V.V.V.S. Murty

4.7k total citations · 2 hit papers
42 papers, 3.8k citations indexed

About

V.V.V.S. Murty is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, V.V.V.S. Murty has authored 42 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 10 papers in Surgery and 10 papers in Genetics. Recurrent topics in V.V.V.S. Murty's work include Testicular diseases and treatments (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (4 papers). V.V.V.S. Murty is often cited by papers focused on Testicular diseases and treatments (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (4 papers). V.V.V.S. Murty collaborates with scholars based in United States, Kuwait and United Kingdom. V.V.V.S. Murty's co-authors include Ethan Dmitrovsky, Akira Kakizuka, Kazuhiko Umesono, Raymond P. Warrell, SR Frankel, Wilson H. Miller, Ronald M. Evans, R. S. K. Chaganti, George J. Bosl and Eftìhia Cayanis and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

V.V.V.S. Murty

42 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PML

1991 1.2k citations Akira Kakizuka, Wilson H. Miller et al. Cell profile →
Cloning and Genomic Organization of Beclin 1, a Candidate Tumor Suppressor Gene on Chromosome 17q21

1999 646 citations Vincent M. Aita, Xiao Liang et al. Genomics profile →

Peers

Countries citing papers authored by V.V.V.S. Murty

Since Specialization

Citations

This map shows the geographic impact of V.V.V.S. Murty's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by V.V.V.S. Murty with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V.V.V.S. Murty more than expected).

Fields of papers citing papers by V.V.V.S. Murty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V.V.V.S. Murty. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by V.V.V.S. Murty. The network helps show where V.V.V.S. Murty may publish in the future.

