J.M. Rary

2.2k total citations · 1 hit paper
25 papers, 2.0k citations indexed

About

J.M. Rary is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, J.M. Rary has authored 25 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 6 papers in Cancer Research. Recurrent topics in J.M. Rary's work include Genomic variations and chromosomal abnormalities (8 papers), DNA Repair Mechanisms (7 papers) and Carcinogens and Genotoxicity Assessment (6 papers). J.M. Rary is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), DNA Repair Mechanisms (7 papers) and Carcinogens and Genotoxicity Assessment (6 papers). J.M. Rary collaborates with scholars based in United States. J.M. Rary's co-authors include Samuel H. Boyer, S S Wachtel, W. Roy Breg, Digamber S. Borgaonkar, Kirby D. Smith, Louis M. Kunkel, O. J. Miller, Raymond R. Tice, Edward L. Schneider and M. A. Bender and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Annals of Neurology.

In The Last Decade

J.M. Rary

25 papers receiving 1.8k 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.

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

1977 1.3k citations Louis M. Kunkel, Kirby D. Smith et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J.M. Rary United States	14	1.1k	537	426	229	220	25	2.0k
Roberto Taramelli Italy	28	1.1k 1.0×	252 0.5×	337 0.8×	77 0.3×	270 1.2×	82	1.9k
F. Arwert Netherlands	25	1.5k 1.3×	519 1.0×	425 1.0×	163 0.7×	104 0.5×	47	2.2k
E.B. Robson United Kingdom	23	694 0.6×	499 0.9×	65 0.2×	140 0.6×	213 1.0×	60	1.9k
Genichi Watanabe Japan	26	1.9k 1.7×	423 0.8×	369 0.9×	66 0.3×	168 0.8×	58	3.0k
Nahid Hemati United States	13	2.5k 2.2×	505 0.9×	324 0.8×	70 0.3×	343 1.6×	16	3.7k
Giuseppe Raschellà Italy	29	1.8k 1.6×	238 0.4×	660 1.5×	76 0.3×	102 0.5×	68	2.7k
Sizhong Zhang China	23	887 0.8×	626 1.2×	288 0.7×	114 0.5×	216 1.0×	111	1.8k
Lee Carpenter United Kingdom	26	1.7k 1.5×	286 0.5×	153 0.4×	112 0.5×	494 2.2×	36	2.4k
François Gaudet United States	16	3.5k 3.1×	708 1.3×	468 1.1×	189 0.8×	212 1.0×	23	4.1k
Bradley A. Ozenberger United States	16	1.4k 1.3×	314 0.6×	407 1.0×	112 0.5×	223 1.0×	19	2.6k

Countries citing papers authored by J.M. Rary

Since Specialization

Citations

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

Fields of papers citing papers by J.M. Rary

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.M. Rary. 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 J.M. Rary. The network helps show where J.M. Rary may publish in the future.

Co-authorship network of co-authors of J.M. Rary

This figure shows the co-authorship network connecting the top 25 collaborators of J.M. Rary. A scholar is included among the top collaborators of J.M. Rary 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 J.M. Rary. J.M. Rary 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

Bender, M. A., et al.. (1985). G2 chromosomal radiosensitivity in ataxia telangiectasia lymphocytes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 152(1). 39–47. 30 indexed citations

Bender, M. A., et al.. (1985). G0 chromosomal radiosensitivity in ataxia telangiectasia lymphocytes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 150(1-2). 277–282. 51 indexed citations

Chaves‐Carballo, Enrique, et al.. (1985). Neurologic aspects of the 9p− syndrome. Pediatric Neurology. 1(1). 57–59. 3 indexed citations

Anderson, Randy L., et al.. (1983). Double balanced chromosomal translocation carrier (6;8), (13;14)—a case report. Journal of Heredity. 74(6). 450–452. 8 indexed citations

Anderson, Robert L., et al.. (1982). The prenatal diagnosis of the 48,xxyy syndrome. Prenatal Diagnosis. 2(2). 123–125. 4 indexed citations

Rary, J.M., et al.. (1979). Cell-cycle duration and sister-chromatid exchange frequency in cultured human lymphocytes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 63(2). 345–349. 60 indexed citations

Rary, J.M., et al.. (1979). G2 chromosomal radiosensitivity in Fanconi's anemia. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 63(1). 189–199. 65 indexed citations

Rary, J.M., et al.. (1978). The fallability of X-chromatin as a screening test for anomalies of the X chromosome.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 51(1). 107–8. 3 indexed citations

Tice, Raymond R., et al.. (1978). Effect of cocultivation on sister chromatid exchange frequencies in Bloom's syndrome and normal fibroblast cells. Nature. 273(5663). 538–540. 52 indexed citations

10.

Roos, Raymond P., C. James Kirkpatrick, Natan Gadoth, Wulfred Berman, & J.M. Rary. (1977). An immunological and cytogenetic investigation of tuberous sclerosis. Annals of Neurology. 1(2). 192–194. 5 indexed citations

11.

Howard‐Peebles, Patricia N., et al.. (1977). Translocation 9q/13q resulting in duplication (trisomy 9pter→9q22) and deficiency (monosomy 13pter→13q12). Clinical Genetics. 11(1). 46–52. 13 indexed citations

12.

Kunkel, Louis M., Kirby D. Smith, Samuel H. Boyer, et al.. (1977). Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.. Proceedings of the National Academy of Sciences. 74(3). 1245–1249. 1270 indexed citations breakdown →

13.

García, Jairo E., et al.. (1977). A 5/X chromosomal translocation in a patient with premature menopause. Journal of Heredity. 68(2). 75–80. 15 indexed citations

14.

Kelly, Thaddeus E., et al.. (1976). Incontinentia pigmenti: a chromosomal breakage syndrome. Journal of Heredity. 67(3). 171–172. 11 indexed citations

15.

Tice, Raymond R., Edward L. Schneider, & J.M. Rary. (1976). The utilization of bromodeoxyuridine incorporation into DNA for the analysis of cellular kinetics. Experimental Cell Research. 102(2). 232–236. 192 indexed citations

16.

Rary, J.M., M. A. Bender, & Thaddeus E. Kelly. (1975). A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasia. Journal of Heredity. 66(1). 33–35. 25 indexed citations

17.

Kelly, Thaddeus E. & J.M. Rary. (1974). Mosaic tetraploidy in a two‐year‐old female. Clinical Genetics. 6(3). 221–224. 25 indexed citations

18.

Rary, J.M., et al.. (1974). Prenatal Cytogenetic Analysis of Women With High Risk For Genetic Disorders. Journal of Heredity. 65(4). 209–212. 6 indexed citations

19.

Rary, J.M., et al.. (1968). The Cytogenetics of Swine in the Tellico Wildlife Management Area, Tennessee. Journal of Heredity. 59(3). 201–204. 15 indexed citations

20.

McFee, A.F., et al.. (1966). Variation in Chromosome Number Among European Wild Pigs. Cytogenetic and Genome Research. 5(1-2). 75–81. 54 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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