Purvi Mohanty[Author] - Search Results

Year	Number of Results
2016	2
2019	1
2020	1
2021	2
2022	4
2023	2
2024	1

1

Comprehensive analysis of genetic factors predicting overall survival in Myelodysplastic syndromes.

Maurya N, Mohanty P, Dhangar S, Panchal P, Jijina F, Mathan SLP, Shanmukhaiah C, Madkaikar M, Vundinti BR. Maurya N, et al. Among authors: mohanty p. Sci Rep. 2022 Apr 8;12(1):5925. doi: 10.1038/s41598-022-09864-9. Sci Rep. 2022. PMID: 35396491 Free PMC article.

2

Over expression of mTOR gene predicts overall survival in myelodysplastic syndromes.

Maurya N, Mohanty P, Panchal P, Shanmukhaiah C, Vundinti BR. Maurya N, et al. Among authors: mohanty p. Mol Biol Rep. 2023 Jan;50(1):235-244. doi: 10.1007/s11033-022-07973-2. Epub 2022 Nov 2. Mol Biol Rep. 2023. PMID: 36322239

3

Investigating the clinical, hematological and cytogenetic profile of endoreduplicated hypodiploids in BCP-ALL.

Shetty D, Amare PK, Mohanty P, Talker E, Chaubal K, Jain H, Tembhare P, Patkar N, Chaturvedi A, Subramanian PG, Moulik N, Dhamne C, Jain H, Bagal B, Narula G, Sengar M, Khattry N, Banavali S. Shetty D, et al. Among authors: mohanty p. Blood Cells Mol Dis. 2020 Nov;85:102465. doi: 10.1016/j.bcmd.2020.102465. Epub 2020 Jul 11. Blood Cells Mol Dis. 2020. PMID: 32693366

4

Copy number gain of JAK2 on marker chromosome in a case of relapsed pediatric B-ALL.

Shetty D, Talker E, Dhamne C, Mohanty P, Chaubal K, Tembhare P, Patkar N, Subramanian PG, Moulik NR, Narula G, Banavali S. Shetty D, et al. Among authors: mohanty p. Pediatr Blood Cancer. 2022 Oct;69(10):e29658. doi: 10.1002/pbc.29658. Epub 2022 Apr 4. Pediatr Blood Cancer. 2022. PMID: 35373889 No abstract available.

5

FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients.

Solanki A, Mohanty P, Shukla P, Rao A, Ghosh K, Vundinti BR. Solanki A, et al. Among authors: mohanty p. PLoS One. 2016 Jan 22;11(1):e0147016. doi: 10.1371/journal.pone.0147016. eCollection 2016. PLoS One. 2016. PMID: 26799702 Free PMC article.

6

Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia.

George M, Solanki A, Mohanty P, Dhangar S, Rajendran A, Mohan S, Vundinti BR. George M, et al. Among authors: mohanty p. Mol Biol Rep. 2021 Mar;48(3):2519-2525. doi: 10.1007/s11033-021-06293-1. Epub 2021 Mar 28. Mol Biol Rep. 2021. PMID: 33778919

7

Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changes.

Mohanty P, Shetty D, Liehr T, Mrasek K, Khattry N. Mohanty P, et al. Int J Lab Hematol. 2022 Dec;44(6):993-994. doi: 10.1111/ijlh.13872. Epub 2022 May 9. Int J Lab Hematol. 2022. PMID: 35534180 No abstract available.

8

Importance of conventional cytogenetics in the identification of ins(19;X)(q13.1;p11.2q28) and t(1;11)(q10;p10), both, novel cytogenetic abnormalities in a pediatric AML case.

Shetty D, Mohanty P, Talker E, Jain H, Chaubal K, Tembhare P, Patkar N, Subramanian P, Moulik NR, Dhamne C, Narula G, Banavali S. Shetty D, et al. Among authors: mohanty p. Cancer Genet. 2021 Aug;256-257:17-20. doi: 10.1016/j.cancergen.2021.03.002. Epub 2021 Mar 21. Cancer Genet. 2021. PMID: 33823403

9

Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes.

Mohanty P, Korgaonkar S, Shanmukhaiah C, Ghosh K, Vundinti BR. Mohanty P, et al. Blood Cells Mol Dis. 2016 Jul;59:52-7. doi: 10.1016/j.bcmd.2016.04.005. Epub 2016 Apr 13. Blood Cells Mol Dis. 2016. PMID: 27282568

10

A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening.

Mohanty P, Jadhav P, Shanmukhaiah C, Kumar S, Vundinti BR. Mohanty P, et al. Int J Dermatol. 2019 Dec;58(12):1468-1471. doi: 10.1111/ijd.14424. Epub 2019 Mar 13. Int J Dermatol. 2019. PMID: 30868555 No abstract available.

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