| Germline variation in BRCA1/2 is highly ethnic‐specific: Evidence from over 30,000 Chinese hereditary breast and ovarian cancer patients SP Bhaskaran, K Chandratre, H Gupta, L Zhang, X Wang, J Cui, YC Kim, ... International journal of cancer 145 (4), 962-973, 2019 | 73 | 2019 |
| Prevalence of BRCA1/BRCA2 pathogenic variation in Chinese Han population H Dong, K Chandratre, Y Qin, J Zhang, X Tian, C Rong, N Wang, M Guo, ... Journal of Medical Genetics 58 (8), 565-569, 2021 | 32 | 2021 |
| Variants of DNA mismatch repair genes derived from 33,998 Chinese individuals with and without cancer reveal their highly ethnic-specific nature L Zhang, SP Bhaskaran, T Huang, H Dong, K Chandratre, X Wu, Z Qin, ... European Journal of Cancer 125, 12-21, 2020 | 13 | 2020 |
| Common genetic variants contribute to incomplete penetrance: evidence from cancer-free BRCA1 mutation carriers B Downs, S Sherman, J Cui, YC Kim, C Snyder, M Christensen, J Luo, ... European Journal of Cancer 107, 68-78, 2019 | 11 | 2019 |
| Prenatal screening for co-inheritance of sickle cell anemia and β-thalassemia traits D Dhawan, S Chaudhary, K Chandratre, A Ghosh, N Sojitra Clin Med Biochem Open Access 2 (01), 2471-2663.1000108, 2016 | 9 | 2016 |
| Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition H Gupta, K Chandratre, S Sinha, T Huang, X Wu, J Cui, MQ Zhang, ... BMC genomics 21, 1-12, 2020 | 6 | 2020 |
| Whole gene sequencing based screening approach to detect β-thalassemia mutations S Chaudhary, D Dhawan, N Sojitra, P Chauhan, K Chandratre, ... Biol Med (Aligarh) 9 (383), 2, 2017 | 5 | 2017 |
| Whole-genome sequencing of Brevundimonas diminuta XGC1, isolated from a tuberculosis patient in Gujarat, India A Ghosh, K Chandratre, A Chaudhary, S Chaudhary, N Badani, ... Genome Announcements 3 (3), 10.1128/genomea. 00686-15, 2015 | 4 | 2015 |
| Computational modeling and analysis of the morphogenetic domain signaling networks regulating C. elegans embryogenesis B Niu, TN Bach, X Chen, KR Chandratre, JI Murray, Z Zhao, M Zhang Computational and Structural Biotechnology Journal 20, 3653-3666, 2022 | 2 | 2022 |
| Molecular diagnosis of inherited retinal diseases with non-specific clinical phenotypes using whole exome sequencing A Ghosh, D Dhawan, K Chandratre, S Chaudhary, B Shah, S Vudathala, ... J Bioinforma Proteomics Rev 2 (2), 1-3, 2016 | 2 | 2016 |
| Accurate prediction of cohesin-mediated 3D genome organization from 2D chromatin features A Abbas, K Chandratre, Y Gao, J Yuan, MQ Zhang, RS Mani bioRxiv, 2022.11. 23.517572, 2022 | 1 | 2022 |
| Abstract LB011: Landscape of promoter centric chromatin interactions and co-regulated gene network provide insights for transcriptional regulation in prostate cancer KR Chandratre, S Ramanad, A abbas Elmahdi, Y Gao, RS Mani, M Zhang Cancer Research 84 (7_Supplement), LB011-LB011, 2024 | | 2024 |
| ChIPr: accurate prediction of cohesin-mediated 3D genome organization from 2D chromatin features A Abbas, K Chandratre, Y Gao, J Yuan, MQ Zhang, RS Mani Genome Biology 25 (1), 15, 2024 | | 2024 |
| Abstract A054: Accurate prediction of cohesin-mediated 3D genome organization using 2D chromatin features K Chandratre Cancer Research 83 (11_Supplement), A054-A054, 2023 | | 2023 |
| A simple procedure for extracting DNA from Coagulated Blood Samples for DNA banking Journal of Cerebrovascular disease, 2018 | | 2018 |
