Christian Medical College Vellore, Ida Scudder Road, Vellore – 632004, Tamil Nadu, India
Publications
Coexistence of aberrant hematopoietic and stromal elements in myelodysplastic syndromes
Tuberculosis among allogeneic bone marrow transplant recipients in India
Frequency of rare BCR-ABL1 fusion transcripts in chronic myeloid leukemia patients
Outcome of treatment with a low cost protocol in adults with T cell acute lymphoblastic leukemia in a tertiary care center in India
Atypical BCR-ABL1 fusion transcripts in adult B-acute lymphoblastic leukemia, including a novel fusion transcript-e8a1
Acute monoblastic leukemia with abnormal eosinophils and inversion (16): A rare entity
Coexistence of aberrant hematopoietic and stromal elements in myelodysplastic syndromes
Tuberculosis among allogeneic bone marrow transplant recipients in India
Frequency of rare BCR-ABL1 fusion transcripts in chronic myeloid leukemia patients
Outcome of treatment with a low cost protocol in adults with T cell acute lymphoblastic leukemia in a tertiary care center in India
Atypical BCR-ABL1 fusion transcripts in adult B-acute lymphoblastic leukemia, including a novel fusion transcript-e8a1
Acute monoblastic leukemia with abnormal eosinophils and inversion (16): A rare entity
ATP-binding casette transporter expression in acute myeloid leukemia: association with in vitro cytotoxicity and prognostic markers
Population pharmacokinetics of Daunorubicin in adult patients with acute myeloid leukemia
RNA expression of genes involved in cytarabine metabolism and transport predicts cytarabine response in acute myeloid leukemia
Fluorescence in situ hybridization patterns of BCR/ABL1 fusion in chronic myelogenous leukemia at diagnosis
Novel NPM1 mutation in the 3'-untranslated region identified in two patients with acute myeloid leukemia
Role of minimal residual disease monitoring in acute promyelocytic leukemia treated with arsenic trioxide in frontline therapy
Clinicopathological features of hepatosplenic T cell lymphoma: a single centre experience from India
Cytogenetic analysis of acute myeloid leukemia with t(8;21) from a tertiary care center in India with correlation between clinicopathologic characteristics and molecular analysis
Prevalence of chromosomal abnormalities and Y chromosome microdeletion among men with severe semen abnormalities and its correlation with successful sperm retrieval
The t(6;9)(p22;q34) in myeloid neoplasms: a retrospective study of 16 cases
Prevalence of chromosomal abnormalities and Y chromosome microdeletion among men with severe semen abnormalities and its correlation with successful sperm retrieval
Impact of FLT3 mutations and secondary cytogenetic changes on the outcome of patients with newly diagnosed acute promyelocytic leukemia treated with a single agent arsenic trioxide regimen.
Generation of an integration-free iPSC line (CSCRi005-A) from erythroid progenitor cells of a healthy Indian male individual
Fludarabine-based conditioning for allogeneic stem cell transplantation for multiply transfused patients with Fanconi's anemia
Hematological and molecular remission with combination chemotherapy in a patient with PLZF-RARalpha acute promyelocytic leukemia (APML)
Hepatotoxicity profile of single agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia, its impact on clinical outcome and the effect of genetic polymorphisms on the incidence of hepatotoxicity
Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: durable remissions with minimal toxicity
Heterogeneity of Mesenchymal Stromal Cells in Myelodysplastic Syndrome-with Multilineage Dysplasia (MDS-MLD)
The t(8;14)(q24.1;q32) and its variant translocations: A study of 34 cases
Acute myeloid leukaemia: challenges and real world data from India
Comparison of newly diagnosed and relapsed patients with acute promyelocytic leukemia treated with arsenic trioxide: insight into mechanisms of resistance
A novel X-chromosomal microdeletion encompassing congenital hemidysplasia with ichthyosiform erythroderma and limb defects
Mosaic double aneuploidy: Down syndrome and XYY.
Incontinentia pigmenti, an x-linked dominant disorder, in a 2-year-old boy with Klinefelter syndrome
Plasma imatinib levels and ABCB1 polymorphism influences early molecular response and failure-free survival in newly diagnosed chronic phase CML patients
Coexistence of aberrant hematopoietic and stromal elements in myelodysplastic syndromes.
Generation of an integration-free iPSC line (CSCRi005-A) from erythroid progenitor cells of a healthy Indian male individual.
Spectrum of Chromosomal Abnormalities Detected by Conventional Cytogenetic Analysis Following Invasive Prenatal Testing of Fetuses with Abnormal Ultrasound Scans
Juvenile ankylosing spondylitis in Turner syndrome
Cytogenetic profile of 1791 adult acute myeloid leukemia in India
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis.
