V. Ramesh Babu

782 total citations
22 papers, 632 citations indexed

About

V. Ramesh Babu is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, V. Ramesh Babu has authored 22 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in V. Ramesh Babu's work include Genomic variations and chromosomal abnormalities (8 papers), Bladder and Urothelial Cancer Treatments (4 papers) and Prenatal Screening and Diagnostics (4 papers). V. Ramesh Babu is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Bladder and Urothelial Cancer Treatments (4 papers) and Prenatal Screening and Diagnostics (4 papers). V. Ramesh Babu collaborates with scholars based in United States and Finland. V. Ramesh Babu's co-authors include Daniel L. Van Dyke, Lester Weiss, M J Worsham, Anne E. Wiktor, Brian J. Miles, Charles E. Jackson, Jacquelyn Roberson, Maria J. Worsham, Golder N. Wilson and Thomas E. Carey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Urology and International Journal of Cancer.

In The Last Decade

V. Ramesh Babu

22 papers receiving 612 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
V. Ramesh Babu	324	270	120	119	103	22	632
Susi Scappaticci	262 0.8×	374 1.4×	67 0.6×	153 1.3×	124 1.2×	47	784
M. Sagi	492 1.5×	314 1.2×	104 0.9×	48 0.4×	68 0.7×	22	756
Jonathan P. Park	267 0.8×	462 1.7×	83 0.7×	63 0.5×	177 1.7×	36	898
Anneke Y. van der Veen	304 0.9×	553 2.0×	189 1.6×	75 0.6×	215 2.1×	36	872
Cecilia Surace	201 0.6×	328 1.2×	128 1.1×	75 0.6×	68 0.7×	33	595
Anne Marie Ottesen	390 1.2×	371 1.4×	109 0.9×	70 0.6×	54 0.5×	15	733
Hanne Rose	480 1.5×	318 1.2×	161 1.3×	209 1.8×	98 1.0×	30	900
M. L. Kwee	320 1.0×	426 1.6×	72 0.6×	57 0.5×	59 0.6×	24	640
Sabrina Tosi	205 0.6×	550 2.0×	125 1.0×	91 0.8×	151 1.5×	52	1.1k
Georg Klaus Hinkel	528 1.6×	498 1.8×	46 0.4×	85 0.7×	51 0.5×	41	933

Countries citing papers authored by V. Ramesh Babu

Since Specialization

Citations

This map shows the geographic impact of V. Ramesh Babu'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. Ramesh Babu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Ramesh Babu more than expected).

Fields of papers citing papers by V. Ramesh Babu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. Ramesh Babu. 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. Ramesh Babu. The network helps show where V. Ramesh Babu may publish in the future.

Co-authorship network of co-authors of V. Ramesh Babu

This figure shows the co-authorship network connecting the top 25 collaborators of V. Ramesh Babu. A scholar is included among the top collaborators of V. Ramesh Babu 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. Ramesh Babu. V. Ramesh Babu 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

Finucane, Brenda, et al.. (1993). Mosaicism for deletion 17p11.2 in a boy with the Smith‐Magenis syndrome. American Journal of Medical Genetics. 45(4). 447–449. 20 indexed citations

Kim, Eun H., et al.. (1992). Trisomy 22 with congenital diaphragmatic hernia and absence of corpus callosum in a liveborn premature infant. American Journal of Medical Genetics. 44(4). 437–438. 21 indexed citations

Dyke, Daniel L. Van, Anne E. Wiktor, Dorothy A. Miller, et al.. (1992). Ullrich‐Turner syndrome with a small ring X chromosome and presence of mental retardation. American Journal of Medical Genetics. 43(6). 996–1005. 72 indexed citations

Roberson, Jacquelyn, et al.. (1991). Mother and son with deletion of 3p25‐pter. American Journal of Medical Genetics. 39(2). 130–132. 18 indexed citations

