| Breakpoint mapping of a novel de novo translocation t (X; 20)(q11. 1; p13) by positional cloning and long read sequencing UR Dutta, SN Rao, VK Pidugu, VS Vineeth, A Bhattacherjee, AD Bhowmik, ... Genomics 111 (5), 1108-1114, 2019 | 34 | 2019 |
| Exome sequencing for perinatal phenotypes: the significance of deep phenotyping S Aggarwal, VS Vineeth, A Das Bhowmik, A Tandon, A Kulkarni, ... Prenatal Diagnosis 40 (2), 260-273, 2020 | 21 | 2020 |
| Transcriptomic Analysis of Chloroquine-Sensitive and Chloroquine-Resistant Strains of Plasmodium falciparum: Toward Malaria Diagnostics and Therapeutics for … HA Antony, V Pathak, SC Parija, K Ghosh, A Bhattacherjee OMICS: A Journal of Integrative Biology 20 (7), 424-432, 2016 | 17 | 2016 |
| Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patients S Nampoothiri, D Yesodharan, A Bhattacherjee, H Ahamed, RD Puri, ... JIMD reports 56 (1), 82-94, 2020 | 13 | 2020 |
| Compensatory Mutations Occur Within the Electrostatic Interaction Range of Deleterious Mutations in Protein Structure SK Amrita Bhattacherjee, Saurav Mallik Journal of Molecular Evolution, 1-3, 2014 | 8* | 2014 |
| Whole transcriptome expression analysis and comparison of two different strains of Plasmodium falciparum using RNA-Seq HA Antony, V Pathak, SC Parija, K Ghosh, A Bhattacherjee Genomics Data 8, 110-112, 2016 | 7 | 2016 |
| Sequence and 3D structure based analysis of TNT degrading proteins in Arabidopsis thaliana A Bhattacherjee, RS Mandal, S Das, S Kundu Journal of molecular modeling 20, 1-9, 2014 | 6 | 2014 |
| Cytogenomic Characterization of a Novel de novo Balanced Reciprocal Translocation t (1; 12) by Genome Sequencing Leading to Fusion Gene Formation of EYA3/EFCAB4b UR Dutta, A Bhattacherjee, A Bahal, LP Posanapally, KA Lone, S Bathula, ... Molecular Syndromology 13 (5), 370-380, 2022 | 3 | 2022 |
| Identification and in-silico analysis of a novel disease-causing variant in the GUSB gene for Mucopolysaccharidosis VII presenting as non-immune fetal hydrops A Bhattacherjee, P Ranganath, D Pasumarthi, AB Dalal Gene Reports 16, 100437, 2019 | 3 | 2019 |
| Co-Occurrence of Leber Congenital Amaurosis and Meckel Syndrome Type 1 in a Fetus: Is There a Lesson to Be Learned K Tallapaka, S Aggarwal, A Bhattacherjee, A Das Bhowmik, A Dalal Molecular Syndromology 10 (3), 177-182, 2019 | 1 | 2019 |
| Genotype first approach & familial segregation analysis help in the elucidation of disease-causing variant for fucosidosis A Bhattacherjee, E Desa, KA Lone, A Jaiswal, S Tyagi, A Dalal Indian Journal of Medical Research 157 (4), 363-366, 2023 | | 2023 |
| Ghosal Hematodiaphyseal Dysplasia: An Unusual but Easy-to-Diagnose Genetic Cause of Anemia A Bhattacherjee, AB Dalal, P Ranganath | | |
| Whole Genome Sequencing as a Diagnostic Tool: Utility and Challenges A Bhattacherjee | | |
| Accepted: 7th November, 2014 Journal of Molecular Evolution A Bhattacherjee, S Mallik, S Kundu | | |
Ashwin DalalHead, Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, HyderabadVerified email at cdfd.org.in
