V.G. Dev

2.7k total citations
55 papers, 2.3k citations indexed

About

V.G. Dev is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, V.G. Dev has authored 55 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 27 papers in Genetics and 22 papers in Plant Science. Recurrent topics in V.G. Dev's work include Chromosomal and Genetic Variations (22 papers), Genomics and Chromatin Dynamics (15 papers) and Genomic variations and chromosomal abnormalities (11 papers). V.G. Dev is often cited by papers focused on Chromosomal and Genetic Variations (22 papers), Genomics and Chromatin Dynamics (15 papers) and Genomic variations and chromosomal abnormalities (11 papers). V.G. Dev collaborates with scholars based in United States, Switzerland and Canada. V.G. Dev's co-authors include D.A. Miller, O. J. Miller, Ramana Tantravahi, C M Croce, P. W. Allderdice, O.J. Miller, Bernard F. Erlanger, Richard E. Kouri, John J. Hutton and Majambu Mbikay and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

V.G. Dev

53 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
V.G. Dev United States	23	1.5k	1.0k	1.0k	116	90	55	2.3k
R.A. Buckland United Kingdom	19	1.5k 1.0×	1.3k 1.2×	1.2k 1.1×	116 1.0×	104 1.2×	27	2.6k
Orlando J. Miller United States	27	1.8k 1.2×	1.2k 1.2×	682 0.7×	136 1.2×	106 1.2×	69	2.5k
J. Meyne United States	18	2.5k 1.7×	778 0.8×	1.3k 1.3×	115 1.0×	140 1.6×	28	3.9k
L. Tiepolo Italy	24	1.6k 1.1×	1.8k 1.8×	677 0.7×	277 2.4×	41 0.5×	73	2.6k
Sajiro Makino Japan	22	588 0.4×	868 0.9×	524 0.5×	132 1.1×	122 1.4×	143	1.8k
Tom Holm United States	5	964 0.7×	863 0.9×	316 0.3×	57 0.5×	128 1.4×	6	1.7k
Peter E. Warburton United States	27	2.1k 1.4×	1.1k 1.1×	1.7k 1.7×	129 1.1×	49 0.5×	51	2.7k
Rhea U. Vallente United States	11	1.4k 1.0×	1.5k 1.5×	1.1k 1.1×	203 1.8×	39 0.4×	23	2.2k
S S Wachtel United States	17	1.0k 0.7×	832 0.8×	258 0.3×	186 1.6×	107 1.2×	37	2.1k
Carol M. Rubin United States	13	2.0k 1.4×	557 0.6×	600 0.6×	52 0.4×	199 2.2×	16	2.4k

Countries citing papers authored by V.G. Dev

Since Specialization

Citations

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

Fields of papers citing papers by V.G. Dev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V.G. Dev

This figure shows the co-authorship network connecting the top 25 collaborators of V.G. Dev. A scholar is included among the top collaborators of V.G. Dev 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.G. Dev. V.G. Dev is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Kuchtey, John, et al.. (2010). Primary Congenital Glaucoma Associated With Patau Syndrome With Long Survival. Journal of Pediatric Ophthalmology & Strabismus. 47(1). 1–4. 4 indexed citations

Tsuchiya, Karen D., Mary G. Schueler, & V.G. Dev. (2001). Familial X centromere variant resulting in false‐positive prenatal diagnosis of monosomy X by interphase FISH. Prenatal Diagnosis. 21(10). 852–855. 5 indexed citations

Barakat, Amin J., et al.. (1991). An infant with deletion of the distal long arm of chromosome 15 (q26.1→qter) and loss of insulin‐like growth factor 1 receptor gene. American Journal of Medical Genetics. 38(1). 74–79. 140 indexed citations

Shah, Dinesh, et al.. (1989). Diagnosis of trisomy 18 in monozygotic twins by cordocentesis. American Journal of Obstetrics and Gynecology. 160(1). 214–215. 10 indexed citations