Babu, V. Ramesh & Anne E. Wiktor. (1991). A fluorescence in situ hybridization technique for retrospective cytogenetic analysis. Cytogenetic and Genome Research. 57(1). 16–17. 25 indexed citations

England, Barry G., et al.. (1991). Establishment and characterization of UM‐EC‐2, a tamoxifen‐sensitive, estrogen receptor‐negative human endometrial carcinoma cell line. International Journal of Gynecology & Obstetrics. 34(3). 293–293. 3 indexed citations

Grénman, Seija, Maria J. Worsham, Daniel L. Van Dyke, et al.. (1990). Establishment and characterization of UM-EC-2, a tamoxifen-sensitive, estrogen receptor-negative human endometrial carcinoma cell line. Gynecologic Oncology. 37(2). 188–199. 17 indexed citations

Grénman, Seija, Daniel L. Van Dyke, Maria J. Worsham, et al.. (1990). Phenotypic characterization, karyotype analysis and in vitro tamoxifen sensitivity of new ER‐negative vulvar carcinoma cell lines, UM‐SCV‐1A and UM‐SCV‐1B. International Journal of Cancer. 45(5). 920–927. 32 indexed citations

Babu, V. Ramesh, Brian J. Miles, Joseph C. Cerny, Lester Weiss, & Daniel L. Van Dyke. (1990). Cytogenetic study of four cancers of the prostate. Cancer Genetics and Cytogenetics. 48(1). 83–87. 36 indexed citations

10.

Janakiraman, Nalini, et al.. (1990). Osteomyelosclerosis with granulocytic sarcoma of chest wall. Morphological, ultrastructural, immunologic, and cytogenetic study.. PubMed. 114(4). 426–9. 2 indexed citations

11.

Dyke, Daniel L. Van, et al.. (1990). The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history.. PubMed. 46(6). 1101–11. 106 indexed citations

12.

Robinow, Meinhard, et al.. (1989). Secondary trisomy or mosaic “tetrasomy” 8p. American Journal of Medical Genetics. 32(3). 320–324. 20 indexed citations

13.

Worsham, M J, D.A. Miller, Jeffrey M. DeVries, et al.. (1989). A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres.. PubMed. 44(1). 115–23. 22 indexed citations

14.

Carey, Thomas E., Daniel L. Van Dyke, M J Worsham, et al.. (1989). Characterization of human laryngeal primary and metastatic squamous cell carcinoma cell lines UM-SCC-17A and UM-SCC-17B.. PubMed. 49(21). 6098–107. 57 indexed citations

15.

Crissman, John D., et al.. (1989). Advances in the diagnosis of urothelial neoplasia.. PubMed. 37(1). 19–23. 1 indexed citations

16.

Miles, Brian J., et al.. (1987). Cytogenetic Analysis of Transitional Cell Carcinoma of the Bladder. The Journal of Urology. 137(6). 1 indexed citations

17.

Dyke, Daniel L. Van, V. Ramesh Babu, & Lester Weiss. (1987). Parental age, and how extra isochromosomes (secondary trisomy) arise. Clinical Genetics. 32(1). 75–79. 35 indexed citations

18.

Babu, V. Ramesh, Daniel L. Van Dyke, Wendy L. Flejter, et al.. (1987). Chromosome 20 deletion in multiple endocrine neoplasia type 2: Expanded double‐blind studies. American Journal of Medical Genetics. 27(3). 739–748. 6 indexed citations

19.

Babu, V. Ramesh, et al.. (1987). Tumor behavior in transitional cell carcinoma of the bladder in relation to chromosomal markers and histopathology.. PubMed. 47(24 Pt 1). 6800–5. 65 indexed citations

20.

Dyke, Daniel L. Van, Wendy L. Flejter, M J Worsham, et al.. (1986). A practical metaphase marker of the inactive X chromosome.. PubMed. 39(1). 88–95. 20 indexed citations

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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