijapurkar Manasi
|| Molecular characterization of GP IIb Gene, mutations in Glanzmanns thrombosthenia patients from Western India .
|| D'Souza Edna
|| Non-Invasive approaches for prenatal diagnosis of hemoglobinopathies from maternal blood.
|| Quadros Leera
|| Molecular pathology of hemophilia B in patients from Western India .
|| Parsannawar Devraj
|| Clinical and molecular characterization of HLA-B7 CREG and its comparison with HLA B27 associated sero negative spondarthritis
||Miss Khushnooma Italia
||The effect of pharmacological agent hydroxyurea on the phonotypic and genotypic expression of the hemoglobinopathies.
||Molecular characterization of FLT3 gene mutation in Acute Non-Lymphoblastic Leukemia (ANLL) patients from Western India
|| Sabita Ray
|| Molecular Characterization of ABO' Blood Group antigens in Indian Population.
|| Navin P. Pai
|| Phenotypic and genotypic characterization of Protein C deficiency cases from India
||Comprehensive biochemical and molecular studies on unexplained inherited hemolytic anaemias.
||Selma Zenia D'Silva
||Evaluation of genetic factors related to unconjugated hyperbilirubinemia among the neonates in India.
||Pooja Shrikant Shraddha Dabke
||Evaluation of Alpha Hemoglobin stabilizing protein (AHSP) as a genetic modifier and effect of other linked and unlinked determinants on clinical manifestations of Hemoglobin disorders
||Preethi Satish Nair
||Molecular characterization of haemophilia A patients in Western India
||Modulation of the clinical phenotypes of sickle cell disease by genetic polymorphisms in modifier genes.
||Shantashree S. Vaidya
||Susceptibility to BCR/ABL gene mutations in invitro and ex-vivo studies.
||Snehal Rajan Mhatre
||Molecular characterization of Haemophagocytic lymphohistiocytosis (HLH) in Western India.
||Patricia Maria Pinto
||Genetic and Non-Genetic risk factors for the development of inhibitors in Haemophilia A patients.
||Dipti Subhash Rajani Upadhye
||Understanding the Natural history of Sickle cell disease and experimental therapeutic interventions for modulatory globin gene expression.
||Rucha Kiran Patil
||Role of circulating cell derived microparticles in women with pregnancy loss, both recurrent miscarriage and unexplained fetal loss
||Molecular pathology of Bengal Macrothrombocytopenia and Bernard Soulier Syndrome (BSS)
||Stacy Peter Brigitte Colaco
||Genotyping of subject with borderline HbA2 level under effect of linked and unlinked determinant on Beta thalassemia carriers screening.
||Swati Suneet Suman Garg
||Study of Biology of Leukemic Stem Cells.
||Comprehensive analysis of genetic polymorphism associated with Warfarin handling in Indian patient.