Co-authorship network of co-authors of V.V.V.S. Murty

This figure shows the co-authorship network connecting the top 25 collaborators of V.V.V.S. Murty. A scholar is included among the top collaborators of V.V.V.S. Murty based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with V.V.V.S. Murty. V.V.V.S. Murty is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Coexistence of independent myelodysplastic and Philadelphia chromosome positive clones in a patient treated with hydroxyurea 2002 ·Leukemia Research ·(unknown), V.V.V.S. Murty, Pulivarthi H. Rao, Gwen Nichols	9
2	Human Fas Associated Factor 1, hFAF1, Gene Maps to Chromosome Band 1p32 2000 ·Molecules and Cells ·Seung‐Wook Ryu, (unknown), Sungjoo Kim Yoon, V.V.V.S. Murty, Eunhee Kim	4
3	Trisomy 1q, 2, and 20 in a case of hepatoblastoma 2000 ·Cancer Genetics and Cytogenetics ·(unknown), Pulivarthi H. Rao, (unknown), William Middlesworth, Jay H. Lefkowitch, V.V.V.S. Murty	16
4	Cloning and Genomic Organization of Beclin 1, a Candidate Tumor Suppressor Gene on Chromosome 17q21 breakdown → 1999 ·Genomics ·Vincent M. Aita, Xiao Liang, V.V.V.S. Murty, David L. Pincus, Weiping Yu, Eftìhia Cayanis, (unknown), T. Conrad Gilliam, Beth Levine	646
5	Translocation (4;15)(p16;q24) 1999 ·Cancer Genetics and Cytogenetics ·Kyriakos P. Papadopoulos, V.V.V.S. Murty, Na Lin, Anne Y. Matsushima, (unknown), Pulivarthi H. Rao, Gwen Nichols	1
6	TERATOMA WITH MALIGNANT TRANSFORMATION: DIVERSE MALIGNANT HISTOLOGIES ARISING IN MEN WITH GERM CELL TUMORS 1998 ·The Journal of Urology ·Robert J. Motzer, Alison Amsterdam, Víctor G. Prieto, Joel Sheinfeld, V.V.V.S. Murty, Madhu Mazumdar, George J. Bosl, R. S. K. Chaganti, Victor E. Reuter	289
7	Nonsyntenic Amplification of MYC with CDK4 and MDM2 in a Malignant Mixed Tumor of Salivary Gland 1998 ·Cancer Genetics and Cytogenetics ·Pulivarthi H. Rao, V.V.V.S. Murty, D C Louie, R. S. K. Chaganti	28
8	Chromosomal amplification is associated with cisplatin resistance of human male germ cell tumors. 1998 ·PubMed ·(unknown), Jane Houldsworth, Nallasivam Palanisamy, V.V.V.S. Murty, Victor E. Reuter, Robert J. Motzer, George J. Bosl, R.S.K. Chaganti	75
9	Physical Mapping of a Commonly Deleted Region, the Site of a Candidate Tumor Suppressor Gene, at 12q22 in Human Male Germ Cell Tumors 1996 ·Genomics ·V.V.V.S. Murty, Beatrice Renault, Catherine T. Falk, George J. Bosl, (unknown), R.S.K. Chaganti	32
10	The gene for fibroblast activation protein α (FAP), a putative cell surface-bound serine protease expressed in cancer stroma and wound healing, maps to chromosome band 2q23 1995 ·Genomics ·S Mathew, Matthew J. Scanlan, B.K. Mohan Raj, V.V.V.S. Murty, Pilar Garin‐Chesa, Lloyd J. Old, Wolfgang J. Rettig, R. S. K. Chaganti	62
11	Homozygous Deletions and Loss of Expression of the CDKN2 gene occur frequently in head and neck squamous cell carcinoma cell lines but infrequently in primary tumors 1995 ·Genes Chromosomes and Cancer ·William M. Lydiatt, V.V.V.S. Murty, Bruce J. Davidson, Li Xu, Katerina Dyomina, Peter G. Sacks, Stimson P. Schantz, R.S.K. Chaganti	29
12	Genetic Alterations at 5p15: a Potential Marker for Progression of Precancerous Lesions of the Uterine Cervix 1995 ·JNCI Journal of the National Cancer Institute ·Arindam Mitra, V.V.V.S. Murty, Li Ren, R. S. K. Chaganti, (unknown), (unknown), Pushpa Sodhani, U K Luthra	53
13	ERBB2 (HER2/neu) oncogene is frequently amplified in squamous cell carcinoma of the uterine cervix. 1994 ·PubMed ·Arindam Mitra, V.V.V.S. Murty, (unknown), Pushpa Sodhani, R. S. K. Chaganti	102
14	Transforming Growth Factor Receptor Gene TGFBR2 Maps to Human Chromosome Band 3p22 1994 ·Genomics ·Susan Mathew, V.V.V.S. Murty, Sela Cheifetz, Diane George, Joan Massagué, RS Chaganti	40
15	Subregional mapping of 8 single copy loci to chromosome 6 by fluorescence in situ hybridization 1994 ·Cytogenetic and Genome Research ·Pulivarthi H. Rao, V.V.V.S. Murty, Gianluca Gaïdano, (unknown), Riccardo Dalla‐Favera, RS Chaganti	22
16	Subregional Localization of 20 Single-Copy Loci to Chromosome 6 by Fluorescence in Situ Hybridization 1993 ·Genomics ·Pulivarthi H. Rao, V.V.V.S. Murty, Gianluca Gaïdano, Robert Hauptschein, Riccardo Dalla-Favera, R. S. K. Chaganti	25
17	Detection of cell-cycle stage by fluorescence in situ hybridization: its application in human interphase cytogenetics 1992 ·Cytogenetic and Genome Research ·A.B. Mukherjee, V.V.V.S. Murty, R. S. K. Chaganti	21
18	Assignment of the human TYRP (brown) locus to chromosome region 9p23 by nonradioactive in situ hybridization 1992 ·Genomics ·V.V.V.S. Murty, Brigitte Bouchard, Susan Mathew, Vijayasaradhi Setaluri, Alan N. Houghton	34
19	Subregional mapping of 13 single-copy genes on the long arm of chromosome 12 by fluorescence in Situ hybridization 1992 ·Genomics ·Susan Mathew, V.V.V.S. Murty, Willi Hunziker, RS Chaganti	27
20	Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PML breakdown → 1991 ·Cell ·Akira Kakizuka, Wilson H. Miller, Kazuhiko Umesono, Raymond P. Warrell, SR Frankel, V.V.V.S. Murty, Ethan Dmitrovsky, Ronald M. Evans	1218

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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