Shriram G Bhosle
Overview
Explore the profile of Shriram G Bhosle including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
6
Citations
657
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Petljak M, Alexandrov L, Brammeld J, Price S, Wedge D, Grossmann S, et al.
Cell
. 2019 Mar;
176(6):1282-1294.e20.
PMID: 30849372
Multiple signatures of somatic mutations have been identified in cancer genomes. Exome sequences of 1,001 human cancer cell lines and 577 xenografts revealed most common mutational signatures, indicating past activity...
2.
Maura F, Agnelli L, Leongamornlert D, Bolli N, Chan W, Dodero A, et al.
Am J Hematol
. 2019 Mar;
94(6):628-634.
PMID: 30829413
The histological diagnosis of peripheral T-cell lymphoma (PTCL) can represent a challenge, particularly in the case of closely related entities such as angioimmunoblastic T-lymphoma (AITL), PTCL-not otherwise specified (PTCL-NOS), and...
3.
Iorio F, Behan F, Goncalves E, Bhosle S, Chen E, Shepherd R, et al.
BMC Genomics
. 2018 Aug;
19(1):604.
PMID: 30103702
Background: Genome editing by CRISPR-Cas9 technology allows large-scale screening of gene essentiality in cancer. A confounding factor when interpreting CRISPR-Cas9 screens is the high false-positive rate in detecting essential genes...
4.
Yates L, Knappskog S, Wedge D, Farmery J, Gonzalez S, Martincorena I, et al.
Cancer Cell
. 2017 Aug;
32(2):169-184.e7.
PMID: 28810143
Patterns of genomic evolution between primary and metastatic breast cancer have not been studied in large numbers, despite patients with metastatic breast cancer having dismal survival. We sequenced whole genomes...
5.
Wilkins M, Aldashev A, Wharton J, Rhodes C, Vandrovcova J, Kasperaviciute D, et al.
Circ Cardiovasc Genet
. 2014 Nov;
7(6):920-9.
PMID: 25373139
Background: Human variation in susceptibility to hypoxia-induced pulmonary hypertension is well recognized. High-altitude residents who do not develop pulmonary hypertension may host protective gene mutations. Methods And Results: Exome sequencing...
6.
Kulkarni-Kale U, Bhosle S, Manjari G, Joshi M, Bansode S, Kolaskar A
BMC Bioinformatics
. 2007 Jan;
7 Suppl 5:S12.
PMID: 17254296
Background: Whole genome sequence data is a step towards generating the 'parts list' of life to understand the underlying principles of Biocomplexity. Genome sequencing initiatives of human and model organisms...