Giannone, Leonard, James A. Whitlock, Marsha C. Kinney, S N Wolff, & V.G. Dev. (1988). Use of the BCR probe to demonstrate extramedullary recurrence of CGL with a T cell lymphoid phenotype following bone marrow transplantation.. PubMed. 3(6). 631–5. 9 indexed citations

Dev, V.G., et al.. (1984). 5‐azacytidine decreases the frequency of fragile X expression in peripheral lymphocyte culture. American Journal of Medical Genetics. 17(1). 253–254. 6 indexed citations

Gal, David, J. Peter Forney, V.G. Dev, & John C. Porter. (1982). A new human cell line derived from a poorly differentiated endometrial adenocarcinoma. Gynecologic Oncology. 13(1). 50–57. 9 indexed citations

Smith, R. Guy, V.G. Dev, & W. Allen Shannon. (1981). Characterization of a novel human pre-B leukemia cell line.. The Journal of Immunology. 126(2). 596–602. 37 indexed citations

Dev, V.G., et al.. (1979). Activity of both mouse and Chinese hamster ribosomal RNA genes in somatic cell hybrids. Experimental Cell Research. 123(2). 424–429. 12 indexed citations

10.

Soprano, Kenneth J., V.G. Dev, Carlo M. Croce, & Renato Baserga. (1979). Reactivation of silent rRNA genes by simian virus 40 in human-mouse hybrid cells.. Proceedings of the National Academy of Sciences. 76(8). 3885–3889. 78 indexed citations

11.

Miller, O. J., D.A. Miller, Ramana Tantravahi, & V.G. Dev. (1978). Nucleolus organizer activity and the origin of Robertsonian translocations. Cytogenetic and Genome Research. 20(1-6). 40–50. 28 indexed citations

12.

Tantravahi, Ramana, D.A. Miller, V.G. Dev, & O. J. Miller. (1976). Detection of nucleolus organizer regions in chromosomes of human, chimpanzee, gorilla, orangutan and gibbon. Chromosoma. 56(1). 15–27. 100 indexed citations

13.

Schnedl, W., V.G. Dev, Ramana Tantravahi, et al.. (1975). 5-Methylcytosine in heterochromatic regions of chromosomes: chimpanzee and gorilla compared to the human. Chromosoma. 52(1). 59–66. 53 indexed citations

14.

Dev, V.G., et al.. (1974). Translocation of centromeric heterochromatin in the T(10;13) 199H stock of Mus musculus and localization of chromosome break points. Cytogenetic and Genome Research. 13(3). 256–267. 14 indexed citations

15.

Miller, D.A., I. Lester Firschein, V.G. Dev, Ramana Tantravahi, & O.J. Miller. (1974). The gorilla karyotype: chromosome lengths and polymorphisms. Cytogenetic and Genome Research. 13(6). 536–550. 42 indexed citations

16.

Dev, V.G., D.A. Miller, & O. J. Miller. (1973). CHROMOSOME MARKERS IN MUS MUSCULUS: STRAIN DIFFERENCES IN C-BANDING. Genetics. 75(4). 663–670. 38 indexed citations

17.

Dev, V.G., et al.. (1972). THE BIARMED MUS POSCHIAVINUS CHROMOSOME CARRYING THE H-2 LOCUS, T1posKlj, IS T7Bnr. Genetics. 72(3). 541–543. 4 indexed citations

18.

Dev, V.G., et al.. (1971). The quinacrine fluorescence karyotype of Mus musculus and demonstration of strain differences in secondary constrictions. Cytogenetic and Genome Research. 10(6). 436–451. 44 indexed citations

19.

Kouri, Richard E., et al.. (1971). IDENTIFICATION BY QUINACRINE FLUORESCENCE OF THE CHROMOSOME CARRYING MOUSE LINKAGE GROUP I IN THE CATTANACH TRANSLOCATION. Genetics. 69(1). 129–132. 16 indexed citations

20.

Miller, D.A., et al.. (1971). Assignment of Four Linkage Groups to Chromosomes in Mus musculus and a Cytogenetic Method for Locating Their Centromeric Ends. Proceedings of the National Academy of Sciences. 68(11). 2699–2702. 14 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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