| Impact of additional chromosomal aberrations on the disease progression of chronic myelogenous leukemia R Krishna Chandran, N Geetha, KM Sakthivel, R Suresh Kumar, ... Frontiers in oncology 9, 88, 2019 | 37 | 2019 |
| Characterization of CEBPA Mutations and Polymorphisms and their Prognostic relevance in de novo acute myeloid leukemia patients S Sarojam, S Raveendran, S Vijay, J Sreedharan, G Narayanan, ... Asian Pacific Journal of Cancer Prevention 16 (9), 3785-3792, 2015 | 13 | 2015 |
| FLT3 Mutation as a Significant Prognostic Marker in de novo Acute Myeloid Leukemia Patients: Incidence, Distribution and Association with Cytogenetic Findings in a Study from … S Sarojam, S Vijay, S Raveendran, J Sreedharan, G Narayanan, ... Middle East Journal of Cancer 5 (4), 185-196, 2014 | 8 | 2014 |
| Mutation analysis of IDH1/2 genes in unselected de novo acute myeloid leukaemia patients in India-identification of a Novel IDH2 mutation S Raveendran, S Sarojam, S Vijay, AC Geetha, J Sreedharan, ... Asian Pacific Journal of Cancer Prevention 16 (9), 4095-4101, 2015 | 7 | 2015 |
| A novel SRY gene mutation c.266 A>T (p.E89V) in a 46,XY complete gonadal dysgenesis patient SK Raveendran, L Ramachandran, L Joseph, AK Asokan, S Raj, ... Andrologia 51 (9), e13377, 2019 | 6 | 2019 |
| Enigmatic Inv (9): a case report on rare findings in hematological malignancies S Vijay, G Narayanan, S Sarojam, SK Raveendran, S Hariharan Iranian Red Crescent Medical Journal 18 (4), 2016 | 6 | 2016 |
| Chronic myeloid leukemia: a model disease of the past, present and future. Cells. 2021; 10 (1): 117 VR Minciacchi, R Kumar, DS Krause | 5 | |
| Mutation analysis of WNT4 gene in SRY negative 46, XX DSD patients with Mullerian agenesis and/or gonadal dysgenesis-An Indian study TS Ragitha, KS Sunish, S Gilvaz, S Daniel, PR Varghese, S Raj, J Francis, ... Gene 861, 147236, 2023 | 3 | 2023 |
| Chronic myeloid leukemia: a model disease of the past, present and future. Cells. 2021; 10: 117 VR Minciacchi, R Kumar, DS Krause s Note: MDPI stays neu-tral with regard to jurisdictional clai-ms in …, 2021 | 3 | 2021 |
| Differential gene expression changes and their implication on the disease progression in patients with chronic myeloid leukemia RK Chandran, N Geetha, KM Sakthivel, RS Kumar, KMNJ Krishna, ... Blood Cells, Molecules, and Diseases 77, 51-60, 2019 | 3 | 2019 |
| A Case Report of Concurrent IDH1 and NPM1 Mutations in a Novel t (X; 2)(q28; p22) Translocation in Acute Myeloid Leukaemia without Maturation (AML-M1) S Raveendran, S Sarojam, S Vijay, S Prem, H Sreedharan The Malaysian Journal of Medical Sciences: MJMS 22 (5), 93, 2015 | 3 | 2015 |
| Acute myeloid leukemia patients with variant or unusual translocations involving chromosomes 8 and 21–A comprehensive cytogenetic profiling of three cases with review of literature TVA Raj, P Gopinath, JAG Raj, G Narayanan, SG Nair, DSJ Philip, ... Journal of Cancer Research and Therapeutics 18 (3), 697-703, 2022 | 2 | 2022 |
| Recurrent isochromosome 21 and multiple abnormalities in a patient suspected of having acute myeloid leukemia with eosinophilic differentiation—a rare case from South India S Vijay, S Sarojam, S Raveendran, V Syamala, S Leelakumari, ... Chinese Journal of Cancer 31 (1), 45, 2012 | 2 | 2012 |
| Novel t (7; 10)(p22; p24) along with NPM1 mutation in patient with relapsed acute myeloid leukemia S Sarojam, S Raveendran, G Narayanan, H Sreedharan Annals of Saudi Medicine 33 (6), 619-622, 2013 | 1 | 2013 |
| Identification of heterochromatic variations in nonsyndromic cleft lip and palate S Raj, L Varghese, PV Narayanan, SK Raveendran, PR Varghese, ... Journal of Orofacial Sciences 15 (1), 55-60, 2023 | | 2023 |
| Enigmatic inv (9): a case report on rare findings in hematological malignancies. SV Sangeetha Vijay, GN Geetha Narayanan, SS Santhi Sarojam, ... | | 2016 |
| A novel chromosomal abnormality t (9; 14)(p24; q13) in B-acute lymphoblastic leukemia S Raveendran, S Sarojam, G Narayanan, H Sreedharan Indian Journal of Human Genetics 20 (1), 79, 2014 | | 2014 |
